(Q71262706)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5360899%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

title

[Infantile amaurotic idiocy and related forms as ganglioside storage diseases] (English)

1 reference

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17 October 2019

author name string

K Sandhoff

series ordinal

1

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17 October 2019

H Jatzkewitz

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5360899%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

G Peters

series ordinal

3

1 reference

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17 October 2019

publication date

1 July 1969

1 reference

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17 October 2019

published in

The Science of Nature

1 reference

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17 October 2019

volume

56

1 reference

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17 October 2019

page(s)

356-362

1 reference

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17 October 2019

issue

7

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https://scigraph.springernature.com/pub.10.1007/bf00596925

17 October 2019

exact match

0 references

cites work

On a biochemically special form of infantile amaturotic idiocy

1 reference

12 December 2020

Enzymatic synthesis of ceramide-glucose and ceramide-lactose by glycosyltransferases from embryonic chicken brain.

1 reference

12 December 2020

The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.

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12 December 2020

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

1 reference

12 December 2020

A SIMPLE AND ACCURATE MICROMETHOD FOR QUANTITATIVE DETERMINATION OF GANGLIOSIDE PATTERNS.

1 reference

12 December 2020

Fine structure of the cerebellum of children with lipidoses.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

STRUCTURE COMPARISON OF THE MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN, GARGOYLISM, AND LATE INFANTILE SYSTEMIC LIPIDOSIS. I.

1 reference

12 December 2020

Enzymatic Defect in Fabry's Disease

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12 December 2020

Studies on brain lipids in Tay-Sachs' disease. I. Isolation of two sialic acid-free glycolipids.

1 reference

12 December 2020

FAMILIAL NEUROVISCERAL LIPIDOSIS. AN ANALYSIS OF EIGHT CASES OF A SYNDROME PREVIOUSLY REPORTED AS "HURLER-VARIANT," "PSEUDO-HURLER," AND "TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT"

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12 December 2020

GM1-gangliosidosis (gneralized gangliosidosis). Morphology and chemical pathology.

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12 December 2020

Enzymatic hydrolysis of sphingolipids. VI. Hydrolysis of ceramide glycosides by calf brain beta-N-acetylhexosaminidase.

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12 December 2020

[Resolution of mammalian N-acetyl-beta-D-hexosaminidase into multiple forms by electrofocussing]

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

[The storage of gangliosides in nervous tissue in Tay-Sachs disease and the changes in material preserved in formalin]

1 reference

12 December 2020

Biochemical evaluation of a combined sulfatidosis and gangliosidosis (glycolipidosis) of the brain.

1 reference

12 December 2020

Membranous cytoplasmic granules in infantile amaurotic idiocy

1 reference

12 December 2020

GM1-ganglioside accumulation and beta-galactosidase deficiency in a case of GM1-gangliosidosis (Landing disease).

1 reference

12 December 2020

Cerebral GM1-gangliosidosis: chemical pathology of visceral organs.

1 reference

12 December 2020

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

12 December 2020

Enzymatic synthesis of disialogangliosides from monosialogangliosides by sialyltransferases from embryonic chicken brain.

1 reference

12 December 2020

GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM?

1 reference

12 December 2020

[ON THE ENZYMATIC BREAKDOWN OF N-ACETYLNEURAMINOACID-FREE GANGLIOSIDE RESIDUES (CEREMIDE OLIGOSACCHARIDES)]

1 reference

12 December 2020

A new glycolipid in Tay-Sachs brain.

1 reference

12 December 2020

Studies in Tay-Sachs disease. II. Ultrastructure of the cerebrum.

