(Q53572902)

15 May 2018

editorial

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title

Hurler syndrome: past, present, and future. (English)

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15 May 2018

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Peters C

1

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15 May 2018

Shapiro EG

series ordinal

2

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15 May 2018

Krivit W

series ordinal

3

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15 May 2018

language of work or name

English

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publication date

1 July 1998

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15 May 2018

The Journal of Pediatrics

published in

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15 May 2018

volume

133

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15 May 2018

issue

1

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15 May 2018

page(s)

7-9

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15 May 2018

Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Follow-up of nine patients with Hurler syndrome after bone marrow transplantation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Long-term outcome of Hurler syndrome following bone marrow transplantation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Allogeneic bone marrow transplantation for lysosomal storage diseases. The European Group for Bone Marrow Transplantation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotype.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

A deletion/insertion mutation in the IDUA gene in a Libyan Jewish patient with Hurler syndrome (mucopolysaccharidosis IH).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Light and electron microscopic features of the liver in mucopolysaccharidosis.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Children with mucopolysaccharidosis: perioperative care, morbidity, mortality, and new findings.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Ocular changes in the mucopolysaccharidoses after bone marrow transplantation. A preliminary report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

The future for treatment by bone marrow transplantation for adrenoleukodystrophy, metachromatic leukodystrophy, globoid cell leukodystrophy and Hurler syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Evaluation of coronary artery disease in the Hurler syndrome by angiography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Resting Tl-201 scintigraphy in the evaluation of coronary artery disease in children with Hurler syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Male donor-derived cells in the brains of female sex-mismatched bone marrow transplant recipients: a Y-chromosome specific in situ hybridization study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Surgical treatment of carpal tunnel syndrome and trigger digits in children with mucopolysaccharide storage disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Marrow stromal cells as stem cells for nonhematopoietic tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Assessment of quality-of-life outcomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis I.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970170-2

10.1016/S0022-3476(98)70170-2

7 January 2021

Identifiers

DOI

1 reference

15 May 2018

PubMed ID

9672503

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15 May 2018