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Showing 1 to 2 of 2 for “"Charcot-Marie-Syndrom"”.

  1. Molekulargenetik der autosomal rezessiven Charcot-Marie-Tooth-Neuropathie mit fokal gefalteten Myelinscheiden

    … motor and sensory neuropathies (HMSN) or Charcot-Marie-Tooth neuropathies are the most common hereditary neuromuscular disorder. In most families the disorder follows an autosomal dominant or X-linked mode of inheritance. Autosomal recessive HMSN (AR-HMSN) is rare in Western Europe, …

    aachen Repository record for Molekulargenetik der autosomal rezessiven Charcot-Marie-Tooth-Neuropathie mit fokal gefalteten Myelinscheiden (opens in a new tab)

  2. Klinik und Molekulargenetik der hereditären motorischen und sensiblen Neuropathien im Kindesalter

    Hereditary motor and sensory neuropathy (HMSN) or Charcot-Marie-Tooth (CMT) disease comprises a group of clinically and genetically heterogeneous disorders of the peripheral nervous system. With an overall prevalence of 1 in 2500, CMT is the most common inherited neuromuscular disorder in man. This …

    aachen Repository record for Klinik und Molekulargenetik der hereditären motorischen und sensiblen Neuropathien im Kindesalter (opens in a new tab)