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A Maselli

Showing results (91-100 of 130) with videos related to

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Annals of Neurology|March 3, 2004
Focal caspase activation underlies the endplate myopathy in slow-channel syndromeBhupinder P S Vohra, Jason S Groshong, Ricardo A Maselli, et al.
Plant Physiology|February 5, 2014
Revisiting the evolutionary history and roles of protein phosphatases with Kelch-like domains in plantsGustavo A Maselli, Claudio H Slamovits, Javier I Bianchi, et al.
International Journal of Immunopathology and Pharmacology|June 13, 2008
Non-allergic rhinitis with eosinophils and mast cells constitutes a new severe nasal disorderM Gelardi, A Maselli del Giudice, M L Fiorella, et al.
Human Genetics|November 28, 2013
COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal laminaJuan Arredondo, Marian Lara, Fiona Ng, et al.
Muscle & Nerve|June 3, 2016
Effect of 3,4-diaminopyridine at the murine neuromuscular junctionFiona Ng, Diana C Lee, Leah A Schrumpf, et al.
Journal of Neuromuscular Diseases|June 5, 2026
Congenital myasthenic syndrome due to novel <i>GFPT1</i> variant presenting with head drop and visual impairment: A case reportKatharine Torrey, Rachel Logan, Emmanuelle Tiongson, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|June 12, 2004
Colonic smooth muscle responses in patients with diverticular disease of the colon: effect of the NK2 receptor antagonist SR48968M A Maselli, A L Piepoli, V Guerra, et al.
Muscle & Nerve|November 13, 2014
Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndromeSuresh Ram, Inoka A Devapriya, Grace Fenton, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.
Case Reports in Genetics|October 29, 2025
<i>RAPSN</i>-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same PositionLaura Keehan, Jennefer N Carter, Elijah Kravets, et al.
Pageof 13

Showing results (91-100 of 130) with videos related to

Sort By:
Pageof 13
Annals of Neurology|March 3, 2004
Focal caspase activation underlies the endplate myopathy in slow-channel syndromeBhupinder P S Vohra, Jason S Groshong, Ricardo A Maselli, et al.
Plant Physiology|February 5, 2014
Revisiting the evolutionary history and roles of protein phosphatases with Kelch-like domains in plantsGustavo A Maselli, Claudio H Slamovits, Javier I Bianchi, et al.
International Journal of Immunopathology and Pharmacology|June 13, 2008
Non-allergic rhinitis with eosinophils and mast cells constitutes a new severe nasal disorderM Gelardi, A Maselli del Giudice, M L Fiorella, et al.
Human Genetics|November 28, 2013
COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal laminaJuan Arredondo, Marian Lara, Fiona Ng, et al.
Muscle & Nerve|June 3, 2016
Effect of 3,4-diaminopyridine at the murine neuromuscular junctionFiona Ng, Diana C Lee, Leah A Schrumpf, et al.
Journal of Neuromuscular Diseases|June 5, 2026
Congenital myasthenic syndrome due to novel <i>GFPT1</i> variant presenting with head drop and visual impairment: A case reportKatharine Torrey, Rachel Logan, Emmanuelle Tiongson, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|June 12, 2004
Colonic smooth muscle responses in patients with diverticular disease of the colon: effect of the NK2 receptor antagonist SR48968M A Maselli, A L Piepoli, V Guerra, et al.
Muscle & Nerve|November 13, 2014
Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndromeSuresh Ram, Inoka A Devapriya, Grace Fenton, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.
Case Reports in Genetics|October 29, 2025
<i>RAPSN</i>-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same PositionLaura Keehan, Jennefer N Carter, Elijah Kravets, et al.
Pageof 13