-
1
-
-
1442265540
-
The International Classification of Headache Disorders
-
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders. Cephalalgia 2004;24(suppl 1):16-151.
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 16-151
-
-
-
2
-
-
16044370232
-
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
-
Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996;87:543-552.
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouwe, M.N.3
-
3
-
-
0035942343
-
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
-
Terwindt GM, Ophoff RA, van Eijk R, et al. Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology 2001;56:1028-1032.
-
(2001)
Neurology
, vol.56
, pp. 1028-1032
-
-
Terwindt, G.M.1
Ophoff, R.A.2
Van Eijk, R.3
-
4
-
-
0037312922
-
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2
-
De Fusco M, Marconi R, Silvestri L, et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 2003;33:192-196.
-
(2003)
Nat Genet
, vol.33
, pp. 192-196
-
-
De Fusco, M.1
Marconi, R.2
Silvestri, L.3
-
5
-
-
0041835844
-
Novel mutations in the Na⊥, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
-
Vanmolkot KR, Kors EE, Hottenga JJ, et al. Novel mutations in the Na⊥, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol 2003;54:360-366.
-
(2003)
Ann Neurol
, vol.54
, pp. 360-366
-
-
Vanmolkot, K.R.1
Kors, E.E.2
Hottenga, J.J.3
-
6
-
-
0033981451
-
Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha (1A) Ca (2+) channel mutation
-
Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, Ferrari MD, Frants RR, Molenaar PC. Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha (1A) Ca (2+) channel mutation. Brain 2000;123:463-471.
-
(2000)
Brain
, vol.123
, pp. 463-471
-
-
Plomp, J.J.1
Vergouwe, M.N.2
Van Den Maagdenberg, A.M.3
Ferrari, M.D.4
Frants, R.R.5
Molenaar, P.C.6
-
7
-
-
0035942346
-
Neuromuscular transmission in migraine. A single-fiber EMG study in clinical subgroups
-
Ambrosini A, de Noordhout AM, Schoenen J. Neuromuscular transmission in migraine. A single-fiber EMG study in clinical subgroups. Neurology 2001;56:1038-1043.
-
(2001)
Neurology
, vol.56
, pp. 1038-1043
-
-
Ambrosini, A.1
De Noordhout, A.M.2
Schoenen, J.3
-
8
-
-
0037343526
-
Acetazolamide acts on neuromuscular transmission abnormalities found in some migraineurs
-
Ambrosini A, Pierelli F, Schoenen. Acetazolamide acts on neuromuscular transmission abnormalities found in some migraineurs. Cephalgia 2003;23:75-78.
-
(2003)
Cephalgia
, vol.23
, pp. 75-78
-
-
Ambrosini, A.1
Pierelli, F.2
Schoenen3
-
9
-
-
0035960623
-
Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission
-
Jen J, Wan J, Graves M, et al. Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission. Neurology 2001;57:1843-1848.
-
(2001)
Neurology
, vol.57
, pp. 1843-1848
-
-
Jen, J.1
Wan, J.2
Graves, M.3
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