1 reference

12 December 2020

[THE QUANTITATIVE DETERMINATION OF GANGLIOSIDES AND THEIR NEURAMINIC ACID-FREE DERIVATIVES IN INFANTILE, JUVENILE AND FORMS OF AMAUROTIC IDIOCY AND AN UNUSUAL LATE INFANTILE BIOCHEMICAL FORM]

1 reference

12 December 2020

Tay-Sachs disease. A generalized metabolic disorder

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

[ON THE FINE STRUCTURE OF STORED SUBSTANCES IN THE INFANTILE FORM OF FAMILIAL AMAUROTIC IDIOCY]

1 reference

12 December 2020

Studies inn Tay-Sachs disease. V. The membrane of the membranous cytoplasmic body

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

Molecular composition of the major glycolipids in globoid cell leukodystrophy.

1 reference

12 December 2020

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

1 reference

12 December 2020

The subcellular localization of gangliosides in the brain.

1 reference

12 December 2020

Alexander's disease--really a leucodystrophy?

1 reference

12 December 2020

Brain ceramide hexosides in Tay-Sachs disease and generalized gangliosidosis (GM1-gangliosidosis).

1 reference

12 December 2020

[Landing's disease or early infantile amaurotic idiocy with generalized gangliosidosis of the GM 1 type]

1 reference

12 December 2020

1 reference

12 December 2020

A CLINICAL, BIOCHEMICAL AND ELECTRON MICROSCOPIC STUDY OF LATE INFANTILE AMAUROTIC FAMILY IDIOCY.

1 reference

12 December 2020

STUDIES IN GLOBOID (KRABBE) LEUKODYSTROPHY. II. CONTROLLED THIN-LAYER CHROMATOGRAPHIC STUDIES OF GLOBOID BODY FRACTIONS IN SEVEN PATIENTS.

1 reference

12 December 2020

THE GLYCOLIPIDS OF THE BRAIN OF TAY-SACHS' DISEASE.--THE CHEMICAL STRUCTURES OF A GLOBOSIDE AND MAIN GANGLIOSIDE.

1 reference

12 December 2020

FORMATION OF THE MEMBRANOUS CYTOPLASMIC BODIES IN TAY-SACHS DISEASE: AN IN VITRO STUDY.

1 reference

12 December 2020

Composition of brain ganglio-sides.

1 reference

12 December 2020

A particle-bound sialyl lactosidoceramide splitting mammalian sialidase

1 reference

12 December 2020

Enzymatic abnormalities in diseases of sphingolipid metabolism.

1 reference

12 December 2020

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

1 reference

12 December 2020

[Concerning brain gangliosides in Tay-Sachs disease]

1 reference

12 December 2020

1 reference

12 December 2020

The pattern of mammalian brain gangliosides. II. Evaluation of the extraction procedures, postmortem changes and the effect of formalin preservation.

1 reference

12 December 2020

The chemistry of gangliosides: a review.

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

Incorporation of selected isotopes into lipids of humans with cerebral lipidoses: studies on D-glucosamine-1-14C.

1 reference

12 December 2020

The chemical structure of normal human brain and Tay-Sachs gangliosides

1 reference

12 December 2020

The lysosomal localization of sphingolipid hydrolases

1 reference

12 December 2020

Biochemical and histochemical observations on Krabbe's disease. (Globoid body diffuse sclerosis).

1 reference

12 December 2020

The amaurotic idiocies: correlation between biochemical data and clinical courses

1 reference

12 December 2020

Enzymatic hydrolysis of sphingolipids. V. Hydrolysis of monosialoganglioside and hexosylceramides by rat brain beta-galactosidase.

1 reference

12 December 2020

Studies in Tay-Sachs disease. IV. Membranous cytoplasmic bodies.

1 reference

12 December 2020

Gangliosides and acetylcholinesterase in isolated membranes of the rat-brain cortex.

1 reference

12 December 2020

CHROMATOGRAPHIC SEPARATION OF HUMAN BRAIN GANGLIOSIDES.

1 reference

12 December 2020

Subacute sclerosing leukoencephalitis. II. Chemical studies including abnormal myelin and an abnormal ganglioside pattern.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00596925

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5360899%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference