-
1
-
-
0345671971
-
-
The International classification of headache disorders, 2nd edn.
-
International Headache Society Headache Classification Subcommittee (2004) The International classification of headache disorders, 2nd edn. Cephalalgia 24 [Suppl 1]:1-150
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 1-150
-
-
-
2
-
-
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
-
3
-
-
0021799194
-
Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia
-
Fitzsimons RB, Wolfenden WH (1985) Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia. Brain 108:555-577
-
(1985)
Brain
, vol.108
, pp. 555-577
-
-
Fitzsimons, R.B.1
Wolfenden, W.H.2
-
4
-
-
0025017477
-
Familial migraine coma: A case study
-
Munte TF, Muller-Vahl H (1990) Familial migraine coma: a case study. J Neurol 237:59-61
-
(1990)
J Neurol
, vol.237
, pp. 59-61
-
-
Munte, T.F.1
Muller-Vahl, H.2
-
5
-
-
0031896548
-
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine
-
Dutch Migraine Genetics Research Group
-
Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, Eijk R van, Frants RR, Ferrari MD (1998) Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group. Neurology 50:1105-1110
-
(1998)
Neurology
, vol.50
, pp. 1105-1110
-
-
Terwindt, G.M.1
Ophoff, R.A.2
Haan, J.3
Vergouwe, M.N.4
Van Eijk, R.5
Frants, R.R.6
Ferrari, M.D.7
-
6
-
-
0034711743
-
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene
-
Chabriat H, Vahedi K, Clark CA, Poupon C, Ducros A, Denier C, Le Bihan D, Bousser MG (2000) Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene. Neurology 54:510-512
-
(2000)
Neurology
, vol.54
, pp. 510-512
-
-
Chabriat, H.1
Vahedi, K.2
Clark, C.A.3
Poupon, C.4
Ducros, A.5
Denier, C.6
Le Bihan, D.7
Bousser, M.G.8
-
7
-
-
0036157992
-
Wide clinical variability in a family with a CACNA1A T666m mutation: Hemiplegic migraine, coma, and progressive ataxia
-
Wada T, Kobayashi N, Takahashi Y, Aoki T, Watanabe T, Saitoh S (2002) Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia. Pediatr Neurol 26:47-50
-
(2002)
Pediatr Neurol
, vol.26
, pp. 47-50
-
-
Wada, T.1
Kobayashi, N.2
Takahashi, Y.3
Aoki, T.4
Watanabe, T.5
Saitoh, S.6
-
8
-
-
0028887901
-
Familial hemiplegic migraine versus migraine with prolonged aura: An uncertain diagnosis in a family report
-
Marchioni E, Galimberti CA, Soragna D, Ferrandi D, Maurelli M, Ratti MT, Bo P, Montalbetti L, Albergati A, Savoldi F (1995) Familial hemiplegic migraine versus migraine with prolonged aura: an uncertain diagnosis in a family report. Neurology 45:33-37
-
(1995)
Neurology
, vol.45
, pp. 33-37
-
-
Marchioni, E.1
Galimberti, C.A.2
Soragna, D.3
Ferrandi, D.4
Maurelli, M.5
Ratti, M.T.6
Bo, P.7
Montalbetti, L.8
Albergati, A.9
Savoldi, F.10
-
9
-
-
0036320705
-
Prolonged hemiplegic migraine associated with unilateral hyperperfusion on perfusion weighted magnetic resonance imaging
-
Lindahl AJ, Allder S, Jefferson D, Allder S, Moody A, Martel A (2002) Prolonged hemiplegic migraine associated with unilateral hyperperfusion on perfusion weighted magnetic resonance imaging. J Neurol Neurosurg Psychiatry 73:202-203
-
(2002)
J Neurol Neurosurg Psychiatry
, vol.73
, pp. 202-203
-
-
Lindahl, A.J.1
