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Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|May 17, 2026
Salivary Bicarbonate Fails to Mirror Systemic Acid-Base Balance in Pediatric Patients at Risk of Metabolic DisturbancesNicola Bertazza Partigiani, Marco Moi, Alessandro D'Uva, et al.Journal of Child Neurology|January 8, 2013
Intrathecal synthesis of oligoclonal bands in rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome: new evidence supporting immunological pathogenesisStefano Sartori, Elena Priante, Andrea Pettenazzo, et al.Journal of Child Neurology|March 2, 2012
Chiari 2 without spinal dysraphism: does it blow a hole in the pathogenesis?Valentina Citton, Irene Toldo, Laura Balao, et al.Neuropediatrics|January 8, 2015
Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancyChiara Bertossi, Matteo Cassina, Ambra Cappellari, et al.Journal of Child Neurology|December 17, 2008
Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvementIrene Toldo, Renzo Manara, Paola Cogo, et al.Journal of Child Neurology|March 20, 2010
Spinal cord infarction due to fibrocartilaginous embolization: the role of diffusion weighted imaging and short-tau inversion recovery sequencesRenzo Manara, Milena Calderone, Maria Savina Severino, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2007
Increased level of N-acetylaspartylglutamate (NAAG) in the CSF of a patient with Pelizaeus-Merzbacher-like disease due to mutation in the GJA12 geneStefano Sartori, Alberto B Burlina, Leonardo Salviati, et al.Brain & Development|November 26, 2013
Delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literatureSara Azzolini, Margherita Nosadini, Marta Balzarin, et al.Journal of Child Neurology|January 8, 2011
Pre- and postprandial electroencephalography in glucose transporter type 1 deficiency syndrome: an illustrative case to discuss the concept of carbohydrate responsivenessGiulia Parolin, Paola Drigo, Irene Toldo, et al.Neurogenetics|October 13, 2006
A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like diseaseLeonardo Salviati, Eva Trevisson, Maria Cristina Baldoin, et al.Pageof 10