Literature DB >> 13305346

[Genetics of myopathy].

P E BECKER.   

Abstract

Entities:  

Keywords:  HEREDITY; MUSCLES/diseases

Mesh:

Year:  1955        PMID: 13305346

Source DB:  PubMed          Journal:  Dtsch Z Nervenheilkd        ISSN: 0367-004X


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  16 in total

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

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

2.  [Estimation of mutation rate in muscular dystrophy].

Authors:  P E BECKER; F LENZ
Journal:  Z Mensch Vererb Konstitutionsl       Date:  1955

3.  [A myasthenic syndrome frequently encountered in tobacco chewers].

Authors:  R COULONJOU; A SALAUN
Journal:  Sem Hop       Date:  1952-12-30

4.  [Postoperative myxedema with a myotonic syndrome].

Authors:  H WICKE
Journal:  Medizinische       Date:  1953-02-14

5.  Dystrophia myotonica as a generalized disease.

Authors:  O MAAS; A S PATERSON
Journal:  Monatsschr Psychiatr Neurol       Date:  1947

6.  Comparison of thymic hyperplasia in myasthenia gravis and exophthalmic goiter.

Authors:  A L BRYAN; J R McDONALD; O T CLAGETT
Journal:  Arch Pathol (Chic)       Date:  1948-09

7.  Treatment of myasthenia gravis.

Authors:  C T STONE; J A RIDER
Journal:  J Am Med Assoc       Date:  1949-09-10

8.  [Not Available].

Authors:  M KLINGER
Journal:  Schweiz Arch Neurol Psychiatr       Date:  1948

9.  Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.

Authors:  F E STEPHENS; F H TYLER
Journal:  Am J Hum Genet       Date:  1951-06       Impact factor: 11.025

10.  Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia.

Authors:  F H TYLER; F E STEPHENS; F D GUNN; G T PERKOFF
Journal:  J Clin Invest       Date:  1951-05       Impact factor: 14.808

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  5 in total

1.  SEVERE MUSCULAR DYSTROPHY IN GIRLS.

Authors:  H A JOHNSTON
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

2.  Aldolase activity in the plasma or serum of normal children and families with muscular dystrophy.

Authors:  B E CLAYTON; K M WILSON; C O CARTER
Journal:  Arch Dis Child       Date:  1963-06       Impact factor: 3.791

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

Authors:  F FUNK
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1962

4.  New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

Authors:  M Zatz; S B Itskan; R Sanger; O Frota-Pessoa; P H Saldanha
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

5.  Detection of carriers of benign X-linked muscular dystrophy.

Authors:  A E Emery; E R Clack; S Simon; J L Taylor
Journal:  Br Med J       Date:  1967-12-02
  5 in total

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