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Results 1 - 6 of 6 for "Charcot-Marie-Tooth" "disease," dominant intermediate C
  1. ... vocal cord paresis, autosomal recessive Genetic Testing Registry: Charcot-Marie-Tooth disease, dominant intermediate c Genetic Testing Registry: Charcot-Marie-Tooth disease, dominant ...
  2. ... spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal muscular ... disease Friedreich’s ataxia Dejerine-Sottas disease Metabolic Diseases ...
  3. Charcot-Marie-Tooth and Related Diseases (Muscular Dystrophy Association) - PDF  
    ... spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal ... Charcot-Marie-Tooth disease Friedreich’s ataxia Dejerine-Sottas disease MDA’s Purpose ...
  4. Myotonic Muscular Dystrophy (Muscular Dystrophy Association) - PDF  
    ... spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal muscular ... disease Friedreich’s ataxia Dejerine-Sottas disease Metabolic Diseases ...
  5. Limb-Girdle Muscular Dystrophies (LGMD) (Muscular Dystrophy Association) - PDF  
    ... spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal muscular ... disease Friedreich’s ataxia Dejerine-Sottas disease Metabolic Diseases ...
  6. ... spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal muscular ... disease Friedreich’s ataxia Dejerine-Sottas disease Metabolic Diseases ...