-
1
-
-
0000676962
-
Epidemiology of migraine in England
-
TJ Steiner, WF Stewart, K Kolodner, J Liberman, RB Lipton Epidemiology of migraine in England Cephalalgia 19 1999 305 306
-
(1999)
Cephalalgia
, vol.19
, pp. 305-306
-
-
Steiner, T.J.1
Stewart, W.F.2
Kolodner, K.3
Liberman, J.4
Lipton, R.B.5
-
2
-
-
0034093231
-
The global burden of disease study: Implications for neurology
-
M Menken, TL Munsat, JF Toole The global burden of disease study: implications for neurology Arch Neurol 57 2000 418 420
-
(2000)
Arch Neurol
, vol.57
, pp. 418-420
-
-
Menken, M.1
Munsat, T.L.2
Toole, J.F.3
-
4
-
-
0036260284
-
The neuronal channelopathies
-
DM Kullmann The neuronal channelopathies Brain 125 2002 1177 1195
-
(2002)
Brain
, vol.125
, pp. 1177-1195
-
-
Kullmann, D.M.1
-
5
-
-
0037312922
-
+ pump α2 subunit associated with familial hemiplegic migraine type 2
-
+ pump α2 subunit associated with familial hemiplegic migraine type 2 Nat Genet 33 2003 192 196
-
(2003)
Nat Genet
, vol.33
, pp. 192-196
-
-
De Fusco, M.1
Marconi, R.2
Silvestri, L.3
-
6
-
-
2642518755
-
Recent findings in headache genetics
-
EE Kors, KR Vanmolkot, J Haan, RR Frants, AM van den Maagdenberg, MD Ferrari Recent findings in headache genetics Curr Opin Neurol 17 2004 283 288
-
(2004)
Curr Opin Neurol
, vol.17
, pp. 283-288
-
-
Kors, E.E.1
Vanmolkot, K.R.2
Haan, J.3
Frants, R.R.4
Van Den Maagdenberg, A.M.5
Ferrari, M.D.6
-
7
-
-
23044459961
-
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
-
D Dichgans, T Freilinger, G Eckstein Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine Lancet 2005 DOI:10.1016/S0140-6736(05)66786-4
-
(2005)
Lancet
-
-
Dichgans, D.1
Freilinger, T.2
Eckstein, G.3
-
8
-
-
0037465375
-
Evidence for a separate type of migraine with aura: Sporadic hemiplegic migraine
-
LL Thomsen, E Ostergaard, J Olesen, MB Russell Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine Neurology 60 2003 595 601
-
(2003)
Neurology
, vol.60
, pp. 595-601
-
-
Thomsen, L.L.1
Ostergaard, E.2
Olesen, J.3
Russell, M.B.4
-
9
-
-
0345671971
-
The international classification of headache disorders, 2nd edn
-
Headache Classification Committee of The International Headache Society
-
Headache Classification Committee of The International Headache Society The international classification of headache disorders, 2nd edn Cephalalgia 24 suppl 1 2004 1 160
-
(2004)
Cephalalgia
, vol.24
, Issue.1 SUPPL.
, pp. 1-160
-
-
-
10
-
-
0034883732
-
Prevalence and burden of migraine in the United States: Data from the American Migraine Study II
-
RB Lipton, WF Stewart, S Diamond, ML Diamond, M Reed Prevalence and burden of migraine in the United States: data from the American Migraine Study II Headache 41 2001 646 657
-
(2001)
Headache
, vol.41
, pp. 646-657
-
-
Lipton, R.B.1
Stewart, W.F.2
Diamond, S.3
Diamond, M.L.4
Reed, M.5
-
11
-
-
0037465547
-
Sporadic hemiplegic migraine: Stamp collecting or food for thought?
-
PJ Goadsby Sporadic hemiplegic migraine: stamp collecting or food for thought? Neurology 60 2003 536 537
-
(2003)
Neurology
, vol.60
, pp. 536-537
-
-
Goadsby, P.J.1
-
12
-
-
0032126806
-
The familial periodic paralyses and nondystrophic myotonias
-
L Ptacek The familial periodic paralyses and nondystrophic myotonias Am J Med 105 1998 58 70
-
(1998)
Am J Med
, vol.105
, pp. 58-70
-
-
Ptacek, L.1
-
13
-
-
0037071896
-
Molecular basis of an inherited epilepsy
-
C Lossin, DW Wang, TH Rhodes, CG Vanoye, AL George Jr Molecular basis of an inherited epilepsy Neuron 34 2002 877 884
-
(2002)
Neuron
, vol.34
, pp. 877-884
-
-
Lossin, C.1
Wang, D.W.2
Rhodes, T.H.3
Vanoye, C.G.4
George Jr., A.L.5
-
14
-
-
0034987073
-
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
-
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy Am J Hum Genet 68 2001 1327 1332
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1327-1332
-
-
Claes, L.1
Del-Favero, J.2
Ceulemans, B.3
Lagae, L.4
Van Broeckhoven, C.5
De Jonghe, P.6
-
16
-
-
12144286750
-
A Cacna1a knock-in migraine mouse model with increased susceptibility to cortical spreading depression
-
AMJM van den Maagdenberg, D Pietrobon, T Pizzorusso A Cacna1a knock-in migraine mouse model with increased susceptibility to cortical spreading depression Neuron 41 2004 701 710
-
(2004)
Neuron
, vol.41
, pp. 701-710
-
-
Den Maagdenberg Amjm, V.1
Pietrobon, D.2
Pizzorusso, T.3
-
18
-
-
0028521142
-
Comorbidity of migraine: The connection between migraine and epilepsy
-
RB Lipton, R Ottman, BL Ehrenberg, WA Hauser Comorbidity of migraine: the connection between migraine and epilepsy Neurology 44 suppl 7 1994 S28 S32
-
(1994)
Neurology
, vol.44
, Issue.7 SUPPL.
-
-
Lipton, R.B.1
Ottman, R.2
Ehrenberg, B.L.3
Hauser, W.A.4
-
19
-
-
0041835844
-
+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
-
+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions Ann Neurol 54 2003 360 366
-
(2003)
Ann Neurol
, vol.54
, pp. 360-366
-
-
Vanmolkot, K.R.J.1
Kors, E.E.2
Hottenga, J.J.3
-
20
-
-
33544461337
-
A new mutation on the ATPA2 gene in one Italian family with basilar-type migraine linked to the FHM2 locus
-
A Ambrosini, M D'Onofrio, GS Grieco A new mutation on the ATPA2 gene in one Italian family with basilar-type migraine linked to the FHM2 locus Neurology 64 suppl 1 2005 A132 abstr
-
(2005)
Neurology
, vol.64
, Issue.1 SUPPL.
, pp. 132
-
-
Ambrosini, A.1
D'Onofrio, M.2
Grieco, G.S.3
-
22
-
-
0035811775
-
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
-
A Ducros, C Denier, A Joutel The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel N Engl J Med 345 2001 17 24
-
(2001)
N Engl J Med
, vol.345
, pp. 17-24
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
-
23
-
-
0034641194
-
Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine
-
H Kaube, J Herzog, T Kaufer, M Dichgans, HC Diener Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine Neurology 55 2000 139 141
-
(2000)
Neurology
, vol.55
, pp. 139-141
-
-
Kaube, H.1
Herzog, J.2
Kaufer, T.3
Dichgans, M.4
Diener, H.C.5
|