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Browse Orphanet Journal of Rare Diseases for Top 20 most accessed articles of all time


 Top 20 most accessed articles for last 30 days / past year / all time

1.
Accesses
22622
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]

2.
Accesses
11283
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]

3.
Accesses
9235
Review    
CHARGE syndrome
Kim D Blake, Chitra Prasad
Orphanet Journal of Rare Diseases 2006, 1:34 (7 September 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

4.
Accesses
9227
Review    
Systemic lupus erythematosus
Jessica J Manson, Anisur Rahman
Orphanet Journal of Rare Diseases 2006, 1:6 (27 March 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

5.
Accesses
8652
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]

6.
Accesses
8439
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]

7.
Accesses
7643
Review    
Pyoderma gangrenosum a review
Uwe Wollina
Orphanet Journal of Rare Diseases 2007, 2:19 (15 April 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

8.
Accesses
7535
Review    
Retinitis pigmentosa
Christian Hamel
Orphanet Journal of Rare Diseases 2006, 1:40 (11 October 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]

9.
Accesses
7028
Review    
Celiac disease
Wolfgang Holtmeier, Wolfgang F Caspary
Orphanet Journal of Rare Diseases 2006, 1:3 (1 March 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

10.
Accesses
6817
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]

11.
Accesses
6724
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]

12.
Accesses
6577
Review    
Alpha thalassaemia-mental retardation, X linked
Richard Gibbons
Orphanet Journal of Rare Diseases 2006, 1:15 (4 May 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]

13.
Accesses
6532
Review    
Klinefelter syndrome and other sex chromosomal aneuploidies
Jeannie Visootsak, John M Graham Jr
Orphanet Journal of Rare Diseases 2006, 1:42 (24 October 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

14.
Accesses
6286
Review    
Paraneoplastic neurological syndromes
Jérôme Honnorat, Jean-Christophe Antoine
Orphanet Journal of Rare Diseases 2007, 2:22 (4 May 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

15.
Accesses
6033
Review    
Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria)
Ralph Gräsbeck
Orphanet Journal of Rare Diseases 2006, 1:17 (19 May 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

16.
Accesses
5959
Review    
Oesophageal atresia
Lewis Spitz
Orphanet Journal of Rare Diseases 2007, 2:24 (11 May 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

17.
Accesses
5761
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]

18.
Accesses
5671
Review    
Primary biliary cirrhosis
Teru Kumagi, E Jenny Heathcote
Orphanet Journal of Rare Diseases 2008, 3:1 (23 January 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

19.
Accesses
5671
Review    
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
Griet Van Buggenhout, Jean-Pierre Fryns
Orphanet Journal of Rare Diseases 2006, 1:26 (10 July 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

20.
Accesses
5427
Review    
Ollier disease
Caroline Silve, Harald Jüppner
Orphanet Journal of Rare Diseases 2006, 1:37 (22 September 2006)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [2 comments]

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