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Neural Regeneration Research|March 27, 2020
Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubesMassimo Santoro, Roberto Piacentini, Alessia Perna, et al.
Cardiology|January 31, 2012
Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2Anna Modoni, Maria Laura Ester Bianchi, Nicola Vitulano, et al.
Molecular Genetics and Metabolism|January 26, 2007
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutation causing a double pathogenic effectMassimo Santoro, Anna Modoni, Mario Sabatelli, et al.
BMC Neurology|March 17, 2022
COVID-19 atypical Parsonage-Turner syndrome: a case reportMaria Beatrice Zazzara, Anna Modoni, Alessandra Bizzarro, et al.
Cancer Chemotherapy and Pharmacology|September 28, 2010
Polymorphism of CAG motif of SK3 gene is associated with acute oxaliplatin neurotoxicityMichele Basso, Anna Modoni, Daniele Spada, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletionsFrancesca Odoardi, Michele Rana, Aldobrando Broccolini, et al.
Neuropathology and Applied Neurobiology|July 30, 2013
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubesMassimo Santoro, Roberto Piacentini, Marcella Masciullo, et al.
Journal of the Neurological Sciences|June 29, 2007
Sleep quality in Facioscapulohumeral muscular dystrophyGiacomo Della Marca, Roberto Frusciante, Catello Vollono, et al.
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