Literature DB >> 13778896

The primary spino-cerebellar atrophies and their associated defects, with a study of the foot deformity.

J H TYRER, J M SUTHERLAND.   

Abstract

Entities:  

Keywords:  FOOT/abnormalities; FRIEDREICH'S ATAXIA/complications; MUSCULAR ATROPHY/etiology; SPINAL CORD/diseases

Mesh：

Year:  1961        PMID： 13778896     DOI： 10.1093/brain/84.2.289

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


× No keyword cloud information.
  9 in total

Review 1.  Hereditary spastic paraparesis: a review of new developments.

Authors:  C McDermott; K White; K Bushby; P Shaw
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-08       Impact factor: 10.154

2.  Spinocerebellar degenerations.

Authors:  R K CHANDRA; S K KHETARPAL; O P GHAI
Journal:  Indian J Pediatr       Date:  1962-10       Impact factor: 1.967

3.  Significance of Extensor Plantar Responses in Muscular Dystrophy.

Authors:  M J Eadie; J H Tyrer; J M Sutherland
Journal:  Arch Dis Child       Date:  1963-02       Impact factor: 3.791

4.  The heart in Friedreich's ataxia.

Authors:  R Hewer
Journal:  Br Heart J       Date:  1969-01

5.  Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.

Authors:  A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-06       Impact factor: 10.154

6.  [Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].

Authors:  G Spalke; R Heene; D Herold
Journal:  J Neurol       Date:  1975       Impact factor: 4.849

Review 7.  [HEART DISEASE IN FRIEDREICH'S ATAXIA. (SURVEY OF THE CASES REPORTED SINCE 1929 AND 10 PERSONAL OBSERVATIONS)].

Authors:  P KOLB; C S SO; H BLOEMER
Journal:  Arch Kreislaufforsch       Date:  1963-12

8.  Familial cerebellar ataxia presenting with down beat nystagmus.

Authors:  G D Schott
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

9.  Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case.

Authors:  D Inzitari; N Rizzuto; P Antuono; D Sità
Journal:  Ital J Neurol Sci       Date:  1981-08
  9 in total

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