Table of contents of journal:

Results: 13

Sodium and calcium channelopathies of sarcolemma: periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia

Authors: Mitrovic, N Lerche, H

Citation: N. Mitrovic et H. Lerche, Sodium and calcium channelopathies of sarcolemma: periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 3-32

Muscle chloride channelopathies: myotonia congenita

Authors: Rudel, R

Citation: R. Rudel, Muscle chloride channelopathies: myotonia congenita, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 33-53

Molecular aspects of malignant hyperthermia and central core disease

Authors: Lynch, PJ McCarthy, TV

Citation: Pj. Lynch et Tv. Mccarthy, Molecular aspects of malignant hyperthermia and central core disease, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 55-84

Mutations affecting muscle nicotinic acetylcholine receptors and their role in congenital myasthenic syndromes

Authors: Beeson, D Newsom-Davis, J

Citation: D. Beeson et J. Newsom-davis, Mutations affecting muscle nicotinic acetylcholine receptors and their role in congenital myasthenic syndromes, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 85-114

Ion channel defects in primary electrical diseases of the heart

Authors: Kirsch, GE

Citation: Ge. Kirsch, Ion channel defects in primary electrical diseases of the heart, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 115-151

Migraine and ataxias

Authors: Ducros, A Denier, C Tournier-Lasserve, E

Citation: A. Ducros et al., Migraine and ataxias, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 155-179

Genetic analysis of idiopathic epilepsies: the role of ion channel mutations

Authors: Steinlein, OK

Citation: Ok. Steinlein, Genetic analysis of idiopathic epilepsies: the role of ion channel mutations, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 181-197

The inhibitory glycine receptor as a model of hereditary channelopathies

Authors: Becker, K Becker, CM Breitinger, HG

Citation: K. Becker et al., The inhibitory glycine receptor as a model of hereditary channelopathies, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 199-224

Cystic fibrosis

Authors: Greger, R

Citation: R. Greger, Cystic fibrosis, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 227-253

Dent's disease: an hereditary nephrolithiasis caused by dysfunction of a voltage-gated chloride channel

Authors: Fahlke, C

Citation: C. Fahlke, Dent's disease: an hereditary nephrolithiasis caused by dysfunction of a voltage-gated chloride channel, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 255-276

Liddle's syndrome and pseudohypoaldosteronism type I

Authors: Grunder, S

Citation: S. Grunder, Liddle's syndrome and pseudohypoaldosteronism type I, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 277-297

The role of ATP-sensitive K+ channels in familial hyperinsulinism

Authors: Glaser, B Aguilar-Bryan, L

Citation: B. Glaser et L. Aguilar-bryan, The role of ATP-sensitive K+ channels in familial hyperinsulinism, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 299-325

Hereditary hypokalemic salt-losing tubulopathies

Authors: Jeck, N Konrad, M Seyberth, HW

Citation: N. Jeck et al., Hereditary hypokalemic salt-losing tubulopathies, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 327-354

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