Cognitive outcomes and age of detection of severe mucopolysaccharidosis type 1. (Q38765618)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

title

Cognitive outcomes and age of detection of severe mucopolysaccharidosis type 1 (English)

1 reference

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9 April 2020

1

1 reference

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9 April 2020

Wendy K K Lam

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Alex R Kemper

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

author name string

Lisa D Wiggins

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

language of work or name

English

0 references

publication date

26 January 2017

1 reference

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9 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

volume

19

1 reference

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9 April 2020

page(s)

975-982

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9 April 2020

issue

9

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https://scigraph.springernature.com/pub.10.1038/gim.2016.223

9 April 2020

exact match

0 references

cites work

Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships

1 reference

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Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatment

31 August 2018

1 reference

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Hematopoietic cell transplantation for mucopolysaccharidosis patients is safe and effective: results after implementation of international guidelines.

31 August 2018

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

31 August 2018

1 reference

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Long-term functional outcomes of children with hurler syndrome treated with unrelated umbilical cord blood transplantation

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5763496

Early treatment is associated with improved cognition in Hurler syndrome.

31 August 2018

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Transplantation in inborn errors of metabolism: current considerations and future perspectives

31 August 2018

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Early initiation of enzyme replacement therapy for the mucopolysaccharidoses

31 August 2018

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Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler-Scheie syndrome

31 August 2018

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

31 August 2018

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An exploratory study of brain function and structure in mucopolysaccharidosis type I: long term observations following hematopoietic cell transplantation (HCT)

31 August 2018

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Current international perspectives on hematopoietic stem cell transplantation for inherited metabolic disorders.

31 August 2018

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Cognitive and neuroradiological improvement in three patients with attenuated MPS I treated by laronidase.

31 August 2018

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Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II.

31 August 2018

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Mucopolysaccharidosis I: management and treatment guidelines

31 August 2018

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

31 August 2018

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The clinical outcome of Hurler syndrome after stem cell transplantation.

31 August 2018

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Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human alpha-L-iduronidase (laronidase).

31 August 2018

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Cord-blood transplants from unrelated donors in patients with Hurler's syndrome

31 August 2018

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The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations

31 August 2018

1 reference

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

31 August 2018

1 reference

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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

31 August 2018

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

31 August 2018

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31 August 2018

1 reference

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

31 August 2018

1 reference

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Laronidase (Aldurazyme): enzyme replacement therapy for mucopolysaccharidosis type I

31 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2016.223

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/GIM.2016.223

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28125077%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

1 reference