Literature DB >> 13190076

On the classification, natural history and treatment of the myopathies.

J N WALTON, F J NATTRASS.   

Abstract

Entities:  

Keywords:  MUSCLES/diseases

Mesh:

Year:  1954        PMID: 13190076     DOI: 10.1093/brain/77.2.169

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


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  101 in total

Review 1.  Concise review: mesoangioblast and mesenchymal stem cell therapy for muscular dystrophy: progress, challenges, and future directions.

Authors:  Suzanne E Berry
Journal:  Stem Cells Transl Med       Date:  2014-11-12       Impact factor: 6.940

2.  SERUM ENZYME STUDIES IN MUSCLE DISEASE. II. SERUM CREATINE KINASE ACTIVITY IN MUSCULAR DYSTROPHY AND IN OTHER MYOPATHIC AND NEUROPATHIC DISORDERS.

Authors:  J M PEARCE; R J PENNINGTON; J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-04       Impact factor: 10.154

3.  MUSCULAR DYSTROPHY.

Authors:  B M BENNETT; E NAKAMURA
Journal:  Br Med J       Date:  1964-07-18

4.  [CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE].

Authors:  H W ROTTHAUWE; S KOWALEWSKI
Journal:  Klin Wochenschr       Date:  1965-02-01

5.  ELECTROENCEPHALOGRAPHIC STUDIES IN HEREDITARY MYOPATHY.

Authors:  D D BARWICK; J W OSSELTON; J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1965-04       Impact factor: 10.154

6.  Duplication of the mitral valve.

Authors:  J P TREMBLAY; L C SIMARD
Journal:  Can Med Assoc J       Date:  1955-06-01       Impact factor: 8.262

7.  Recovery from "muscular dystrophy" [Résumé].

Authors:  F J NATTRASS
Journal:  Proc R Soc Med       Date:  1955-02

8.  The differential diagnosis of flaccid paralysis.

Authors:  P H SANDIFER
Journal:  Proc R Soc Med       Date:  1955-03

9.  Sources of error in the biochemical diagnosis of muscular dystrophy.

Authors:  W A THOMSON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1962-08       Impact factor: 10.154

10.  Congenital myopathy with myasthenic features and congenital cataract in two siblings.

Authors:  Y Nishida; T Kobayashi; M Machi; T Yamada; T Kitaguchi; K Oda; I Goto
Journal:  J Neurol       Date:  1989-03       Impact factor: 4.849

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