Literature DB >> 5494204

Spinal muscular atrophy of the scapulo-peroneal-type.

L Schuchmann.   

Abstract

Entities:  

Mesh:

Year:  1970        PMID: 5494204     DOI: 10.1007/bf00438809

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN: 0044-2917


× No keyword cloud information.
  4 in total

1.  Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

Authors:  E KUGELBERG; L WELANDER
Journal:  AMA Arch Neurol Psychiatry       Date:  1956-05

2.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

3.  A spinal muscular atrophy with scapuloperoneal distribution.

Authors:  E S Emery; G M Fenichel; G Eng
Journal:  Arch Neurol       Date:  1968-02

4.  Scapuloperoneal muscular atrophy.

Authors:  H E Kaeser
Journal:  Brain       Date:  1965-06       Impact factor: 13.501

  4 in total
  4 in total

1.  X-linked scapuloperoneal syndrome.

Authors:  P K Thomas; D B Calne; C F Elliott
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-04       Impact factor: 10.154

2.  Neurogenic scapuloperoneal syndrome in childhood.

Authors:  R Mercelis; J Demeester; J J Martin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-10       Impact factor: 10.154

Review 3.  The nosology of the spinal muscular atrophies.

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

4.  The differential diagnosis of scapuloperoneal amyotrophy.

Authors:  G Spalke; H Hökendorf; P von Roques
Journal:  J Neurol       Date:  1976-06-14       Impact factor: 4.849

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.