Follow-up of nine patients with Hurler syndrome after bone marrow transplantation. (Q50504785)

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13 November 2019

title

Follow-up of nine patients with Hurler syndrome after bone marrow transplantation (English)

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13 November 2019

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N Guffon

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13 November 2019

G Souillet

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13 November 2019

I Maire

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13 November 2019

J Straczek

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13 November 2019

P Guibaud

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13 November 2019

language of work or name

English

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publication date

1 July 1998

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The Journal of Pediatrics

13 November 2019

published in

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13 November 2019

volume

133

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13 November 2019

issue

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13 November 2019

page(s)

119-125

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

13 November 2019

cites work

1 reference

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Long-term outcome of Hurler syndrome following bone marrow transplantation

7 January 2021

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

7 January 2021

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

7 January 2021

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7 January 2021

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Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.

7 January 2021

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Prenatal diagnosis of Hurler disease by analysis of alpha-iduronidase in chorionic villi

7 January 2021

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

7 January 2021

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Fluorescence-assisted mismatch analysis (FAMA) for exhaustive screening of the alpha-galactosidase A gene and detection of carriers in Fabry disease

7 January 2021

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Characterization of a panel of highly variable minisatellites cloned from human DNA

7 January 2021

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Pseudodeficiency of alpha-iduronidase

7 January 2021

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Normal intraocular pressure after a bone marrow transplant in glaucoma associated with mucopolysaccharidosis type I-H.

7 January 2021

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

7 January 2021

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Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotype

7 January 2021

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

7 January 2021

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Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow.

7 January 2021

1 reference

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10.1016/S0022-3476(98)70201-X

7 January 2021

Identifiers

DOI

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13 November 2019

1 reference

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