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Annals of Surgical Oncology|March 16, 2007
Treatment and outcome of 82 patients with angiosarcomaJohn A Abraham, Francis J Hornicek, Adam M Kaufman, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 31, 2016
The role of biochemical of bone turnover markers in osteoporosis and metabolic bone disease: a consensus paper of the Belgian Bone ClubE Cavalier, P Bergmann, O Bruyère, et al.Cancer Research|May 28, 2021
STK11/LKB1 Loss of Function Is Associated with Global DNA Hypomethylation and <i>S</i>-Adenosyl-Methionine Depletion in Human Lung AdenocarcinomaMichael J Koenig, Bernice A Agana, Jacob M Kaufman, et al.Frontiers in Genetics|February 28, 2014
The struggle to find reliable results in exome sequencing data: filtering out Mendelian errorsZubin H Patel, Leah C Kottyan, Sara Lazaro, et al.Journal of Translational Medicine|August 23, 2012
IRF5 gene polymorphisms in melanomaLorenzo Uccellini, Valeria De Giorgi, Yingdong Zhao, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 21, 2016
The role of calcium supplementation in healthy musculoskeletal ageing : An expert consensus meeting of the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) and the International Foundation for Osteoporosis (IOF)N C Harvey, E Biver, J-M Kaufman, et al.The Lancet. Haematology|March 6, 2017
Derivation and external validation of the PLASMIC score for rapid assessment of adults with thrombotic microangiopathies: a cohort studyPavan K Bendapudi, Shelley Hurwitz, Ashley Fry, et al.Genes and Immunity|April 24, 2009
Meta-analysis and imputation identifies a 109 kb risk haplotype spanning TNFAIP3 associated with lupus nephritis and hematologic manifestationsJ S Bates, C J Lessard, J M Leon, et al.Transfusion|May 31, 2020
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestryWilliam J Lane, Nicholas S Gleadall, Judith Aeschlimann, et al.Plos One|March 6, 2008
Common variants within MECP2 confer risk of systemic lupus erythematosusAmr H Sawalha, Ryan Webb, Shizhong Han, et al.Pageof 88