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Literature DB >> 6053568

Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form.

G M Fenichel, E S Emery, P Hunt.

Abstract

Entities: Disease

Mesh：

Year: 1967 PMID： 6053568 DOI： 10.1001/archneur.1967.00470270035005

Source DB: PubMed Journal: Arch Neurol ISSN： 0003-9942

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11 in total

1. Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.

Authors: T Siddique; H Roper; M A Pericak-Vance; J Shaw; K L Warner; W Y Hung; K L Phillips; P Lunt; W J Cumming; A D Roses
Journal: J Med Genet Date: 1989-08 Impact factor: 6.318

2. Hearing loss in facioscapulohumeral dystrophy.

Authors: T Voit; A Lamprecht; H G Lenard; H H Goebel
Journal: Eur J Pediatr Date: 1986-09 Impact factor: 3.183

3. Creatine phosphokinase in facioscapulohumeral muscular dystrophy.

Authors: B P Hughes
Journal: Br Med J Date: 1971-08

Review 4. The nosology of the spinal muscular atrophies.

Authors: A E Emery
Journal: J Med Genet Date: 1971-12 Impact factor: 6.318

5. Familial bulbospinal neuronopathy with optic atrophy: a distinct entity.

Authors: G Paradiso; F Micheli; A L Taratuto; I C Parera
Journal: J Neurol Neurosurg Psychiatry Date: 1996-08 Impact factor: 10.154

6. Chronic spinal muscular atrophy of facioscapulohumeral type.

Authors: T Furukawa; Y Toyokura
Journal: J Med Genet Date: 1976-08 Impact factor: 6.318

7. New method for the estimation of the number of motor units in a muscle. 2. Duchenne, limb-girdle and facioscapulohumeral, and myotonic muscular dystrophies.

Authors: J P Ballantyne; S Hansen
Journal: J Neurol Neurosurg Psychiatry Date: 1974-11 Impact factor: 10.154