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Claudio Bruno

Showing results (111-120 of 302) with videos related to

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Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
JIMD Reports|April 10, 2015
Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 MutationRoberta Biancheri, Eleonora Lamantea, Mariasavina Severino, et al.
Neurobiology of Disease|August 2, 2025
Nusinersen corrects L-arginine deficiency in the cerebrospinal fluid of patients with severe spinal muscular atrophyAmber Hassan, Raffaella di Vito, Anna Caretto, et al.
Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Communications Medicine|February 16, 2026
Nusinersen rescues taurine deficiency in patients with type 1 Spinal Muscular AtrophyRaffaella di Vito, Amber Hassan, Tommaso Nuzzo, et al.
Neuropediatrics|May 31, 2023
Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1Chiara Panicucci, Sara Casalini, Monica Traverso, et al.
Brain & Development|February 16, 2023
Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patientsChiara Panicucci, Sara Casalini, Beatrice M Damasio, et al.
Frontiers in Pediatrics|April 24, 2025
Evaluating treatment and care outcomes for neuromuscular diseases in a pediatric intermediate care settingGiacomo Brisca, Marina F Strati, Francesca Canzoneri, et al.
Trends in Psychiatry and Psychotherapy|June 3, 2024
Atomoxetine: toxicological aspects of a new treatment for Attention Deficit Hyperactivity Disorder in BrazilGabriel Christian de Farias Morais, Shopnil Akash, Edilson Dantas da Silva, et al.
Pageof 31

Showing results (111-120 of 302) with videos related to

Sort By:
Pageof 31
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
JIMD Reports|April 10, 2015
Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 MutationRoberta Biancheri, Eleonora Lamantea, Mariasavina Severino, et al.
Neurobiology of Disease|August 2, 2025
Nusinersen corrects L-arginine deficiency in the cerebrospinal fluid of patients with severe spinal muscular atrophyAmber Hassan, Raffaella di Vito, Anna Caretto, et al.
Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Communications Medicine|February 16, 2026
Nusinersen rescues taurine deficiency in patients with type 1 Spinal Muscular AtrophyRaffaella di Vito, Amber Hassan, Tommaso Nuzzo, et al.
Neuropediatrics|May 31, 2023
Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1Chiara Panicucci, Sara Casalini, Monica Traverso, et al.
Brain & Development|February 16, 2023
Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patientsChiara Panicucci, Sara Casalini, Beatrice M Damasio, et al.
Frontiers in Pediatrics|April 24, 2025
Evaluating treatment and care outcomes for neuromuscular diseases in a pediatric intermediate care settingGiacomo Brisca, Marina F Strati, Francesca Canzoneri, et al.
Trends in Psychiatry and Psychotherapy|June 3, 2024
Atomoxetine: toxicological aspects of a new treatment for Attention Deficit Hyperactivity Disorder in BrazilGabriel Christian de Farias Morais, Shopnil Akash, Edilson Dantas da Silva, et al.
Pageof 31