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Thrombosis Journal|July 16, 2019
Validation of the Khorana score in acute myeloid leukemia patients: a single-institution experienceAbu-Sayeef Mirza, Seongseok Yun, Najla Al Ali, et al.Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Human germline biallelic loss-of-function OSMR variants cause severe allergic diseaseMehul Sharma, Simran Samra, Yihui Liu, et al.Blood|April 20, 2021
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulationOttavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, et al.Nature Genetics|November 8, 2016
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy numberJonathan J Lyons, Xiaomin Yu, Jason D Hughes, et al.Frontiers in Immunology|May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunityBreanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.Nature Immunology|January 20, 2025
Variants and vaccines impact nasal immunity over three waves of SARS-CoV-2Jaclyn M L Walsh, Vincent N Miao, Anna H Owings, et al.Nature Genetics|October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.Hemasphere|December 13, 2021
Updated Diagnostic Criteria and Classification of Mast Cell Disorders: A Consensus ProposalPeter Valent, Cem Akin, Karin Hartmann, et al.Nature Genetics|December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseQing Zhou, Hongying Wang, Daniella M Schwartz, et al.Nature Genetics|June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.Pageof 9