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Literature DB >> 11207185

Ion channels and neurology.

S M Zuberi¹, M G Hanna.

Abstract

Mesh：

Substances：
Ion Channels

Year: 2001 PMID： 11207185 PMCID： PMC1718682 DOI： 10.1136/adc.84.3.277

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

Keyword Cloud
References

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23 in total

1. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Authors: A Escayg; B T MacDonald; M H Meisler; S Baulac; G Huberfeld; I An-Gourfinkel; A Brice; E LeGuern; B Moulard; D Chaigne; C Buresi; A Malafosse
Journal: Nat Genet Date: 2000-04 Impact factor: 38.330

2. A quantitative description of membrane current and its application to conduction and excitation in nerve.

Authors: A L HODGKIN; A F HUXLEY
Journal: J Physiol Date: 1952-08 Impact factor: 5.182

3. Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.

Authors: R Singh; I E Scheffer; K Crossland; S F Berkovic
Journal: Ann Neurol Date: 1999-01 Impact factor: 10.422

4. KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.

Authors: H S Wang; Z Pan; W Shi; B S Brown; R S Wymore; I S Cohen; J E Dixon; D McKinnon
Journal: Science Date: 1998-12-04 Impact factor: 47.728

Review 5. Calcium channels in neurological disease.

Authors: D A Greenberg
Journal: Ann Neurol Date: 1997-09 Impact factor: 10.422

6. A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

Authors: S M Zuberi; L H Eunson; A Spauschus; R De Silva; J Tolmie; N W Wood; R C McWilliam; J B Stephenson; J P Stephenson; D M Kullmann; M G Hanna
Journal: Brain Date: 1999-05 Impact factor: 13.501

Ion channels and neurology.

1. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

2. A quantitative description of membrane current and its application to conduction and excitation in nerve.

3. Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.

4. KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.

Review 5. Calcium channels in neurological disease.

6. A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

7. Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.

8. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

9. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

10. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.