(Q35116756)

6 August 2017

title

Mild form of Hunter's syndrome: clinical delineation based on 31 cases (English)

1 reference

6 August 2017

Young ID

1

1 reference

6 August 2017

Harper PS

series ordinal

2

1 reference

6 August 2017

language of work or name

English

0 references

publication date

1 November 1982

1 reference

Archives of Disease in Childhood

6 August 2017

published in

1 reference

6 August 2017

volume

57

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6 August 2017

issue

11

1 reference

6 August 2017

page(s)

828-836

1 reference

Gargoylism (Chondro-osteo-dystrophy, Hepatosplenomegaly, Deafness) in Two Brothers.

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

A Rare Disease in Two Brothers

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

The cardiovascular system in gargoylism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

The pathology and chemistry of a case of gargoylism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Gargoylism with cardiovascular involvement in two brothers

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

A sex-linked variant of gargoylism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Multiple peripheral nerve entrapments. An unusual phenotypical variant of the Hunter syndrome (mucopolysaccharidosis II) in a family.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

The systemic mucopolysaccharidoses.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Two cases of Hunter's syndrome--the anaesthetic and operative difficulties in oral surgery.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Peripheral Nerve Involvement in Hunter Syndrome (Mucopolysaccharidosis II)

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Long-term complications in Hunter's syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Myelopathy in mucopolysaccharidosis type II (Hunter syndrome).

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628015

Gargoylism (dysostosis multiplex): two adult cases with one autopsy

27 September 2018

1 reference

12 December 2020

Ultrastructural ocular pathology of Hunter's syndrome. Systemic mucopolysaccharidosis type II

1 reference

12 December 2020

Clinical and probable genetic heterogeneity within mucopolysaccharidosis. II. Report of a family with a mild form

1 reference

12 December 2020

Pulmonary disability in the Hurler syndrome (lipochondrodystrophy): a study of two cases

1 reference

12 December 2020

Psychosocial problems in Hunter's syndrome

1 reference

12 December 2020

Arachnoid cysts in the Hurler-Hunter syndrome

1 reference

12 December 2020

An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.57.11.828

1 reference

6 August 2017

1 reference

6 August 2017

1 reference