New players in the genetics of stroke

被引：34

作者：

Tournier-Lasserve, E ^{[1
]}

机构：

[1] Assistance Publ Hop Paris, F-75010 Paris, France

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2002年 / 347卷 / 21期

关键词：

D O I：

10.1056/NEJMcibr022035

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1711 / 1712

页数：2

共 6 条

[1] 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

[2] Genetics and ischaemic stroke [J].

Hassan, A ;

Markus, HS .

BRAIN, 2000, 123 :1784-1812

[3] Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia [J].

Joutel, A ;

Corpechot, C ;

Ducros, A ;

Vahedi, K ;

Chabriat, H ;

Mouton, P ;

Alamowitch, S ;

Domenga, V ;

Cecillion, M ;

Marechal, E ;

Maciazek, J ;

Vayssiere, C ;

Cruaud, C ;

Cabanis, EA ;

Ruchoux, MM ;

Weissenbach, J ;

Bach, JF ;

Bousser, MG ;

TournierLasserve, E .

NATURE, 1996, 383 (6602) :707-710

[4] Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas [J].

Laberge-le Couteulx, S ;

Jung, HH ;

Labauge, P ;

Houtteville, JP ;

Lescoat, C ;

Cecillon, M ;

Marechal, E ;

Joutel, A ;

Bach, JF ;

Tournier-Lasserve, E .

NATURE GENETICS, 1999, 23 (02) :189-193

[5] MENDELIAN ETIOLOGIES OF STROKE [J].

NATOWICZ, M ;

KELLEY, RI .

ANNALS OF NEUROLOGY, 1987, 22 (02) :175-192

[6] Genomewide-linkage and haplotype-association studies map intracranial aneurysm to chromosome 7q11 [J].

Onda, H ;

Kasuya, H ;

Yoneyama, T ;

Takakura, K ;

Hori, T ;

Takeda, J ;

Nakajima, T ;

Inoue, I .

AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) :804-819

← 1 →