Showing results (201-210 of 247) with videos related to

Sort By:
Pageof 25
Journal of Clinical Medicine|June 19, 2024
Magnetic Resonance Imaging of Central Nervous System Manifestations of Type 1 Neurofibromatosis: Pictorial Review and Retrospective Study of Their Frequency in a Cohort of PatientsStefano Di Pietro, Linda Reali, Emanuela Tona, et al.
Italian Journal of Pediatrics|February 18, 2022
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variabilityPiero Pavone, Xena Giada Pappalardo, Naira Mustafa, et al.
Genes|December 30, 2025
Genetic, Clinical and Neuroradiological Spectrum of MED-Related Disorders: An Updated ReviewAlessandro Fazio, Roberta Leonardi, Lorenzo Aliotta, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 20, 2008
Neurofibromatosis type 1 and infantile spasmsMartino Ruggieri, Paola Iannetti, Maurizio Clementi, et al.
Quantitative Imaging in Medicine and Surgery|December 13, 2016
Cutis tricolor: a literature review and report of five new casesMartino Ruggieri, Agata Polizzi, Carmelo Schepis, et al.
Frontiers in Pediatrics|November 21, 2022
Neuroblastic tumors and neurofibromatosis type 1: A retrospective multicenter study in Italy and systematic review of the literatureFederica Puglisi, Rachele Soma, Marta Podda, et al.
Human Mutation|October 27, 2007
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)M Upadhyaya, Lan Kluwe, G Spurlock, et al.
Italian Journal of Pediatrics|April 22, 2024
Point-of-care ultrasound (POCUS) pediatric resident training course: a cross-sectional surveyManuela Lo Bianco, Santiago Presti, Maria Carla Finocchiaro, et al.
American Journal of Medical Genetics. Part A|September 20, 2012
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patientsMartino Ruggieri, Pietro Milone, Piero Pavone, et al.
European Journal of Pediatrics|October 20, 2009
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7qPiero Pavone, Martino Ruggieri, Ilaria Lombardo, et al.
Pageof 25