| Document Date: 2009-04-24 10:06:07
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MedicalCondition Nemaline myopathy / Congenital myotonic dystrophy / Fibre-type disproportion Non-specific myopathy Mitochondrial myopathies Lipid storage myopathies / Emery-Dreifuss syndrome / Chronic inflammatory demyelinating / muscular dystrophy / Myotonia / Congenital Myopathies / Schwartz-Jampel syndrome / Periodic paralysis / Central core disease / Dominant SMA variants Hereditary / muscular atrophies / phosphofructokinase deficiency / Myotonic dystrophy / Charcot-Marie-Tooth disease / muscular atrophy Inflammatory / Inclusion body myositis / Pseudomyotonia / core disease / Carnitine palmityl transferase deficiency / Kugelberg Welander disease / Neuromyotonia / Adult spinal muscular atrophy / Pompe’s disease / peripheral neuropathy / polyneuropathy / Limb-girdle muscular dystrophies Myotonic disorders / Glycogen storage disease / phosporylase deficiency / Myositis / acid maltase deficiency / Muscular dystrophies / Juvenile dermatomyositis / Carnitine deficiency / Guillain Barre syndrome / Werdnig Hoffman disease / metabolic disorders / Myofibrillar myopathies / Kennedy’s syndrome / Myotubular (centronuclear) myopathy / connective tissue disease / Congenital muscular dystrophies / brancher enzyme deficiency / Dermatomyositis / CIDP / debrancher enzyme deficiency / Myasthenia gravis / Polymyositis / Disorders / Paramyotonia congenita / / Person Cori Forbes / /
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MC32V1 December 2006/Updated April 08