Screening for GALC to make neonatal diagnosis and initial neonatal stem cell treatment with umbilical cord blood (Q73165965)

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1 November 2019

editorial

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title

Screening for GALC to make neonatal diagnosis and initial neonatal stem cell treatment with umbilical cord blood (English)

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1 November 2019

author name string

Patricia A Galvin-Parton

series ordinal

1

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1 November 2019

publication date

1 April 2003

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Pediatric Transplantation

1 November 2019

published in

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volume

7

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issue

2

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1 November 2019

page(s)

83-85

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Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe disease

1 November 2019

cites work

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Molecular genetics of Krabbe disease (globoid cell leukodystrophy): Diagnostic and clinical implications

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Lysosomal storage diseases

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Gene therapy of lysosomal storage disorders

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Hematopoietic stem-cell transplantation in globoid-cell leukodystrophy

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7 January 2021

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

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7 January 2021

Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism

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7 January 2021

Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometry

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7 January 2021

Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experience.

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7 January 2021

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

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7 January 2021

10.1034/J.1399-3046.2003.00032.X

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12654046 AND SRC:MED&resulttype=core&format=json

1 November 2019

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