Allder, S.2
Jefferson, D.3
Allder, S.4
Moody, A.5
Martel, A.6
-
10
-
-
0037206675
-
Multimodal functional imaging of prolonged neurological deficits in a patient suffering from familial hemiplegic migraine
-
Gutschalk A, Kollmar R, Mohr A, Henze M, Ille N, Schwaninger M, Hartmann M, Hahnel S, Haberkorn U, Rupp A, Meyding-Lamade U (2002) Multimodal functional imaging of prolonged neurological deficits in a patient suffering from familial hemiplegic migraine. Neurosci Lett 332:115-118
-
(2002)
Neurosci Lett
, vol.332
, pp. 115-118
-
-
Gutschalk, A.1
Kollmar, R.2
Mohr, A.3
Henze, M.4
Ille, N.5
Schwaninger, M.6
Hartmann, M.7
Hahnel, S.8
Haberkorn, U.9
Rupp, A.10
Meyding-Lamade, U.11
-
11
-
-
0031992194
-
Familial hemiplegic migraine with irreversible brain damage
-
Hayashi R, Tachikawa H, Watanabe R, Honda M, Katsumata Y (1998) Familial hemiplegic migraine with irreversible brain damage. Intern Med 37:166-168
-
(1998)
Intern Med
, vol.37
, pp. 166-168
-
-
Hayashi, R.1
Tachikawa, H.2
Watanabe, R.3
Honda, M.4
Katsumata, Y.5
-
12
-
-
0034988145
-
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
-
Kors EE, Terwindt GM, Vermeulen FL, Fitzsimons RB, Jardine PE, Heywood P, Love S, Maagdenberg AM van den, Haan J, Frants RR, Ferrari MD (2001) Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol 49:753-760
-
(2001)
Ann Neurol
, vol.49
, pp. 753-760
-
-
Kors, E.E.1
Terwindt, G.M.2
Vermeulen, F.L.3
Fitzsimons, R.B.4
Jardine, P.E.5
Heywood, P.6
Love, S.7
Van Den Maagdenberg, A.M.8
Haan, J.9
Frants, R.R.10
Ferrari, M.D.11
-
15
-
-
0021107841
-
Footballer's migraine - A report of 2 cases
-
Sandyk R (1983) Footballer's migraine - a report of 2 cases. S Afr Med J 63:434
-
(1983)
S Afr Med J
, vol.63
, pp. 434
-
-
Sandyk, R.1
-
16
-
-
0030013798
-
Familial hemiplegic migraine: A clinical comparison of families linked and unlinked to chromosome 19
-
Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD (1996) Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19. Cephalalgia 16:153-155
-
(1996)
Cephalalgia
, vol.16
, pp. 153-155
-
-
Terwindt, G.M.1
Ophoff, R.A.2
Haan, J.3
Frants, R.R.4
Ferrari, M.D.5
-
18
-
-
0033832538
-
Hemiplegic migraine induced by exertion
-
Razavi M, Razavi B, Fattal D, Afifi A, Adams HP Jr (2000) Hemiplegic migraine induced by exertion. Arch Neurol 57:1363-1365
-
(2000)
Arch Neurol
, vol.57
, pp. 1363-1365
-
-
Razavi, M.1
Razavi, B.2
Fattal, D.3
Afifi, A.4
Adams Jr., H.P.5
-
19
-
-
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
-
20
-
-
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, Eijk R van, Oefner PJ, Huffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, Ommen GJ van, Hofker MH, Ferrari MD, Frants RR (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87:543-552
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouwe, M.N.3
Van Eijk, R.4
Oefner, P.J.5
Huffman, S.M.6
Lamerdin, J.E.7
Mohrenweiser, H.W.8
Bulman, D.E.9
Ferrari, M.10
Haan, J.11
Lindhout, D.12
Van Ommen, G.J.13
Hofker, M.H.14
Ferrari, M.D.15
Frants, R.R.16
-
21
-
-
0037312922
-
Haploin-sufficiency 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) Haploin-sufficiency 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
