Email updates

Keep up to date with the latest news and content from Orphanet Journal of Rare Diseases and BioMed Central.

Open Access Review

Central core disease

Heinz Jungbluth

Author Affiliations

Evelina Children's Hospital, Department of Paediatric Neurology, St. Thomas' Hospital, London, UK

Orphanet Journal of Rare Diseases 2007, 2:25  doi:10.1186/1750-1172-2-25

The electronic version of this article is the complete one and can be found online at: http://www.OJRD.com/content/2/1/25


Received:5 March 2007
Accepted:15 May 2007
Published:15 May 2007

© 2007 Jungbluth; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy. Prevalence is unknown but the condition is probably more common than other congenital myopathies. CCD typically presents in infancy with hypotonia and motor developmental delay and is characterized by predominantly proximal weakness pronounced in the hip girdle; orthopaedic complications are common and malignant hyperthermia susceptibility (MHS) is a frequent complication. CCD and MHS are allelic conditions both due to (predominantly dominant) mutations in the skeletal muscle ryanodine receptor (RYR1) gene, encoding the principal skeletal muscle sarcoplasmic reticulum calcium release channel (RyR1). Altered excitability and/or changes in calcium homeostasis within muscle cells due to mutation-induced conformational changes of the RyR protein are considered the main pathogenetic mechanism(s). The diagnosis of CCD is based on the presence of suggestive clinical features and central cores on muscle biopsy; muscle MRI may show a characteristic pattern of selective muscle involvement and aid the diagnosis in cases with equivocal histopathological findings. Mutational analysis of the RYR1 gene may provide genetic confirmation of the diagnosis. Management is mainly supportive and has to anticipate susceptibility to potentially life-threatening reactions to general anaesthesia. Further evaluation of the underlying molecular mechanisms may provide the basis for future rational pharmacological treatment. In the majority of patients, weakness is static or only slowly progressive, with a favourable long-term outcome.

Disease name

Central core disease

Definition

Central core disease (CCD) (MIM * 117000) [1] is an inherited neuromuscular disorder defined by a) areas with reduced oxidative activity running along the longitudinal axis of the muscle fibre ("central cores") and b) clinical features of a congenital myopathy.

CCD was originally reported in a family with congenital hypotonia, non-progressive weakness and central areas of amorphous appearance within muscle fibres stained with the modified Gomori trichrome technique [2]. The term CCD was introduced later [3] and reflects the characteristic absence of oxidative enzyme activity in the core area due to mitochondrial depletion [4].

Epidemiology

Epidemiological data are only available for the congenital myopathies as a group but not for specific conditions. The incidence of all congenital myopathies is estimated at around 6.0/100,000 live births, or onetenth of all cases of neuromuscular disorders [5]. Regional studies in Northern Ireland [6] and Western Sweden [7] suggest a prevalence between 3.5 – 5.0/100,000 in a paediatric population.

CCD is probably the most common congenital myopathy; the condition is likely to be under recognised considering that some individuals with suggestive clinical features and an identical genetic background do not necessarily exhibit the characteristic histopathological features, particularly when biopsied at an early age.

Clinical description

Presentation of dominantly inherited CCD is typically in infancy with hypotonia or in early childhood with motor developmental delay [8]; however, marked clinical variability, often within the same family, has been recognised [9-12]. Muscle stiffness and weakness on exertion are recognised presenting features [13,14]. More severe presentations within the range of the foetal akinesia sequence [15] have been reported associated with recessive inheritance. There is no association between the number of cores on muscle biopsy and the degree of muscle weakness [16].

Distribution of weakness is typically proximal with prominent involvement of the hip girdle and also axial muscles [8]; rare patients may show focal wasting [17]. Inability to bury eyelashes completely may be the only manifestation of typically mild facial involvement. Bulbar involvement is untypical in the dominant form and extra-ocular muscle involvement has been considered a clinical exclusion criterion by some authors [18]; however, both features may be observed in the most severely affected neonates due to recessive inheritance [15].

Orthopaedic complications are common in CCD [19] and comprise congenital dislocation of the hips [20], scoliosis which may be present from birth [12] and foot deformities including talipes equinovarus and pes planus [19]. Many affected individuals have marked ligamentous laxity, occasionally associated with patellar instability [19], whereas contractures other than tendon Achilles tightness are rare.

Structural cardiac abnormalities other than mitral valve prolapse have rarely been reported [13], but cardiomyopathies are not a feature of CCD associated with RYR1 mutations. Central cores on muscle biopsy have been observed in a group of patients with hypertrophic cardiomyopathy secondary to mutations in the beta-myosin heavy chain (MYH7) gene, however, these patients typically do not have associated muscle weakness or any other features of typical CCD [21]. Central and minicores in association with a dilated cardiomyopathy may also rarely been observed in patients with mutations in the skeletal muscle α-actin (ACTA1) gene [22], more frequently associated with nemaline myopathy.

Respiratory involvement in dominant CCD is exceptional but may be severe in neonatal cases due to recessive RYR1 mutations [15].

Malignant hyperthermia, a pharmacogenetic disorder of skeletal muscle characterised by an abnormal response to muscle relaxants such as succinylcholine and volatile anaesthetics, is a frequent complication [23-25]. Malignant hyperthermia is a severe and occasionally fatal reaction characterised by muscular rigidity, rhabdomyolysis, rapid increase in body temperature and signs of generalised metabolic decompensation; survivors may suffer severe renal and neurologic damage. Many patients with CCD test positive for the malignant hyperthermia susceptibility (MHS) trait on in vitro contracture test (IVCT) [13,26] and should therefore be considered at risk for malignant hyperthermia during general anaesthesia.

Almost all patients with CCD achieve the ability to walk independently, except the most severe neonatal cases and some of those with congenital dislocation of the hips [27,28]. CCD typically follows a static or only slowly progressive course, even over prolonged periods of follow-up [29]. Intermittent deterioration of symptoms has been reported during or after pregnancy [30].

Serum creatine kinase (CK) activity is usually normal, but may be elevated up to 6 to 14 times normal in rare cases [11,31,32]. Muscle ultrasound often shows a striking increase in echogenicity even in paucisymptomatic individuals [33]. A characteristic pattern of selective involvement on muscle magnetic resonance imaging (MRI) has been reported in patients with typical CCD [34] and is distinct from that observed in other congenital myopathies such as nemaline myopathy [35]; muscle MRI may therefore be particularly useful for aiding genetic diagnosis in cases with mixed pathologies featuring both cores and rods [36,37].

Aetiology

CCD is due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene at chromosome 19q13.1, also implicated in the malignant hyperthermia susceptibility (MHS) trait, initially recognised as a familial autosomal dominant trait by Denborough and Lovell [23] in Australia.

