-
1
-
-
79954880590
-
Sporadic and familial hemiplegic migraine: Pathophysiological mechanisms, clinical characteristics, diagnosis, and management
-
Russell MB, Ducros A (2011) Sporadic and familial hemiplegic migraine: Pathophysiological mechanisms, clinical characteristics, diagnosis, and management. Lancet Neurol 10:457-470
-
(2011)
Lancet Neurol
, vol.10
, pp. 457-470
-
-
Russell, M.B.1
Ducros, A.2
-
2
-
-
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, Atorino L, Rampoldi L, Morgante L, Ballabio A, Aridon P, Casari G (2003) Haploinsufficiency of ATP1A2 encoding the Na ?/K ? pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 33:192-196
-
(2003)
Nat Genet
, vol.33
, pp. 192-196
-
-
De Fusco, M.1
Marconi, R.2
Silvestri, L.3
Atorino, L.4
Rampoldi, L.5
Morgante, L.6
Ballabio, A.7
Aridon, P.8
Casari, G.9
-
3
-
-
32044460644
-
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation
-
Vanmolkot KR, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJ, van den Boogerd EH, Stam AH, Haan J, De Vries BB, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AM (2006) Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation. Ann Neurol 59:310-314
-
(2006)
Ann Neurol
, vol.59
, pp. 310-314
-
-
Vanmolkot, K.R.1
Stroink, H.2
Koenderink, J.B.3
Kors, E.E.4
Van Den Heuvel, J.J.5
Van Den Boogerd, E.H.6
Stam, A.H.7
Haan, J.8
De Vries, B.B.9
Terwindt, G.M.10
Frants, R.R.11
Ferrari, M.D.12
Van Den Maagdenberg, A.M.13
-
4
-
-
5444222541
-
A G301R Na ?/K ?-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs
-
Spadaro M, Ursu S, Lehmann-Horn F, Veneziano L, Liana V, Antonini G, Giovanni A, Giunti P, Paola G, Frontali M, Jurkat-Rott K (2004) A G301R Na ?/K ?-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. Neurogenetics 5:177-185
-
(2004)
Neurogenetics
, vol.5
, pp. 177-185
-
-
Spadaro, M.1
Ursu, S.2
Lehmann-Horn, F.3
Veneziano, L.4
Liana, V.5
Antonini, G.6
Giovanni, A.7
Giunti, P.8
Paola, G.9
Frontali, M.10
Jurkat-Rott, K.11
-
5
-
-
0019985430
-
Episodes of acute confusion or psychosis in familial hemiplegic migraine
-
Feely MP, O'Hare J, Veale D, Callaghan N (1982) Episodes of acute confusion or psychosis in familial hemiplegic migraine. Acta Neurol Scand 65:369-375
-
(1982)
Acta Neurol Scand
, vol.65
, pp. 369-375
-
-
Feely, M.P.1
O'Hare, J.2
Veale, D.3
Callaghan, N.4
-
6
-
-
0032890557
-
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis
-
Spranger M, Spranger S, Schwab S, Benninger C, Dichgans M (1999) Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis. Eur Neurol 41:150-152
-
(1999)
Eur Neurol
, vol.41
, pp. 150-152
-
-
Spranger, M.1
Spranger, S.2
Schwab, S.3
Benninger, C.4
Dichgans, M.5
-
7
-
-
0035811775
-
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
-
Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, Darcel F, Vicaut E, Bousser MG, Tournier-Lasserve E (2001) The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med 345:17-24
-
(2001)
N Engl J Med
, vol.345
, pp. 17-24
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
Cecillon, M.4
Lescoat, C.5
Vahedi, K.6
Darcel, F.7
Vicaut, E.8
Bousser, M.G.9
Tournier-Lasserve, E.10
-
8
-
-
73449083058
-
Neurological picture. Cortical oedema: A link between delusional misidentification syndromes and hemiplegic migraine
-
Moreira T, Menetrey A, Carota A (2010) Neurological picture. Cortical oedema: A link between delusional misidentification syndromes and hemiplegic migraine. J Neurol Neurosurg Psychiatry 81:52-53
-
(2010)
J Neurol Neurosurg Psychiatry
, vol.81
, pp. 52-53
-
-
Moreira, T.1
Menetrey, A.2
Carota, A.3
-
9
-
-
36448998130
-
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine
-
Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KR, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro J (2007) Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine. J Hum Genet 52:990-998
-
(2007)
J Hum Genet
, vol.52
, pp. 990-998
-
-
Castro, M.J.1
Stam, A.H.2
Lemos, C.3
Barros, J.4
Gouveia, R.G.5
Martins, I.P.6
Koenderink, J.B.7
Vanmolkot, K.R.8
Mendes, A.P.9
Frants, R.R.10
Ferrari, M.D.11
Sequeiros, J.12
Pereira-Monteiro, J.13
-
10
-
-
0032869936
-
Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1
-
Echenne B, Ducros A, Rivier F, Joutel A, Humbertclaude V, Roubertie A, Azaïs M, Bousser MG, Tournier-Lasserve E (1999) Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1. Neuropediatrics 30:214-217
-
(1999)
Neuropediatrics
, vol.30
, pp. 214-217
-
-
Echenne, B.1
Ducros, A.2
Rivier, F.3
Joutel, A.4
Humbertclaude, V.5
Roubertie, A.6
Azaïs, M.7
Bousser, M.G.8
Tournier-Lasserve, E.9
-
11
-
-
37249054940
-
Two novel functional mutations in the Na?, K?-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
-
CastroM-J,NunesB, deVries B, LemosC,VanmolkotKRJ, van den Heuvel JJMW, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM, van den Maagdenberg AMJM (2008) Two novel functional mutations in the Na?, K?-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. Clin Genet 73:37-43
-
(2008)
Clin Genet
, vol.73
, pp. 37-43
-
-
Castro, M.-J.1
Nunes, B.2
De Vries, B.3
Lemos, C.4
Vanmolkot, K.R.J.5
Van Den Heuvel, J.J.M.W.6
Temudo, T.7
Barros, J.8
Sequeiros, J.9
Frants, R.R.10
Koenderink, J.B.11
Pereira-Monteiro, J.M.12
Van Den Maagdenberg, A.M.J.M.13
-
12
-
-
53049090545
-
Mentales zeitreisen-neurokognitive grundlagen des zukunftsdenkens
-
Weiler JA, Daum I (2008) Mentales zeitreisen-neurokognitive grundlagen des zukunftsdenkens. Fortschr Neurol Psychiatr 76:539-548
-
(2008)
Fortschr Neurol Psychiatr
, vol.76
, pp. 539-548
-
-
Weiler, J.A.1
Daum, I.2
|