1. Accesses 28738 |
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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2. Accesses 16747 |
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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3. Accesses 13389 |
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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4. Accesses 12734 |
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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5. Accesses 12486 |
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]
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6. Accesses 11655 |
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]
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7. Accesses 11234 |
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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8. Accesses 11009 |
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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9. Accesses 10769 |
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]
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10. Accesses 10069 |
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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11. Accesses 10047 |
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] [Cited on BioMed Central]
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12. Accesses 10031 |
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]
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13. Accesses 10003 |
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]
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14. Accesses 9727 |
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]
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15. Accesses 9717 |
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]
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16. Accesses 9333 |
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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17. Accesses 9098 |
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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18. Accesses 9095 |
Review
  Oesophageal atresia Lewis Spitz Orphanet Journal of Rare Diseases 2007, 2:24 (11 May 2007) [Abstract] [Full Text] [PDF] [PubMed] [Related articles]
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19. Accesses 9002 |
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]
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20. Accesses 8944 |
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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