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Francesca Gualandi

Showing results (61-70 of 169) with videos related to

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Giornale Italiano Di Cardiologia (2006)|February 25, 2026
[Cardiogenetics in Piacenza: integrated care and telemedicine for precision medicine]Francesco Di Spigno, Francesca Gualandi, Alessandro Arata, et al.
Infection|September 21, 2018
Efficacy of lamivudine prophylaxis in preventing hepatitis B virus reactivation in patients with resolved infection undergoing allogeneic SCT and receiving rituximabEmanuela Zappulo, Laura Ambra Nicolini, Carmen Di Grazia, et al.
Neuromuscular Disorders : NMD|September 13, 2016
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcriptAlice Todeschini, Francesca Gualandi, Cecilia Trabanelli, et al.
The Lancet. Oncology|August 12, 2008
Direct intrabone transplant of unrelated cord-blood cells in acute leukaemia: a phase I/II studyFrancesco Frassoni, Francesca Gualandi, Marina Podestà, et al.
Genomics|November 1, 2002
Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin geneLuisa Toffolatti, Barbara Cardazzo, Carlo Nobile, et al.
Frontiers in Immunology|May 24, 2021
Autologous Hematopoietic Stem Cell Transplantation for Behçet's Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow TransplantationMathieu Puyade, Amit Patel, Yeong Jer Lim, et al.
Diagnostic Microbiology and Infectious Disease|January 28, 2012
Galactomannan testing might be useful for early diagnosis of fusariosisMałgorzata Mikulska, Elisa Furfaro, Valerio Del Bono, et al.
Journal of Cardiovascular Development and Disease|September 26, 2021
Left Ventricular Myocardial Noncompaction with Advanced Atrioventricular Conduction Disorder and Ventricular Arrhythmias in a Young Patient: Role of MIB1 GeneCristina Balla, Martina De Raffele, Maria Angela Deserio, et al.
Transplantation and Cellular Therapy|April 24, 2023
Total Marrow Irradiation for Second Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Advanced Acute LeukemiaAlida Dominietto, Stefano Vagge, Carmen di Grazia, et al.
BMC Medical Genetics|March 23, 2010
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathiesMatteo Bovolenta, Marcella Neri, Elena Martoni, et al.
Pageof 17

Showing results (61-70 of 169) with videos related to

Sort By:
Pageof 17
Giornale Italiano Di Cardiologia (2006)|February 25, 2026
[Cardiogenetics in Piacenza: integrated care and telemedicine for precision medicine]Francesco Di Spigno, Francesca Gualandi, Alessandro Arata, et al.
Infection|September 21, 2018
Efficacy of lamivudine prophylaxis in preventing hepatitis B virus reactivation in patients with resolved infection undergoing allogeneic SCT and receiving rituximabEmanuela Zappulo, Laura Ambra Nicolini, Carmen Di Grazia, et al.
Neuromuscular Disorders : NMD|September 13, 2016
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcriptAlice Todeschini, Francesca Gualandi, Cecilia Trabanelli, et al.
The Lancet. Oncology|August 12, 2008
Direct intrabone transplant of unrelated cord-blood cells in acute leukaemia: a phase I/II studyFrancesco Frassoni, Francesca Gualandi, Marina Podestà, et al.
Genomics|November 1, 2002
Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin geneLuisa Toffolatti, Barbara Cardazzo, Carlo Nobile, et al.
Frontiers in Immunology|May 24, 2021
Autologous Hematopoietic Stem Cell Transplantation for Behçet's Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow TransplantationMathieu Puyade, Amit Patel, Yeong Jer Lim, et al.
Diagnostic Microbiology and Infectious Disease|January 28, 2012
Galactomannan testing might be useful for early diagnosis of fusariosisMałgorzata Mikulska, Elisa Furfaro, Valerio Del Bono, et al.
Journal of Cardiovascular Development and Disease|September 26, 2021
Left Ventricular Myocardial Noncompaction with Advanced Atrioventricular Conduction Disorder and Ventricular Arrhythmias in a Young Patient: Role of MIB1 GeneCristina Balla, Martina De Raffele, Maria Angela Deserio, et al.
Transplantation and Cellular Therapy|April 24, 2023
Total Marrow Irradiation for Second Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Advanced Acute LeukemiaAlida Dominietto, Stefano Vagge, Carmen di Grazia, et al.
BMC Medical Genetics|March 23, 2010
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathiesMatteo Bovolenta, Marcella Neri, Elena Martoni, et al.
Pageof 17