-
1
-
-
74549161471
-
Proposals for new standardized general diagnostic criteria for the secondary headaches
-
Olesen J, Steiner T, Bousser M-G, Diener H-C, Dodick D, First MB, et al. Proposals for new standardized general diagnostic criteria for the secondary headaches. Cephalalgia. 2009 ; 29: 1331-1336
-
(2009)
Cephalalgia
, vol.29
, pp. 1331-1336
-
-
Olesen, J.1
Steiner, T.2
Bousser, M.-G.3
Diener, H.-C.4
Dodick, D.5
First, M.B.6
-
2
-
-
74549207436
-
The future of headache classification and classification research
-
Olesen J. The future of headache classification and classification research. Cephalalgia. 2009 ; 29: 1240-1241
-
(2009)
Cephalalgia
, vol.29
, pp. 1240-1241
-
-
Olesen, J.1
-
3
-
-
34547877951
-
Migraine attributed to genetic disorder
-
Sacco S, Carolei A. Migraine attributed to genetic disorder. Funct Neurol. 2007 ; 22: 117-118 (Pubitemid 47249618)
-
(2007)
Functional Neurology
, vol.22
, Issue.2
, pp. 117-118
-
-
Sacco, S.1
Carolei, A.2
-
4
-
-
33846620591
-
The genetic spectrum of a population-based sample of familial hemiplegic migraine
-
DOI 10.1093/brain/awl334
-
Thomsen LL, Kirchmann M, Bjornsson A, Stefansson H, Jensen RM, Fasquel AC, et al. The genetic spectrum of a population-based sample of familial hemiplegic migraine. Brain. 2007 ; 130: 346-356 (Pubitemid 46181089)
-
(2007)
Brain
, vol.130
, Issue.2
, pp. 346-356
-
-
Thomsen, L.L.1
Kirchmann, M.2
Bjornsson, A.3
Stefansson, H.4
Jensen, R.M.5
Fasquel, A.C.6
Petursson, H.7
Stefansson, M.8
Frigge, M.L.9
Kong, A.10
Gulcher, J.11
Stefansson, K.12
Olesen, J.13
-
5
-
-
77957280532
-
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
-
Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E. 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
Barbance, C.4
Depienne, C.5
Tournier-Lasserve, E.6
-
6
-
-
33645062190
-
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
-
Ambrosini A, D'Onofrio M, Grieco GS, Di Mambro A, Montagna G, Fortini D, et al. Familial basilar migraine associated with a new mutation in the ATP1A2 gene. Neurology. 2005 ; 65: 1826-1828
-
(2005)
Neurology
, vol.65
, pp. 1826-1828
-
-
Ambrosini, A.1
D'Onofrio, M.2
Grieco, G.S.3
Di Mambro, A.4
Montagna, G.5
Fortini, D.6
-
7
-
-
77957812064
-
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura
-
Lafrenière RG, Cader MZ, Poulin JF, Andres-Enguix I, Simoneau M, Gupta N, et al. A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. Nat Med. 2010 ; 16: 1157-1160
-
(2010)
Nat Med
, vol.16
, pp. 1157-1160
-
-
Lafrenière, R.G.1
Cader, M.Z.2
Poulin, J.F.3
Andres-Enguix, I.4
Simoneau, M.5
Gupta, N.6
-
8
-
-
77957287197
-
Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): Are they appropriate?
-
Sacco S, Degan D, Carolei A. Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): are they appropriate?. J Headache Pain. 2010 ; 11: 181-186
-
(2010)
J Headache Pain
, vol.11
, pp. 181-186
-
-
Sacco, S.1
Degan, D.2
Carolei, A.3
-
9
-
-
54949142139
-
Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: Basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome
-
Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann N Y Acad Sci. 2008 ; 1142: 133-158
-
(2008)
Ann N y Acad Sci
, vol.1142
, pp. 133-158
-
-
Sproule, D.M.1
Kaufmann, P.2
-
10
-
-
47249142894
-
New roles for the major human 3′-5′ exonuclease TREX1 in human disease
-
Kavanagh D, Spitzer D, Kothari PH, Shaikh A, Liszewski MK, Richards A, et al. New roles for the major human 3'-5' exonuclease TREX1 in human disease. Cell Cycle. 2008 ; 7: 1718-1725 (Pubitemid 351988737)
-
(2008)
Cell Cycle
, vol.7
, Issue.12
, pp. 1718-1725
-
-
Kavanagh, D.1
Spitzer, D.2
Kothari, P.H.3
Shaikh, A.4
Liszewski, M.K.5
Richards, A.6
Atkinson, J.P.7
-
11
-
-
77955173802
-
COL4A1 mutations as a monogenic cause of cerebral small vessel disease. A systematic review
-
Lanfranconi S, Markus HS. COL4A1 mutations as a monogenic cause of cerebral small vessel disease. A systematic review. Stroke. 2010 ; 41: e513 - e518
-
(2010)
Stroke
, vol.41
-
-
Lanfranconi, S.1
Markus, H.S.2
-
12
-
-
1442265540
-
The international classification of headache disorders. 2nd ed
-
The international classification of headache disorders. 2nd ed. Cephalalgia. 2004 ; 24 (Suppl. 1). 9-160
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 9-160
-
-
|