-
22
-
-
0027306090
-
A gene for familial hemiplegic migraine maps to chromosome 19
-
Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al (1993) A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet 5:40-45
-
(1993)
Nat Genet
, vol.5
, pp. 40-45
-
-
Joutel, A.1
Bousser, M.G.2
Biousse, V.3
Labauge, P.4
Chabriat, H.5
Nibbio, A.6
Maciazek, J.7
Meyer, B.8
Bach, M.A.9
Weissenbach, J.10
-
23
-
-
0344406276
-
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family
-
Alonso I, Barros J, Tuna A, Coelho J, Sequeiros J, Silveira I, Coutinho P (2003) Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. Arch Neurol 60:610-614
-
(2003)
Arch Neurol
, vol.60
, pp. 610-614
-
-
Alonso, I.1
Barros, J.2
Tuna, A.3
Coelho, J.4
Sequeiros, J.5
Silveira, I.6
Coutinho, P.7
-
24
-
-
0028024395
-
Familial hemiplegic migraine in The Netherlands
-
Haan J, Terwindt GM, Bos PL, Ophoff RA, Frants RR, Ferrari MD, Dutch Migraine Genetics Research Group (1994) Familial hemiplegic migraine in The Netherlands. Clin Neurol Neurosurg 96:244-249
-
(1994)
Clin Neurol Neurosurg
, vol.96
, pp. 244-249
-
-
Haan, J.1
Terwindt, G.M.2
Bos, P.L.3
Ophoff, R.A.4
Frants, R.R.5
Ferrari, M.D.6
-
25
-
-
0033551452
-
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia
-
Battistini S, Stenirri S, Piatti M, Gelfi C, Righetti PG, Rocchi R, Giannini F, Battistini N, Guazzi GC, Ferrari M, Carrera P (1999) A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia. Neurology 53:38-43
-
(1999)
Neurology
, vol.53
, pp. 38-43
-
-
Battistini, S.1
Stenirri, S.2
Piatti, M.3
Gelfi, C.4
Righetti, P.G.5
Rocchi, R.6
Giannini, F.7
Battistini, N.8
Guazzi, G.C.9
Ferrari, M.10
Carrera, P.11
-
26
-
-
0034633752
-
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
-
Vahedi K, Denier C, Ducros A, Bousson PV, Levy C, Chabriat H, Haguenau PM, Tournier-Lasserve E, Bousser MG (2000) CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy. Neurology 55:1040-1042
-
(2000)
Neurology
, vol.55
, pp. 1040-1042
-
-
Vahedi, K.1
Denier, C.2
Ducros, A.3
Bousson, P.V.4
Levy, C.5
Chabriat, H.6
Haguenau, P.M.7
Tournier-Lasserve, E.8
Bousser, M.G.9
-
27
-
-
0038823677
-
Serial MRI in a case of familial hemiplegic migraine
-
Butteriss DJ, Ramesh V, Birchall D (2003) Serial MRI in a case of familial hemiplegic migraine. Neuroradiology 45:300-303
-
(2003)
Neuroradiology
, vol.45
, pp. 300-303
-
-
Butteriss, D.J.1
Ramesh, V.2
Birchall, D.3
-
28
-
-
0031470730
-
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
-
Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, Verier A, Echenne B, Lopez de Munain A, Bousser MG, Tournier-Lasserve E (1997) Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ann Neurol 42:885-890
-
(1997)
Ann Neurol
, vol.42
, pp. 885-890
-
-
Ducros, A.1
Joutel, A.2
Vahedi, K.3
Cecillon, M.4
Ferreira, A.5
Bernard, E.6
Verier, A.7
Echenne, B.8
Lopez De Munain, A.9
Bousser, M.G.10
Tournier-Lasserve, E.11
-
29
-
-
0037371121
-
Familial hemiplegic migraine type 2 is linked to 0.9 Mb region on chromosome 1q23
-
