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 (71-80 of 91) with videos related to

Pageof 10
Sort By:
EMBO Molecular Medicine|November 7, 2015
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophyGiulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
Blood|March 6, 2024
Circulating hematopoietic stem/progenitor cell subsets contribute to human hematopoietic homeostasisPamela Quaranta, Luca Basso-Ricci, Raisa Jofra Hernandez, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 24, 2021
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunityCinzia Milito, Vassilios Lougaris, Giuliana Giardino, et al.
Nature Medicine|January 22, 2019
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemiaSarah Marktel, Samantha Scaramuzza, Maria Pia Cicalese, et al.
Frontiers in Immunology|April 30, 2019
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Frontiers in Immunology|June 20, 2019
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophyAlessandra Biffi, Eugenio Montini, Laura Lorioli, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndromeAlessandro Aiuti, Luca Biasco, Samantha Scaramuzza, et al.
The Lancet. Haematology|April 15, 2019
Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical studyFrancesca Ferrua, Maria Pia Cicalese, Stefania Galimberti, et al.
Nature Communications|April 30, 2024
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCIDDaniela Cesana, Maria Pia Cicalese, Andrea Calabria, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
EMBO Molecular Medicine|November 7, 2015
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophyGiulio Cossu, Stefano C Previtali, Sara Napolitano, et al.
Blood|March 6, 2024
Circulating hematopoietic stem/progenitor cell subsets contribute to human hematopoietic homeostasisPamela Quaranta, Luca Basso-Ricci, Raisa Jofra Hernandez, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 24, 2021
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunityCinzia Milito, Vassilios Lougaris, Giuliana Giardino, et al.
Nature Medicine|January 22, 2019
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemiaSarah Marktel, Samantha Scaramuzza, Maria Pia Cicalese, et al.
Frontiers in Immunology|April 30, 2019
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Frontiers in Immunology|June 20, 2019
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophyAlessandra Biffi, Eugenio Montini, Laura Lorioli, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndromeAlessandro Aiuti, Luca Biasco, Samantha Scaramuzza, et al.
The Lancet. Haematology|April 15, 2019
Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical studyFrancesca Ferrua, Maria Pia Cicalese, Stefania Galimberti, et al.
Nature Communications|April 30, 2024
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCIDDaniela Cesana, Maria Pia Cicalese, Andrea Calabria, et al.
Pageof 10