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Ueber atypische Formen der Thomsen'schen Krankheit (Myotonia congenita)


Ueber atypische Formen der Thomsen'schen Krankheit (Myotonia congenita)



European Archives of Psychiatry and Clinical Neuroscience 42(2): 704-751



ISSN/ISBN: 0940-1334

DOI: 10.1007/bf02231515


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(PDF emailed within 0-6 h: $19.90)

Accession: 060589955

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Related references

Zur Histologie des myotonisch hypertrophischen Muskels der Thomsen'schen Krankheit (Myotonia congenita). Virchows Archiv 163(3): 380-403, 1901

Eine Familie Mit Myotonia Congenita (Thomsen'sche Krankheit). Genetica 17(3-4): 253-269, 1935

Mutations in the CLCN1 gene leading to myotonia congenita Thomsen and generalized myotonia Becker. American Journal of Human Genetics 55(3 Suppl. ): A226, 1994

The Identity Of Myotonia Congenita (Thomsen'S Disease), Dystrophia Myotonica (Myotonia Atrophica) And Paramyotonia. Brain 62(2): 198-212, 1939

Ein casuistischer Beitrag zur Lehre von der Thomsen'schen Krankheit. Journal of Neurology 15(3-4): 274-285, 1899

A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita thomsen. Acta Neurologica Scandinavica 51(3): 225-232, 1975

Thomsen and myotonia congenita. Medical History 12(2): 190-194, 1968

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Heterogeneity of dominant myotonia congenita thomsen. American Journal of Human Genetics 27(6): 17A, 1975