An association between CCD and MHS had been suspected early, as individuals with MHS may have central cores on muscle biopsy [38], and patients with CCD may be prone to malignant hyperthermia episodes [13,39,40]. The RYR1 gene had been considered as a candidate for malignant hyperthermia based on the finding of a founder mutation in the porcine isoform resulting in the porcine stress syndrome (PSS), a naturally occurring animal model with almost identical clinical features [41]. Following demonstration of linkage to the human RYR1 locus in some families with MHS [42-45] and CCD [46-48], subsequent identification of mutations in the RYR1 gene suggested that the two conditions are allelic disorders [49-51].

RYR1 is organized in 106 exons [52] and encodes the skeletal muscle ryanodine receptor (RyR1), a large protein of 5037 amino acids visible on electron microscopy. RyR1 is a ligand-gated release channel for Ca++ stored in the terminal cisterna with a crucial role in excitation-contraction (E-C) coupling by regulating cytosolic calcium levels. RyR1 calcium release is primarily triggered by voltage-induced conformational changes of the abutting dihydropyridine receptor (DHPR), and secondarily by a number of exogeneous and endogeneous effector molecules (for review, [53]). RyR1 N-terminal portions are myoplasmic and constitute the visible foot structure that interacts with the DHPR, whereas the actual calcium release channel is located in the C-terminal part of the protein [54,55].

More than 80 mutations have been identified in the RYR1 gene to date [56-63], most of them missense mutations. A few small deletions [59,60,64] and cryptic splicing site mutations [63,65] have been documented. The majority of RYR1 mutations associated with MHS or CCD described to date were dominant mutations; homozygosity or heterozygosity for RYR1 mutations has been previously documented in association with MHS [66,67] and have been recently reported in a severe form of CCD presenting with a foetal akinesia syndrome [15] and few mild cases [16].

Genotype-phenotype correlations associated with mutations in the RYR1 gene are complex and may be partly explained by the degree of functional differentiation within this large protein. Dominant RYR1 mutations affecting the cytoplasmic N-terminal (MHS/CCD region 1, amino acids 35 – 614) and central (MHS/CCD region 2, amino acids 2163 – 2458) domains of the protein give predominantly rise to the MHS phenotype [68], whereas the CCD phenotype is closely associated with dominant RYR1 C-terminal (MHS/CCD region 3, amino acids 4550 – 4940) mutations [16,58-61]. CCD-related dominant RYR1 mutations affecting the N-terminal and central portions of the protein and RYR1 C-terminal mutations giving rise to MHS represent exceptions to this rule but have only been reported in a few families [50,51,69-71]. Recessively inherited mutations are more widespread throughout the RYR1 gene and appear to be more frequently associated with the histopathological appearance of Multi-minicore Disease (MmD) [27,63-65,72] rather than CCD [16]. Data regarding the frequency of CCD-related RYR1 mutations are currently emerging.

Although many mutations are private, the Arg4861Cys substitution has been identified in three unrelated CCD families and mutations affecting RYR1 exons 100 – 101 appear to be particularly common [16,61,62]. Since most previous genetic studies in MHS and CCD were limited to a partial screening strategy due to the large size of the RYR1 gene, future studies involving the entire RYR1 coding sequence are likely to identify new mutational hotspots.

Mutation-induced conformational changes of the RyR1 protein are thought to alter excitability and/or calcium homeostasis within muscle cells, but the precise molecular mechanisms underlying genotype-phenotype correlations associated with specific RYR1 mutations are currently still emerging. Two models for receptor malfunction have been proposed, depletion of sarcoplasmic reticulum calcium stores with resulting increase in cytosolic calcium levels ("leaky channel" hypothesis) [73], and disturbance of excitation-contraction coupling (E-C uncoupling hypothesis) [74]; these models are not mutually exclusive and may be equally valid depending on the specific effect of individual mutations on the structurally complex RyR1 protein.

The functional effects of specific RYR1 mutations have been studied in response to IVCT, in cultured myotubes from patients and in various homologous and heterologous expression systems. Early studies already suggested an association between specific RYR1 mutations and IVCT response [75], and indicated a correlation between the particular RYR1 gene mutation in a family and the severity of MH or liability to CCD [26,76]. In vitro studies on human myotubes demonstrated both increased [77,78] and reduced [79,80] agonist sensitivity depending on the precise location of the RYR1 mutation investigated. Studies on a RYR1 C-terminus mutation (I4898T) associated with a severe CCD phenotype demonstrated reduced intracellular calcium release without increasing the sensitivity to caffeine or halothane [36] and a marked disturbance of excitation-contraction coupling [81]; the latter may also apply for other C-terminal mutations [82]. Studies of RYR1 mutants expressed in myotubes of RYR1 knockout ("dyspedic") mice [83,84] indicate that mixed MHS/CCD mutations are associated with increased channel activity sufficient to deplete sarcoplasmic reticulum calcium stores, elevated intracellular calcium levels and reduced maximum voltage gated calcium release [79], whereas MH-only mutations appear to increase basal release channel activity insufficiently to alter net sarcoplasmic reticulum calcium content ("compensated leak"). Expression of a functional RyR1 protein in B-lymphocytes has been recently described and offers a novel approach to study the pathogenesis of RYR1 mutations in vitro. B-lymphocytes harbouring CCD-related RYR1 mutations show depletion of sarcoplasmic reticulum stores secondary to unprompted calcium release [59,85]; increased release of inflammatory cytokines in the same study population [86] may also point at a role of RYR1 in immunomodulation.

Although most studies have confirmed the association between CCD and mutations in the RYR1 gene, possible genetic heterogeneity is indicated by recombination events between CCD and RYR1 in one family [87], and failure to identify a mutation despite screening of the entire RYR1 coding sequence in a severely affected neonate with histopathologic and clinical features of CCD [15].

Diagnostic methods

The diagnosis of CCD depends on the presence of typical histopathological findings on muscle biopsy in combination with suggestive clinical features; muscle MR imaging may complement clinical assessment.

Histochemical staining of muscle biopsy samples shows the absence of oxidative and glycolytic enzymatic activity from central core regions [4] (Figure 1). Central cores may be single or multiple, central or eccentric [88,89], but commonly run along a significant extent of the longitudinal muscle fiber axis [90,91]; the latter feature distinguishes central cores most clearly from multi- or minicores which share focal reduction of oxidative activity as a common histopathological feature. Central cores are typically found in type 1 fibres; marked type 1 predominance or uniformity and hypotrophy are typical and may be the only abnormal features at presentation [89,92]. An increase in internal nucleation is often associated and substantial increases in fat and connective tissue have been described in some patients [89], corresponding to a marked degree of increased signal intensity on muscle MRI [35]. The degree of histopathologic changes may be variable depending on sampling site and the age of the patient.

thumbnailFigure 1. Histopathologic appearance of typical central core disease: NADH-TR, transverse section from the rectus femoris. Marked predominance of dark staining, high oxidative type 1 fibres with cores affecting the majority of fibres. Cores are typically well demarcated and centrally located (→), but may occasionally be multiple and of eccentric location.

