Update on the genetics of stroke and cerebrovascular disease 2004

被引:10
作者
Alberts, MJ
Tournier-Lasserve, E
机构
[1] Northwestern Univ, Stroke Program, Dept Neurol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] CHU Lariboisiere, Paris, France
[3] INSERM, Paris, France
关键词
D O I
10.1161/01.STR.0000153066.74217.31
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
[No abstract available]
引用
收藏
页码:179 / 181
页数:3
相关论文
共 32 条
[1]  
BERGAMETTI F, 2004, AM J HUM GENET, V76
[2]   Meta-analysis of genetic studies in ischemic stroke - Thirty-two genes involving approximately 18 000 cases and 58 000 controls [J].
Casas, JP ;
Hingorani, AD ;
Bautista, LE ;
Sharma, P .
ARCHIVES OF NEUROLOGY, 2004, 61 (11) :1652-1661
[3]   A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke [J].
Cipollone, F ;
Toniato, E ;
Martinotti, S ;
Fazia, M ;
Iezzi, A ;
Cuccurullo, C ;
Pini, B ;
Ursi, S ;
Vitullo, G ;
Averna, M ;
Arca, M ;
Montali, A ;
Campagna, F ;
Ucchino, S ;
Spigonardo, F ;
Taddei, S ;
Virdis, A ;
Ciabattoni, G ;
Notarbartolo, A ;
Cuccurullo, F ;
Mezzetti, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (18) :2221-2228
[4]   Retinal abnormalities in CADASIL:: a retrospective study of 18 patients [J].
Cumurciuc, R ;
Massin, P ;
Pâques, M ;
Krisovic, V ;
Gaudric, A ;
Bousser, MG ;
Chabriat, H .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2004, 75 (07) :1058-1060
[5]   Clinical features of cerebral cavernous malformations patients with KRIT1 mutations [J].
Denier, C ;
Labauge, P ;
Brunereau, L ;
Cavé-Riant, F ;
Marchelli, F ;
Arnoult, M ;
Cecillon, M ;
Maciazek, J ;
Joutel, A ;
Tournier-Lasserve, E .
ANNALS OF NEUROLOGY, 2004, 55 (02) :213-220
[6]   Mutations within the MGC4607 gene cause cerebral cavernous malformations [J].
Denier, C ;
Goutagny, S ;
Labauge, P ;
Krivosic, V ;
Arnoult, M ;
Cousin, A ;
Benabid, AL ;
Comoy, J ;
Frerebeau, P ;
Gilbert, B ;
Houtteville, JP ;
Jan, M ;
Lapierre, F ;
Loiseau, H ;
Menei, P ;
Mercier, P ;
Moreau, JJ ;
Nivelon-Chevallier, A ;
Parker, F ;
Redondo, AM ;
Scarabin, JM ;
Tremoulet, M ;
Zerah, M ;
Maciazek, J ;
Tournier-Lasserve, E .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (02) :326-337
[7]   Distribution pattern of Notch3 mutations suggests a gain-of-function mechanism for CADASIL [J].
Donahue, CP ;
Kosik, KS .
GENOMICS, 2004, 83 (01) :59-65
[8]   Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm [J].
Farnham, JM ;
Camp, NJ ;
Neuhausen, SL ;
Tsuruda, J ;
Parker, D ;
MacDonald, J ;
Cannon-Albright, LA .
HUMAN GENETICS, 2004, 114 (03) :250-255
[9]   Potential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke [J].
Flossmann, E ;
Schulz, UGR ;
Rothwell, PM .
CEREBROVASCULAR DISEASES, 2005, 19 (01) :1-10
[10]   Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke [J].
Flossmann, E ;
Schulz, UGR ;
Rothwell, PM .
STROKE, 2004, 35 (01) :212-227