A genetic study of subacute and chronic spinal muscular atrophy in childhood-Reference-Cited by-同舟云学术

A genetic study of subacute and chronic spinal muscular atrophy in childhood

Published:1978-07 Issue:3 Volume:37 Page:227-248
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Pearn John,Bundey Sarah,Carter C.O.,Wilson J.,Gardner-Medwin D.,Walton J.N.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference44 articles.

1. Atrophia musculorum spinalis pseudomyopathica — Hereditäre neurogene proximale Amyotrophie von Hugelberg und Welander;Becker;Z. menschl. Vererb.-u Konstit.-Lehre,1964

2. Familial correlations for age at onset and age at death in Huntington's disease;Brackenridge;J. med. Genet.,1972

3. Hereditary factors in infantile progressive muscular atrophy;Brandt;Amer. J. Dis. Child.,1949

4. Werdnig-Hoffmann's Infantile Progressive Muscular Atrophy;Brandt,1950

5. Contribution a l'étude de la paralysie musculaire progressive de la forme familiale;Bruns;Rev. neurol.,1900

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3. A Randomized, Placebo-Controlled Trial of Creatine in Children With Spinal Muscular Atrophy;Journal of Clinical Neuromuscular Disease;2007-03

4. Inherited Neuronal Atrophy and Degeneration Predominantly of Lower Motor Neurons * *This chapter is reprinted from the third edition because the invited author was unable to meet extended deadlines for revision. A recent review of spinal muscular atrophies by Sabine Rudnik-Schöneborn and colleagues can be found in Myology, third edition, edited by A. G. Engel and C. Franzini-Armstrong (McGraw-Hill, 2004). Several tables from that chapter appear here.;Peripheral Neuropathy;2005

5. Pulmonary manifestations of neuromuscular disease with special reference to Duchenne muscular dystrophy and spinal muscular atrophy;PEDIATR PULM;2000