Typical findings on electron microscopy include reduction or absence of mitochondria, variable degrees of myofibrillar disorganisation and accumulation of abnormal Z band material within the usually sharply demarcated core area [9]. Some ("structured") cores preserve a degree of myofibrillar organisation and therefore retain some ATPase activity; other ("unstructured") cores do not and can be found in the same muscle biopsy [32,90]. The sarcoplasmic reticulum and Ttubule structures may be increased within the core area [93].

Abnormal expression of various sarcomeric and intermediate filament proteins, particularly desmin, has been demonstrated within or around the core-area in a number of immunohistochemical studies; corresponding to type 1 predominance on histochemical stains, slow myosin isoforms may be upregulated [89,94-96]. An antibody to the actin cross-linking protein filamin C has been recently identified as a strong but non-specific marker of central cores [97].

In cases with equivocal histopathological features, muscle MR imaging may complement clinical assessment and indicate involvement of the RYR1 gene, as RYR1 C-terminal mutations may be associated with a consistent pattern of selective muscle involvement [35] (Figure 2) distinct from that observed in other congenital myopathies such as nemaline myopathy [34].

thumbnailFigure 2. * Muscle involvement in the lower limbs in CCD secondary to dominant RYR1 mutations: T1-weighted MR imaging, transverse sections of the proximal thigh (A-C) and the proximal lower leg (D-F) in an eleven (A) and a thirteen year old boy (B,E), and a twelve (C,F) and seventeen year old girl (D). In the thigh (A-C), there is marked increase in abnormal signal within vasti, sartorius and adductor magnus with relative sparing of rectus femoris, adductor longus, gracilis and semitendinosus. In the lower leg, there is increase in abnormal signal in soleus (D-F), and – in more severe cases (E-F) – peroneal group and gastrocnemius medialis. Tibialis anterior and gastrocnemius lateralis are relatively spared. (VL = vastus lateralis, VI = vastus intermedius, VM = vastus medialis, RF = rectus femoris, AL = adductor longus, AM = adductor magnus, S = sartorius, G = gracilis, St = semitendinosus). * Reprinted from Neuromuscul Disord 2004, 14: Jungbluth H, Davis MR, Muller C, Counsell S, Allsop J, Chattopadhyay A, Messina S, Mercuri E, Laing NG, Sewry CA, Bydder G, Muntoni F. Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Pages: 785–790. Copyright Owner Elsevier, Copyright (2004), with permission from Elsevier".

Differential diagnosis

The diagnosis of CCD is usually straightforward in cases where clinical features are suggestive and typical central cores are present on muscle biopsy; however, the typical histopathological picture may only evolve over time and may not always be present when muscle biopsy has been performed at an early age. Also, core-formation is a non-specific finding which may be observed in other clinical contexts such as tenotomy, denervation ("target-fibers") [98] or malignant hyperthermia susceptible individuals without other features of a congenital myopathy [99]; it has to be emphasised that the presence of central cores on muscle biopsy without associated weakness is not sufficient to constitute a diagnosis of CCD.

The distinction from Multi-minicore Disease (MmD) may be particularly difficult, as recent studies suggest a histopathological continuum between the two conditions in a subset of patients rather than distinct entities. Although the great majority of MmD is caused by recessive mutations in the selenoprotein N (SEPN1) gene [100], recessive RYR1 mutations have been recently identified in distinct subgroups of MmD [27,63,65,72]. However, MmD-associated mutations give rise to clinical features such as external ophthalmoplegia, bulbar involvement and a moderate degree of respiratory impairment which are not commonly observed in typical CCD.

Other conditions which may feature central cores on muscle biopsy include hypertrophic cardiomyopathy (HCM) associated with missense mutations in the β-myosin heavychain gene, MYH7 [21]; in contrast to CCD, muscle weakness is, however, exceptional and there are no associated musculoskeletal deformities. Mutations in the ACTA1 gene, more commonly associated with nemaline myopathy, have been recently implicated in an autosomal dominant myopathy with both central and minicores [22]; however, some patients in this pedigree had an associated cardiomyopathy, which is not a feature in RYR1-related CCD.

The common occurrence of central cores and features of other congenital myopathies such as nemaline rods or minicores has been recognised for a long time, poses a diagnostic challenge [37,101-103] and emphasises that histopathological interpretation has to take into account the clinical context.

Genetic counselling

Genetic counselling should be offered to all families and individuals in whom a diagnosis of CCD has been made. Although the majority of cases appear to be associated with dominant inheritance, care should be taken in interpreting the mode of inheritance in isolated cases, as both sporadic occurrence and, more recently, recessive inheritance [16,27,72] have been documented; an unusually severe presentation with antenatal onset in particular should raise the possibility of a recessively inherited form of CCD.

Molecular genetic confirmation of the diagnosis is possible by mutational analysis of the RYR1 gene; diagnostic RYR1 screening has been established for malignant hyperthermia patients by a number of laboratories associated with the European Malignant Hyperthermia Group (EMHG) [104] but does require a modified approach for patients with central core disease as many CCD-related RYR1 mutations do not localise to known MH hotspots. Technical difficulties associated with the large size of this gene may be partly alleviated by focusing on the C-terminal mutational hotspot [16,61,62], particularly exons 100 and 101, closely associated with the typical dominant form of CCD; however, recessive inheritance due to compound heterozygosity for two different RYR1 mutations can not be excluded if only a partial screening strategy is applied and sequencing of the entire RYR1 coding sequence may be required in patients without confirmed hotspot mutation.

Management

No curative treatment is currently available for CCD and management is essentially supportive based on a multidisciplinary approach.

Regular physiotherapy is aimed at the preservation of muscle power and function and the prevention of contractures, particularly those of the tendon Achilles which are commonly observed in CCD. Considering often prominent axial involvement, exercises promoting endurance and truncal stability such as swimming and riding [105] may be particularly useful. Considering a tendency to exercise-induced myalgia in CCD, exercises involving a high-resistance load have to be approached with caution and are probably not recommendable. If complications such as congenital dislocation of the hips (CDH), talipes equinovarus or scoliosis are present at birth or evolve in the course of the disease, those may be managed surgically at a centre with experience in the management of neuromuscular disorders once conservative approaches have failed. As in other neuromuscular conditions, post-operative mobilization ought to be rapid in order to avoid adverse effects of prolonged immobilization such as muscle atrophy. In the most severe cases where walking can not be achieved without additional support, independent ambulation may be promoted by appropriate rehabilitative measures such as provision of weight bearing calipers.

