The following pages link to Congenital myasthenic syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Lambert–Eaton myasthenic syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Myasthenia gravis (links | edit)
- Neuromyotonia (links | edit)
- Sphynx cat (links | edit)
- CMS (links | edit)
- Acetylcholine receptor (links | edit)
- Glycogen storage disease type V (links | edit)
- Glycogen storage disease (links | edit)
- Ephedrine (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Salbutamol (links | edit)
- Transferase (links | edit)
- Choline acetyltransferase (links | edit)
- Neuromuscular junction (links | edit)
- Nicotinic acetylcholine receptor (links | edit)
- Pyridostigmine (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Hypotonia (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Becker muscular dystrophy (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Myopathy (links | edit)
- Nemaline myopathy (links | edit)
- Channelopathy (links | edit)
- Facioscapulohumeral muscular dystrophy (links | edit)
- Myotonia congenita (links | edit)
- Mitochondrial myopathy (links | edit)
- Kearns–Sayre syndrome (links | edit)
- Hypertonia (links | edit)
- Walker–Warburg syndrome (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- MELAS syndrome (links | edit)
- Zaspopathy (links | edit)
- History of the Romani people (links | edit)
- Neuromuscular disease (links | edit)
- Centronuclear myopathy (links | edit)
- Agrin (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- Dok-7 (links | edit)
- MERRF syndrome (links | edit)
- Distal myopathy (links | edit)
- Micrognathism (links | edit)
- Amifampridine (links | edit)
- Myotonic dystrophy (links | edit)
- Endocrine disease (links | edit)
- Congenital myopathy (links | edit)
- Bethlem myopathy (links | edit)