The gangliosidoses (Q36612600)

15 August 2017

1 reference

title

The gangliosidoses (English)

1 reference

15 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A170187

21 December 2022

author name string

B. W. Volk

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A170187

20 May 2022

M. Adachi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A170187

20 May 2022

L. Schneck

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A170187

20 May 2022

language of work or name

English

0 references

publication date

1 September 1975

1 reference

full work available at URL

15 August 2017

https://api.elsevier.com/content/article/PII:S0046817775800414?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

https://api.elsevier.com/content/article/PII:S0046817775800414?httpAccept=text/plain

20 May 2022

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

20 May 2022

1 reference

15 August 2017

6

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15 August 2017

5

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15 August 2017

555-569

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ON ARRESTED CEREBRAL DEVELOPMENT, WITH SPECIAL REFERENCE TO ITS CORTICAL PATHOLOGY.1

15 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Enzyme alterations and lipid storage in three variants of Tay-Sachs disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Demonstration of an alteration of ganglioside metabolism in Tay-Sachs disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

The hydrolysis of Tay-Sachs ganglioside (TSG) by human N-acetyl-beta-D-hexosaminidase A

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

The metabolism of Tay-Sachs ganglioside: catabolic studies with lysosomal enzymes from normal and Tay-Sachs brain tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Tay-Sachs disease. A generalized metabolic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Chemical pathology of G-m-1-gangliosidosis (generalized gangliosidosis).

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Ultrastructural alterations of endocrine glands in Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT AND ITS RELATION TO GARGOYLISM

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

FINE STRUCTURAL LOCALIZATION OF ACID PHOSPHATASE ACTIVITY IN NEURONS OF TAY-SACHS DISEASE

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Alterations of astrocytic organelles in various lipidoses and allied diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Tay-Sachs Disease: Prenatal Diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Ultrastructure manifestations of G M1 and G M2 gangliosidosis in fetal tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Ultrastructural demonstration of neuronal storage in fetal Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

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%2FS0046-8177%2875%2980041-4

7 January 2021

Tay-Sachs disease with hexosaminidase deficiency. Clinical, morphological and biochemical findings in a case with visceral storage of renal globosides

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Gm2-gangliosidosis with total hexosaminidase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Juvenile GM2-gangliosidosis: Clinical variant of Tay-Sachs disease or a new disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Tay-Sachs disease: neurophysiological studies in 20 children.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

EYE MOVEMENTS IN TAY-SACHS DISEASE

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

THE EARLY ELECTROENCEPHALOGRAPHIC AND SEIZURE CHARACTERISTICS OF TAY-SACHS' DISEASE

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Gangliosides in the cerebrospinal fluid and the Tay-Sachs disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Generalized gangliosidosis: impaired cleavage of galactose from a mucopolysaccharide and a glycoprotien.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Tay‐Sachs' disease with visceral involvement and its relationship to Niemann‐Pick's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Familial neurovisceral lipidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis).

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Prenatal diagnosis of G M1 -gangliosidosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Gm1-gangliosidosis type I: In utero detection and fetal manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

[A disorder of ganglioside metabolism with storage of ceramide lactoside, monosialo ceramide lactoside and Tay-Sachs ganglioside in the brain]

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

GM3 (hematoside) sphingolipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Spongy degeneration of the central nervous system (Van Bogaert and Bertrand type; Canavan's disease)A review

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

1 reference

7 January 2021

Prenatal diagnosis of Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

ENZYME HISTOCHEMICAL STUDIES OF TAY-SACHS DISEASE

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Studies on cerebral lipidosis. Prenatal diagnosis of Tay-Sachs disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2875%2980041-4

7 January 2021

Pathologic anatomy

26

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

Fine structure of the myenteric plexus in various lipidoses

21 December 2022

39

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

Auditory Responses in Tay-Sachs Disease

21 December 2022

60

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

Electrocardiographic and biochemical abnormalities in Tay-Sachs disease

21 December 2022

64

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase A

21 December 2022

87

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(75)80041-4

21 December 2022

Identifiers

1 reference

release_vzhz7j4cwrefjkhtq3vo3lrhzy

15 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vzhz7j4cwrefjkhtq3vo3lrhzy

24 November 2022

mapped directly with Wikidata item

1 reference