Literature DB >> 14314241

MUSCLE LACTATE DEHYDROGENASE PATTERNS IN TWO TYPES OF X-LINKED MUSCULAR DYSTROPHY.

C M PEARSON, N C KAR, J B PETER, T L MUNSAT.   

Abstract

Keywords:  CHILD; ELECTROPHORESIS; GENETICS, HUMAN; LACTATE DEHYDROGENASE; MUSCLES; MUSCULAR DYSTROPHY; PATHOLOGY

Mesh：

Substances：

Year:  1965        PMID： 14314241     DOI： 10.1016/0002-9343(65)90248-2

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  4 in total

1.  [Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

Authors:  H Moser
Journal:  Humangenetik       Date:  1971

2.  [A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].

Authors:  H W Rotthauwe; S Kowalewski
Journal:  Humangenetik       Date:  1966

3.  LDH isozyme pattern in induced muscle disease (Coxsackie Group A virus infection).

Authors:  S Kelly; A Belorit
Journal:  Experientia       Date:  1967-07-15

4.  [Congenital muscular dystrophy].

Authors:  F Vassella; M Mumenthaler; E Rossi; H Moser; U Wiesmann
Journal:  Dtsch Z Nervenheilkd       Date:  1967
  4 in total

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