Marconi R, De Fusco M, Aridon P, Plewnia K, Rossi M, Carapelli S, Ballabio A, Morgante L, Musolino R, Epifanio A, Micieli G, De Michele G, Casari G (2003) Familial hemiplegic migraine type 2 is linked to 0.9 Mb region on chromosome 1q23. Ann Neurol 53:376-381
-
(2003)
Ann Neurol
, vol.53
, pp. 376-381
-
-
Marconi, R.1
De Fusco, M.2
Aridon, P.3
Plewnia, K.4
Rossi, M.5
Carapelli, S.6
Ballabio, A.7
Morgante, L.8
Musolino, R.9
Epifanio, A.10
Micieli, G.11
De Michele, G.12
Casari, G.13
-
30
-
-
0041835844
-
Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign infantile convulsions
-
Vanmolkot KR, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WA, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, Maagdenberg AM van den (2003) Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign infantile convulsions. Ann Neurol 54:360-366
-
(2003)
Ann Neurol
, vol.54
, pp. 360-366
-
-
Vanmolkot, K.R.1
Kors, E.E.2
Hottenga, J.J.3
Terwindt, G.M.4
Haan, J.5
Hoefnagels, W.A.6
Black, D.F.7
Sandkuijl, L.A.8
Frants, R.R.9
Ferrari, M.D.10
Van Den Maagdenberg, A.M.11
-
31
-
-
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, Azais 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
Azais, M.7
Bousser, M.G.8
Tournier-Lasserve, E.9
-
32
-
-
0036524555
-
A typical migraine susceptibility region localizes to chromosome 1q31
-
Lea RA, Shepherd AG, Curtain RP, Nyholt DR, Quinlan S, Brimage PJ, Griffiths LR (2002) A typical migraine susceptibility region localizes to chromosome 1q31. Neurogenetics 4:17-22
-
(2002)
Neurogenetics
, vol.4
, pp. 17-22
-
-
Lea, R.A.1
Shepherd, A.G.2
Curtain, R.P.3
Nyholt, D.R.4
Quinlan, S.5
Brimage, P.J.6
Griffiths, L.R.7
-
33
-
-
0026446099
-
A second generation linkage map on the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M (1992) A second generation linkage map on the human genome. Nature 359:777-778
-
(1992)
Nature
, vol.359
, pp. 777-778
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
35
-
-
0035968165
-
Importance of transmembrane segment M3 of the sarcoplasmic reticulum Ca2+-ATPase for control of the gateway to the Ca2+ sites
-
Andersen JP, Sorensen TL, Povlsen K, Vilsen B (2001) Importance of transmembrane segment M3 of the sarcoplasmic reticulum Ca2+-ATPase for control of the gateway to the Ca2+ sites. J Biol Chem 276:23312-23321
-
(2001)
J Biol Chem
, vol.276
, pp. 23312-23321
-
-
Andersen, J.P.1
Sorensen, T.L.2
Povlsen, K.3
Vilsen, B.4
-
36
-
-
0030682445
-
Familial hemiplegic migraine with crossed cerebellar diaschisis and unilateral meningeal enhancement
-
Crawford JS, Konkol RJ (1997) Familial hemiplegic migraine with crossed cerebellar diaschisis and unilateral meningeal enhancement. Headache 37:590-593
-
(1997)
Headache
, vol.37
, pp. 590-593
-
-
Crawford, J.S.1
Konkol, R.J.2
-
37
-
-
0036274795
-
Familial hemiplegic migraine: Clinical features and probable linkage to chromosome 1 in an Italian family
-
Cevoli S, Pierangeli G, Monari L, Valentino ML, Bernardoni P, Mochi M, Cortelli P, Montagna P (2002) Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family. Neurol Sci 23:7-10
-
(2002)
Neurol Sci
, vol.23
, pp. 7-10
-
-
Cevoli, S.1
Pierangeli, G.2
Monari, L.3
Valentino, M.L.4
Bernardoni, P.5
Mochi, M.6
Cortelli, P.7
Montagna, P.8
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