SCOPUS 정보 검색 플랫폼

Neurology

Volumn 77, Issue 22, 2011, Pages 1960-1964

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

(8) Matthews, E a Portaro, S b Ke, Q c Sud, R a Haworth, A a Davis, M B a Griggs, R C c Hanna, M G a

a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY (United Kingdom)

b UNIVERSITY OF MESSINA (Italy)

c UNIVERSITY OF ROCHESTER (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE;

ARTICLE; CLINICAL EVALUATION; DISEASE SEVERITY; DNA SEQUENCE; DRUG EFFICACY; GENE MUTATION; GENETIC ANALYSIS; GENETIC CORRELATION; GENOTYPE; HUMAN; HYPOKALEMIC PERIODIC PARALYSIS; MAJOR CLINICAL STUDY; MORBIDITY; PREDICTIVE VALUE; PRIORITY JOURNAL; RETROSPECTIVE STUDY; TREATMENT RESPONSE;

EID: 82955228816 PISSN: 00283878 EISSN: 1526632X Source Type: Journal
DOI: 10.1212/WNL.0b013e31823a0cb6 Document Type: Article

Times cited : (84)

References (14)

1
- 0028234647
- Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
- DOI 10.1016/0092-8674(94)90135-X
- Ptacek LJ, Tawil R, Griggs RC, et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994;77:863-868. (Pubitemid 24187684)
- (1994) Cell , vol.77 , Issue.6 , pp. 863-868
- Ptacek, L.J.¹ Tawil, R.² Griggs, R.C.³ Engel, A.G.⁴ Layzer, R.B.⁵ Kwiecinski, H.⁶ McManis, P.G.⁷ Santiago, L.⁸ Moore, M.⁹ Fouad, G.¹⁰ Bradley, P.¹¹ Leppert, M.F.¹²

2
- 0027965420
- A calcium channel mutation causing hypokalemic periodic paralysis
- Jurkat-Rott K, Lehmann-Horn F, Elbaz A, et al. A calcium channel mutation causing hypokalemic periodic paralysis. Hum Mol Genet 1994;3:1415-1419. (Pubitemid 24255482)
- (1994) Human Molecular Genetics , vol.3 , Issue.8 , pp. 1415-1419
- Jurkat-Rott, K.¹ Lehmann-Horn, F.² Elbaz, A.³ Heine, R.⁴ Gregg, R.G.⁵ Hogan, K.⁶ Powers, P.A.⁷ Lapie, P.⁸ Vale-Santos, J.E.⁹ Weissenbach, J.¹⁰ Fontaine, B.¹¹

3
- 0032801833
- A novel sodium channel mutation in a family with hypokalemic periodic paralysis
- Bulman DE, Scoggan KA, van Oene MD, et al. A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology 1999;53: 1932-1936.
- (1999) Neurology , vol.53 , pp. 1932-1936
- Bulman, D.E.¹ Scoggan, K.A.² Van Oene, M.D.³

4
- 67649397890
- Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
- Matthews E, Labrum R, Sweeney MG, et al. Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis. Neurology 2009;72:1544-1547.
- (2009) Neurology , vol.72 , pp. 1544-1547
- Matthews, E.¹ Labrum, R.² Sweeney, M.G.³

5
- 0014413462
- Acetazolamide prophylaxis in hypokalemic periodic paralysis
- Resnick JS, Engel WK, Griggs RC, Stam AC. Acetazolamide prophylaxis in hypokalemic periodic paralysis. N Engl J Med 1968;278:582-586.
- (1968) N Engl J Med , vol.278 , pp. 582-586
- Resnick, J.S.¹ Engel, W.K.² Griggs, R.C.³ Stam, A.C.⁴

6
- 8844247914
- SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide
- Venance SL, Jurkat-Rott K, Lehmann-Horn F, Tawil R. SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide. Neurology 2004;63: 1977. (Pubitemid 39532410)
- (2004) Neurology , vol.63 , Issue.10 , pp. 1977
- Venance, S.L.¹ Jurkat-Rott, K.² Lehmann-Horn, F.³ Tawil, R.⁴

