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Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

scientific article published on 20 April 2020

Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia

artículo científico publicado en 2020

Enabling External Inquiries to an Existing Patient Registry by Using the Open Source Registry System for Rare Diseases: Demonstration of the System Using the European Society for Immunodeficiencies Registry

scientific article published on 07 October 2020

Front-line imatinib treatment in children and adolescents with chronic myeloid leukemia: results from a phase III trial

scientific article published on 20 June 2018

Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice

artículo científico publicado en 2021

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

artículo científico publicado en 2020

Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.

artículo científico publicado en 2018

Leukemia-induced dysfunctional TIM-3+CD4+ bone marrow T cells increase risk of relapse in pediatric B-precursor ALL patients

artículo científico publicado en 2020

Patients with rare diseases: from therapeutic orphans to pioneers of personalized treatments.

artículo científico publicado en 2017

Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition

artículo científico publicado en 2019

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