Clinically significant respiratory involvement is exceptional in typical cases of dominant CCD; however, considering the small risk of respiratory impairment, we would advocate regular monitoring of respiratory capacity and annual overnight oxygen saturation studies if forced vital capacity (FVC) is less than 60% of the expected value, and more frequently if FVC is less than 40% [106]. Respiratory infections should be treated actively. In the most severely affected, often recessive CCD cases with antenatal onset, respiratory involvement may be severe enough to require invasive ventilation [15,65]. Although in some of these infants respiratory impairment may be life-limiting, others appear to stabilise or even improve after a period of ventilation; active treatment decision therefore ought to be made on an individual basis applying the same criteria as for other children with neonatally severe conditions.

An associated cardiomyopathy has not been reported in typical CCD due to mutations in the RYR1 gene; however, cardiomyopathies associated with mutations in the MYH7 [21] and the ACTA1 [22] genes may feature central cores on muscle biopsy but do not share the typical clinical features of CCD. Cardiac ultrasound studies therefore ought to be considered in cases where clinical presentation is unusual.

Patients with CCD are at risk of malignant hyperthermia, an abnormal response to muscle relaxants such as succinylcholine and volatile anaesthetics [24,25]. The anaesthetist ought to be aware of the diagnosis of CCD and plan the anaesthesia accordingly, avoiding potentially MH-triggering agents. Clinically manifest MH reactions may be aborted by the RyR1 agonist Dantrolene if administered early in the course of a reaction. Not all patients with CCD will be at risk of MH [36,72] and ideally the MHS status ought to be determined by IVCT testing in individual cases; however, this may not always be practical as the IVCT is not offered for young children and involves an open muscle biopsy under general anaesthesia. It may be more appropriate to assume MH susceptibility in CCD patients in the absence of firm evidence to the contrary and discuss the issue with affected individuals and their families accordingly.

In affected females, the potential for intermittent deterioration of symptoms during or after pregnancy [30] ought to be anticipated and discussed with the patient.

In addition to supportive management and prevention of malignant hyperthermia reactions during general anaesthesia, the β-agonist salbutamol has been recently investigated as a pharmacological agent in the treatment of CCD with encouraging results [107]. However, results of this pilot study will have to be validated in a larger randomized controlled trial as a basis for future recommendation.

Prognosis

The typical form of dominantly inherited CCD is usually associated with a mild to moderate degree of disability and carries an overall favourable prognosis, although the degree of severity may be variable, occasionally within the same family. Apart from the most severe cases and some of those with congenital orthopaedic complications [27,28] almost all patients achieve the ability to walk independently. The course of CCD is static or only slowly progressive, even over prolonged periods of follow-up [29].

In the most severely affected, often recessive CCD cases with antenatal onset, respiratory impairment may be life-limiting despite active management, although others appear to stabilise or even improve after a period of ventilation [65].

Unresolved questions

CCD and the MHS trait are closely associated with mutations in the RYR1 gene, but clear genotype-phenotype correlations are still emerging. Screening of the entire RYR1 coding sequence in an increasing number of patients may identify new mutational hotspots in future, and alleviate the difficulties associated with the large size of this gene by a more rationalised screening strategy.

Although the pathogenetic basis of CCD and the malignant hyperthermia susceptibility trait is currently only partially understood, available experimental evidence suggests a mutation-specific disruption of excitation-contraction-coupling and/or disturbance of intracellular calcium homeostasis. Future work is likely to advance our understanding of these key processes in contractile cells, and to elucidate mutation-specific effects resulting in congenital myopathy phenotypes and/or malignant hyperthermia. Further understanding of the molecular basis of CCD and MHS may also provide the basis for rational pharmacological treatments. Unresolved questions concern the pathogenesis of central cores, the impact of specific mutations on RyR1 assembly, the precise role of RyR1 in non-muscle cells such as B-lymphocytes and the effect of mutations on those tissues, and other calcium dependent signalling pathways other than E-C coupling.

References

  1. McKusick VA: Mendelian Inheritance in Man. 12th edition edition. Edited by Press TJHU. Baltimore , Johns Hopkins University Press; 1998.

  2. Magee KR, Shy GM: A new congenital non-progressive myopathy.

    Brain 1956, 79(4):610-621. PubMed Abstract | Publisher Full Text OpenURL

  3. Greenfield JG, Cornman T, Shy GM: The prognostic value of the muscle biopsy in the floppy infant.

    Brain 1958, 81(4):461-484. PubMed Abstract | Publisher Full Text OpenURL

  4. Dubowitz V, Pearse AG: Oxidative enzymes and phosphorylase in central-core disease of muscle.

    Lancet 1960, 2:23-24. PubMed Abstract | Publisher Full Text OpenURL

  5. Wallgren-Pettersson C: Congenital nemaline myopathy: a longitudinal study. In Commentationes Physico Mathematicae. University of Helsinki; 1990. OpenURL

  6. Hughes MI, Hicks EM, Nevin NC, Patterson VH: The prevalence of inherited neuromuscular disease in Northern Ireland.

    Neuromuscul Disord 1996, 6(1):69-73. PubMed Abstract | Publisher Full Text OpenURL

  7. Darin N, Tulinius M: Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden.

    Neuromuscul Disord 2000, 10(1):1-9. PubMed Abstract | Publisher Full Text OpenURL

  8. Dubowitz V: Muscle disorders in childhood. Volume 2nd. London , WB Saunders; 1995.

  9. Dubo witz V, Roy S: Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child.

    Brain 1970, 93(1):133-146. PubMed Abstract | Publisher Full Text OpenURL

  10. Bethlem J, van Wijngaarden GK, Meijer AE, Fleury P: Observations on central core disease.

    J Neurol Sci 1971, 14(3):293-299. PubMed Abstract | Publisher Full Text OpenURL

  11. Patterson VH, Hill TR, Fletcher PJ, Heron JR: Central core disease: clinical and pathological evidence of progression within a family.

    Brain 1979, 102(3):581-594. PubMed Abstract | Publisher Full Text OpenURL

  12. Merlini L, Mattutini P, Bonfiglioli S, Granata C: Non-progressive central core disease with severe congenital scoliosis: a case report.

    Dev Med Child Neurol 1987, 29(1):106-109. PubMed Abstract OpenURL

  13. Shuaib A, Paasuke RT, Brownell KW: Central core disease. Clinical features in 13 patients.

    Medicine (Baltimore) 1987, 66(5):389-396. PubMed Abstract OpenURL

  14. Bethlem J, van Gool J, Hulsmann WC, Meijer AE: Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres.

    Brain 1966, 89(3):569-588. PubMed Abstract | Publisher Full Text OpenURL

  15. Romero NB, Monnier N, Viollet L, Cortey A, Chevallay M, Leroy JP, Lunardi J, Fardeau M: Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.

