Neurological potassium channelopathies

QJM: An International Journal of Medicine

Volumn 93, Issue 12, 2000, Pages 787-797

  Benatar, M ^a  

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE; ACETYLCHOLINE; ADENOSINE TRIPHOSPHATE; ANTIBODY; ANTICONVULSIVE AGENT; CALCIUM ION; CHLORIDE ION; NEUROTRANSMITTER; POTASSIUM CHANNEL; POTASSIUM ION; SODIUM ION;

ALPHA CHAIN; ANIMAL CELL; ATAXIA; BENIGN CHILDHOOD EPILEPSY; BETA CHAIN; CONTROLLED STUDY; GENE MUTATION; HUMAN; HYPOKALEMIC PERIODIC PARALYSIS; ION PERMEABILITY; LONG QT SYNDROME; MEMBRANE DEPOLARIZATION; MEMBRANE STEADY POTENTIAL; MOUSE; MUSCLE EXCITATION; MYOKYMIA; NERVE POTENTIAL; NEUROLOGIC DISEASE; NEUROTRANSMITTER RELEASE; NONHUMAN; POTASSIUM CURRENT; POTASSIUM TRANSPORT; PRIORITY JOURNAL; RAT; REPOLARIZATION; REVIEW;

EID: 0033638751     PISSN: 14602725     EISSN: None     Source Type: Journal    
DOI: 10.1093/qjmed/93.12.787     Document Type: Review

References (46)

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2. + channel β-subunit
3. Cloned potassium channels from eukaryotes and prokaryotes
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5. Morvan's fibrillary chorea: A paraneoplastic manifestation of thymoma
6. A syndrome of continuous muscle-fibre activity
7. Electromyographic and nerve conduction findings in a patient with neuromyotonia, normocalcaemic tetancy and small-cell lung cancer
8. Autoimmune aetiology for acquired neuromyotonia (Isaacs' syndrome)
9. + channels of peripheral nerves
10. + channels are implicated in neuromyotonia
11. Serum of Isaac's syndrome suppresses potassium channels in PC12 cell lines
12. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
13. Episodic ataxia mutations in KV1.1 alter potassium channel function by dominant negative effects or haploinsufficiency
14. Episodic ataxia results from voltage-dependent potassium channels with altered function
15. Ultrastructural localization of Shaker-related potassium channel subunits and synapse-associated protein 90 to sepate-like junctions in rat cerebellar Pinceaux
16. Patch-clamp recordings from cerebellar basket cell bodies and their presynaptic terminals reveal an asymmetric distribution of voltage-gated potassium channels
17. A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
18. Seizure characteristics in chromosome 20 benign familial neonatal convulsions
19. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
20. A novel potassium channel gene, KNQ2, is mutated in an inherited epilepsy of newborns
21. A potassium channel mutation in neonatal human epilepsy
22. + channels cause epilepsy
23. KCNQ2 and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel
24. + current due to a novel mutation in KCNQ2 causes neonatal convulsions
25. Molecular basis of the long-QT syndrome associated with deafness
26. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
27. KCNE1 mutations cause Jervell and Lange-Nielsen syndrome
28. IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
29. Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome
30. + channel mutations found in inherited cardiac arrhythmias
31. Mutations in the hminK gene cause long QT syndrome and suppress I(KS) function
32. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
33. Dihydropyridine receptor mutations cause hypokalaemic periodic paralysis
34. Calcium channelopathies
35. Potassium channels in hypokalaemic periodic paralysis: A key to the pathogenesis?
36. + channels in patients with hypokalemic periodic paralysis
37. + current
38. +-depleted rat, an animal model of hypokalemic periodic paralysis
39. Trial of the prophylactive effect of diazoxide in the treatment of familial periodic hypkalemia
40. Ion channel defects and aberrant excitability in myotonia and periodic paralysis
41. Ion channel genes and human neurological disease: Recent progress, prospects and challenges
42. Isolation of a potassium channel gene, hSKCa3, containing polymorphic CAG repeat: A candidate gene for schizophrenia and bipolar disorder
43. A piece in the puzzle: An ion channel candidate gene for schizophrenia
44. A gene for autosomal dominant paraxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2cM between D1S443 and S1S197
45. Abnormal function of potassium channels in platelets of patients with Alzheimer's disease