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Lancet (London, England)
|
June 13, 2016
Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial
Maria Sessa, Laura Lorioli, Francesca Fumagalli, et al.
Bone Marrow Transplantation
|
January 31, 2018
Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy
Valeria Calbi, Francesca Fumagalli, Giulia Consiglieri, et al.
Bone Marrow Transplantation
|
June 1, 2019
Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapy
Francesca Tucci, Marta Frittoli, Federica Barzaghi, et al.
The Journal of Allergy and Clinical Immunology
|
September 16, 2024
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities
Dimitri Bulté, Federica Barzaghi, Cristina Mesa-Nuñez, et al.
Frontiers in Immunology
|
December 17, 2020
Mild SARS-CoV-2 Infection After Gene Therapy in a Child With Wiskott-Aldrich Syndrome: A Case Report
Sabina Cenciarelli, Valeria Calbi, Federica Barzaghi, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2020
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
Emilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Diabetologia
|
January 24, 2023
Genetic determinants of type 1 diabetes in individuals with weak evidence of islet autoimmunity at disease onset
Paola Carrera, Ilaria Marzinotto, Riccardo Bonfanti, et al.
Frontiers in Immunology
|
October 17, 2022
Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency
Federica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, et al.
Frontiers in Immunology
|
August 29, 2019
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network
Emilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
EMBO Molecular Medicine
|
December 3, 2016
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy
Giulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
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Search research articles
Search
Showing results (61-70 of 91) with videos related to
Sort By:
Page
of 10
Lancet (London, England)
|
June 13, 2016
Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial
Maria Sessa, Laura Lorioli, Francesca Fumagalli, et al.
Bone Marrow Transplantation
|
January 31, 2018
Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy
Valeria Calbi, Francesca Fumagalli, Giulia Consiglieri, et al.
Bone Marrow Transplantation
|
June 1, 2019
Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapy
Francesca Tucci, Marta Frittoli, Federica Barzaghi, et al.
The Journal of Allergy and Clinical Immunology
|
September 16, 2024
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities
Dimitri Bulté, Federica Barzaghi, Cristina Mesa-Nuñez, et al.
Frontiers in Immunology
|
December 17, 2020
Mild SARS-CoV-2 Infection After Gene Therapy in a Child With Wiskott-Aldrich Syndrome: A Case Report
Sabina Cenciarelli, Valeria Calbi, Federica Barzaghi, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2020
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
Emilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Diabetologia
|
January 24, 2023
Genetic determinants of type 1 diabetes in individuals with weak evidence of islet autoimmunity at disease onset
Paola Carrera, Ilaria Marzinotto, Riccardo Bonfanti, et al.
Frontiers in Immunology
|
October 17, 2022
Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency
Federica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, et al.
Frontiers in Immunology
|
August 29, 2019
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network
Emilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
EMBO Molecular Medicine
|
December 3, 2016
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy
Giulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
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of 10