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Stefania Corti

Showing results (231-240 of 287) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Limb girdle muscular dystrophy due to <i>LAMA2</i> gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosisFrancesca Magri, Roberta Brusa, Luca Bello, et al.
Cellular and Molecular Life Sciences : CMLS|August 5, 2023
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective studyIrene Faravelli, Delia Gagliardi, Elena Abati, et al.
Progress in Neurobiology|April 27, 2020
miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosisAlessia Loffreda, Monica Nizzardo, Alessandro Arosio, et al.
BMC Medical Genetics|March 15, 2011
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencingFrancesca Magri, Roberto Del Bo, Maria G D'Angelo, et al.
Npj Aging|July 10, 2025
p300 inhibition delays premature cellular senescenceElisabetta Di Fede, Esi Taci, Silvia Castiglioni, et al.
Neuromuscular Disorders : NMD|June 30, 2012
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patientsFrancesca Magri, Roberto Del Bo, Maria Grazia D'Angelo, et al.
Cell Calcium|December 1, 2019
STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular boneThilini H Gamage, Emma Lengle, Gjermund Gunnes, et al.
Cellular and Molecular Life Sciences : CMLS|March 14, 2022
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomesMafalda Rizzuti, Valentina Melzi, Delia Gagliardi, et al.
Neurobiology of Aging|July 28, 2009
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohortRoberto Del Bo, Stefania Corti, Domenico Santoro, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Expanding the genetic landscape of Dusty Core Disease: new RYR1 variants in Italian patientsSimona Zanotti, Francesca Magri, Sabrina Salani, et al.
Pageof 29

Showing results (231-240 of 287) with videos related to

Sort By:
Pageof 29
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Limb girdle muscular dystrophy due to <i>LAMA2</i> gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosisFrancesca Magri, Roberta Brusa, Luca Bello, et al.
Cellular and Molecular Life Sciences : CMLS|August 5, 2023
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective studyIrene Faravelli, Delia Gagliardi, Elena Abati, et al.
Progress in Neurobiology|April 27, 2020
miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosisAlessia Loffreda, Monica Nizzardo, Alessandro Arosio, et al.
BMC Medical Genetics|March 15, 2011
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencingFrancesca Magri, Roberto Del Bo, Maria G D'Angelo, et al.
Npj Aging|July 10, 2025
p300 inhibition delays premature cellular senescenceElisabetta Di Fede, Esi Taci, Silvia Castiglioni, et al.
Neuromuscular Disorders : NMD|June 30, 2012
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patientsFrancesca Magri, Roberto Del Bo, Maria Grazia D'Angelo, et al.
Cell Calcium|December 1, 2019
STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular boneThilini H Gamage, Emma Lengle, Gjermund Gunnes, et al.
Cellular and Molecular Life Sciences : CMLS|March 14, 2022
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomesMafalda Rizzuti, Valentina Melzi, Delia Gagliardi, et al.
Neurobiology of Aging|July 28, 2009
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohortRoberto Del Bo, Stefania Corti, Domenico Santoro, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Expanding the genetic landscape of Dusty Core Disease: new RYR1 variants in Italian patientsSimona Zanotti, Francesca Magri, Sabrina Salani, et al.
Pageof 29