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Neuroradiology|April 22, 2022
Spinal involvement in pediatric familial cavernous malformation syndromeAna Filipa Geraldo, Aysha Luis, Cesar Augusto P F Alves, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Focal dermal hypoplasia (Goltz-Gorlin syndrome): a new case with a novel variant in the PORCN gene (c.1250T>C:p.F417S) and unusual spinal anomalyLivia Garavelli, Graziella Simonte, Simonetta Rosato, et al.
Neuroradiology|October 5, 2022
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort studyAna Filipa Geraldo, Cesar Augusto P F Alves, Aysha Luis, et al.
American Journal of Medical Genetics. Part A|April 20, 2017
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experienceClaudia Santoro, Federico Di Rocco, Manoelle Kossorotoff, et al.
Journal of Neurosurgery. Pediatrics|June 7, 2024
White matter characteristics in children with cerebral palsy prior to selective dorsal rhizotomy: a multicenter diffusion tensor imaging studyWeihong Yuan, Charles B Stevenson, Paolo Moretti, et al.
Cancers|March 29, 2023
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213Marzia Ognibene, Marcello Scala, Michele Iacomino, et al.
Cancers|April 30, 2021
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort StudyMarcello Scala, Irene Schiavetti, Francesca Madia, et al.
Nature Ecology & Evolution|May 25, 2026
Human shielding from wolves facilitates jackal expansion across EuropeNathan Ranc, Christopher C Wilmers, Luigi Maiorano, et al.
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