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Molecules (Basel, Switzerland)|June 10, 2022
Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their AnalogsVincenzo Tragni, Guido Primiano, Albina Tummolo, et al.Leukemia & Lymphoma|September 28, 2011
WT1 overexpression at diagnosis may predict favorable outcome in patients with de novo non-M3 acute myeloid leukemiaMaurizio Miglino, Nicoletta Colombo, Gianmatteo Pica, et al.Protein Science : a Publication of the Protein Society|June 20, 2026
Structural basis of ligand selectivity in FAD/NAD(P)H-dependent dehydrogenases: insights from trypanothione reductase and type II NADH dehydrogenaseGiulia Chiara Maria Perrone, Serena Spadone, Anna Lucia Francavilla, et al.The New England Journal of Medicine|August 16, 2023
Gene Therapy in Patients with the Crigler-Najjar SyndromeLorenzo D'Antiga, Ulrich Beuers, Giuseppe Ronzitti, et al.NEJM Evidence|February 6, 2024
Liver-Directed Adeno-Associated Virus-Mediated Gene Therapy for Mucopolysaccharidosis Type VINicola Brunetti-Pierri, Rita Ferla, Virginia Maria Ginocchio, et al.Bone Marrow Transplantation|April 30, 2020
Haploidentical hematopoietic stem cell transplantation in aplastic anemia: a systematic review and meta-analysis of clinical outcome on behalf of the severe aplastic anemia working party of the European group for blood and marrow transplantation (SAAWP of EBMT)Ghada ElGohary, Riad El Fakih, Regis de Latour, et al.Bone Marrow Transplantation|October 31, 2002
Allogeneic bone marrow transplantation (BMT) for adults with acute lymphoblastic leukemia (ALL): predictive role of minimal residual disease monitoring on relapseM Miglino, G Berisso, R Grasso, et al.British Journal of Haematology|February 22, 2020
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?Paola Quarello, Emanuela Garelli, Adriana Carando, et al.British Journal of Haematology|July 17, 2019
FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 geneMaurizio Miano, Enrico Cappelli, Agnese Pezzulla, et al.Frontiers in Immunology|April 28, 2022
Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The "Fil Rouge" of Treg Between IPEX Features and Other Clinical Entities?Micaela Gentile, Maurizio Miano, Paola Terranova, et al.Pageof 93