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Preventive Veterinary Medicine|May 8, 2007
UK surveillance: provision of quality assured information from combined datasetsG A Paiba, S R Roberts, C W Houston, et al.American Heart Journal|March 1, 1994
Coronary arteriographic findings in black patients and risk markers for coronary artery diseaseR L Peniston, L Adams-Campbell, J W Fletcher, et al.Leukemia & Lymphoma|May 30, 2001
Fludarabine and cytarabine as a sequential infusion regimen for treatment of adults with recurrent, refractory or poor prognosis acute leukemiaB Vidarsson, R Abonour, E C Williams, et al.Diabetes Research and Clinical Practice|January 16, 2022
A practical approach to continuous glucose monitoring (rtCGM) and FreeStyle Libre systems (isCGM) in children and young people with Type 1 diabetesA Soni, N Wright, J C Agwu, et al.Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.International Journal of Obesity (2005)|August 17, 2013
Gene expression profiling in subcutaneous, visceral and epigastric adipose tissues of patients with extreme obesityG S Gerhard, A M Styer, W E Strodel, et al.Blood Cells, Molecules & Diseases|January 1, 1996
Mutation analysis in hereditary hemochromatosisE Beutler, T Gelbart, C West, et al.Journal of Thrombosis and Haemostasis : JTH|October 8, 2016
The association of anti-platelet factor 4/heparin antibodies with early and delayed thromboembolism after cardiac surgeryI J Welsby, E F Krakow, J A Heit, et al.Genes, Brain, and Behavior|August 13, 2009
Genetic architecture for hole-board behaviors across substantial time intervals in young, middle-aged and old miceJ E Foreman, A Lionikas, D H Lang, et al.Cell|November 1, 1996
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4R A Ophoff, G M Terwindt, M N Vergouwe, et al.Pageof 9