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The Journal of Allergy and Clinical Immunology|October 31, 2021
Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohortArjan C Lankester, Benedicte Neven, Nizar Mahlaoui, et al.
Science (New York, N.Y.)|August 4, 2022
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathiesDaniel Reichart, Eric L Lindberg, Henrike Maatz, et al.
Annals of Intensive Care|April 26, 2023
Attributable mortality due to nosocomial sepsis in Brazilian hospitals: a case-control studyFernando G Zampieri, Alexandre B Cavalcanti, Leandro U Taniguchi, et al.
Clinics (Sao Paulo, Brazil)|November 24, 2021
Poor Sleep quality and health-related quality of life impact in adolescents with and without chronic immunosuppressive conditions during COVID-19 quarantineAlberto C Helito, Livia Lindoso, Sofia M Sieczkowska, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|March 31, 2015
A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibilityF David Carmona, Sarah L Mackie, Jose-Ezequiel Martín, et al.
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