Martin Helme The main article for this category is Channelopathy. Subcategories This category has only the following subcategory. C Cystic fibrosis (3 C, 28 P) Pages in category "Channelopathies" The following 51 pages are in this category, out of 51 total. This list may not reflect recent changes. * ChannelopathyA Achromatopsia Andersen–Tawil syndrome Autoimmune autonomic ganglionopathy Autosomal dominant nocturnal frontal lobe epilepsy Autosomal dominant polycystic kidney diseaseB Bartter syndrome Benign familial neonatal seizures Brugada syndromeC Calciumopathy Catecholaminergic polymorphic ventricular tachycardia Channelome Template:Channelopathy Childhood absence epilepsy Congenital hyperinsulinism Congenital insensitivity to pain Congenital stationary night blindness Cystic fibrosisD Dent's diseaseE Episodic ataxia ErythromelalgiaF Familial atrial fibrillation Familial hemiplegic migraine Focal segmental glomerulosclerosisG Generalized epilepsy with febrile seizures plusH Hemiplegic migraine Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Hypomagnesemia with secondary hypocalcemiaJ Juvenile myoclonic epilepsyL Lambert–Eaton myasthenic syndrome Long QT syndromeM Maculopathy Malignant hyperthermia Mucolipidosis type IV Myotonia congenitaN Nonsyndromic deafnessP Paramyotonia congenita Paroxysmal extreme pain disorder Periodic paralysis Posterior column ataxia-retinitis pigmentosa syndrome Potassium-aggravated myotonia PseudohypoaldosteronismR Retinitis pigmentosa Rolandic epilepsy Romano–Ward syndromeS Short QT syndrome Spinocerebellar ataxia type 6 Spinocerebellar ataxia type-13 Sporadic hemiplegic migraineT Timothy syndrome No tags for this post. Navigeerimine Raul KirjanenKivisildnik
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