Blood Diseases
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Last Posted: Nov 21, 2018
- Prevalence of inherited blood disorders and associations with malaria and anemia in Malawian children.
McGann Patrick T et al. Blood advances 2018 Nov 2(21) 3035-3044 - Prevalence of FVIII inhibitors in severe haemophilia A patients: Effect of treatment and genetic factors in an Indian population.
David Sachin et al. Haemophilia : the official journal of the World Federation of Hemophilia 2018 Nov - Sickle Cell Disease Clinical Trials and Phenotypes.
Ezekekwu Chinedu A et al. Journal of tropical diseases & public health 2018 6(2) 259 - Pharmacogenetics to prevent heparin-induced thrombocytopenia: what do we know?
Karnes Jason H et al. Pharmacogenomics 2018 Nov - Thousands of sickle cell and hemophilia patients are waiting for gene therapies. Can manufacturers keep up?
E Mullin, Stat News, November 5, 2018 - About genetic diagnosis of hereditary hemochromatosis.
Michel Henri et al. Annales de biologie clinique 2018 Apr 76(2) 131 - Noninvasive fetal RHD genotyping of RhD negative pregnant women for targeted anti-D therapy in Australia: A cost-effectiveness analysis.
Gordon Louisa G et al. Prenatal diagnosis 2017 37(12) 1245-1253 - Emerging Genetic Therapy for Sickle Cell Disease.
Orkin Stuart H et al. Annual review of medicine 2018 Oct - Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review
RP Naik et al, Annals of Internal Medicine, October 2018 - Systematic review study supports that sickle cell trait increases risk for some health conditions- More research needed to clarify all health outcomes associated with SCT
J Mjoseth, NHGRI, October 30, 2018 - Classification and Personalized Prognosis in Myeloproliferative Neoplasms.
Grinfeld Jacob et al. The New England journal of medicine 2018 379(15) 1416-1430 - Who is more likely to develop CKD?
NIDDK Information, 2018 - [Sickle Cell Disease in Newborns in Germany: Analysis of the AOK Health Insurance Data].
Pattloch Dagmar et al. Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)) 2018 Oct - A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia.
Johnson Ben et al. Research and practice in thrombosis and haemostasis 2018 Oct 2(4) 640-652 - Hereditary Hemochromatosis
Hereditary hemochromatosis is a genetic disorder that can cause severe liver disease and other health problems
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