    Brain 2003, 126(Pt 11):2341-2349. PubMed Abstract | Publisher Full Text OpenURL

  16. Wu S, Ibarra MC, Malicdan MC, Murayama K, Ichihara Y, Kikuchi H, Nonaka I, Noguchi S, Hayashi YK, Nishino I: Central core disease is due to RYR1 mutations in more than 90% of patients.

    Brain 2006, 129(Pt 6):1470-1480. PubMed Abstract | Publisher Full Text OpenURL

  17. Dubowitz V, Platts M: Central core disease of muscle with focal wasting.

    J Neurol Neurosurg Psychiatry 1965, 28(5):432-437. PubMed Abstract OpenURL

  18. Middleton LT, Moser H: Mini core disease and central core disease. In Diagnostic Criteria for Neuromuscular Disorders. 2nd edition. edition. Edited by Emery E. London , Royal Society of Medicine; 1998:73-74. OpenURL

  19. Gamble JG, Rinsky LA, Lee JH: Orthopaedic aspects of central core disease.

    J Bone Joint Surg Am 1988, 70(7):1061-1066. PubMed Abstract OpenURL

  20. Ramsey PL, Hensinger RN: Congenital dislocation of the hip associated with central core disease.

    J Bone Joint Surg Am 1975, 57(5):648-651. PubMed Abstract OpenURL

  21. Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND: Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

    Proc Natl Acad Sci U S A 1993, 90(9):3993-3997. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  22. Kaindl AM, Ruschendorf F, Krause S, Goebel HH, Koehler K, Becker C, Pongratz D, Muller-Hocker J, Nurnberg P, Stoltenburg-Didinger G, Lochmuller H, Huebner A: Missense mutations of ACTA1 cause dominant congenital myopathy with cores.

    J Med Genet 2004, 41(11):842-848. PubMed Abstract | Publisher Full Text OpenURL

  23. Denborough MA, Forster JF, Lovell RR, Maplestone PA, Villiers JD: Anaesthetic deaths in a family.

    Br J Anaesth 1962, 34:395-396. PubMed Abstract | Publisher Full Text OpenURL

  24. Denborough MA, Forster JF, Hudson MC, Carter NG, Zapf P: Biochemical changes in malignant hyperpyrexia.

    Lancet 1970, 1(7657):1137-1138. PubMed Abstract | Publisher Full Text OpenURL

  25. Rueffert H, Olthoff D, Deutrich C, Schober R, Froster UG: A new mutation in the skeletal ryanodine receptor gene (RYR1) is potentially causative of malignant hyperthermia, central core disease, and severe skeletal malformation.

    Am J Med Genet A 2004, 124(3):248-254. PubMed Abstract | Publisher Full Text OpenURL

  26. Robinson RL, Brooks C, Brown SL, Ellis FR, Halsall PJ, Quinnell RJ, Shaw MA, Hopkins PM: RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypes.

    Hum Mutat 2002, 20(2):88-97. PubMed Abstract | Publisher Full Text OpenURL

  27. Jungbluth H, Muller CR, Halliger-Keller B, Brockington M, Brown SC, Feng L, Chattopadhyay A, Mercuri E, Manzur AY, Ferreiro A, Laing NG, Davis MR, Roper HP, Dubowitz V, Bydder G, Sewry CA, Muntoni F: Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.

    Neurology 2002, 59(2):284-287. PubMed Abstract OpenURL

  28. Manzur AY, Sewry CA, Ziprin J, Dubowitz V, Muntoni F: A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance.

    Neuromuscul Disord 1998, 8(7):467-473. PubMed Abstract | Publisher Full Text OpenURL

  29. Lamont PJ, Dubowitz V, Landon DN, Davis M, Morgan-Hughes JA: Fifty year follow-up of a patient with central core disease shows slow but definite progression.

    Neuromuscul Disord 1998, 8(6):385-391. PubMed Abstract | Publisher Full Text OpenURL

  30. Rudnik-Schoneborn S, Glauner B, Rohrig D, Zerres K: Obstetric aspects in women with facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, and congenital myopathies.

    Arch Neurol 1997, 54(7):888-894. PubMed Abstract OpenURL

  31. Mrozek K, Strugalska M, Fidzianska A: A sporadic case of central core disease.

    J Neurol Sci 1970, 10(4):339-348. PubMed Abstract | Publisher Full Text OpenURL

  32. Isaacs H, Heffron JJ, Badenhorst M: Central core disease. A correlated genetic, histochemical, ultramicroscopic, and biochemical study.

    J Neurol Neurosurg Psychiatry 1975, 38(12):1177-1186. PubMed Abstract OpenURL

  33. Heckmatt JZ, Dubowitz V: Ultrasound imaging and directed needle biopsy in the diagnosis of selective involvement in muscle disease.

    J Child Neurol 1987, 2(3):205-213. PubMed Abstract OpenURL

  34. Jungbluth H, Sewry CA, Counsell S, Allsop J, Chattopadhyay A, Mercuri E, North K, Laing N, Bydder G, Pelin K, Wallgren-Pettersson C, Muntoni F: Magnetic resonance imaging of muscle in nemaline myopathy.

    Neuromuscul Disord 2004, 14(12):779-784. PubMed Abstract | Publisher Full Text OpenURL

  35. Jungbluth H, Davis MR, Muller C, Counsell S, Allsop J, Chattopadhyay A, Messina S, Mercuri E, Laing NG, Sewry CA, Bydder G, Muntoni F: Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations.

    Neuromuscul Disord 2004, 14(12):785-790. PubMed Abstract | Publisher Full Text OpenURL

  36. Lynch PJ, Tong J, Lehane M, Mallet A, Giblin L, Heffron JJ, Vaughan P, Zafra G, MacLennan DH, McCarthy TV: A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.

    Proc Natl Acad Sci U S A 1999, 96(7):4164-4169. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  37. Scacheri PC, Hoffman EP, Fratkin JD, Semino-Mora C, Senchak A, Davis MR, Laing NG, Vedanarayanan V, Subramony SH: A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.

    Neurology 2000, 55(11):1689-1696. PubMed Abstract OpenURL

  38. Denborough MA, Dennett X, Anderson RM: Central-core disease and malignant hyperpyrexia.

    Br Med J 1973, 1(5848):272-273. PubMed Abstract | PubMed Central Full Text OpenURL

  39. Eng GD, Epstein BS, Engel WK, McKay DW, McKay R: Malignant hyperthermia and central core disease in a child with congenital dislocating hips.

