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Maria Luisa Escolar

Observed names: Escolar, Maria, Escolar, Maria L., Escolar, Maria Luisa, M ESCOLAR, M L Escolar, M. Escolar, M. L. Escolar, M.L. Escolar, MARIA ESCOLAR, Maria Escolar, Maria L Escolar, Maria L. Escolar
Observed institutions: University of North Carolina at Chapel Hill, University of Pittsburgh, Duke University, George Washington University, Duke Medical Center, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Theriva Biologics (United States), San Francisco Unified School District, X4 Pharmaceuticals, Inc. (United States)
ORCID: 0000-0003-1530-6777
Observed ORCID: 0000-0003-1530-6777
OpenAlex ID: A5064601509
Transplantation of Umbilical-Cord Blood in Babies with Infantile Krabbe's Disease
2005 · Maria L. Escolar, Michele D. Poe, et al. · New England Journal of Medicine · 709
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Cord-Blood Transplants from Unrelated Donors in Patients with Hurler's Syndrome
2004 · Susan L. Staba, Maria L. Escolar, et al. · New England Journal of Medicine · 478
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Unrelated donor umbilical cord blood transplantation for inherited metabolic disorders in 159 pediatric patients from a single center: influence of cellular composition of the graft on transplantation outcomes
2008 · Vinod K. Prasad, Adam Mendizabal, et al. · Blood · 262
Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning
2013 · Jaap Jan Boelens, Mieke Aldenhoven, et al. · Blood · 206
Multidisciplinary Management of Hunter Syndrome
2009 · Joseph Muenzer, M. Beck, et al. · PEDIATRICS · 192
Newborn Screening for Krabbe Disease: the New York State Model
2009 · Patricia K. Duffner, Michele Caggana, et al. · Pediatric Neurology · 187
Survival and Functional Outcomes in Boys with Cerebral Adrenoleukodystrophy with and without Hematopoietic Stem Cell Transplantation
2018 · Gerald V. Raymond, Patrick Aubourg, et al. · Transplantation and Cellular Therapy · 142
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Neurodevelopmental Outcomes of Umbilical Cord Blood Transplantation in Metachromatic Leukodystrophy
2013 · Holly R. Martin, Michele D. Poe, et al. · Transplantation and Cellular Therapy · 123
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Natural Progression of Neurological Disease in Mucopolysaccharidosis Type II
2011 · Joshua B. Holt, Michele D. Poe, et al. · PEDIATRICS · 123
DTI registration in atlas based fiber analysis of infantile Krabbe disease
2011 · Yi Wang, Aditya Gupta, et al. · NeuroImage · 121
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Risk Factor Analysis of Outcomes after Unrelated Cord Blood Transplantation in Patients with Hurler Syndrome
2009 · Jaap Jan Boelens, Vanderson Rocha, et al. · Transplantation and Cellular Therapy · 111
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Newborn screening for Krabbe disease in New York State: the first eight years’ experience
2016 · Joseph J. Orsini, Denise M. Kay, et al. · Genetics in Medicine · 108
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Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State
2016 · Melissa P. Wasserstein, Mary Andriola, et al. · Genetics in Medicine · 102
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Early treatment is associated with improved cognition in H urler syndrome
2014 · Michele D. Poe, Sarah L. Chagnon, et al. · Annals of Neurology · 101
Developmental outcomes of cord blood transplantation for Krabbe disease
2017 · Matthew D. Wright, Michele D. Poe, et al. · Neurology · 100
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Outcomes of Unrelated Umbilical Cord Blood Transplantation for X-Linked Adrenoleukodystrophy
2007 · Donald Beam, Michele D. Poe, et al. · Transplantation and Cellular Therapy · 99
Developmental and behavioral aspects of mucopolysaccharidoses with brain manifestations — Neurological signs and symptoms
2017 · Elsa G. Shapiro, Simon A. Jones, et al. · Molecular Genetics and Metabolism · 95
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Allogeneic hematopoietic SCT for alpha-mannosidosis: an analysis of 17 patients
2011 · M Mynarek, J Tolar, et al. · Bone Marrow Transplantation · 93
A Staging System for Infantile Krabbe Disease to Predict Outcome After Unrelated Umbilical Cord Blood Transplantation
2006 · Maria L. Escolar, Michele D. Poe, et al. · PEDIATRICS · 91
Natural history of Sanfilippo syndrome type A
2013 · Dakota Buhrman, Kavita Thakkar, et al. · Journal of Inherited Metabolic Disease · 86
Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies
2017 · Laura A. Adang, Omar Sherbini, et al. · Molecular Genetics and Metabolism · 74
Early disease progression of Hurler syndrome
2017 · Bridget T. Kiely, Jennifer L. Kohler, et al. · Orphanet Journal of Rare Diseases · 74
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Krabbe Disease Treated with Hematopoietic Stem Cell Transplantation: Serial Assessment of Anisotropy Measurements—Initial Experience
2005 · Peter McGraw, Luxia Liang, et al. · Radiology · 72
Treatment of brain disease in the mucopolysaccharidoses
2017 · Maurizio Scarpa, Paul J. Orchard, et al. · Molecular Genetics and Metabolism · 71
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Metachromatic Leukodystrophy: A Case of Triplets With the Late Infantile Variant and a Systematic Review of the Literature
2009 · Asif Mahmood, Jay Berry, et al. · Journal of Child Neurology · 71
Works count: 209
Citation count: 5,980
H-index: 42
I10-index: 80
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