Projects per year
Fingerprint Dive into the research topics where Pediatrics - Neuropsychology is active. These topic labels come from the works of this organization's members. Together they form a unique fingerprint.
Mucopolysaccharidosis I
Medicine & Life Sciences
Attention Deficit Disorder with Hyperactivity
Medicine & Life Sciences
Adrenoleukodystrophy
Medicine & Life Sciences
Brain
Medicine & Life Sciences
Learning Disorders
Medicine & Life Sciences
Mucopolysaccharidoses
Medicine & Life Sciences
Mucopolysaccharidosis III
Medicine & Life Sciences
Bone Marrow Transplantation
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Profiles
Oluwatosin O Alabi
- Pediatrics - Neuropsychology - Post-Doctoral Associate
Person: Professional-in-Training
Jennifer E Boike Armerding
- Pediatrics - Neuropsychology - Psychology Fellow Specialist
Person: Professional-in-Training
Projects 2006 2023
Biomarker correlates of neurocognitive outcomes in the cerebrospinal fluid in MPS I
2/1/19 → 1/31/20
Project: Research project
Cerebrospinal Fluid
Biomarkers
An Open-Label, Single-Arm, Multicenter Study of Intracerebral Administration of Adeno-Associated Viral Vectors Serotype rh10 Carrying the Human N-sulfoglucosamine sulfohydrolase(SGSH) cDNA for the Treatment ofMucopolysaccharidosis Type IIIA
Whitley, C. B., Belani, K. G. & Eisengart, J.
1/25/19 → 2/28/21
Project: Research project
Mucopolysaccharidosis III
Multicenter Studies
Complementary DNA
Serogroup
N-sulfoglucosamine sulfohydrolase
Research Output 1986 2019
2
Citations
(Scopus)
Adverse Childhood Experiences and Weight Status among Adolescents
Davis, L., Barnes, A. J., Gross, A. C., Ryder, J. R. & Shlafer, R. J., Jan 1 2019, In : Journal of Pediatrics. 204, p. 71-76.e1Research output: Contribution to journal › Article
Weights and Measures
Morbid Obesity
Obesity
Students
Thinness
A longitudinal study of neurocognition and behavior in patients with Hurler-Scheie syndrome heterozygous for the L238Q mutation
Ahmed, A., Ou, L., Rudser, K., Shapiro, E., Eisengart, J., King, K. E., Chen, A., Dickson, P. & Whitley, C. B., Sep 1 2019, In : Molecular Genetics and Metabolism Reports. 20, 100484.Research output: Contribution to journal › Article
Open Access
Mucopolysaccharidosis I
Longitudinal Studies
Iduronidase
Mutation
Computational Biology
1
Citation
(Scopus)
A report on state-wide implementation of newborn screening for X-linked Adrenoleukodystrophy
Wiens, K., Berry, S. A., Choi, H., Gaviglio, A., Gupta, A. O., Hietala, A., Kenney-Jung, D. L., Lund, T. C., Miller, W., Pierpont, R., Raymond, G., Winslow, H., Zierhut, H. & Orchard, P. J., Jul 1 2019, In : American Journal of Medical Genetics, Part A. 179, 7, p. 1205-1213 9 p.Research output: Contribution to journal › Article
Open Access
Adrenoleukodystrophy
Newborn Infant
Adrenal Insufficiency
Lysophosphatidylcholines
Pedigree