(Q39789786)

14 September 2017

title

Biochemical profiling to predict disease severity in metachromatic leukodystrophy (English)

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14 September 2017

4

J J Hopwood

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14 September 2017

M A F Tan

1

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14 September 2017

M Fuller

series ordinal

2

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14 September 2017

Z A M H Zabidi-Hussin

series ordinal

3

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14 September 2017

P J Meikle

series ordinal

5

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14 September 2017

publication date

15 September 2009

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Molecular Genetics and Metabolism

14 September 2017

published in

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14 September 2017

volume

99

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14 September 2017

issue

2

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14 September 2017

page(s)

142-148

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Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases

14 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and S

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Slow progression of juvenile metachromatic leukodystrophy 6 years after bone marrow transplantation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spots.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Measurement of protein using bicinchoninic acid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Effect of lysosomal storage on bis(monoacylglycero)phosphate.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Urinary Lipid Profiling for the Identification of Fabry Hemizygotes and Heterozygotes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Newborn screening for lysosomal storage disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Multiplex enzyme assay screening of dried blood spots for lysosomal storage disorders by using tandem mass spectrometry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Umbilical cord blood transplantation for juvenile metachromatic leukodystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Enzyme replacement improves ataxic gait and central nervous system histopathology in a mouse model of metachromatic leukodystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno-associated viral vector serotype 1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Molecular basis of different forms of metachromatic leukodystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Metachromatic leukodystrophy - mutation analysis provides further evidence of genotype-phenotype correlation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Elevated sulfatide excretion in compound heterozygotes of metachromatic leukodystrophy and ASA-pseudodeficiency allele

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

Secondary accumulation of gangliosides in lysosomal storage disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.09.006

10.1016/J.YMGME.2009.09.006

7 January 2021

Identifiers

DOI

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release_mjqrwkjofve7rhhukhodbiy3yi

14 September 2017

Fatcat ID

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