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  • 34All Results
  • Evidence-Based Medicine GuidelinesEvidence-Based Medicine Guidelines
  • EE+ POEM ArchiveEE+ POEM Archive
  • Cochrane AbstractsCochrane Abstracts
Hereditary myopathies
34 results
1 - 34
  • EBMG Hereditary myopathies
    • Essentials
    • Suspicion of a myopathy
    • Myositis
      • Evidence Summaries
    • Mitochondrial myopathies
    • Metabolic myopathies
    • Secondary myopathies
    • Examination
    • Treatment and rehabilitation
      • Evidence Summaries
    • Myopathies in early childhood
    • Myodystrophies with nervous origin and spinal muscular atrophies
    • Inherited polyneuropathies and disorders of the neuromuscular junction
    • Progressive muscular dystrophies
    • Myotonic dystrophies
      • Evidence Summaries
    • Distal myopathies
  • EBMG Polyneuropathies
    • Hereditary neuropathies
  • EBMG Myositis
    • Differential diagnosis
    • Polymyositis (PM)
  • EBMG Rhabdomyolysis
    • Aetiology
  • CochraneCreatine for treating muscle disorders New search for studies and content updated (no change to conclusions)
    • Abstract
  • EBMG Neurological disorders and alcohol
    • Others
  • EBMG Peripheral neuropathies: examination of the patient
    • Differential diagnostics
  • EBMG Ptosis
    • Aetiology and clinical features
  • EBMG Developmental coordination disorder (DCD)
    • Diagnosis
  • EBMG Dyspnoea
    • Dyspnoea that has developed over weeks or months
  • EBMG Dysphagia and globus sensation (globus pharyngeus)
    • Aetiology of dysphagia
  • CochraneRespiratory muscle training in children and adults with neuromuscular disease New
    • Reviewer's Conclusions
  • EBMG Ventricular ectopic beats
    • Treatment
  • CochraneTreatment for inclusion body myositis: Cochrane systematic review
    • Abstract
  • EBMG Treatment of dyslipidaemias
    • Choice of medication based on type of dyslipidaemia
  • EBMG** Update Information **
    • Latest Update
  • 1 - 34 of 34 records
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