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Francesca Gualandi

Showing results (71-80 of 169) with videos related to

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Haematologica|September 10, 2002
Treatment of acute graft versus host disease with low dose-alternate day anti-thymocyte globulinFrancesco Graziani, Maria Teresa Van Lint, Alida Dominietto, et al.
Journal of Cellular Physiology|November 22, 2012
Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophyCamilla Pellegrini, Alessandra Zulian, Francesca Gualandi, et al.
Bone Marrow Transplantation|August 22, 2019
Graft versus host disease in unmanipulated haploidentical marrow transplantation with a modified post-transplant cyclophosphamide (PT-CY) regimen: an update on 425 patientsAndrea Bacigalupo, Anna Maria Raiola, Alida Dominietto, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|June 17, 2005
Autologous stem cell transplantation as rescue therapy in malignant forms of multiple sclerosisGiovanni Luigi Mancardi, Alessandra Murialdo, Paolo Rossi, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|July 11, 2014
Patterns of late gadolinium enhancement in Duchenne muscular dystrophy carriersVincenzo Giglio, Paolo Emilio Puddu, Giovanni Camastra, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 12, 2007
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporinsAlessia Angelin, Tania Tiepolo, Patrizia Sabatelli, et al.
The Journal of Investigative Dermatology|October 1, 2010
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathiesPatrizia Sabatelli, Sudheer K Gara, Paolo Grumati, et al.
Circulation. Genomic and Precision Medicine|March 11, 2020
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and LaminopathiesAnnarita Armaroli, Cristina Balla, Cecilia Trabanelli, et al.
Plos One|October 3, 2012
The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoformsMatteo Bovolenta, Daniela Erriquez, Emanuele Valli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 2, 2017
Somatic mosaicism represents an underestimated event underlying collagen 6-related disordersAdele D'Amico, Fabiana Fattori, Giorgio Tasca, et al.
Pageof 17

Showing results (71-80 of 169) with videos related to

Sort By:
Pageof 17
Haematologica|September 10, 2002
Treatment of acute graft versus host disease with low dose-alternate day anti-thymocyte globulinFrancesco Graziani, Maria Teresa Van Lint, Alida Dominietto, et al.
Journal of Cellular Physiology|November 22, 2012
Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophyCamilla Pellegrini, Alessandra Zulian, Francesca Gualandi, et al.
Bone Marrow Transplantation|August 22, 2019
Graft versus host disease in unmanipulated haploidentical marrow transplantation with a modified post-transplant cyclophosphamide (PT-CY) regimen: an update on 425 patientsAndrea Bacigalupo, Anna Maria Raiola, Alida Dominietto, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|June 17, 2005
Autologous stem cell transplantation as rescue therapy in malignant forms of multiple sclerosisGiovanni Luigi Mancardi, Alessandra Murialdo, Paolo Rossi, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|July 11, 2014
Patterns of late gadolinium enhancement in Duchenne muscular dystrophy carriersVincenzo Giglio, Paolo Emilio Puddu, Giovanni Camastra, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 12, 2007
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporinsAlessia Angelin, Tania Tiepolo, Patrizia Sabatelli, et al.
The Journal of Investigative Dermatology|October 1, 2010
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathiesPatrizia Sabatelli, Sudheer K Gara, Paolo Grumati, et al.
Circulation. Genomic and Precision Medicine|March 11, 2020
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and LaminopathiesAnnarita Armaroli, Cristina Balla, Cecilia Trabanelli, et al.
Plos One|October 3, 2012
The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoformsMatteo Bovolenta, Daniela Erriquez, Emanuele Valli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 2, 2017
Somatic mosaicism represents an underestimated event underlying collagen 6-related disordersAdele D'Amico, Fabiana Fattori, Giorgio Tasca, et al.
Pageof 17