Chaos in classification of the spinal muscular atrophies of childhood

Neuromuscular Disorders

Volumn 1, Issue 2, 1991, Pages 77-80

  Dubowitz, Victor ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLASSIFICATION; EDITORIAL; HUMAN; SPINAL MUSCULAR ATROPHY;

HUMAN; MUSCULAR ATROPHY, SPINAL;

EID: 0026271910     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-8966(91)90051-S     Document Type: Editorial

References (21)

1. Zwei fruhinfantile hereditaren Falle von progressiver Muskelatrophie unter dem Bilde der Dystrophie, aber auf neurotischer Grundlage
2. Die fruhinfantile progressive spinale Amyotrophie
3. Ueber chronische spinale Muskelatrophie im Kindesalter, auf familiarer Basis
4. Weiterer Beitrag zur Lehre von der hereditaren progressive spinalen Muskelatrophie im Kindesalter
5. Dritter Beitrag zur Lehre von der hereditaren progressiven spinalen Muskelatrophie im Kindesalter
6. Werdnig-Hoffmann's infantile progressive muscular atrophy
7. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy
8. Infantile muscular atrophy
9. Infantile muscular atrophy. A prospective study with particular reference to a slowly progressive variety
10. Infantile muscular atrophy: a broad spectrum
11. Hereditary proximal spinal muscular atrophy: single or multiple genes?
12. Neurogenic muscular atrophy of infancy with prolonged survival
13. The nosology of the spinal muscular atrophies
14. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type III (Kugelberg-Welander disease)
15. Infantile and juvenile spinal muscular atrophy
16. The genetic identity of acute infantile spinal muscular atrophy
17. Acute Werdnig-Hoffmann disease
18. Genetic homogeniety between acute and chronic forms of spinal muscular atrophy
19. Linkage analysis in spinal muscular atrophy by six closely flanking markers on chromosome 5
20. No evidence for non-allelic genetic heterogeneity of acute (SMA I) or chronic (SMA II & III) spinal muscular atrophy
21. Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2–13.3 (SMA 5q)