hjerneslag
akutt forstyrrelse i hjernens blodsirkulasjon
lea
jápminsivva
symptom eller tegn
sajádat
menneskehjerne[1]
dálkkasdieđalaš fágasuorgi
neurologiija
nevrokirurgi
doavtterdutkan
ROSIER scale
Orpington Prognostic Scale
dikšumis geavahuvvon dálkkas
pentoxifylline[15]
anatomisk lokasjon
menneskehjerne
genetisk assosiasjon
beskrevet i kilde
Brockhaus-Efron leksikon
tema for: Q24333862, Q59882236
Encyklopedisk ordbok fra Brockhaus-Efron
tema for: Q24729663
Store sovjetiske encyklopedi (1926–1947)
tema for: Q43401168
Kazakhstan. National encyclopedia
The Domestic Encyclopædia; Or, A Dictionary Of Facts, And Useful Knowledge
tema for: Domestic Encyclopædia (1802)/Apoplexy
Armenian Soviet Encyclopedia, vol. 5
siidu: 168
Wikiprošeavtta fáddálisttus
Wikipedia:Liste over artikler vi bør ha
Wikipedia:Luettelo keskeisistä tietosanakirja-artikkeleista/Laajennettu
goas: 31 golggotmánnu 2022
risikofaktor
WordLift-URL
ICPC-2
K90
eksakt samsvar
eará ášši go
Stroke
angivelig det samme som
cerebrovaskulære sykdommer
Commons-kategoriija
Stroke
fáttá váldokategoriija
Category:Stroke
Gáldu
- ↑ a á b c č Disease Ontology, 2 golggotmánnu 2017, DOID:6713
- ↑ BBC Things
- ↑ Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=4953, 13 geassemánnu 2021
- ↑ a á Symptom Ontology, 21 skábmamánnu 2020, 0000734
- ↑ http://www.patient.co.uk/patientplus/s.htm
- ↑ a á b c č d đ e OpenAlex, 26 ođđajagimánnu 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ Freebase-data fra Google, 28 golggotmánnu 2013
- ↑ KBpedia, 9 suoidnemánnu 2020
- ↑ GF WordNet
- ↑ Israels nasjonalbibliotek
- ↑ Gemeinsame Normdatei
- ↑ UMLS 2023, 25 miessemánnu 2023, inferred by common MeSH mappings on source and on Wikidata
- ↑ Biblioteca Nazionale Centrale di Firenze
- ↑ Symptom Ontology, 22 skábmamánnu 2020, 0000734
- ↑ N0000146791, 17 borgemánnu 2016, NDF-RT, eaŋgalsgiella
- ↑ 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 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 čakčamánnu 2017
- ↑ KALRN: a central regulator of synaptic function and synaptopathies, oversiktsartikkel
- ↑ 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, Máilmmi dearvvasvuohtaorganisašuvdna, 30 suoidnemánnu 2016
- ↑ 29273594
- ↑ a á 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/