1.
Accesses
20778 |
Review
 
Brachydactyly
Samia A Temtamy, Mona S Aglan
Orphanet Journal of Rare Diseases 2008, 3:15 (13 June 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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2.
Accesses
8491 |
Review
Corneal dystrophies
Gordon K Klintworth
Orphanet Journal of Rare Diseases 2009, 4:7 (23 February 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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3.
Accesses
8478 |
Review
Amyotrophic lateral sclerosis
Lokesh C Wijesekera, P Nigel Leigh
Orphanet Journal of Rare Diseases 2009, 4:3 (3 February 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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4.
Accesses
6226 |
Review
Jacobsen syndrome
Teresa Mattina, Concetta Simona Perrotta, Paul Grossfeld
Orphanet Journal of Rare Diseases 2009, 4:9 (7 March 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]
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5.
Accesses
5987 |
Review
Gitelman syndrome
Nine VAM Knoers, Elena N Levtchenko
Orphanet Journal of Rare Diseases 2008, 3:22 (30 July 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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6.
Accesses
5940 |
Review
Cri du Chat syndrome
Paola Cerruti Mainardi
Orphanet Journal of Rare Diseases 2006, 1:33 (5 September 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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7.
Accesses
5141 |
Review
Sweet's syndrome  a comprehensive review of an acute febrile neutrophilic dermatosis
Philip R Cohen
Orphanet Journal of Rare Diseases 2007, 2:34 (26 July 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]
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8.
Accesses
4493 |
Review
Amelogenesis imperfecta
Peter JM Crawford, Michael Aldred, Agnes Bloch-Zupan
Orphanet Journal of Rare Diseases 2007, 2:17 (4 April 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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9.
Accesses
4288 |
Review
Osteopetrosis
Zornitza Stark, Ravi Savarirayan
Orphanet Journal of Rare Diseases 2009, 4:5 (20 February 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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10.
Accesses
4021 |
Review
Malignant hyperthermia
Henry Rosenberg, Mark Davis, Danielle James, Neil Pollock, Kathryn Stowell
Orphanet Journal of Rare Diseases 2007, 2:21 (24 April 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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11.
Accesses
4004 |
Review
Hereditary sensory and autonomic neuropathies: types II, III, and IV
Felicia B Axelrod, Gabrielle Gold-von Simson
Orphanet Journal of Rare Diseases 2007, 2:39 (3 October 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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12.
Accesses
3895 |
Review
Myasthenia gravis
Vern C Juel, Janice M Massey
Orphanet Journal of Rare Diseases 2007, 2:44 (6 November 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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13.
Accesses
3883 |
Review
Noonan syndrome
Ineke van der Burgt
Orphanet Journal of Rare Diseases 2007, 2:4 (14 January 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]
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14.
Accesses
3876 |
Review
McCune-Albright syndrome
Claudia E Dumitrescu, Michael T Collins
Orphanet Journal of Rare Diseases 2008, 3:12 (19 May 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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15.
Accesses
3774 |
Review
Idiopathic pulmonary fibrosis
Eric B Meltzer, Paul W Noble
Orphanet Journal of Rare Diseases 2008, 3:8 (26 March 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]
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16.
Accesses
3734 |
Review
Mixed cryoglobulinemia
Clodoveo Ferri
Orphanet Journal of Rare Diseases 2008, 3:25 (16 September 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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17.
Accesses
3700 |
Review
Neurofibromatosis type 2 (NF2): A clinical and molecular review
D Gareth R Evans
Orphanet Journal of Rare Diseases 2009, 4:16 (19 June 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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18.
Accesses
3608 |
Review
Ehlers-Danlos syndrome type IV
Dominique P Germain
Orphanet Journal of Rare Diseases 2007, 2:32 (19 July 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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19.
Accesses
3583 |
Review
Familial adenomatous polyposis
Elizabeth Half, Dani Bercovich, Paul Rozen
Orphanet Journal of Rare Diseases 2009, 4:22 (12 October 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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20.
Accesses
3536 |
Review
Tetralogy of Fallot
Frederique Bailliard, Robert H Anderson
Orphanet Journal of Rare Diseases 2009, 4:2 (13 January 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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