(Q45109885)

9 December 2017

title

Experimental polymer storage disease in rabbits. An approach to the histogenesis of sphingolipidoses (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A803739

29 July 2022

author name string

K. Miyasaki

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A803739

29 July 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=803739

29 July 2022

publication date

1 January 1975

1 reference

Virchows Archiv. A, Pathological anatomy and histology

9 December 2017

published in

1 reference

9 December 2017

volume

365

1 reference

9 December 2017

issue

4

1 reference

9 December 2017

page(s)

351-365

1 reference

Lipomucopolysaccharidosis--a second look

9 December 2017

cites work

1 reference

12 December 2020

Fabry's Disease: Alpha-Galactosidase Deficiency

1 reference

12 December 2020

Glycosphingolipidosis. Accumulation of ceramide trihexoside and globoside

1 reference

12 December 2020

GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM?

1 reference

12 December 2020

Ultrastructural study of experimental globoid cells.

1 reference

12 December 2020

THE METABOLISM OF GLUCOCEREBROSIDES. I. PURIFICATION AND PROPERTIES OF A GLUCOCEREBROSIDE-CLEAVING ENZYME FROM SPLEEN TISSUE

1 reference

12 December 2020

The genetic mucolipidoses. Diagnosis and differential diagnosis

1 reference

12 December 2020

The metabolism of ceramide trihexosides. I. Purification and properties of an enzyme that cleaves the terminal galactose molecule of galactosylgalactosylglucosylceramide

1 reference

12 December 2020

Deficiency of sphingomyelin-cleaving enzyme activity in tissue cultures derived from patients with Niemann-Pick disease

1 reference

12 December 2020

Lactosyl Ceramidosis: Catabolic Enzyme Defect of Glycosphingolipid Metabolism

1 reference

12 December 2020

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

1 reference

12 December 2020

Enzymatic Defect in Fabry's Disease

1 reference

12 December 2020

Experimental splenic tumors in the rabbit by intravenous injection of a polyvinylacetate emulsion

1 reference

12 December 2020

The metabolism of glucocerebrosides. 3. Purification and properties of a glucosyl- and galactosylceramide-cleaving enzyme from rat intestinal tissue.

1 reference

12 December 2020

Metachromatic Leukodystrophy: Diagnosis with Samples of Venous Blood

1 reference

12 December 2020

Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.

1 reference

12 December 2020

Globoid cell leucodystrophy (Krabbe's disease): deficiency of galactocerebroside beta-galactosidase

1 reference

12 December 2020

Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease

1 reference

12 December 2020

ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM

1 reference

12 December 2020

Pathologic findings in Sandhoff disease

1 reference

12 December 2020

A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM

1 reference

12 December 2020

The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick diseae

1 reference

12 December 2020

Cerebroside galactosidase of brain.

1 reference

12 December 2020

Cerebral GM1-gangliosidosis: chemical pathology of visceral organs.

1 reference

12 December 2020

The metabolism of sphingomyelin. I. Purification and properties of a sphingomyelin-cleaving enzyme from rat liver tissue.

1 reference

12 December 2020

Detection of the defect of Gaucher's disease and its carrier state in peripheral-blood leucocytes

1 reference

12 December 2020

The genetic mucolipidoses.

1 reference

12 December 2020

EVIDENCE FOR THE GENETIC BLOCK IN METACHROMATIC LEUCODYSTROPHY (ML).

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00471182

1 reference

9 December 2017

1 reference