Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 3 (of 3 Records)

Query Trace: Neonatal Stroke[original query]
Symptomatic ischemic stroke in full-term neonates : role of acquired and genetic prothrombotic risk factors.
Stroke; a journal of cerebral circulation 2000 Oct 31 (10): 2437-41.
Günther G, Junker R, Sträter R, Schobess R, Kurnik K, Heller C, Kosch A, Nowak-Göttl U,
Candidate gene polymorphisms do not differ between newborns with stroke and normal controls.
Stroke; a journal of cerebral circulation 2006 Nov 37 (11): 2678-83.
Miller Steven P, Wu Yvonne W, Lee Janet, Lammer Edward J, Iovannisci David M, Glidden David V, Bonifacio Sonia L, Collins Abigail, Shaw Gary M, Barkovich A James, Ferriero Donna
Molecular characterization of factor V leiden G1691A and prothrombin G20210A mutations in Saudi newborns with stroke.
Biochemical genetics 2011 Oct 49 (9-10): 601-10.
Gawish Gihan E
TOP