(Q72874275)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6255724%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients (English)

1 reference

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29 October 2019

author name string

J E Goldman

1

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29 October 2019

T Yamanaka

2

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29 October 2019

I Rapin

3

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29 October 2019

M Adachi

4

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29 October 2019

K Suzuki

5

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29 October 2019

K Suzuki

6

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29 October 2019

publication date

1 January 1980

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29 October 2019

published in

Acta Neuropathologica

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29 October 2019

volume

52

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29 October 2019

issue

3

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29 October 2019

page(s)

189-202

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https://scigraph.springernature.com/pub.10.1007/bf00705807

29 October 2019

exact match

0 references

cites work

Adult (chronic) GM2 gangliosidosis. Atypical spinocerebellar degeneration in a Jewish sibship

1 reference

12 December 2020

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

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

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

Cerebral lipids in a case of systemic Gm2-gangliosidosis of a late infantile type.

1 reference

12 December 2020

[Sandhoff's disease (GM2 gangliosidosis, type 2). Clinical, biochemical and anatomo-clinical study]

1 reference

12 December 2020

Alterations of astrocytic organelles in various lipidoses and allied diseases.

1 reference

12 December 2020

Gm2-gangliosidosis with total hexosaminidase deficiency.

1 reference

12 December 2020

Characterization of an activating factor required for hydrolysis of Gm2 ganglioside catalyzed by hexosaminidase A

1 reference

12 December 2020

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

1 reference

12 December 2020

Quantitative estimation of sialic acids. II. A colorimetric resorcinol-hydrochloric acid method

1 reference

12 December 2020

STUDY OF IONIC STRUCTURES IN PHOSPHOLIPIDS BY INFRARED SPECTRA

1 reference

12 December 2020

The quantitative analysis of plasmalogens by paper chromatography

1 reference

12 December 2020

The lipid composition of purified bovine brain myelin

1 reference

12 December 2020

GM2 gangliosidosis with total beta-N-acetyl-hexosaminidase deficit or Sandhoff's disease

1 reference

12 December 2020

Tay-Sachs disease (amaurotic familial idiocy) in a non-Jewish male: a case report

1 reference

12 December 2020

Gaucher's disease: deficiency of 'acid' -glucosidase and reconstitution of enzyme activity in vitro

1 reference

12 December 2020

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

1 reference

12 December 2020

The Activator of Cerebroside Sulphatase. Purification from Human Liver and Identification as a Protein

1 reference

12 December 2020

AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2

1 reference

12 December 2020

ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM

1 reference

12 December 2020

G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis

1 reference

12 December 2020

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

1 reference

12 December 2020

An activator stimulating the enzymic hydrolysis of sphingoglycolipids

1 reference

12 December 2020

Purification, Biochemical and Immunological Characterisation of Hexosaminidase A from Variant AB of Infantile GM2 Gangliosidosis

1 reference

12 December 2020

GM2-gangliosidosis, AB variant: clinico-pathological study of a case

1 reference

12 December 2020

Progress in investigations of sphingolipidoses

1 reference

12 December 2020

THE CHEMICAL COMPOSITION OF BOVINE CNS MYELIN

1 reference

12 December 2020

Ectopic dendritic growth in mature pyramidal neurones in human ganglioside storage disease

1 reference

12 December 2020

A new color reaction for the quantitation of serum cholesterol

1 reference

12 December 2020

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

1 reference

12 December 2020

Distortion of neuronal geometry and formation of aberrant synapses in neuronal storage disease

1 reference

12 December 2020

A simple method for the isolation and purification of total lipides from animal tissues

1 reference

12 December 2020

High-performance thin-layer chromatography and densitometric determination of brain ganglioside compositions of several species

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Studies in Tay-Sachs disease. I. B. Clinical and pathologic descriptions

1 reference

12 December 2020

The quantitative estimation of cerebrosides in nervous tissue

1 reference

12 December 2020

Adult-onset GM2 gangliosidosis Seizures, dementia, and normal pressure hydrocephalus associated with glycolipid storage in the brain and arachnoid granulation

1 reference

12 December 2020

CHROMATOGRAPHlC SEPARATION OF HUMAN BRAIN GANGLIOSIDES*

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00705807

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6255724%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference