(Q36612600)

English

The gangliosidoses

scientific article published on September 1, 1975

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1 reference

Europe PubMed Central

The gangliosidoses (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

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

Europe PubMed Central

PubMed publication ID

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

Europe PubMed Central

PubMed publication ID

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

Europe PubMed Central

PubMed publication ID

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

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publication date

1 September 1975

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

full work available at URL

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

1 reference

10.1016/S0046-8177(75)80041-4

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

20 May 2022

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

1 reference

10.1016/S0046-8177(75)80041-4

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

20 May 2022

Human Pathology

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

555-569

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Tay-Sachs disease. A generalized metabolic disorder

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Tay-Sachs Disease: Prenatal Diagnosis

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Gm2-gangliosidosis with total hexosaminidase deficiency.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

EYE MOVEMENTS IN TAY-SACHS DISEASE

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Familial neurovisceral lipidosis

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis of G M1 -gangliosidosis.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

[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

based on heuristic

inferred from DOI database lookup

GM3 (hematoside) sphingolipodystrophy

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

GM1 gangliosidosis

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis of Tay-Sachs disease.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

ENZYME HISTOCHEMICAL STUDIES OF TAY-SACHS DISEASE

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Pathologic anatomy

26

1 reference

10.1016/S0046-8177(75)80041-4

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

21 December 2022

Fine structure of the myenteric plexus in various lipidoses

39

1 reference

10.1016/S0046-8177(75)80041-4

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

21 December 2022

Auditory Responses in Tay-Sachs Disease

60

1 reference

10.1016/S0046-8177(75)80041-4

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

21 December 2022

Electrocardiographic and biochemical abnormalities in Tay-Sachs disease

64

1 reference

10.1016/S0046-8177(75)80041-4

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

21 December 2022

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

87

1 reference

10.1016/S0046-8177(75)80041-4

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

21 December 2022

Identifiers

10.1016/S0046-8177(75)80041-4

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

release_vzhz7j4cwrefjkhtq3vo3lrhzy

1 reference

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

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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