7
- 10444273389
- New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
- Vicart S, Sternberg D, Fournier E, et al. New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 2004;63:2120-2127. (Pubitemid 39636261)
- (2004) Neurology , vol.63 , Issue.11 , pp. 2120-2127
- Vicart, S.¹ Sternberg, D.² Fournier, E.³ Ochsner, F.⁴ Laforet, P.⁵ Kuntzer, T.⁶ Eymard, B.⁷ Hainque, B.⁸ Fontaine, B.⁹

8
- 0033958202
- Randomized trials of dichlorphenamide in the periodic paralyses
- DOI 10.1002/1531-8249(200001)47:1<46::AID-ANA9>3.0.CO;2-H
- Tawil R, McDermott MP, Brown R Jr, et al. Randomized trials of dichlorphenamide in the periodic paralyses: Working Group on Periodic Paralysis. Ann Neurol 2000;47:46-53. (Pubitemid 30033649)
- (2000) Annals of Neurology , vol.47 , Issue.1 , pp. 46-53
- Tawil, R.¹ McDermott, M.P.² Brown Jr., R.³ Shapiro, B.C.⁴ Ptacek, L.J.⁵ McManis, P.G.⁶ Dalakas, M.C.⁷ Spector, S.A.⁸ Mendell, J.R.⁹ Hahn, A.F.¹⁰ Griggs, R.C.¹¹

9
- 44949154442
- Treatment for periodic paralysis
- Sansone V, Meola G, Links TP, Panzeri M, Rose MR. Treatment for periodic paralysis. Cochrane Database Syst Rev 2008;1:CD005045.
- (2008) Cochrane Database Syst Rev , vol.1
- Sansone, V.¹ Meola, G.² Links, T.P.³ Panzeri, M.⁴ Rose, M.R.⁵

10
- 0036211354
- + channel mutations causing hypokalaemic periodic paralysis type II
- + channel mutations causing hypokalaemic periodic paralysis type II. Brain 2002;125:835-843. (Pubitemid 34279778)
- (2002) Brain , vol.125 , Issue.4 , pp. 835-843
- Kuzmenkin, A.¹ Muncan, V.² Jurkat-Rott, K.³ Hang, C.⁴ Lerche, H.⁵ Lehmann-Horn, F.⁶ Mitrovic, N.⁷

11
- 34347211819
- + channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore
- DOI 10.1085/jgp.200709755
- + channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore. J Gen Physiol 2007;130: 11-20. (Pubitemid 47001069)
- (2007) Journal of General Physiology , vol.130 , Issue.1 , pp. 11-20
- Struyk, A.F.¹ Cannon, S.C.²

12
- 33847344389
- Gating pore current in an inherited ion channelopathy
- DOI 10.1038/nature05598, PII NATURE05598
- Sokolov S, Scheuer T, Catterall WA. Gating pore current in an inherited ion channelopathy. Nature 2007; 446:76-78. (Pubitemid 46348048)
- (2007) Nature , vol.446 , Issue.7131 , pp. 76-78
- Sokolov, S.¹ Scheuer, T.² Catterall, W.A.³

13
- 77954529022
- Muscle channelopathies: Does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?
- Matthews E, Hanna MG. Muscle channelopathies: Does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis? J Physiol 2010; 588:1879 -1886.
- (2010) J Physiol , vol.588 , pp. 1879-1886
- Matthews, E.¹ Hanna, M.G.²

14
- 30344434616
- The primary periodic paralyses: Diagnosis, pathogenesis and treatment
- DOI 10.1093/brain/awh639
- Venance SL, Cannon SC, Fialho D, et al. The primary periodic paralyses: Diagnosis, pathogenesis and treatment. Brain 2006;129:8-17. (Pubitemid 43063755)
- (2006) Brain , vol.129 , Issue.1 , pp. 8-17
- Venance, S.L.¹ Cannon, S.C.² Fialho, D.³ Fontaine, B.⁴ Hanna, M.G.⁵ Ptacek, L.J.⁶ Tristani-Firouzi, M.⁷ Tawil, R.⁸ Griggs, R.C.⁹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.