(Q53827923)

20 May 2018

title

The role of lysosomes in the pathogeny of storage diseases. (English)

1 reference

20 May 2018

author name string

H G Hers

series ordinal

1

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20 May 2018

publication date

1 January 1972

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20 May 2018

published in

Biochimie

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20 May 2018

volume

54

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20 May 2018

issue

5

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20 May 2018

page(s)

753-757

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20 May 2018

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).

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Gml-ganglioside accumulation and β-galactosidase deficiency in a case of Gml-gangliosidosis (Landing disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Functions of lysosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Fabry's Disease: Alpha-Galactosidase Deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Tissue fractionation studies. 16. Intracellular distribution and properties of alpha-glucosidases in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Accumulation of a glycerolphospholipid in classical niemann-pick disease

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2872%2980179-2

7 January 2021

10.1016/S0300-9084(72)80179-2

Identifiers

DOI

0 references

1 reference

20 May 2018