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La Revue Du Praticien
|
May 21, 2013
[Gene therapy: where do we stand?]
Marina Cavazzana-Calvo
Human Gene Therapy
|
September 12, 2018
Gene Therapy for Hemoglobinopathies
Marina Cavazzana, Fulvio Mavilio
Cell Stem Cell
|
April 5, 2024
The difficult translational pathway from animal models to patients
Marina Cavazzana, Annarita Miccio
The Journal of Clinical Investigation
|
June 6, 2007
Gene therapy for severe combined immunodeficiency: are we there yet?
Marina Cavazzana-Calvo, Alain Fischer
Stem Cells Translational Medicine
|
March 20, 2019
Concise Review: Boosting T-Cell Reconstitution Following Allogeneic Transplantation-Current Concepts and Future Perspectives
Laura Simons, Marina Cavazzana, Isabelle André
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 6, 2017
Gene Therapy for β-Hemoglobinopathies
Marina Cavazzana, Chiara Antoniani, Annarita Miccio
Hematology/Oncology Clinics of North America
|
September 13, 2017
Gene Therapy Approaches to Hemoglobinopathies
Giuliana Ferrari, Marina Cavazzana, Fulvio Mavilio
Blood
|
August 31, 2019
Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies
Elisa Magrin, Annarita Miccio, Marina Cavazzana
British Journal of Haematology
|
November 22, 2012
Haematopoietic stem cell transplantation for SCID patients: where do we stand?
Marina Cavazzana-Calvo, Isabelle André-Schmutz, Alain Fischer
Current Gene Therapy
|
September 24, 2014
Gene therapy for Wiskott-Aldrich Syndrome
Marita Bosticardo, Francesca Ferrua, Marina Cavazzana, et al.
Page
of 24
Search research articles
Search
Showing results (1-10 of 232) with videos related to
Sort By:
Page
of 24
La Revue Du Praticien
|
May 21, 2013
[Gene therapy: where do we stand?]
Marina Cavazzana-Calvo
Human Gene Therapy
|
September 12, 2018
Gene Therapy for Hemoglobinopathies
Marina Cavazzana, Fulvio Mavilio
Cell Stem Cell
|
April 5, 2024
The difficult translational pathway from animal models to patients
Marina Cavazzana, Annarita Miccio
The Journal of Clinical Investigation
|
June 6, 2007
Gene therapy for severe combined immunodeficiency: are we there yet?
Marina Cavazzana-Calvo, Alain Fischer
Stem Cells Translational Medicine
|
March 20, 2019
Concise Review: Boosting T-Cell Reconstitution Following Allogeneic Transplantation-Current Concepts and Future Perspectives
Laura Simons, Marina Cavazzana, Isabelle André
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 6, 2017
Gene Therapy for β-Hemoglobinopathies
Marina Cavazzana, Chiara Antoniani, Annarita Miccio
Hematology/Oncology Clinics of North America
|
September 13, 2017
Gene Therapy Approaches to Hemoglobinopathies
Giuliana Ferrari, Marina Cavazzana, Fulvio Mavilio
Blood
|
August 31, 2019
Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies
Elisa Magrin, Annarita Miccio, Marina Cavazzana
British Journal of Haematology
|
November 22, 2012
Haematopoietic stem cell transplantation for SCID patients: where do we stand?
Marina Cavazzana-Calvo, Isabelle André-Schmutz, Alain Fischer
Current Gene Therapy
|
September 24, 2014
Gene therapy for Wiskott-Aldrich Syndrome
Marita Bosticardo, Francesca Ferrua, Marina Cavazzana, et al.
Page
of 24