Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation. (Q37329301)

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scientific article published on 30 January 2016

Language	Label	Description	Also known as
English	Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation.	scientific article published on 30 January 2016

Statements

scholarly article

1 reference

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6 March 2020

Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation (English)

1 reference

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6 March 2020

Hurler syndrome

1 reference

based on heuristic

inferred from title

6

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6 March 2020

9

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6 March 2020

author name string

A S Kunin-Batson

1

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6 March 2020

E G Shapiro

2

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6 March 2020

K D Rudser

3

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6 March 2020

C A Lavery

4

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6 March 2020

K J Bjoraker

5

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6 March 2020

R F Wynn

7

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6 March 2020

A Vellodi

8

1 reference

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6 March 2020

P J Orchard

10

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6 March 2020

J E Wraith

11

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6 March 2020

language of work or name

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publication date

30 January 2016

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6 March 2020

Journal of Inherited Metabolic Disorders Reports

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6 March 2020

29

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6 March 2020

95-102

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6 March 2020

Enzyme replacement is associated with better cognitive outcomes after transplant in Hurler syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059216

6 September 2017

Transplant outcomes in mucopolysaccharidoses

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6 September 2017

Mucopolysaccharidosis I: management and treatment guidelines

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6 September 2017

Health-related quality of life in survivors of BMT for paediatric malignancy: a systematic review of the literature

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6 September 2017

The clinical outcome of Hurler syndrome after stem cell transplantation.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059216

6 September 2017

Socioeconomic determinants of health related quality of life in childhood and adolescence: results from a European study

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Can mucopolysaccharidosis type I disease severity be predicted based on a patient's genotype? A comprehensive review of the literature

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6 September 2017

Unrelated donor hematopoietic cell transplantation: marrow or umbilical cord blood?

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6 September 2017

Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres

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6 September 2017

Neuropsychological outcomes of several storage diseases with and without bone marrow transplantation

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14 September 2017

Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndrome.

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28 September 2017

Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study.

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26 June 2018

Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group

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26 June 2018

The contribution of neurocognitive functioning to quality of life after childhood acute lymphoblastic leukemia.

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2 September 2018

Bone marrow transplantation in children with Hunter syndrome: outcome after 7 to 17 years.

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2 September 2018

Outcome in six children with mucopolysaccharidosis type IH, Hurler syndrome, after haematopoietic stem cell transplantation (HSCT).

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2 September 2018

Combination of enzyme replacement and hematopoietic stem cell transplantation as therapy for Hurler syndrome.

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2 September 2018

Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources

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2 September 2018

Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients.

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2 September 2018

Acute health-related quality of life in children undergoing stem cell transplant: II. Medical and demographic determinants.

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2 September 2018

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2 September 2018

Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation

1 reference

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12 December 2020

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The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I

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Understanding health disparities: the role of race and socioeconomic status in children's health

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Identifiers

10.1007/8904_2015_521

1 reference

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6 March 2020

1 reference

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6 March 2020

1 reference

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6 March 2020

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