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Francesca Gualandi

Showing results (41-50 of 169) with videos related to

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International Journal of Molecular Sciences|February 10, 2024
Charcot-Marie-Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber NeuropathyFranco Gemignani, Antonio Percesepe, Francesca Gualandi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 14, 2015
Low intensity lympho-ablative regimen followed by autologous hematopoietic stem cell transplantation in severe forms of multiple sclerosis: A MRI-based clinical studyDaniela Curro', Luisa Vuolo, Francesca Gualandi, et al.
Journal of Clinical Microbiology|March 30, 2002
Aspergillus galactomannan antigen in the cerebrospinal fluid of bone marrow transplant recipients with probable cerebral aspergillosisClaudio Viscoli, Marco Machetti, Paola Gazzola, et al.
Biomedicines|August 26, 2023
Brugada Syndrome: More than a Monogenic ChannelopathyAntonella Liantonio, Matteo Bertini, Antonietta Mele, et al.
Neurogenetics|August 27, 2013
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3Ginevra Zanni, Chiara Scotton, Chiara Passarelli, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 27, 2018
De-Escalation and Discontinuation of Empirical Antibiotic Treatment in a Cohort of Allogeneic Hematopoietic Stem Cell Transplantation Recipients during the Pre-Engraftment PeriodGiulia Gustinetti, Anna Maria Raiola, Riccardo Varaldo, et al.
BMC Medical Genetics|March 30, 2012
The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathyMarcella Neri, Emanuele Valli, Giovanna Alfano, et al.
The Neurologist|August 31, 2012
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiencyGaetano Vattemi, Marcella Neri, Matteo Marini, et al.
Human Gene Therapy|May 22, 2010
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for x-linked dilated cardiomyopathyPaola Rimessi, Marina Fabris, Matteo Bovolenta, et al.
Human Gene Therapy|September 21, 2012
Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathyFrancesca Gualandi, Elisa Manzati, Patrizia Sabatelli, et al.
Pageof 17

Showing results (41-50 of 169) with videos related to

Sort By:
Pageof 17
International Journal of Molecular Sciences|February 10, 2024
Charcot-Marie-Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber NeuropathyFranco Gemignani, Antonio Percesepe, Francesca Gualandi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 14, 2015
Low intensity lympho-ablative regimen followed by autologous hematopoietic stem cell transplantation in severe forms of multiple sclerosis: A MRI-based clinical studyDaniela Curro', Luisa Vuolo, Francesca Gualandi, et al.
Journal of Clinical Microbiology|March 30, 2002
Aspergillus galactomannan antigen in the cerebrospinal fluid of bone marrow transplant recipients with probable cerebral aspergillosisClaudio Viscoli, Marco Machetti, Paola Gazzola, et al.
Biomedicines|August 26, 2023
Brugada Syndrome: More than a Monogenic ChannelopathyAntonella Liantonio, Matteo Bertini, Antonietta Mele, et al.
Neurogenetics|August 27, 2013
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3Ginevra Zanni, Chiara Scotton, Chiara Passarelli, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 27, 2018
De-Escalation and Discontinuation of Empirical Antibiotic Treatment in a Cohort of Allogeneic Hematopoietic Stem Cell Transplantation Recipients during the Pre-Engraftment PeriodGiulia Gustinetti, Anna Maria Raiola, Riccardo Varaldo, et al.
BMC Medical Genetics|March 30, 2012
The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathyMarcella Neri, Emanuele Valli, Giovanna Alfano, et al.
The Neurologist|August 31, 2012
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiencyGaetano Vattemi, Marcella Neri, Matteo Marini, et al.
Human Gene Therapy|May 22, 2010
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for x-linked dilated cardiomyopathyPaola Rimessi, Marina Fabris, Matteo Bovolenta, et al.
Human Gene Therapy|September 21, 2012
Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathyFrancesca Gualandi, Elisa Manzati, Patrizia Sabatelli, et al.
Pageof 17