-
1
-
-
0029980056
-
Migraine without aura and migraine with aura are distinct clinical entities: A study of four hundred and eighty-four male and female migraineurs from the general population
-
Russell MB Rasmussen BK Fenger K Olesen J Migraine without aura and migraine with aura are distinct clinical entities: a study of four hundred and eighty-four male and female migraineurs from the general population Cephalalgia 1996 16 239 245
-
(1996)
Cephalalgia
, vol.16
, pp. 239-245
-
-
Russell, M.B.1
Rasmussen, B.K.2
Fenger, K.3
Olesen, J.4
-
2
-
-
0019435433
-
Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine
-
Olesen J Larsen B Lauritzen M Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine Ann Neurol 1981 9 344 352
-
(1981)
Ann Neurol
, vol.9
, pp. 344-352
-
-
Olesen, J.1
Larsen, B.2
Lauritzen, M.3
-
3
-
-
0027161898
-
Familial occurrence of migraine without aura and migraine with aura
-
Russell MB Hilden J Sorensen SA Olesen J Familial occurrence of migraine without aura and migraine with aura Neurology 1993 43 1369 1373
-
(1993)
Neurology
, vol.43
, pp. 1369-1373
-
-
Russell, M.B.1
Hilden, J.2
Sorensen, S.A.3
Olesen, J.4
-
4
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko O Bailey J Bonnen P et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel Nat Genet 1997 15 62 69
-
(1997)
Nat Genet
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
-
5
-
-
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
-
6
-
-
0037312922
-
Haploinsufficiency of ATP1A2 encoding the Na(+)/K(+) pump alpha2 subunit associated with familial hemiplegic migraine type 2
-
Fusco MD 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
-
-
Fusco, M.D.1
Marconi, R.2
Silvestri, L.3
-
7
-
-
0242266995
-
Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder
-
Thomsen LL Ostergaard E Romer SF et al. Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder Cephalalgia 2003 23 921 928
-
(2003)
Cephalalgia
, vol.23
, pp. 921-928
-
-
Thomsen, L.L.1
Ostergaard, E.2
Romer, S.F.3
-
8
-
-
4644251247
-
Clinical characteristics of 362 patients with familial migraine with aura
-
Eriksen M Thomsen L Olesen J Clinical characteristics of 362 patients with familial migraine with aura Cephalalgia 2004 24 564 575
-
(2004)
Cephalalgia
, vol.24
, pp. 564-575
-
-
Eriksen, M.1
Thomsen, L.2
Olesen, J.3
-
9
-
-
0036598557
-
An epidemiological survey of hemiplegic migraine
-
Thomsen LL Eriksen MK Romer SF et al. An epidemiological survey of hemiplegic migraine Cephalalgia 2002 22 361 375
-
(2002)
Cephalalgia
, vol.22
, pp. 361-375
-
-
Thomsen, L.L.1
Eriksen, M.K.2
Romer, S.F.3
-
11
-
-
0037465375
-
Evidence for a separate type of migraine with aura: Sporadic hemiplegic migraine
-
Thomsen LL Ostergaard E Olesen J Russell MB Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine Neurology 2003 60 595 601
-
(2003)
Neurology
, vol.60
, pp. 595-601
-
-
Thomsen, L.L.1
Ostergaard, E.2
Olesen, J.3
Russell, M.B.4
-
12
-
-
0346031709
-
Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain
-
ICHD-1. Headache Classification Committee of the International Headache Society
-
ICHD-1. Headache Classification Committee of the International Headache Society Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain Cephalalgia 1988 8 1 96
-
(1988)
Cephalalgia
, vol.8
, pp. 1-96
-
-
-
13
-
-
0026668280
-
Symptomatic and nonsymptomatic headaches in a general population
-
Rasmussen BK Olesen J Symptomatic and nonsymptomatic headaches in a general population Neurology 1992 42 1225 1231
-
(1992)
Neurology
, vol.42
, pp. 1225-1231
-
-
Rasmussen, B.K.1
Olesen, J.2
-
14
-
-
0029988603
-
A nosographic analysis of the migraine aura in a general population
-
Russell MB Olesen J A nosographic analysis of the migraine aura in a general population Brain 1996 119 Pt 2 355 361
-
(1996)
Brain
, vol.119
, Issue.2 PART
, pp. 355-361
-
-
Russell, M.B.1
Olesen, J.2
-
15
-
-
0345671971
-
The International Classification of Headache Disorders 2nd ed
-
ICHD-2
-
ICHD-2 The International Classification of Headache Disorders 2nd ed Cephalalgia 2004 24 1 160
