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JIMD Reports, Volume 29

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Cover of 'JIMD Reports, Volume 29'

Table of Contents

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    Book Overview
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    Chapter 297 Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia
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    Chapter 336 LC-MS/MS Analysis of Cerebrospinal Fluid Metabolites in the Pterin Biosynthetic Pathway
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    Chapter 372 Erratum to: LC-MS/MS Analysis of Cerebrospinal Fluid Metabolites in the Pterin Biosynthetic Pathway
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    Chapter 493 CoQ10 Deficiency Is Not a Common Finding in GLUT1 Deficiency Syndrome.
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    Chapter 495 Continual Low-Dose Infusion of Sulfamidase Is Superior to Intermittent High-Dose Delivery in Ameliorating Neuropathology in the MPS IIIA Mouse Brain.
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    Chapter 507 A Short Synthetic Peptide Mimetic of Apolipoprotein A1 Mediates Cholesterol and Globotriaosylceramide Efflux from Fabry Fibroblasts.
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    Chapter 508 Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age
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    Chapter 509 Renal Involvement in a French Paediatric Cohort of Patients with Lysinuric Protein Intolerance
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    Chapter 513 Correlation Between Flexible Fiberoptic Laryngoscopic and Polysomnographic Findings in Patients with Mucopolysaccharidosis Type VI.
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    Chapter 517 A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect.
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    Chapter 519 Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1 ) Deficiency as a Cause of Recurrent Ketoacidosis
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    Chapter 520 The Lactose and Galactose Content of Cheese Suitable for Galactosaemia: New Analysis
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    Chapter 521 Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation.
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    Chapter 525 Atypical Clinical Presentations of TAZ Mutations: An Underdiagnosed Cause of Growth Retardation?
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    Chapter 526 Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants. - PubMed - NCBI
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    Chapter 529 Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrosp... - PubMed - NCBI
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    Chapter 574 Erratum to: Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase Deficiency
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Chapter title
Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation.
Chapter number 521
Book title
JIMD Reports, Volume 29
Published in
JIMD Reports, January 2016
DOI 10.1007/8904_2015_521
Pubmed ID
Book ISBNs
978-3-66-253277-5, 978-3-66-253278-2
Authors

Kunin-Batson, A S, Shapiro, E G, Rudser, K D, Lavery, C A, Bjoraker, K J, Jones, S A, Wynn, R F, Vellodi, A, Tolar, J, Orchard, P J, Wraith, J E, A. S. Kunin-Batson, E. G. Shapiro, K. D. Rudser, C. A. Lavery, K. J. Bjoraker, S. A. Jones, R. F. Wynn, A. Vellodi, J. Tolar, P. J. Orchard, J. E. Wraith, Kunin-Batson, A. S., Shapiro, E. G., Rudser, K. D., Lavery, C. A., Bjoraker, K. J., Jones, S. A., Wynn, R. F., Vellodi, A., Tolar, J., Orchard, P. J., Wraith, J. E.

Abstract

The long-term cognitive and functional outcomes of children with mucopolysaccharidosis type I (MPS-IH) post-hematopoietic cell transplant (HCT) are not well documented, and the role of genetic and treatment factors in these outcomes has yet to be defined. In this multi-site, international study, we (1) characterize the cognitive and functional status of 47 individuals (ages 2-25, mean of 10.6 years) with MPS-IH who are 1-24 years post HCT (mean = 9 years) and (2) examine contributions of genotype, transplant characteristics, and sociodemographic factors to cognitive ability, adaptive behavior, and quality of life. The overall cognitive ability of our sample was mildly impaired, more than two standard deviations below general population norms. Parent reported adaptive behaviors (i.e., communication, daily living, and motor skills) were similarly impaired with a relative strength in socialization. Quality of life, as reported by parents, fell more than two standard deviations below population norms for physical functioning; however, psychosocial quality of life (emotional well-being) approximated population norms. In linear regression analysis, adjusted for demographic and treatment factors, mutation severity was associated with lower cognitive ability (p = 0.005) and adaptive functioning (p = 0.004), but not parent ratings of children's quality of life. Older age at HCT was associated with poorer physical quality of life (p = 0.002); lower socioeconomic status (p = 0.028) and unrelated bone marrow HCT (p = 0.010) were associated with poorer psychosocial quality of life. Implications for screening and early intervention for children at risk for poorer cognitive and functional outcomes are described.

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The data shown below were compiled from readership statistics for 51 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 51 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 10 20%
Student > Master 6 12%
Researcher 5 10%
Student > Doctoral Student 4 8%
Student > Postgraduate 4 8%
Other 8 16%
Unknown 14 27%
Readers by discipline Count As %
Medicine and Dentistry 12 24%
Agricultural and Biological Sciences 6 12%
Psychology 5 10%
Immunology and Microbiology 2 4%
Social Sciences 2 4%
Other 9 18%
Unknown 15 29%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 February 2016.
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#18,437,241
of 22,842,950 outputs
Outputs from JIMD Reports
#437
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#287,005
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Outputs of similar age from JIMD Reports
#10
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