    Arch Neurol 1978, 35(4):189-197. PubMed Abstract OpenURL

  40. Frank JP, Harati Y, Butler IJ, Nelson TE, Scott CI: Central core disease and malignant hyperthermia syndrome.

    Ann Neurol 1980, 7(1):11-17. PubMed Abstract | Publisher Full Text OpenURL

  41. Fujii J, Otsu K, Zorzato F, de Leon S, Khanna VK, Weiler JE, O'Brien PJ, MacLennan DH: Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia.

    Science 1991, 253(5018):448-451. PubMed Abstract | Publisher Full Text OpenURL

  42. MacLennan DH, Duff C, Zorzato F, Fujii J, Phillips M, Korneluk RG, Frodis W, Britt BA, Worton RG: Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia.

    Nature 1990, 343(6258):559-561. PubMed Abstract | Publisher Full Text OpenURL

  43. McCarthy TV, Healy JM, Heffron JJ, Lehane M, Deufel T, Lehmann-Horn F, Farrall M, Johnson K: Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2.

    Nature 1990, 343(6258):562-564. PubMed Abstract | Publisher Full Text OpenURL

  44. Healy SJ, Heffron JJ, Lehane M, Bradley DG, Johnson K, McCarthy TV: Diagnosis of susceptibility to malignant hyperthermia with flanking DNA markers.

    Bmj 1991, 303(6812):1225-1228. PubMed Abstract | PubMed Central Full Text OpenURL

  45. Ball SP, Johnson KJ: The genetics of malignant hyperthermia.

    J Med Genet 1993, 30(2):89-93. PubMed Abstract OpenURL

  46. Haan EA, Freemantle CJ, McCure JA, Friend KL, Mulley JC: Assignment of the gene for central core disease to chromosome 19.

    Hum Genet 1990, 86(2):187-190. PubMed Abstract | Publisher Full Text OpenURL

  47. Kausch K, Lehmann-Horn F, Janka M, Wieringa B, Grimm T, Muller CR: Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19.

    Genomics 1991, 10(3):765-769. PubMed Abstract | Publisher Full Text OpenURL

  48. Mulley JC, Kozman HM, Phillips HA, Gedeon AK, McCure JA, Iles DE, Gregg RG, Hogan K, Couch FJ, MacLennan DH, et al.: Refined genetic localization for central core disease.

    Am J Hum Genet 1993, 52(2):398-405. PubMed Abstract | PubMed Central Full Text OpenURL

  49. Gillard EF, Otsu K, Fujii J, Khanna VK, de Leon S, Derdemezi J, Britt BA, Duff CL, Worton RG, MacLennan DH: A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia.

    Genomics 1991, 11(3):751-755. PubMed Abstract | Publisher Full Text OpenURL

  50. Zhang Y, Chen HS, Khanna VK, De Leon S, Phillips MS, Schappert K, Britt BA, Browell AK, MacLennan DH: A mutation in the human ryanodine receptor gene associated with central core disease.

    Nat Genet 1993, 5(1):46-50. PubMed Abstract | Publisher Full Text OpenURL

  51. Quane KA, Healy JM, Keating KE, Manning BM, Couch FJ, Palmucci LM, Doriguzzi C, Fagerlund TH, Berg K, Ording H, et al.: Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia.

    Nat Genet 1993, 5(1):51-55. PubMed Abstract | Publisher Full Text OpenURL

  52. Phillips MS, Fujii J, Khanna VK, DeLeon S, Yokobata K, de Jong PJ, MacLennan DH: The structural organization of the human skeletal muscle ryanodine receptor (RYR1) gene.

    Genomics 1996, 34(1):24-41. PubMed Abstract | Publisher Full Text OpenURL

  53. Meissner G: Regulation of mammalian ryanodine receptors.

    Front Biosci 2002, 7:d2072-80. PubMed Abstract | Publisher Full Text OpenURL

  54. Wagenknecht T, Grassucci R, Frank J, Saito A, Inui M, Fleischer S: Three-dimensional architecture of the calcium channel/foot structure of sarcoplasmic reticulum.

    Nature 1989, 338(6211):167-170. PubMed Abstract | Publisher Full Text OpenURL

  55. Murray BE, Ohlendieck K: Cross-linking analysis of the ryanodine receptor and alpha1-dihydropyridine receptor in rabbit skeletal muscle triads.

    Biochem J 1997, 324 ( Pt 2):689-696. PubMed Abstract | PubMed Central Full Text OpenURL

  56. McCarthy TV, Quane KA, Lynch PJ: Ryanodine receptor mutations in malignant hyperthermia and central core disease.

    Hum Mutat 2000, 15(5):410-417. PubMed Abstract | Publisher Full Text OpenURL

  57. Jurkat-Rott K, McCarthy T, Lehmann-Horn F: Genetics and pathogenesis of malignant hyperthermia.

    Muscle Nerve 2000, 23(1):4-17. PubMed Abstract | Publisher Full Text OpenURL

  58. Treves S, Anderson AA, Ducreux S, Divet A, Bleunven C, Grasso C, Paesante S, Zorzato F: Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders.

    Neuromuscul Disord 2005, 15(9-10):577-587. PubMed Abstract | Publisher Full Text OpenURL

  59. Tilgen N, Zorzato F, Halliger-Keller B, Muntoni F, Sewry C, Palmucci LM, Schneider C, Hauser E, Lehmann-Horn F, Muller CR, Treves S: Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis.

    Hum Mol Genet 2001, 10(25):2879-2887. PubMed Abstract | Publisher Full Text OpenURL

  60. Monnier N, Romero NB, Lerale J, Landrieu P, Nivoche Y, Fardeau M, Lunardi J: Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.

    Hum Mol Genet 2001, 10(22):2581-2592. PubMed Abstract | Publisher Full Text OpenURL

  61. Davis MR, Haan E, Jungbluth H, Sewry C, North K, Muntoni F, Kuntzer T, Lamont P, Bankier A, Tomlinson P, Sanchez A, Walsh P, Nagarajan L, Oley C, Colley A, Gedeon A, Quinlivan R, Dixon J, James D, Muller CR, Laing NG: Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene.

    Neuromuscul Disord 2003, 13(2):151-157. PubMed Abstract | Publisher Full Text OpenURL

  62. Jungbluth H, Beggs A, Bonnemann C, Bushby K, Ceuterick-de Groote C, Estournet-Mathiaud B, Goemans N, Guicheney P, Lescure A, Lunardi J, Muntoni F, Quinlivan R, Sewry C, Straub V, Treves S, Ferreiro A: 111th ENMC International Workshop on Multi-minicore Disease. 2nd International MmD Workshop, 9-11 November 2002, Naarden, The Netherlands.

