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

页码：342 / 344

页数：3

共 27 条

[1] Familial clustering of intracerebral hemorrhage: A prospective study in north Carolina
Alberts, MJ
McCarron, MO
Hoffmann, KL
Graffagnino, C
[J]. NEUROEPIDEMIOLOGY, 2002, 21 (01) : 18 - 21
[2] Genetic liability in stroke - A long-term follow-up study of Danish twins
Bak, S
Gaist, D
Sindrup, SH
Skytthe, A
Christensen, K
[J]. STROKE, 2002, 33 (03) : 769 - 774
[3] Genetic association studies - Genes in search of diseases
Bird, TD
Jarvik, GP
Wood, NW
[J]. NEUROLOGY, 2001, 57 (07) : 1153 - 1154
[4] No association of factor XIII Val34Leu polymorphism with primary intracerebral hemorrhage and healthy controls in Korean population
Cho, KH
Kim, BC
Kim, MK
Shin, BA
[J]. JOURNAL OF KOREAN MEDICAL SCIENCE, 2002, 17 (02) : 249 - 253
[5] Localization of a susceptibility gene for common forms of stroke to 5q12
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
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (03) : 593 - 603
[6] Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysis
Grond-Ginsbach, C
Klima, B
Weber, R
Striegel, J
Fischer, C
Hacke, W
Brandt, T
Hausser, I
[J]. ANNALS OF NEUROLOGY, 2002, 52 (03) : 359 - 364
[7] Sequence analysis of the COL5A2 gene in patients with spontaneous cervical artery dissections
Grond-Ginsbach, C
Wigger, F
Morcher, M
von Pein, F
Grau, A
Hausser, I
Brandt, T
[J]. NEUROLOGY, 2002, 58 (07) : 1103 - 1105
[8] Angiotensin converting enzyme insertion/deletion genotype is associated with leukoaraiosis in lacunar syndromes
Hassan, A
Lansbury, A
Catto, AJ
Guthrie, A
Spencer, J
Craven, C
Grant, PJ
Bamford, JM
[J]. 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
Hassan, A
Sham, PC
Markus, HS
[J]. 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
Hindorff, LA
Schwartz, SM
Siscovick, DS
Psaty, BM
Longstreth, WT
Reiner, AP
[J]. JOURNAL OF CARDIOVASCULAR RISK, 2002, 9 (02): : 131 - 137

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