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Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 12, 2011
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenitaAnna Modoni, Adele D'Amico, Bruno Dallapiccola, et al.Journal of Neurology|December 25, 2012
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansionsMassimo Santoro, Marcella Masciullo, Roberta Pietrobono, et al.Frontiers in Neurology|June 30, 2020
High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional StudyAlessia Perna, Daria Maccora, Salvatore Rossi, et al.The Journal of Sexual Medicine|July 3, 2009
Abnormal sexual behavior during sleepGiacomo Della Marca, Serena Dittoni, Roberto Frusciante, et al.Neurogenetics|July 9, 2020
Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxiaMassimo Santoro, Alessia Perna, Piergiorgio La Rosa, et al.Frontiers in Neurology|May 16, 2020
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4Serena Pagliarani, Sabrina Lucchiari, Marina Scarlato, et al.Journal of Neurology|January 8, 2016
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factorsMaria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, et al.Journal of the Neurological Sciences|April 24, 2012
Myotonia congenita: novel mutations in CLCN1 gene and functional characterizations in Italian patientsGianna Ulzi, Marzia Lecchi, Valeria Sansone, et al.Blood Advances|August 8, 2025
Routine Prophylaxis with Levetiracetam offers no benefit in CD19 CAR-T for LBCL: a Multicenter Propensity-matched StudyEugenio Galli, Roberta Di Blasi, Alice Di Rocco, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progressionMario Pescatori, Aldobrando Broccolini, Carlo Minetti, et al.Pageof 5