-
(2004)
Cephalalgia
, vol.24
, pp. 1-160
-
-
-
16
-
-
4644343975
-
New international classification of migraine with aura (ICHD-2) applied to 362 migraine patients
-
Eriksen M Thomsen L Olesen J New international classification of migraine with aura (ICHD-2) applied to 362 migraine patients Eur J Neurol 2004 11 583 591
-
(2004)
Eur J Neurol
, vol.11
, pp. 583-591
-
-
Eriksen, M.1
Thomsen, L.2
Olesen, J.3
-
19
-
-
0035811775
-
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
-
Ducros A Denier C Joutel A et al. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel N Engl J Med 2001 345 17 24
-
(2001)
N Engl J Med
, vol.345
, pp. 17-24
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
-
20
-
-
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
-
21
-
-
2442713897
-
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
-
Jurkat-Rott K Freilinger T Dreier JP et al. Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants Neurology 2004 62 1857 1861
-
(2004)
Neurology
, vol.62
, pp. 1857-1861
-
-
Jurkat-Rott, K.1
Freilinger, T.2
Dreier, J.P.3
-
22
-
-
0036279411
-
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
-
Terwindt G Kors E Haan J et al. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine Arch Neurol 2002 59 1016 1018
-
(2002)
Arch Neurol
, vol.59
, pp. 1016-1018
-
-
Terwindt, G.1
Kors, E.2
Haan, J.3
-
23
-
-
0000265923
-
Sporadic hemiplegic migraine with de novo CACNA1A missense mutation
-
Vahedi K Denier C Ducros A et al. Sporadic hemiplegic migraine with de novo CACNA1A missense mutation Neurology 1999 52 A274
-
(1999)
Neurology
, vol.52
, pp. 274
-
-
Vahedi, K.1
Denier, C.2
Ducros, A.3
-
24
-
-
18244372492
-
A susceptibility locus for migraine with aura, on chromosome 4q24
-
Wessman M Kallela M Kaunisto MA et al. A susceptibility locus for migraine with aura, on chromosome 4q24 Am J Hum Genet 2002 70 652 662
-
(2002)
Am J Hum Genet
, vol.70
, pp. 652-662
-
-
Wessman, M.1
Kallela, M.2
Kaunisto, M.A.3
-
25
-
-
0033364409
-
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
-
Ducros A Denier C Joutel A et al. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia Am J Hum Genet 1999 64 89 98
-
(1999)
Am J Hum Genet
, vol.64
, pp. 89-98
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
-
26
-
-
0033551481
-
Genetic heterogeneity in Italian families with familial hemiplegic migraine
-
Carrera P Piatti M Stenirri S et al. Genetic heterogeneity in Italian families with familial hemiplegic migraine Neurology 1999 53 26 33
-
(1999)
Neurology
, vol.53
, pp. 26-33
-
-
Carrera, P.1
Piatti, M.2
Stenirri, S.3
-
27
-
-
0028841501
-
Is familial hemiplegic migraine a hereditary form of basilar migraine¿
-
Haan J Terwindt GM Ophoff RA et al. Is familial hemiplegic migraine a hereditary form of basilar migraine¿ Cephalalgia 1995 15 477 481
-
(1995)
Cephalalgia
, vol.15
, pp. 477-481
-
-
Haan, J.1
Terwindt, G.M.2
Ophoff, R.A.3
-
32
-
-
0023005605
-
Observations on prodromes of classic migraine in a headache clinic population
-
Bana DS Graham JR Observations on prodromes of classic migraine in a headache clinic population Headache 1986 26 216 219
-
(1986)
Headache
, vol.26
, pp. 216-219
-
-
Bana, D.S.1
Graham, J.R.2
-
34
-
-
0031015471
-
Clinical characteristics and long-term outcome of migraine with aura in children and adolescents
-
Ballotin U Borgatti R Zambrino C Lanzi G Clinical characteristics and long-term outcome of migraine with aura in children and adolescents Dev Med Child Neurol 1997 39 26 30
-
(1997)
Dev Med Child Neurol
, vol.39
, pp. 26-30
-
-
Ballotin, U.1
Borgatti, R.2
Zambrino, C.3
Lanzi, G.4
-
36
-
-
33645083633
-
Diagnosis and differential diagnosis
-
In*Olesen J.*Tfelt-Hansen P.*Welch K.M.A. Philadelphia. Lippincott Williams and Wilkins eds
-
Keith Campbell C Sakai F Diagnosis and differential diagnosis In Olesen J Tfelt-Hansen P Welch KMA eds The Headaches Philadelphia Lippincott Williams and Wilkins 2000 359 365
-
(2000)
The Headaches
, pp. 359-365
-
-
Keith Campbell, C.1
Sakai, F.2
|