Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy (Q24651989)

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English	Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy	scientific article

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scholarly article

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8 references

12 March 2019

14 March 2019

21 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

28 September 2019

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy (English)

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enzyme replacement therapy

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mucopolysaccharidosis II

8 references

12 March 2019

14 March 2019

21 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

28 September 2019

1 reference

28 September 2019

object named as

Jiri Zeman

10

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author name string

J Edmond Wraith

1

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Maurizio Scarpa

2

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Michael Beck

3

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Olaf A Bodamer

4

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Linda De Meirleir

5

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Nathalie Guffon

6

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Allan Meldgaard Lund

7

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Gunilla Malm

8

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Ans T Van der Ploeg

9

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language of work or name

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publication date

March 2008

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1 March 2008

8 references

12 March 2019

14 March 2019

21 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

28 September 2019

European Journal of Pediatrics

8 references

12 March 2019

14 March 2019

21 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

28 September 2019

167

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267-77

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3

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https://scigraph.springernature.com/pub.10.1007/s00431-007-0635-4

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A Rare Disease in Two Brothers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

7 April 2017

A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

7 April 2017

The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

7 April 2017

Large animal models and gene therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Otorhinolaryngological manifestations of the mucopolysaccharidoses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Mucopolysaccharidosis type II in females: case report and review of literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

The frequency of lysosomal storage diseases in The Netherlands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Molecular and phenotypic variation in patients with severe Hunter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Disc oedema in association with Hunter's syndrome: ocular histopathological findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Upper airway obstruction in Hunter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 September 2017

Disordered breathing during sleep in patients with mucopolysaccharidoses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Failure to control the airway in a patient with Hunter's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

New perspectives in type 2 Gaucher disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Carpal tunnel syndrome in the mucopolysaccharidoses and mucolipidoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Magnetic resonance imaging of the brain, neck and cervical spine in mild Hunter's syndrome (mucopolysaccharidoses type II).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Anaesthesia for children with mucopolysaccharidoses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Ultrastructure of the rectal wall in Hunter's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

30 May 2018

Reduction of GAG storage in MPS II mouse model following implantation of encapsulated recombinant myoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

Gene therapy ameliorates cardiovascular disease in dogs with mucopolysaccharidosis VII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

Long-term follow-up following bone marrow transplantation for Hunter disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

Pebbling of the skin: a marker of Hunter's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

MRI in the mild type of mucopolysaccharidosis II (Hunter's syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

Hearing loss in Hunter's syndrome--mucopolysaccharidosis II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234442

28 November 2018

Cardiac structural involvement in mucopolysaccharidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uveal effusion in Hunter's syndrome. Evidence that abnormal sclera is responsible for the uveal effusion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Follow-up of patients with Hunter syndrome: the Hunter Outcome Survey (HOS) registry]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presenting features of mucopolysaccharidosis type IH (Hurler syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive Mongolian spots associated with Hunter syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis I, the cherry red-spot--myoclonus syndrome and neuraminidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute airway obstruction in Hunter syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cumulative incidence rates of the mucopolysaccharidoses in Germany

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hunter's syndrome: a study in airway obstruction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral epiretinal membranes: a new finding in Hunter syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of the Hunter syndrome with progeny

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychosocial problems in Hunter's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden death in Hunter syndrome caused by complete atrioventricular block

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First-trimester diagnosis of hunter syndrome: Very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18038146

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-007-0635-4

1 reference

Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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