Literature DB >> 13960293

[A rarely observed familial form of progressive muscular dystrophy in adulthood].

F FUNK.   

Abstract

Entities:  

Keywords:  GENETICS, HUMAN; MUSCULAR DYSTROPHY

Mesh:

Year:  1962        PMID: 13960293     DOI: 10.1007/BF00356302

Source DB:  PubMed          Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr


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  10 in total

1.  Discrimination of genetic entities in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

2.  Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

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

3.  Studies on serum aldolase activity in neuromuscular disorders. I. Clinical applications.

Authors:  S M ARONSON; B W VOLK
Journal:  Am J Med       Date:  1957-03       Impact factor: 4.965

4.  Autosomal recessive inheritance of Duchennetype muscular dystrophy.

Authors:  H W KLOEPFER; C TALLEY
Journal:  Ann Hum Genet       Date:  1958-02       Impact factor: 1.670

5.  [A case of late progressive myopathy of Nevin type].

Authors:  R GARCIN; J LAPRESLE
Journal:  Rev Neurol (Paris)       Date:  1958-01       Impact factor: 2.607

6.  Two cases of myopathy limited to the quadriceps.

Authors:  J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1956-05       Impact factor: 10.154

7.  [Genetics of myopathy].

Authors:  P E BECKER
Journal:  Dtsch Z Nervenheilkd       Date:  1955

8.  [A new x-chromosomal muscular dystrophy].

Authors:  P E BECKER; F KIENER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1955

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

Authors:  J N WALTON; F J NATTRASS
Journal:  Brain       Date:  1954       Impact factor: 13.501

10.  Myopathia distalis tarda hereditaria; 249 examined cases in 72 pedigrees.

Authors:  L WELANDER
Journal:  Acta Med Scand Suppl       Date:  1951
  10 in total

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