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Complement factor H Y402H gene polymorphism, C-reactive protein, and risk of incident myocardial infarction, ischaemic stroke, and venous thromboembolism : A nested case-control study

Author
ZEE, Robert Y. L1 2 3 ; DIEHL, Kirsti A1 2 3 ; RIDKER, Paul M1 2 3
[1] Laboratory of Genetic Epidemiology, Center for Cardiovascular Disease Prevention, Brigham and Women's Hospital, Harvard Medical School, 900 Commonwealth Avenue East, Boston, MA 02215, United States
[2] Donald W. Reynolds Center for Cardiovascular Research, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States
[3] LeDucq Center for Molecular and Genetic Epidemiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States
Source

Atherosclerosis. 2006, Vol 187, Num 2, pp 332-335, 4 p ; ref : 10 ref

ISSN
0021-9150
Scientific domain
Cardiology, blood circulation, phlebology
Publisher
Elsevier, Amsterdam
Publication country
Netherlands
Document type
Article
Language
English
Author keyword
CFH Polymorphism Risk factor Thromboembolism
Keyword (fr)
Accident cérébrovasculaire Anticoagulant Appareil circulatoire pathologie Athérosclérose Complément Embolie Etude cas témoin Etude cohorte Facteur risque Génotype Homme Héparine Infarctus myocarde Ischémie Médecin Polymorphisme Protéine C réactive Tabagisme Thromboembolie Thrombose profonde Thrombose veineuse Variant génétique Cardiopathie Cérébrovasculaire pathologie Encéphale pathologie Glycosaminoglycane Myocarde pathologie Système nerveux central pathologie Système nerveux pathologie Vaisseau sanguin pathologie Veine pathologie
Keyword (en)
Stroke Anticoagulant Cardiovascular disease Atherosclerosis Complement Embolism Case control study Cohort study Risk factor Genotype Human Heparin Myocardial infarction Ischemia Physician Polymorphism C reactive protein Tobacco smoking Thromboembolism Deep vein thrombosis Venous thrombosis Genetic variant Heart disease Cerebrovascular disease Cerebral disorder Glycosaminoglycan Myocardial disease Central nervous system disease Nervous system diseases Vascular disease Venous disease
Keyword (es)
Accidente cerebrovascular Anticoagulante Aparato circulatorio patología Ateroesclerosis Complemento Embolia Estudio caso control Estudio cohorte Factor riesgo Genotipo Hombre Heparina Infarto miocardio Isquemia Médico Polimorfismo Proteína reactiva Tabaquismo Tromboembolia Trombosis venosa profunda Trombosis venosa Variante genética Cardiopatía Vaso sanguíneo encéfalo patología Encéfalo patología Glicosaminoglicano Miocardio patología Sistema nervosio central patología Sistema nervioso patología Vaso sanguíneo patología Vena patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12A Heart / 002B12A03 Coronary heart disease

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12B Blood and lymphatic vessels / 002B12B01 Atherosclerosis (general aspects, experimental research)

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12B Blood and lymphatic vessels / 002B12B03 Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous

Discipline
Cardiology. Circulatory system
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
17940372

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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