    Neuromuscul Disord 2004, 14(11):754-766. PubMed Abstract | Publisher Full Text OpenURL

  63. Jungbluth H, Zhou H, Hartley L, Halliger-Keller B, Messina S, Longman C, Brockington M, Robb SA, Straub V, Voit T, Swash M, Ferreiro A, Bydder G, Sewry CA, Muller C, Muntoni F: Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.

    Neurology 2005, 65(12):1930-1935. PubMed Abstract | Publisher Full Text OpenURL

  64. Sambuughin N, McWilliams S, de Bantel A, Sivakumar K, Nelson TE: Single-amino-acid deletion in the RYR1 gene, associated with malignant hyperthermia susceptibility and unusual contraction phenotype.

    Am J Hum Genet 2001, 69(1):204-208. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  65. Monnier N, Ferreiro A, Marty I, Labarre-Vila A, Mezin P, Lunardi J: A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia.

    Hum Mol Genet 2003, 12(10):1171-1178. PubMed Abstract | Publisher Full Text OpenURL

  66. Deufel T, Sudbrak R, Feist Y, Rubsam B, Du Chesne I, Schafer KL, Roewer N, Grimm T, Lehmann-Horn F, Hartung EJ, et al.: Discordance, in a malignant hyperthermia pedigree, between in vitro contracture-test phenotypes and haplotypes for the MHS1 region on chromosome 19q12-13.2, comprising the C1840T transition in the RYR1 gene.

    Am J Hum Genet 1995, 56(6):1334-1342. PubMed Abstract | PubMed Central Full Text OpenURL

  67. Lynch PJ, Krivosic-Horber R, Reyford H, Monnier N, Quane K, Adnet P, Haudecoeur G, Krivosic I, McCarthy T, Lunardi J: Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindred.

    Anesthesiology 1997, 86(3):620-626. PubMed Abstract | Publisher Full Text OpenURL

  68. Sei Y, Sambuughin NN, Davis EJ, Sachs D, Cuenca PB, Brandom BW, Tautz T, Rosenberg H, Nelson TE, Muldoon SM: Malignant hyperthermia in North America: genetic screening of the three hot spots in the type I ryanodine receptor gene.

    Anesthesiology 2004, 101(4):824-830. PubMed Abstract | Publisher Full Text OpenURL

  69. Quane KA, Keating KE, Manning BM, Healy JM, Monsieurs K, Heffron JJ, Lehane M, Heytens L, Krivosic-Horber R, Adnet P, et al.: Detection of a novel common mutation in the ryanodine receptor gene in malignant hyperthermia: implications for diagnosis and heterogeneity studies.

    Hum Mol Genet 1994, 3(3):471-476. PubMed Abstract | Publisher Full Text OpenURL

  70. Galli L, Orrico A, Cozzolino S, Pietrini V, Tegazzin V, Sorrentino V: Mutations in the RYR1 gene in Italian patients at risk for malignant hyperthermia: evidence for a cluster of novel mutations in the C-terminal region.

    Cell Calcium 2002, 32(3):143-151. PubMed Abstract | Publisher Full Text OpenURL

  71. Shepherd S, Ellis F, Halsall J, Hopkins P, Robinson R: RYR1 mutations in UK central core disease patients: more than just the C-terminal transmembrane region of the RYR1 gene.

    J Med Genet 2004, 41(3):e33. PubMed Abstract | Publisher Full Text OpenURL

  72. Ferreiro A, Monnier N, Romero NB, Leroy JP, Bonnemann C, Haenggeli CA, Straub V, Voss WD, Nivoche Y, Jungbluth H, Lemainque A, Voit T, Lunardi J, Fardeau M, Guicheney P: A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene.

    Ann Neurol 2002, 51(6):750-759. PubMed Abstract | Publisher Full Text OpenURL

  73. Tong J, McCarthy TV, MacLennan DH: Measurement of resting cytosolic Ca2+ concentrations and Ca2+ store size in HEK-293 cells transfected with malignant hyperthermia or central core disease mutant Ca2+ release channels.

    J Biol Chem 1999, 274(2):693-702. PubMed Abstract | Publisher Full Text OpenURL

  74. Dirksen RT, Avila G: Altered ryanodine receptor function in central core disease: leaky or uncoupled Ca(2+) release channels?

    Trends Cardiovasc Med 2002, 12(5):189-197. PubMed Abstract | Publisher Full Text OpenURL

  75. Manning BM, Quane KA, Ording H, Urwyler A, Tegazzin V, Lehane M, O'Halloran J, Hartung E, Giblin LM, Lynch PJ, Vaughan P, Censier K, Bendixen D, Comi G, Heytens L, Monsieurs K, Fagerlund T, Wolz W, Heffron JJ, Muller CR, McCarthy TV: Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation.

    Am J Hum Genet 1998, 62(3):599-609. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  76. Keating KE, Quane KA, Manning BM, Lehane M, Hartung E, Censier K, Urwyler A, Klausnitzer M, Muller CR, Heffron JJ, et al.: Detection of a novel RYR1 mutation in four malignant hyperthermia pedigrees.

    Hum Mol Genet 1994, 3(10):1855-1858. PubMed Abstract | Publisher Full Text OpenURL

  77. Girard T, Treves S, Censier K, Mueller CR, Zorzato F, Urwyler A: Phenotyping malignant hyperthermia susceptibility by measuring halothane-induced changes in myoplasmic calcium concentration in cultured human skeletal muscle cells.

    Br J Anaesth 2002, 89(4):571-579. PubMed Abstract | Publisher Full Text OpenURL

  78. Wehner M, Rueffert H, Koenig F, Meinecke CD, Olthoff D: The Ile2453Thr mutation in the ryanodine receptor gene 1 is associated with facilitated calcium release from sarcoplasmic reticulum by 4-chloro-m-cresol in human myotubes.

    Cell Calcium 2003, 34(2):163-168. PubMed Abstract | Publisher Full Text OpenURL

  79. Du GG, Khanna VK, MacLennan DH: Mutation of divergent region 1 alters caffeine and Ca(2+) sensitivity of the skeletal muscle Ca(2+) release channel (ryanodine receptor).

    J Biol Chem 2000, 275(16):11778-11783. PubMed Abstract | Publisher Full Text OpenURL

  80. Du GG, Khanna VK, Guo X, MacLennan DH: Central core disease mutations R4892W, I4897T and G4898E in the ryanodine receptor isoform 1 reduce the Ca2+ sensitivity and amplitude of Ca2+-dependent Ca2+ release.

    Biochem J 2004, 382(Pt 2):557-564. PubMed Abstract | PubMed Central Full Text OpenURL

  81. Avila G, O'Brien JJ, Dirksen RT: Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor.

    Proc Natl Acad Sci U S A 2001, 98(7):4215-4220. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  82. Avila G, O'Connell KM, Dirksen RT: The pore region of the skeletal muscle ryanodine receptor is a primary locus for excitation-contraction uncoupling in central core disease.

