(Q51983425)

19 April 2018

title

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

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19 April 2018

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A Vellodi

1

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19 April 2018

E Young

2

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19 April 2018

A Cooper

3

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19 April 2018

V Lidchi

4

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19 April 2018

B Winchester

5

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19 April 2018

J E Wraith

6

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19 April 2018

publication date

1 June 1999

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19 April 2018

Journal of Inherited Metabolic Disease

published in

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19 April 2018

volume

22

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19 April 2018

page(s)

638-648

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19 April 2018

issue

5

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19 April 2018

https://scigraph.springernature.com/pub.10.1023/a:1005525931994

exact match

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cites work

Bone marrow transplantation in Hunter syndrome (mucopolysaccharidosis type II): two-year follow-up of the first Italian patient and review of the literature

1 reference

12 December 2020

A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity

1 reference

12 December 2020

Long-term follow-up of a patient transplanted for Hunter's disease type IIB: a case report and literature review.

1 reference

12 December 2020

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

1 reference

12 December 2020

Rising IQ scores in British children: recent evidence

1 reference

12 December 2020

Mutation analysis in 20 patients with Hunter disease

1 reference

12 December 2020

The natural history of the severe form of Hunter's syndrome: a study based on 52 cases.

1 reference

12 December 2020

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

1 reference

12 December 2020

Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning

1 reference

12 December 2020

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

1 reference

12 December 2020

Bone marrow transplantation in Hunter syndrome.

1 reference

12 December 2020

Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II).

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12 December 2020

Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats--similarities to astrocyte grafts

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12 December 2020

Long-term effects of bone marrow transplantation for inborn errors of metabolism: a study of four patients with lysosomal storage diseases.

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12 December 2020

Molecular and phenotypic variation in patients with severe Hunter syndrome

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12 December 2020

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

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12 December 2020

A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient.

1 reference

12 December 2020

Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome

1 reference

12 December 2020

Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm

1 reference

12 December 2020

Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase gene

1 reference

12 December 2020

Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)

1 reference

12 December 2020

The laboratory diagnosis of sanfilippo disease

1 reference

12 December 2020

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

1 reference

12 December 2020

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005525931994

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19 April 2018

Dimensions Publication ID

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19 April 2018