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Francesca Gualandi

Showing results (91-100 of 169) with videos related to

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Journal of Biomedicine & Biotechnology|October 24, 2012
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx miceElena Bassi, Sofia Falzarano, Marina Fabris, et al.
Oxidative Medicine and Cellular Longevity|October 27, 2011
Cyclosporine A in Ullrich congenital muscular dystrophy: long-term resultsLuciano Merlini, Patrizia Sabatelli, Annarita Armaroli, et al.
Neuromuscular Disorders : NMD|September 1, 2019
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional studyFilomena Caria, Matilde Cescon, Francesca Gualandi, et al.
Frontiers in Physiology|November 8, 2021
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic DiseasesMaria Sofia Falzarano, Rachele Rossi, Andrea Grilli, et al.
Molecular and Cellular Neurosciences|July 2, 2017
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctionsPaola Imbrici, Concetta Altamura, Francesca Gualandi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 4, 2012
Unmanipulated haploidentical bone marrow transplantation and posttransplantation cyclophosphamide for hematologic malignancies after myeloablative conditioningAnna Maria Raiola, Alida Dominietto, Anna Ghiso, et al.
Heart Rhythm|March 11, 2024
Cardiac conduction disorders in young adults: Clinical characteristics and genetic background of an underestimated populationCristina Balla, Alice Margutti, Beatrice De Carolis, et al.
Human Mutation|September 18, 2009
Exon skipping-mediated dystrophin reading frame restoration for small mutationsPietro Spitali, Paola Rimessi, Marina Fabris, et al.
The Journal of Pediatrics|May 8, 2012
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlationMarika Pane, Maria Elena Lombardo, Paolo Alfieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 10, 2020
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypesMarcin M Machnicki, Valeria Guglielmi, Elia Pancheri, et al.
Pageof 17

Showing results (91-100 of 169) with videos related to

Sort By:
Pageof 17
Journal of Biomedicine & Biotechnology|October 24, 2012
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx miceElena Bassi, Sofia Falzarano, Marina Fabris, et al.
Oxidative Medicine and Cellular Longevity|October 27, 2011
Cyclosporine A in Ullrich congenital muscular dystrophy: long-term resultsLuciano Merlini, Patrizia Sabatelli, Annarita Armaroli, et al.
Neuromuscular Disorders : NMD|September 1, 2019
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional studyFilomena Caria, Matilde Cescon, Francesca Gualandi, et al.
Frontiers in Physiology|November 8, 2021
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic DiseasesMaria Sofia Falzarano, Rachele Rossi, Andrea Grilli, et al.
Molecular and Cellular Neurosciences|July 2, 2017
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctionsPaola Imbrici, Concetta Altamura, Francesca Gualandi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 4, 2012
Unmanipulated haploidentical bone marrow transplantation and posttransplantation cyclophosphamide for hematologic malignancies after myeloablative conditioningAnna Maria Raiola, Alida Dominietto, Anna Ghiso, et al.
Heart Rhythm|March 11, 2024
Cardiac conduction disorders in young adults: Clinical characteristics and genetic background of an underestimated populationCristina Balla, Alice Margutti, Beatrice De Carolis, et al.
Human Mutation|September 18, 2009
Exon skipping-mediated dystrophin reading frame restoration for small mutationsPietro Spitali, Paola Rimessi, Marina Fabris, et al.
The Journal of Pediatrics|May 8, 2012
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlationMarika Pane, Maria Elena Lombardo, Paolo Alfieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 10, 2020
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypesMarcin M Machnicki, Valeria Guglielmi, Elia Pancheri, et al.
Pageof 17