Search research articles
Contact Us
Filters
Showing results (231-240 of 245) with videos related to
Page
of 25
Sort By:
Human Mutation
|
August 14, 2014
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates
Daniela Rossi, Bianca Vezzani, Lucia Galli, et al.
Neuromuscular Disorders : NMD
|
December 19, 2025
Identification of novel potentially causative RYR1 variants in individuals with malignant hyperthermia susceptibility
Daniela Rossi, Carlotta Pranzo, Sara Roccabianca, et al.
European Journal of Medicinal Chemistry
|
September 18, 2018
Identification of dual Sigma1 receptor modulators/acetylcholinesterase inhibitors with antioxidant and neurotrophic properties, as neuroprotective agents
Marta Rui, Giacomo Rossino, Stefania Coniglio, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
April 28, 2023
Quantification and prospective evaluation of serum NfL and GFAP as blood-derived biomarkers of outcome in acute ischemic stroke patients
Federica Ferrari, Daniela Rossi, Alessandra Ricciardi, et al.
ACS Medicinal Chemistry Letters
|
April 19, 2019
Novel Compounds Targeting the RNA-Binding Protein HuR. Structure-Based Design, Synthesis, and Interaction Studies
Serena Della Volpe, Rita Nasti, Michele Queirolo, et al.
Frontiers in Pharmacology
|
February 19, 2024
Neurodegeneration: can metabolites from <i>Eremurus persicus</i> help?
Valeria Cavalloro, Nicoletta Marchesi, Pasquale Linciano, et al.
Human Mutation
|
September 13, 2017
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy
Virginia Barone, Valeria Del Re, Alessandra Gamberucci, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 23, 2006
Multicenter study on hepatitis C virus-related cryoglobulinemic glomerulonephritis
Dario Roccatello, Alessandro Fornasieri, Osvaldo Giachino, et al.
Plos One
|
October 27, 2017
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy
Daniela Rossi, Johanna Palmio, Anni Evilä, et al.
The Journal of General Physiology
|
May 14, 2025
Obscurin deficiency leads to compensated dilated cardiomyopathy and increased arrhythmias
Josè Manuel Pioner, Enrico Pierantozzi, Raffaele Coppini, et al.
Page
of 25
Search research articles
Search
Showing results (231-240 of 245) with videos related to
Sort By:
Page
of 25
Human Mutation
|
August 14, 2014
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates
Daniela Rossi, Bianca Vezzani, Lucia Galli, et al.
Neuromuscular Disorders : NMD
|
December 19, 2025
Identification of novel potentially causative RYR1 variants in individuals with malignant hyperthermia susceptibility
Daniela Rossi, Carlotta Pranzo, Sara Roccabianca, et al.
European Journal of Medicinal Chemistry
|
September 18, 2018
Identification of dual Sigma1 receptor modulators/acetylcholinesterase inhibitors with antioxidant and neurotrophic properties, as neuroprotective agents
Marta Rui, Giacomo Rossino, Stefania Coniglio, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
April 28, 2023
Quantification and prospective evaluation of serum NfL and GFAP as blood-derived biomarkers of outcome in acute ischemic stroke patients
Federica Ferrari, Daniela Rossi, Alessandra Ricciardi, et al.
ACS Medicinal Chemistry Letters
|
April 19, 2019
Novel Compounds Targeting the RNA-Binding Protein HuR. Structure-Based Design, Synthesis, and Interaction Studies
Serena Della Volpe, Rita Nasti, Michele Queirolo, et al.
Frontiers in Pharmacology
|
February 19, 2024
Neurodegeneration: can metabolites from <i>Eremurus persicus</i> help?
Valeria Cavalloro, Nicoletta Marchesi, Pasquale Linciano, et al.
Human Mutation
|
September 13, 2017
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy
Virginia Barone, Valeria Del Re, Alessandra Gamberucci, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 23, 2006
Multicenter study on hepatitis C virus-related cryoglobulinemic glomerulonephritis
Dario Roccatello, Alessandro Fornasieri, Osvaldo Giachino, et al.
Plos One
|
October 27, 2017
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy
Daniela Rossi, Johanna Palmio, Anni Evilä, et al.
The Journal of General Physiology
|
May 14, 2025
Obscurin deficiency leads to compensated dilated cardiomyopathy and increased arrhythmias
Josè Manuel Pioner, Enrico Pierantozzi, Raffaele Coppini, et al.
Page
of 25