-
1
-
-
33947543278
-
Familial Hemiplegic Migraine
-
DOI 10.1016/j.nurt.2007.01.008, PII S1933721307000098
-
Pietrobon D,. Familial hemiplegic migraine. Neurother. 2007; 4: 274-284. (Pubitemid 46467543)
-
(2007)
Neurotherapeutics
, vol.4
, Issue.2
, pp. 274-284
-
-
Pietrobon, D.1
-
2
-
-
77957666465
-
- cotransporter NBCe1 is associated with familial migraine
-
- cotransporter NBCe1 is associated with familial migraine. PNAS. 2010; 107: 15963-15968.
-
(2010)
PNAS
, vol.107
, pp. 15963-15968
-
-
Suzuki, M.1
Van Paesschen, W.2
Stalmans, I.3
-
3
-
-
77957280532
-
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
-
Riant F, Ducros A, Ploton C, et al,. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. Neurology. 2010; 75: 967-972.
-
(2010)
Neurology
, vol.75
, pp. 967-972
-
-
Riant, F.1
Ducros, A.2
Ploton, C.3
-
4
-
-
34247204267
-
Prolonged hemiplegic episodes in children due to mutations in ATP1A2
-
DOI 10.1136/jnnp.2006.103267
-
Jen JC, Klein A, Boltshauser E, et al,. Prolonged hemiplegic episodes in children due to mutations in ATP1A2. J Neurol Neurosurg Psychiatry. 2007; 78: 523-526. (Pubitemid 46662904)
-
(2007)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.78
, Issue.5
, pp. 523-526
-
-
Jen, J.C.1
Klein, A.2
Boltshauser, E.3
Cartwright, M.S.4
Roach, E.S.5
Mamsa, H.6
Baloh, R.W.7
-
5
-
-
79952270988
-
Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation
-
De Sanctis S, Grieco GS, Breda L, et al,. Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation. Headache. 2011; 51: 447-450.
-
(2011)
Headache
, vol.51
, pp. 447-450
-
-
De Sanctis, S.1
Grieco, G.S.2
Breda, L.3
-
6
-
-
70349684936
-
Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation
-
Stam AH, Luijckx GJ, Poll-Thé BT, et al,. Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation. J Neurol Neurosurg Psychiatry. 2009; 80: 1125-1129.
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, pp. 1125-1129
-
-
Stam, A.H.1
Luijckx, G.J.2
Poll-Thé, B.T.3
-
7
-
-
51149087575
-
CACNA1A R1347Q: A frequent recurrent mutation in hemiplegic migraine
-
Stam AH, Vanmolkot KRJ, Kremer HPH, et al,. CACNA1A R1347Q: A frequent recurrent mutation in hemiplegic migraine. Clin Genet. 2008; 74: 481-485.
-
(2008)
Clin Genet
, vol.74
, pp. 481-485
-
-
Stam, A.H.1
Vanmolkot, K.R.J.2
Kremer, H.P.H.3
-
8
-
-
0034633752
-
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
-
Vahedi K, Denier C, Ducros A, et al,. CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy. Neurology. 2000; 55: 1040-1042.
-
(2000)
Neurology
, vol.55
, pp. 1040-1042
-
-
Vahedi, K.1
Denier, C.2
Ducros, A.3
-
9
-
-
32044460644
-
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation
-
DOI 10.1002/ana.20760
-
Vanmolkot KR, Stroink H, Koenderink JB, et al,. Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation. Ann Neurol. 2006; 59: 310-314. (Pubitemid 43202484)
-
(2006)
Annals of Neurology
, vol.59
, Issue.2
, pp. 310-314
-
-
Vanmolkot, K.R.J.1
Stroink, H.2
Koenderink, J.B.3
Kors, E.E.4
Van Den Heuvel, J.J.M.W.5
Van Den Boogerd, E.H.6
Stam, A.H.7
Haan, J.8
De Vries, B.B.A.9
Terwindt, G.M.10
Frants, R.R.11
Ferrari, M.D.12
Van Den Maagdenberg, A.M.J.M.13
-
10
-
-
51649112972
-
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes
-
Cuenca-Leõn E, Corominas R, Fernàndez-Castillo N, et al,. Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes. Cephalalgia. 2008; 28: 1039-1047.
-
(2008)
Cephalalgia
, vol.28
, pp. 1039-1047
-
-
Cuenca-Leõn, E.1
Corominas, R.2
Fernãndez-Castillo, N.3
-
11
-
-
44649087925
-
Analysis of calcium ion homeostasis and mitochondrial function in cerebellar granule cells of adult CaV 2.1 calcium ion channel mutant mice
-
Bawa B, Abbott LC,. Analysis of calcium ion homeostasis and mitochondrial function in cerebellar granule cells of adult CaV 2.1 calcium ion channel mutant mice. Neurotox Res. 2008; 13: 1-18.
-
(2008)
Neurotox Res
, vol.13
, pp. 1-18
-
-
Bawa, B.1
Abbott, L.C.2
-
12
-
-
0017693429
-
Respiratory arrest in familial hemiplegic migraine: A clinical and neuropathological study
-
Neligan P, Harriman DG, Pearce J,. Respiratory arrest in familial hemiplegic migraine: A clinical and neuropathological study. Br Med J. 1977; 2: 732-734. (Pubitemid 8175362)
-
(1977)
British Medical Journal
, vol.2
, Issue.6089
, pp. 732-734
-
-
Neligan, P.1
Harriman, D.G.F.2
Pearce, J.3
-
13
-
-
73249129712
-
Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: A novel de novo CACNA1A gene mutation
-
Malpas TJ, Riant F, Tournier-Lasserve E, et al,. Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: A novel de novo CACNA1A gene mutation. Dev Med Child Neurol. 2010; 52: 103-104.
-
(2010)
Dev Med Child Neurol
, vol.52
, pp. 103-104
-
-
Malpas, T.J.1
Riant, F.2
Tournier-Lasserve, E.3
-
14
-
-
51649100885
-
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood
-
de Vries B, Stam AH, Beker F, et al,. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. Cephalalgia. 2008; 28: 887-891.
-
(2008)
Cephalalgia
, vol.28
, pp. 887-891
-
-
De Vries, B.1
Stam, A.H.2
Beker, F.3
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