Literature DB >> 13339316

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Abstract

Keywords:  PARALYSIS/differential diagnosis

Mesh：

Year:  1956        PMID： 13339316

Source DB:  PubMed          Journal:  Acta Paediatr Suppl        ISSN： 0365-5741


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  19 in total

1.  [AN UNUSUAL VARIATION OF VACUOLAR DEGENERATION OF STRIATED SKELETAL MUSCLE].

Authors:  F MITTELBACH
Journal:  Acta Neuropathol       Date:  1964-05-05       Impact factor: 17.088

2.  [On the hypokalemic form of paroxysmal paralysis. On the problem hereditary of episodic adynamial].

Authors:  G BEKENY; T HASZNOS; F SOLTI
Journal:  Dtsch Z Nervenheilkd       Date:  1961

3.  [ON THE ELECTROLYTE AND ALDOSTERONE METABOLISM IN ADYNAMIA EPISODICA HEREDITARIA, THE HYPERKALEMIC FORM OF PERIODIC PARALYSIS].

Authors:  H G MERTENS; K SCHIMRIGK; U VOLKWEIN; K D VOIGT
Journal:  Klin Wochenschr       Date:  1964-01-15

4.  [Role of adosterone in paroxysmal paralysis].

Authors:  H DIECKMANN; H G MERTENS; K D VOIGT; U VOLKWEIN
Journal:  Klin Wochenschr       Date:  1963-02-15

5.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1957-12       Impact factor: 11.025

6.  Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

Authors:  F Lehmann-Horn; P A Iaizzo; H Hatt; C Franke
Journal:  Pflugers Arch       Date:  1991-04       Impact factor: 3.657

7.  Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis.

Authors:  T S Danowski; E R Fisher; C Vidalon; J W Vester; R Thompson; S Nolan; T Stephan; J H Sunder
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

8.  Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

Authors:  M C Koch; K Ricker; M Otto; T Grimm; K Bender; B Zoll; P S Harper; F Lehmann-Horn; R Rüdel; E P Hoffman
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

9.  Histochemistry and electron microscopy of muscle fibres in a case of congenital paramyotonia.

Authors:  D Schiffer; M T Giordana; G Monga; F Mollo
Journal:  J Neurol       Date:  1976-01-14       Impact factor: 4.849

10.  Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19.

Authors:  M Koch; H Harley; M Sarfarazi; K Bender; T Wienker; B Zoll; P S Harper
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132
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