    J Gen Physiol 2003, 121(4):277-286. PubMed Abstract | Publisher Full Text OpenURL

  83. Buck ED, Nguyen HT, Pessah IN, Allen PD: Dyspedic mouse skeletal muscle expresses major elements of the triadic junction but lacks detectable ryanodine receptor protein and function.

    J Biol Chem 1997, 272(11):7360-7367. PubMed Abstract | Publisher Full Text OpenURL

  84. Dirksen RT, Avila G: Distinct effects on Ca2+ handling caused by malignant hyperthermia and central core disease mutations in RyR1.

    Biophys J 2004, 87(5):3193-3204. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  85. Zorzato F, Yamaguchi N, Xu L, Meissner G, Muller CR, Pouliquin P, Muntoni F, Sewry C, Girard T, Treves S: Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor.

    Hum Mol Genet 2003, 12(4):379-388. PubMed Abstract | Publisher Full Text OpenURL

  86. Ducreux S, Zorzato F, Muller C, Sewry C, Muntoni F, Quinlivan R, Restagno G, Girard T, Treves S: Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core disease.

    J Biol Chem 2004, 279(42):43838-43846. PubMed Abstract | Publisher Full Text OpenURL

  87. Curran JL, Hall WJ, Halsall PJ, Hopkins PM, Iles DE, Markham AF, McCall SH, Robinson RL, West SP, Bridges LR, Ellis FR: Segregation of malignant hyperthermia, central core disease and chromosome 19 markers.

    Br J Anaesth 1999, 83(2):217-222. PubMed Abstract OpenURL

  88. Dubowitz V: Muscle biopsy - A practical approach. London , Baillière Tindall; 1985.

  89. Sewry CA, Muller C, Davis M, Dwyer JS, Dove J, Evans G, Schroder R, Furst D, Helliwell T, Laing N, Quinlivan RC: The spectrum of pathology in central core disease.

    Neuromuscul Disord 2002, 12(10):930-938. PubMed Abstract | Publisher Full Text OpenURL

  90. Telerman-Toppet N, Gerard JM, Coers C: Central core disease. A study of clinically unaffected muscle.

    J Neurol Sci 1973, 19(2):207-223. PubMed Abstract | Publisher Full Text OpenURL

  91. Harriman DGF: The pathology of malignant hyperpyrexia. In Skeletal Muscle Pathology. Edited by Mastaglia FL WJ. Edinburgh , Churchil Livingstone; 1982:575. OpenURL

  92. Tojo M, Ozawa M, Nonaka I: Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family.

    Brain Dev 2000, 22(4):262-264. PubMed Abstract | Publisher Full Text OpenURL

  93. Hayashi K, Miller RG, Brownell AK: Central core disease: ultrastructure of the sarcoplasmic reticulum and T-tubules.

    Muscle Nerve 1989, 12(2):95-102. PubMed Abstract | Publisher Full Text OpenURL

  94. Vita G, Migliorato A, Baradello A, Mazzeo A, Rodolico C, Falsaperla R, Messina C: Expression of cytoskeleton proteins in central core disease.

    J Neurol Sci 1994, 124(1):71-76. PubMed Abstract | Publisher Full Text OpenURL

  95. van der Ven PF, Jap PH, ter Laak HJ, Nonaka I, Barth PG, Sengers RC, Stadhouders AM, Ramaekers FC: Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins.

    J Neurol Sci 1995, 129(2):199-213. PubMed Abstract | Publisher Full Text OpenURL

  96. Sewry CA: The role of immunocytochemistry in congenital myopathies.

    Neuromuscul Disord 1998, 8(6):394-400. PubMed Abstract | Publisher Full Text OpenURL

  97. Bonnemann CG, Thompson TG, van der Ven PF, Goebel HH, Warlo I, Vollmers B, Reimann J, Herms J, Gautel M, Takada F, Beggs AH, Furst DO, Kunkel LM, Hanefeld F, Schroder R: Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle.

    J Neurol Sci 2003, 206(1):71-78. PubMed Abstract | Publisher Full Text OpenURL

  98. Engel WK: Muscle target fibres, a newly recognized sign of denervation.

    Nature 1961, 191:389-390. PubMed Abstract | Publisher Full Text OpenURL

  99. Barone V, Massa O, Intravaia E, Bracco A, Di Martino A, Tegazzin V, Cozzolino S, Sorrentino V: Mutation screening of the RYR1 gene and identification of two novel mutations in Italian malignant hyperthermia families.

    J Med Genet 1999, 36(2):115-118. PubMed Abstract OpenURL

  100. Ferreiro A, Quijano-Roy S, Pichereau C, Moghadaszadeh B, Goemans N, Bonnemann C, Jungbluth H, Straub V, Villanova M, Leroy JP, Romero NB, Martin JJ, Muntoni F, Voit T, Estournet B, Richard P, Fardeau M, Guicheney P: Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies.

    Am J Hum Genet 2002, 71(4):739-749. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  101. Thomas C: Nemaline rod and central core disease: a coexisting Z-band myopathy.

    Muscle Nerve 1997, 20(7):893-896. PubMed Abstract | Publisher Full Text OpenURL

  102. Bethlem J, Arts WF, Dingemans KP: Common origin of rods, cores, miniature cores, and focal loss of cross-striations.

    Arch Neurol 1978, 35(9):555-566. PubMed Abstract OpenURL

  103. Vallat JM, de Lumley L, Loubet A, Leboutet MJ, Corvisier N, Umdenstock R: Coexistence of minicores, cores, and rods in the same muscle biopsy. A new example of mixed congenital myopathy.

    Acta Neuropathol (Berl) 1982, 58(3):229-232. PubMed Abstract | Publisher Full Text OpenURL

  104. European Malignant Hyperthermia Group [http://www.emhg.org] webcite

  105. Hagberg JM, Carroll JE, Brooke MH: Endurance exercise training in a patient with central core disease.

    Neurology 1980, 30(11):1242-1244. PubMed Abstract OpenURL

  106. Wallgren-Pettersson C, Bushby K, Mellies U, Simonds A: 117th ENMC workshop: ventilatory support in congenital neuromuscular disorders -- congenital myopathies, congenital muscular dystrophies, congenital myotonic dystrophy and SMA (II) 4-6 April 2003, Naarden, The Netherlands.

    Neuromuscul Disord 2004, 14(1):56-69. PubMed Abstract | Publisher Full Text OpenURL

  107. Messina S, Hartley L, Main M, Kinali M, Jungbluth H, Muntoni F, Mercuri E: Pilot trial of salbutamol in central core and multi-minicore diseases.

    Neuropediatrics 2004, 35(5):262-266. PubMed Abstract | Publisher Full Text OpenURL