Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: Primary or secondary defect(s)?-Reference-Cited by-同舟云学术

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Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: Primary or secondary defect(s)?

Published:1995-01 Issue:1 Volume:12 Page:21-30
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Tein Ingrid,Sloane Avril E.,Donner Elizabeth J.,Lehotay Dennis C.,Millington David S.,Kelley Richard I.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference67 articles.

1. Classification of spinal muscular atrophies;Pearn;Lancet,1980

2. Disorders of the lower motor neurone;Dubowitz,1978

3. The gene frequency of acute Werdnig-Hoffmann disease (SMA type I). A total population survey in north-east England;Pearn;J Med Genet,1973

4. Acute Werdnig-Hoffmann disease. Acute infantile spinal muscular atrophy;Pearn;Arch Dis Child,1973

5. Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw;Spiegler;Hum Genet,1990

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