Showing results (1501-1510 of 1,590) with videos related to

Sort By:
Pageof 159
Blood|April 25, 2025
Clinical phenotype and pathophysiological mechanisms underlying qualitative Low VWFFerdows Atiq, Robin Blok, Calvin van Kwawegen, et al.
NPJ Precision Oncology|July 9, 2026
Development of a rapid ex vivo tumor platform for drug response prediction in lung cancerRianne D W Vaes, Zhongli Chen, Iris E W G Laven, et al.
Human Genetics|May 10, 2018
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorderLot Snijders Blok, Susan M Hiatt, Kevin M Bowling, et al.
Bone Marrow Transplantation|March 25, 2022
Allogeneic hematopoietic stem cell transplantation for adult HLH: a retrospective study by the chronic malignancies and inborn errors working parties of EBMTRafal Machowicz, Felipe Suarez, Wieslaw Wiktor-Jedrzejczak, et al.
Plos Neglected Tropical Diseases|March 31, 2021
The long-term impact of the Leprosy Post-Exposure Prophylaxis (LPEP) program on leprosy incidence: A modelling studyDavid J Blok, Peter Steinmann, Anuj Tiwari, et al.
European Journal of Neurology|April 10, 2025
European Academy of Neurology (EAN)/European Federation of Autonomic Societies (EFAS)/International Neuro-Urology Society (INUS) Guidelines for Practising Neurologists on the Assessment and Treatment of Neurogenic Urinary and Sexual Symptoms (NEUROGED Guidelines)Jalesh N Panicker, Alessandra Fanciulli, Magdalena Krbot Skoric, et al.
Blood|July 3, 2020
Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adultsRobert Chiesa, Junfeng Wang, Henric-Jan Blok, et al.
Genome Biology|June 12, 2016
The genome of the yellow potato cyst nematode, Globodera rostochiensis, reveals insights into the basis of parasitism and virulenceSebastian Eves-van den Akker, Dominik R Laetsch, Peter Thorpe, et al.
American Journal of Human Genetics|July 16, 2019
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental DisorderLot Snijders Blok, Tjitske Kleefstra, Hanka Venselaar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 5, 2024
Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disabilityLachlan De Hayr, Laura E R Blok, Kerith-Rae Dias, et al.
Pageof 159