-
1
-
-
0033594502
-
Mutations of sodium channels in periodic paralysis
-
Robert C, Griggs M, Louis J. Mutations of sodium channels in periodic paralysis. Neurology 1999; 52: 1309-1310.
-
(1999)
Neurology
, vol.52
, pp. 1309-1310
-
-
Robert, C.1
Griggs, M.2
Louis, J.3
-
2
-
-
0141740617
-
Severe in fantile hyperkalaemic periodic paralysis and paramyotonia congenita: Broadening the clinical spectrum associated with the T704M mutation in SCN4A
-
Brancati F, Valente EM, Davies NP, Sarkozy A, Sweeney MG, LoMonaco M, et al. Severe in fantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A. J Neurol Neurosurg Psychiatry 2003; 74: 1339-1341.
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, pp. 1339-1341
-
-
Brancati, F.1
Valente, E.M.2
Davies, N.P.3
Sarkozy, A.4
Sweeney, M.G.5
LoMonaco, M.6
-
3
-
-
0025649547
-
Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene
-
Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, et al. Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene. Science 1990; 250: 1000-1002.
-
(1990)
Science
, vol.250
, pp. 1000-1002
-
-
Fontaine, B.1
Khurana, T.S.2
Hoffman, E.P.3
Bruns, G.A.4
Haines, J.L.5
Trofatter, J.A.6
-
4
-
-
0035833968
-
Sodium channel gene hypokalemic periodic paralysis: An uncommon cause in the UK
-
Davies NP, Eunson LH, Samuel M, Hanna MG. Sodium channel gene hypokalemic periodic paralysis: An uncommon cause in the UK. Neurology 2001; 57: 1323-1325.
-
(2001)
Neurology
, vol.57
, pp. 1323-1325
-
-
Davies, N.P.1
Eunson, L.H.2
Samuel, M.3
Hanna, M.G.4
-
6
-
-
0024368695
-
Structural parts involved in activation and inactivation of the sodium channel
-
Stühmer W, Conti F, Suzuki H, Wang XD, Noda M, Yahagi N, et al. Structural parts involved in activation and inactivation of the sodium channel. Nature 1989; 339: 597-603.
-
(1989)
Nature
, vol.339
, pp. 597-603
-
-
Stühmer, W.1
Conti, F.2
Suzuki, H.3
Wang, X.D.4
Noda, M.5
Yahagi, N.6
-
7
-
-
0033594502
-
Mutations of sodium channels in periodic paralysis
-
Robert C, Griggs M, Louis J. Mutations of sodium channels in periodic paralysis. Neurology 1999; 52: 1309-1310.
-
(1999)
Neurology
, vol.52
, pp. 1309-1310
-
-
Robert, C.1
Griggs, M.2
Louis, J.3
-
8
-
-
0037336637
-
Crucial role of sodium channel fast inactivation in muscle fibre inexcitability in a rat model of critical illness myopathy
-
Rich MM, Pinter MJ. Crucial role of sodium channel fast inactivation in muscle fibre inexcitability in a rat model of critical illness myopathy. J Physiol 2003; 547: 555-566.
-
(2003)
J Physiol
, vol.547
, pp. 555-566
-
-
Rich, M.M.1
Pinter, M.J.2
-
9
-
-
0035788438
-
Hyperkalemic periodic paralysis and paramyotonia congenita-a novel sodium channel mutation
-
Okuda S, Kanda F, Nishimoto K, Sasaki R, Chihara K. Hyperkalemic periodic paralysis and paramyotonia congenita-a novel sodium channel mutation. J Neurol 2001; 248: 1003-1004.
-
(2001)
J Neurol
, vol.248
, pp. 1003-1004
-
-
Okuda, S.1
Kanda, F.2
Nishimoto, K.3
Sasaki, R.4
Chihara, K.5
-
10
-
-
0023182476
-
AAEE minimonograph #27: Differential diagnosis of myotonic syndromes
-
Streib EW. AAEE minimonograph #27: differential diagnosis of myotonic syndromes. Muscle Nerve 1987; 10: 603-615.
-
(1987)
Muscle Nerve
, vol.10
, pp. 603-615
-
-
Streib, E.W.1
-
11
-
-
37049022801
-
Muscle membrane excitability after exercise in thyrotoxic periodic paralysis and thyrotoxicosis without periodic paralysis
-
Arimura K, Arimura Y, Ng AR, Sakoda S, Higuchi I. Muscle membrane excitability after exercise in thyrotoxic periodic paralysis and thyrotoxicosis without periodic paralysis. Muscle Nerve 2007; 36: 784-788.
-
(2007)
Muscle Nerve
, vol.36
, pp. 784-788
-
-
Arimura, K.1
Arimura, Y.2
Ng, A.R.3
Sakoda, S.4
Higuchi, I.5
-
12
-
-
33845962509
-
Exercise test in the inter-attack period of thyrotoxic periodic paralysis: A useful diagnostic tool
-
Tsai MH, Chang WN, Lu CH, Chuang YC, Chen SD, Lee LH, et al. Exercise test in the inter-attack period of thyrotoxic periodic paralysis: a useful diagnostic tool. Acta Neurol Taiwan 2006; 15: 259-263.
