Literature DB >> 14092155

[ON THE GENETICS OF MYOTONIAS (A PRELIMINARY SURVEY)].

P E BECKER.   

Abstract

Entities:  

Keywords:  EPIDEMIOLOGY; GENETICS, HUMAN; GERMANY, WEST; MYOTONIA; MYOTONIA ATROPHICA; MYOTONIA CONGENITA; PARALYSIS, FAMILIAL PERIODIC

Mesh：

Year:  1963        PMID： 14092155

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN： 0020-9554            Impact factor:   0.743


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  8 in total

1.  [MYOTONIA AND KLINEFELTER SYNDROME].

Authors:  P E BECKER; P EBERLE
Journal:  Humangenetik       Date:  1964

2.  [CHROMOSOME STUDIES IN MYOTONIA].

Authors:  P EBERLE; P E BECKER
Journal:  Humangenetik       Date:  1964

3.  Recessively inherited myotonia congenita.

Authors:  P S Harper; D M Johnston
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

4.  [Overexcitability of the gamma-motor neurons in "stiff-man" syndrome].

Authors:  H G Mertens; K Ricker
Journal:  Klin Wochenschr       Date:  1968-01-01

5.  [Biochemical characteristics and differences in autosomal dominant and autosomal recessive myotonia congenita].

Authors:  E Kuhn; D Seiler
Journal:  Klin Wochenschr       Date:  1970-09-15

6.  [Metabolic studies and exchange of 42 K in a case of periodic hyperkalemic paralysis with myotonic symptoms].

Authors:  W Ulbricht; W Schwartzkopff
Journal:  Dtsch Z Nervenheilkd       Date:  1969

7.  [Genetic contribution to the problem of the late form of Pelizaeus-Merzbacher disease].

Authors:  E Zerbin-Rüdin; J Peiffer
Journal:  Humangenetik       Date:  1964

8.  [Comparative studies of endocrine glands and enzyme activities in dystrophia myotonica and myotonia congenita].

Authors:  K Schimrigk; D Matzelt; H G Mertens
Journal:  Klin Wochenschr       Date:  1966-01-15
  8 in total

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