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Metabolic Brain Disease|April 20, 2022
Evolving therapies in neuronopathic LSDs: opportunities and challengesDeepa S Rajan, Maria L EscolarClinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 4, 2006
Neurophysiologic assessment of mucopolysaccharidosis IIIAatif M Husain, Maria L Escolar, Joanne KurtzbergThe Journal of Pediatrics|May 3, 2011
Early clinical markers of central nervous system involvement in mucopolysaccharidosis type IIJoshua Holt, Michele D Poe, Maria L EscolarAnnals of Neurology|August 9, 2014
Early treatment is associated with improved cognition in Hurler syndromeMichele D Poe, Sarah L Chagnon, Maria L EscolarMolecular Genetics and Metabolism|October 28, 2017
Developmental and behavioral aspects of mucopolysaccharidoses with brain manifestations - Neurological signs and symptomsElsa G Shapiro, Simon A Jones, Maria L EscolarJournal of Inherited Metabolic Disease|November 26, 2013
Natural history of Sanfilippo syndrome type ADakota Buhrman, Kavita Thakkar, Michele Poe, et al.Pediatric Neurology|March 22, 2020
Spontaneous Third Ventriculostomy in Krabbe DiseaseGiulio Zuccoli, Aram Kim, Michele Poe, et al.Pediatrics|April 27, 2011
Natural progression of neurological disease in mucopolysaccharidosis type IIJoshua B Holt, Michele D Poe, Maria L EscolarFrontiers in Neurology|November 12, 2020
Pathogenic Variants in <i>GALC</i> Gene Correlate With Late Onset Krabbe Disease and Vision Loss: Case Series and Review of LiteratureNicholas A Bascou, Maria L Beltran-Quintero, Maria L EscolarPediatric Clinics of North America|May 30, 2015
Emerging treatments for pediatric leukodystrophiesGuy Helman, Keith Van Haren, Maria L Escolar, et al.Pageof 7