Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria Pia Cicalese

Showing results (61-70 of 91) with videos related to

Pageof 10
Sort By:
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 trialMaria 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 therapyValeria Calbi, Francesca Fumagalli, Giulia Consiglieri, et al.
Bone Marrow Transplantation|June 1, 2019
Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapyFrancesca 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 severitiesDimitri 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 ReportSabina 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 immunityEmilia 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 onsetPaola 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 deficiencyFederica 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 NetworkEmilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
EMBO Molecular Medicine|December 3, 2016
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophyGiulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 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 trialMaria 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 therapyValeria Calbi, Francesca Fumagalli, Giulia Consiglieri, et al.
Bone Marrow Transplantation|June 1, 2019
Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapyFrancesca 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 severitiesDimitri 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 ReportSabina 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 immunityEmilia 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 onsetPaola 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 deficiencyFederica 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 NetworkEmilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
EMBO Molecular Medicine|December 3, 2016
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophyGiulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
Pageof 10