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European Journal of Medical Genetics|November 14, 2016
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platformFrancesco Calì, Valeria Chiavetta, Giuseppa Ruggeri, et al.Italian Journal of Pediatrics|April 18, 2024
Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent NeuropsychiatryValeria Calcaterra, Gianluca Tornese, Gianvincenzo Zuccotti, et al.The Lancet. Neurology|August 11, 2007
Clinical features and viral serologies in children with multiple sclerosis: a multinational observational studyBrenda Banwell, Lauren Krupp, Julia Kennedy, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 2, 2022
Prognostic relevance of quantitative and longitudinal MOG antibody testing in patients with MOGAD: a multicentre retrospective studyMatteo Gastaldi, Thomas Foiadelli, Giacomo Greco, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 6, 2024
Clinical, prognostic and pathophysiological implications of MOG-IgG detection in the CSF: the importance of intrathecal MOG-IgG synthesisGiacomo Greco, Mario Risi, Stefano Masciocchi, et al.Frontiers in Neurology|November 23, 2020
Cyclic Vomiting Syndrome in ChildrenUmberto Raucci, Osvaldo Borrelli, Giovanni Di Nardo, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 24, 2022
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative diseaseElisa Calì, Sheng-Jia Lin, Clarissa Rocca, et al.Pageof 25