Misplaced Pages

The following pages link to Paramyotonia congenita

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Showing 50 items.

• Bartter syndrome (links | edit)
• Neuromuscular disease (links | edit)
• Ion transporter (links | edit)
• Vitelliform macular dystrophy (links | edit)
• Centronuclear myopathy (links | edit)
• Congenital absence of the vas deferens (links | edit)
• Pseudohypoaldosteronism (links | edit)
• Emery–Dreifuss muscular dystrophy (links | edit)
• MERRF syndrome (links | edit)
• Mucolipidosis type IV (links | edit)
• Distal myopathy (links | edit)
• Generalized epilepsy with febrile seizures plus (links | edit)
• Nav1.4 (links | edit)
• Benign familial neonatal seizures (links | edit)
• Catecholaminergic polymorphic ventricular tachycardia (links | edit)
• Spinocerebellar ataxia type 6 (links | edit)
• Episodic ataxia (links | edit)
• Spinocerebellar ataxia type-13 (links | edit)
• Congenital stationary night blindness (links | edit)
• Myotonic dystrophy (links | edit)
• Familial atrial fibrillation (links | edit)
• Congenital myopathy (links | edit)
• Bethlem myopathy (links | edit)
• Dent's disease (links | edit)
• Paramyotonia Congenita (redirect page) (links | edit)
  • Misplaced Pages:WikiProject Medicine/Neurology task force/List of articles (links | edit)
• Potassium-aggravated myotonia (links | edit)
• Eulenburg Disease (redirect page) (links | edit)
• Paralysis periodica paramyotonia (redirect page) (links | edit)
• Paramyotonia congenita of von Eulenburg (redirect page) (links | edit)
  • List of diseases (P) (links | edit)
• Von Eulenberg's disease (redirect page) (links | edit)
• Albert Eulenburg (links | edit)
• Chronic progressive external ophthalmoplegia (links | edit)
• Paroxysmal extreme pain disorder (links | edit)
• Thyrotoxic myopathy (links | edit)
• Oculodentodigital dysplasia (links | edit)
• Central core disease (links | edit)
• Ocular albinism (links | edit)
• Neuromuscular junction disease (links | edit)
• Metabolic myopathy (links | edit)
• Ichthyosis hystrix (links | edit)
• Erythrokeratodermia variabilis (links | edit)
• Keratitis–ichthyosis–deafness syndrome (links | edit)
• Clouston's hidrotic ectodermal dysplasia (links | edit)
• Progressive symmetric erythrokeratodermia (links | edit)
• Transient neonatal diabetes (links | edit)
• EAST syndrome (links | edit)
• Ullrich congenital muscular dystrophy (links | edit)
• X-linked myotubular myopathy (links | edit)
• Bart–Pumphrey syndrome (links | edit)
• Thyrotoxic periodic paralysis (links | edit)