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Genetic Testing and Molecular Biomarkers|October 21, 2009
Preliminary results in a study regarding the relationship between perlecan gene polymorphism and spinal muscular atrophy type I diseaseMonica Stavarachi, Mihai Toma, Niculina Butoianu, et al.Journal of Immunoassay & Immunochemistry|April 5, 2017
Myositis non-inflammatory mechanisms: An up-dated reviewEmilia Manole, Alexandra E Bastian, Niculina Butoianu, et al.Maedica|December 9, 2017
Acute Myocardial Injury in a Child with Duchenne Muscular Dystrophy: Pulse Steroid Therapy?Eliza Cinteza, Claudiu Stoicescu, Niculina Butoianu, et al.Maedica|February 24, 2015
Intellectual disability and epilepsy in down syndromeDiana Barca, Oana Tarta-Arsene, Alice Dica, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2025
Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective StudyMaria Nedelcu, Dana Craiu, Elena Neagu, et al.Diseases (Basel, Switzerland)|July 25, 2025
Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center ExperienceAlice Denisa Dică, Dana Craiu, Florentina Ionela Linca, et al.Genes|January 28, 2026
Brain Matters in Duchenne Muscular Dystrophy: DMD Mutation Sites and Their Association with Neurological Comorbidities Through Isoform ImpairmentTeodora Barbarii, Raluca Anca Tudorache, Dana Craiu, et al.American Journal of Human Genetics|August 30, 2016
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic ApneaStéphanie Bauché, Seana O'Regan, Yoshiteru Azuma, et al.Neurology. Genetics|December 30, 2020
Ethnicity-related DMD Genotype Landscapes in European and Non-European CountriesRita Selvatici, Rachele Rossi, Fernanda Fortunato, et al.Journal of Neurology|October 29, 2013
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and EuropeCatherine L Bladen, Rachel Thompson, Jacqueline M Jackson, et al.Pageof 2