Stroke genetics update

被引：25
作者：
Alberts, MJ [1 ]
机构：
[1] Northwestern Univ, Sch Med, Chicago, IL 60611 USA
来源：
STROKE | 2003年 / 34卷 / 02期
关键词：
genetics; mutation; polymorphism;
D O I：
10.1161/01.STR.0000054263.67434.BE
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：342 / 344
页数：3
相关论文
共 27 条
[1]   Familial clustering of intracerebral hemorrhage: A prospective study in north Carolina [J].
Alberts, MJ ;
McCarron, MO ;
Hoffmann, KL ;
Graffagnino, C .
NEUROEPIDEMIOLOGY, 2002, 21 (01) :18-21
[2]   Genetic liability in stroke - A long-term follow-up study of Danish twins [J].
Bak, S ;
Gaist, D ;
Sindrup, SH ;
Skytthe, A ;
Christensen, K .
STROKE, 2002, 33 (03) :769-774
[3]   Genetic association studies - Genes in search of diseases [J].
Bird, TD ;
Jarvik, GP ;
Wood, NW .
NEUROLOGY, 2001, 57 (07) :1153-1154
[4]   No association of factor XIII Val34Leu polymorphism with primary intracerebral hemorrhage and healthy controls in Korean population [J].
Cho, KH ;
Kim, BC ;
Kim, MK ;
Shin, BA .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2002, 17 (02) :249-253
[5]   Localization of a susceptibility gene for common forms of stroke to 5q12 [J].
Gretarsdottir, S ;
Sveinbjörnsdottir, S ;
Jonsson, HH ;
Jakobsson, F ;
Einarsdottir, E ;
Agnarsson, U ;
Shkolny, D ;
Einarsson, G ;
Gudjonsdottir, HM ;
Valdimarsson, EM ;
Einarsson, OB ;
Thorgeirsson, G ;
Hadzic, R ;
Jonsdottir, S ;
Reynisdottir, ST ;
Bjarnadottir, SM ;
Gudmundsdottir, T ;
Gudlaugsdottir, GJ ;
Gill, R ;
Lindpaintner, K ;
Sainz, J ;
Hannesson, HH ;
Sigurdsson, GT ;
Frigge, ML ;
Kong, A ;
Gudnason, V ;
Stefansson, K ;
Gulcher, JR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (03) :593-603
[6]   Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysis [J].
Grond-Ginsbach, C ;
Klima, B ;
Weber, R ;
Striegel, J ;
Fischer, C ;
Hacke, W ;
Brandt, T ;
Hausser, I .
ANNALS OF NEUROLOGY, 2002, 52 (03) :359-364
[7]   Sequence analysis of the COL5A2 gene in patients with spontaneous cervical artery dissections [J].
Grond-Ginsbach, C ;
Wigger, F ;
Morcher, M ;
von Pein, F ;
Grau, A ;
Hausser, I ;
Brandt, T .
NEUROLOGY, 2002, 58 (07) :1103-1105
[8]   Angiotensin converting enzyme insertion/deletion genotype is associated with leukoaraiosis in lacunar syndromes [J].
Hassan, A ;
Lansbury, A ;
Catto, AJ ;
Guthrie, A ;
Spencer, J ;
Craven, C ;
Grant, PJ ;
Bamford, JM .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2002, 72 (03) :343-346
[9]   Planning genetic studies in human stroke - Sample size estimates based on family history data [J].
Hassan, A ;
Sham, PC ;
Markus, HS .
NEUROLOGY, 2002, 58 (10) :1483-1488
[10]   The association of PAI-1 promoter 4G/5G insertion/deletion polymorphism with myocardial infarction and stroke in young women [J].
Hindorff, LA ;
Schwartz, SM ;
Siscovick, DS ;
Psaty, BM ;
Longstreth, WT ;
Reiner, AP .
JOURNAL OF CARDIOVASCULAR RISK, 2002, 9 (02) :131-137
123