Hereditary channelopathies in neurology

Advances in Experimental Medicine and Biology

Volumn 686, Issue , 2010, Pages 305-334

  Lehmann Horn, Frank ^a   Jurkat Rott, Karin ^b   Lerche, Holger ^b   Weber, Yvonne ^b  

^a UNIVERSITY OF ULM   (Germany)

^b NONE

Author keywords

Ataxia; Epilepsy; Migraine; Myasthenia; Myotonia; Neuromyotonia; Pain; Periodic paralysis

Indexed keywords

CALCIUM CHANNEL; CALCIUM CHANNEL T TYPE; CARBAMAZEPINE; CHLORIDE CHANNEL; DANTROLENE; FLECAINIDE; OXCARBAZEPINE; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNE3; POTASSIUM CHANNEL KV1.1; RYANODINE RECEPTOR 1; SODIUM CHANNEL NAV1.1; SODIUM CHANNEL NAV1.2; SODIUM CHANNEL NAV1.3; SODIUM CHANNEL NAV1.6; SODIUM CHANNEL NAV1.7; UNCLASSIFIED DRUG; ION CHANNEL;

ANDERSEN SYNDROME; ARTICLE; ATAXIA; CENTRAL CORE DISEASE; CHANNELOPATHY; CLINICAL FEATURE; CONGENITAL MYASTHENIC SYNDROME; EPILEPSY; FOCAL EPILEPSY; GENE MUTATION; GENETIC SUSCEPTIBILITY; HEREDITARY CHANNELOPATHY; HUMAN; HYPERREFLEXIA; HYPOKALEMIC PERIODIC PARALYSIS; MALIGNANT HYPERTHERMIA; MIGRAINE; MONOGENIC DISORDER; MULTIMINICORE DISEASE; MUSCLE WEAKNESS; MYOKYMIA; MYOTONIA; NEUROLOGY; NEUROPATHIC PAIN; NONHUMAN; PERIODIC PARALYSIS; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; SODIUM CHANNEL MYOTONIA; THOMSEN DISEASE; THYROTOXIC PERIODIC PARALYSIS; GENETICS; MUTATION; NEURALGIA; NEUROLOGIC DISEASE; PATHOLOGICAL REFLEX; RARE DISEASE; REVIEW; STARTLE REFLEX;

ATAXIA; EPILEPSY; HUMANS; ION CHANNELS; ISAACS SYNDROME; MALIGNANT HYPERTHERMIA; MIGRAINE DISORDERS; MUTATION; MYASTHENIC SYNDROMES, CONGENITAL; MYOPATHY, CENTRAL CORE; MYOTONIA CONGENITA; NERVOUS SYSTEM DISEASES; NEURALGIA; PARALYSES, FAMILIAL PERIODIC; RARE DISEASES; REFLEX, ABNORMAL; STARTLE REACTION;

EID: 79952109351     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-90-481-9485-8_18     Document Type: Article

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