-
(2006)
Acta Neurol Taiwan
, vol.15
, pp. 259-263
-
-
Tsai, M.H.1
Chang, W.N.2
Lu, C.H.3
Chuang, Y.C.4
Chen, S.D.5
Lee, L.H.6
-
14
-
-
0037121146
-
Hypokalemic periodic paralysis: Exercise test
-
Santiago-Pérez S, Pérez-Conde MC. Hypokalemic periodic paralysis: exercise test. Rev Neurol 2002; 35: 738-740.
-
(2002)
Rev Neurol
, vol.35
, pp. 738-740
-
-
Santiago-Pérez, S.1
Pérez-Conde, M.C.2
-
15
-
-
0035039125
-
Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica
-
Kim J, Hahn Y, Sohn EH, Lee YJ, Yun JH, Kim JM, et al. Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica. J Neurol Neurosurg Psychiatry 2001; 70: 618-623.
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.70
, pp. 618-623
-
-
Kim, J.1
Hahn, Y.2
Sohn, E.H.3
Lee, Y.J.4
Yun, J.H.5
Kim, J.M.6
-
16
-
-
33745617091
-
Paralysis periodica paramyotonica caused by SCN4A Arg1448Cys mutation
-
Hsu WC, Huang YC, Wang CW, Hsueh CH, Lai LP, Yeh JH. Paralysis periodica paramyotonica caused by SCN4A Arg1448Cys mutation. J Formos Med Assoc 2006; 105: 503-507.
-
(2006)
J Formos Med Assoc
, vol.105
, pp. 503-507
-
-
Hsu, W.C.1
Huang, Y.C.2
Wang, C.W.3
Hsueh, C.H.4
Lai, L.P.5
Yeh, J.H.6
-
17
-
-
0033947677
-
Exercise test in muscle channelopathies and other muscle disorders
-
Kuntzer T, Flocard F, Vial C, Kohler A, Magistris M, Labarre-Vila A, et al. Exercise test in muscle channelopathies and other muscle disorders. Muscle Nerve 2000; 23: 1089-1094.
-
(2000)
Muscle Nerve
, vol.23
, pp. 1089-1094
-
-
Kuntzer, T.1
Flocard, F.2
Vial, C.3
Kohler, A.4
Magistris, M.5
Labarre-Vila, A.6
-
18
-
-
9144223871
-
Electromyography guides toward subgroups of mutations in muscle channelopathies
-
Fournier E, Arzel M, Sternberg D, Vicart S, Laforet P, Eymard B, et al. Electromyography guides toward subgroups of mutations in muscle channelopathies. Ann Neurol 2004; 56: 650-661.
-
(2004)
Ann Neurol
, vol.56
, pp. 650-661
-
-
Fournier, E.1
Arzel, M.2
Sternberg, D.3
Vicart, S.4
Laforet, P.5
Eymard, B.6
-
19
-
-
0032988783
-
The exercise test in Andersen syndrome
-
Katz JS, Wolfe GI, Iannaccone S, Bryan WW, Barohn RJ. The exercise test in Andersen syndrome. Arch Neurol 1999; 56: 352-356.
-
(1999)
Arch Neurol
, vol.56
, pp. 352-356
-
-
Katz, J.S.1
Wolfe, G.I.2
Iannaccone, S.3
Bryan, W.W.4
Barohn, R.J.5
-
20
-
-
54349087160
-
Value of exercise test in the diagnosis of 18 patients with periodic paralysis
-
Ding ZY, Liu M, Cui LY. Value of exercise test in the diagnosis of 18 patients with periodic paralysis. Chin J Neurol (Chin) 2007; 40: 242-245.
-
(2007)
Chin J Neurol (Chin)
, vol.40
, pp. 242-245
-
-
Ding, Z.Y.1
Liu, M.2
Cui, L.Y.3
-
21
-
-
10444273389
-
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
-
Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, et al. New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 2004; 63: 2120-2127.
-
(2004)
Neurology
, vol.63
, pp. 2120-2127
-
-
Vicart, S.1
Sternberg, D.2
Fournier, E.3
Ochsner, F.4
Laforet, P.5
Kuntzer, T.6
-
22
-
-
0026674723
-
Improvement of the exercise test after therapy in thyrotoxic periodic paralysis
-
Jackson CE, Barohn RJ. Improvement of the exercise test after therapy in thyrotoxic periodic paralysis. Muscle Nerve 1992; 15: 1069-1071.
-
(1992)
Muscle Nerve
, vol.15
, pp. 1069-1071
-
-
Jackson, C.E.1
Barohn, R.J.2
-
23
-
-
0031873856
-
Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A)
-
Hanna MG, Stewart J, Schapira AH, Wood NW, Morgan-Hughes JA, Murray NM. Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A). J Neurol Neurosurg Psychiatry 1998; 65: 248-250.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, pp. 248-250
-
-
Hanna, M.G.1
Stewart, J.2
Schapira, A.H.3
Wood, N.W.4
Morgan-Hughes, J.A.5
Murray, N.M.6
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