Unusual clinical features in infantile Spinal Muscular Atrophies-Reference-Cited by-同舟云学术

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Unusual clinical features in infantile Spinal Muscular Atrophies

Published:2008-03 Issue:3 Volume:30 Page:169-178
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Guillot Nathalie,Cuisset Jean-Marie,Cuvellier Jean-Christophe,Hurtevent Jean-François,Joriot Sylvie,Vallee Louis

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference43 articles.

1. Zerres K, Davies KE. 59th ENMC International Workshop: spinal muscular atrophies: recent progress and revised diagnostic criteria. Neuromuscul Disord 1999;9:272–78.

2. Zerres K, Rudnik-Schöneborn S. 93rd ENMC International Workshop: non-5q-spinal muscular atrophies (SMA) – clinical picture (6–8 April 2001, Naarden, The Netherlands). Neuromuscul Disord 2003;13:179–83.

3. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings;Rudnik-Schöneborn;Neuropediatrics,1996

4. Mutation of gene in spinal muscular atrophy respiratory distress type I;Wong;Pediatr Neurol,2006

5. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1;Grohmann;Nat Genet,2001

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