accident vasculaire cérébral
déficit neurologique soudain d'origine vasculaire
egzanp nan
cause de décès
symptôme ou signe médical
lieu
cerveau humain[1]
spécialité médicale
neurologie
neurochirurgie
examens possibles
ROSIER scale
Orpington Prognostic Scale
médicament ou thérapie de traitement
pentoxifylline[15]
région anatomique
cerveau humain
association génétique
décrit par
Dictionnaire encyclopédique Brockhaus et Efron
affirmation détaillée dans: Q24333862, Q59882236
Petit Dictionnaire encyclopédique Brockhaus-Efron
affirmation détaillée dans: Q24729663
Grande Encyclopédie soviétique
affirmation détaillée dans: Q43401168
encyclopédie nationale du Kazakhstan
The Domestic Encyclopædia; Or, A Dictionary Of Facts, And Useful Knowledge
affirmation détaillée dans: Domestic Encyclopædia (1802)/Apoplexy
Armenian Soviet Encyclopedia, vol. 5
page(s): 168
projet Wikimédia s’intéressant à l'élément
Wikipédia:Articles vitaux/Niveau 4
date: 31 oktòb 2022
facteur de risque
incidence
identifiant WordLift
identifiant Classification internationale des soins primaires
K90
correspondance exacte
à ne pas confondre avec
Stroke
réputé identique à
maladie cérébro-vasculaire
catégorie Commons
Stroke
catégorie
Catégorie:Accident vasculaire cérébral
Referans
- ↑ 1,0 1,1 1,2 1,3 et 1,4 ontologie des maladies, 2 oktòb 2017, DOID:6713
- ↑ BBC Things
- ↑ Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=4953, 13 jen 2021
- ↑ 4,0 et 4,1 Symptom Ontology, 21 novanm 2020, 0000734
- ↑ http://www.patient.co.uk/patientplus/s.htm
- ↑ 6,0 6,1 6,2 6,3 6,4 6,5 6,6 et 6,7 OpenAlex, 26 janvye 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ sauvegarde de la base de données Freebase, 28 oktòb 2013
- ↑ KBpedia, 9 jiyè 2020
- ↑ GF WordNet
- ↑ National Library pèp Izrayèl
- ↑ Gemeinsame Normdatei
- ↑ UMLS 2023, 25 me 2023, inferred by common MeSH mappings on source and on Wikidata
- ↑ bibliothèque nationale centrale de Florence
- ↑ Symptom Ontology, 22 novanm 2020, 0000734
- ↑ N0000146791, 17 out 2016, NDF-RT, angle
- ↑ Phenocarta, Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=463, http://www.genome.gov/gwastudies/index.cfm?gene=ZFHX3, 13 septanm 2017
- ↑ Phenocarta, Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=92369, http://www.genome.gov/gwastudies/index.cfm?gene=SPSB4, 13 septanm 2017
- ↑ Phenocarta, Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=217, http://www.genome.gov/gwastudies/index.cfm?gene=ALDH2, 13 septanm 2017
- ↑ Phenocarta, A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=81792, http://www.genome.gov/gwastudies/index.cfm?gene=ADAMTS12, 13 septanm 2017
- ↑ Phenocarta, A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=9509, http://www.genome.gov/gwastudies/index.cfm?gene=ADAMTS2, 13 septanm 2017
- ↑ Phenocarta, Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=9734, http://www.genome.gov/gwastudies/index.cfm?gene=HDAC9, 13 septanm 2017
- ↑ Phenocarta, A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=202, http://www.genome.gov/gwastudies/index.cfm?gene=AIM1, 13 septanm 2017
- ↑ Phenocarta, A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release, http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=3613, http://www.genome.gov/gwastudies/index.cfm?gene=IMPA2, 13 septanm 2017
- ↑ KALRN: a central regulator of synaptic function and synaptopathies, article de revue de littérature
- ↑ Genetic Variant of Kalirin Gene Is Associated with Ischemic Stroke in a Chinese Han Population.
- ↑ http://www.who.int/healthinfo/global_burden_disease/estimates/en/index2.html, Òganizasyon Mondyal Lasante, 30 jiyè 2016
- ↑ 29273594
- ↑ 28,0 et 28,1 Epidemiology of ischemic and hemorrhagic stroke: incidence, prevalence, mortality, and risk factors
- ↑ 33302276
- ↑ https://www.medicalrecords.com/health-a-to-z/stroke-definition-2/
- ↑ https://www.medicalrecords.com/health-a-to-z/stroke-definition/