Latest papers

Hereditary episodic ataxias.

Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy.

Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob disease.

Autoimmune channelopathies: John Newsom-Davis's work and legacy. A summary of the Newsom-Davis Memorial Lecture 2008.

What's new in: "genetics in childhood epilepsy".

Channels active in the excitability of nerves and skeletal muscles across the neuromuscular junction: basic function and pathophysiology.

Common pathophysiologic mechanisms in migraine and epilepsy.

Ion channel diseases in children: manifestations and management.

Muscle channelopathies.

[Human calcium channelopathies. Voltage-gated Ca(2+) channels in etiology, pathogenesis, and pharmacotherapy of neurologic disorders].

Channelopathies in children and adults.

Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.

Slow inactivation: slow but not dull.

Channelopathies: a review.

Voltage-dependent Na(v)1.7 sodium channels: multiple roles in adrenal chromaffin cells and peripheral nervous system.

Drug-induced spatial dispersion of repolarization.

Critical illness myopathy: further evidence from muscle-fiber excitability studies of an acquired channelopathy.

Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy.

Genetics and epilepsy.

Altered functional expression of Purkinje cell calcium channels precedes motor dysfunction in tottering mice.