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Orphanet Journal of Rare Diseases|August 10, 2018
A prospective natural history study of Krabbe disease in a patient cohort with onset between 6 months and 3 years of lifeNicholas Bascou, Anthony DeRenzo, Michele D Poe, et al.Pediatrics|August 23, 2006
A staging system for infantile Krabbe disease to predict outcome after unrelated umbilical cord blood transplantationMaria L Escolar, Michele D Poe, Holly R Martin, et al.Developmental Medicine and Child Neurology|October 19, 2006
Gross motor abilities in children with Hurler syndromeStacey C Dusing, Deborah Thorpe, Angela Rosenberg, et al.Journal of Neuroscience Research|September 18, 2016
Clinical management of Krabbe diseaseMaria L Escolar, Tara West, Alessandra Dallavecchia, et al.Molecular Genetics and Metabolism|November 13, 2017
Assessments of neurocognitive and behavioral function in the mucopolysaccharidosesElsa G Shapiro, Maria L Escolar, Kathleen A Delaney, et al.Neuroradiology|April 11, 2015
Midbrain morphology reflects extent of brain damage in Krabbe diseaseGiulio Zuccoli, Srikala Narayanan, Ashok Panigrahy, et al.Neurology|September 1, 2017
Developmental outcomes of cord blood transplantation for Krabbe disease: A 15-year studyMatthew D Wright, Michele D Poe, Anthony DeRenzo, et al.Blood|November 5, 2020
Long-term neurodevelopmental outcomes of hematopoietic stem cell transplantation for late-infantile Krabbe diseaseIsabel C Yoon, Nicholas A Bascou, Michele D Poe, et al.European Radiology|May 4, 2016
Thickening of the cauda equina roots: a common finding in Krabbe diseaseMisun Hwang, Giulio Zuccoli, Ashok Panigrahy, et al.Frontiers in Molecular Neuroscience|August 15, 2022
Improved Brain Pathology and Progressive Peripheral Neuropathy in a 15 Year Old Survivor of Infantile Krabbe Disease Treated With Umbilical Cord TransplantationJulia Kofler, Maria L Beltran-Quintero, Anne Rugari, et al.Pageof 7