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Results 1 - 10 of 23 for Inclusion body myopathy 2
  1. Genetics Home Reference: Inclusion body myopathy 2 From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Inclusion body myopathy 2 On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Muscle Disorders (National Library of Medicine)  
    Your muscles help you move and help your body work. Different types of muscles have different jobs. There are many problems that can affect muscles. Muscle ...
  3. ... Miyoshi distal myopathy dysferlin abnormalities recessive Nonaka distal myopathy; also called hereditary inclusion-body myositis type 2 (HIBM2) GNE abnormalities recessive Gowers-Laing distal myopathy ...
  4. ... idiopathic inflammatory myopathy? The incidence of idiopathic ... inclusion body myositis is more common in men. What genes ...
  5. Inflammatory Myopathies From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... can occur in children between the ages of 2 and 15 years. Inclusion body myositis usually affects individuals over age 50. What are the signs and symptoms? General symptoms of chronic inflammatory myopathy include slow but progressive muscle weakness that starts ...
  6. Friedreich's Ataxia (FA) (Muscular Dystrophy Association) - PDF  
    ... Werdnig-Hoffmann disease) Intermediate spinal muscular atrophy (Type 2) ... Diseases of Neuromuscular Junction Myasthenia gravis Lambert- ...
  7. Mitochondrial Myopathies (Muscular Dystrophy Association) - PDF  
    ... Werdnig-Hoffmann disease) Intermediate spinal muscular atrophy (Type 2) ... Diseases of Neuromuscular Junction Myasthenia gravis Lambert- ...
  8. Genetics and Neuromuscular Diseases (Muscular Dystrophy Association) - PDF  
    ... Werdnig-Hoffmann disease) Intermediate spinal muscular atrophy (Type 2) ... Diseases of Neuromuscular Junction Myasthenia gravis Lambert- ...
  9. ... Werdnig-Hoffmann disease) Intermediate spinal muscular atrophy (Type 2) ... Diseases of neuromuscular Junction Myasthenia gravis Lambert- ...
  10. Spinal Muscular Atrophy (SMA) (Muscular Dystrophy Association) - PDF  
    ... Werdnig-Hoffmann disease) Intermediate spinal muscular atrophy (Type 2) ... Diseases of Neuromuscular Junction Myasthenia gravis Lambert- ...
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