(Q53788990)

19 May 2018

title

Mucolipidosis II (I-cell disease). A clinical and biochemical study (English)

1 reference

19 May 2018

author name string

Wiesmann UN

series ordinal

1

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19 May 2018

Vassella F

series ordinal

2

1 reference

19 May 2018

Herschkowitz NN

series ordinal

3

1 reference

19 May 2018

publication date

1 January 1974

1 reference

19 May 2018

Acta Paediatrica Scandinavica

published in

1 reference

19 May 2018

volume

63

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19 May 2018

issue

1

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19 May 2018

page(s)

9-16

1 reference

19 May 2018

Abnormal Sulphatase Activities in Two Human Diseases (Metachromatic Leucodystrophy and Gargoylism)

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

I-cell disease: a clinical picture

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

I-cell disease: multiple lysosomal-enzyme defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

Acid hydrolases in skin and plasma in gargoylism. Deficiency of beta-galactosidase in skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

Metachromatic Leukodystrophy: Diagnosis with Samples of Venous Blood

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

The abnormalities of lysosomal enzymes in mucopolysacc- haridoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

Hurler's syndrome: deficiency of a specific beta galactosidase isoenzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1974.TB04343.X

10.1111/J.1651-2227.1974.TB04343.X

21 January 2018

Identifiers

DOI

1 reference

19 May 2018

1 reference

19 May 2018