(Q42463856)

1 November 2017

title

Galactosialidosis: neuropathological findings in a case of the late-infantile type (English)

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1 November 2017

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K Oyanagi

1

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1 November 2017

E Ohama

2

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1 November 2017

K Miyashita

3

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1 November 2017

H Yoshino

4

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1 November 2017

T Miyatake

5

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1 November 2017

M Yamazaki

6

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1 November 2017

F Ikuta

7

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1 November 2017

publication date

1 January 1991

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1 November 2017

published in

Acta Neuropathologica

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1 November 2017

volume

82

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1 November 2017

issue

5

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1 November 2017

page(s)

331-339

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https://scigraph.springernature.com/pub.10.1007/bf00296543

1 November 2017

exact match

0 references

cites work

Pathological study on a severe sialidosis (alpha-neuraminidase deficiency).

1 reference

12 December 2020

Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosis.

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12 December 2020

Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein

1 reference

12 December 2020

An autopsy case of a late form of familial amaurotic idiocy in comparison to the clinical and pathological findings on the two siblings with the same disease

1 reference

12 December 2020

Adult type neuronal storage disease with neuraminidase deficiency

1 reference

12 December 2020

Globoid cell leukodystrophy: Additional deficiency of psychosine galactosidase

1 reference

12 December 2020

Sialidosis: a review of human neuraminidase deficiency

1 reference

12 December 2020

Carrier detection of sialidosis with partial beta-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes

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12 December 2020

A new type of mucolipidosis associated with hereditary thrombocytopathy and color blindness

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12 December 2020

Processing of human beta-galactosidase in GM1-gangliosidosis and Morquio B syndrome

1 reference

12 December 2020

An autopsy case of familial neurovisceral storage disease of late onset

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12 December 2020

The presence of a reduced amount of 32-kd "protective" protein is a distinct biochemical finding in late infantile galactosialidosis

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12 December 2020

A CASE OF JUVENILE LIPIDOSIS: THE SIGNIFICANCE OF ELECTRON MICROSCOPIC AND BIOCHEMICAL OBSERVATIONS OF A CEREBRAL BIOPSY.

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12 December 2020

beta-Galactosidase-neuraminidase deficiency (galactosialidosis): clinical, pathological, and enzymatic studies in a postmortem case

1 reference

12 December 2020

Macular cherry-red spots and beta-galactosidase deficiency in an adult. An autopsy case with progressive cerebellar ataxia, myoclonus, thrombocytopathy, and accumulation of polysaccharide in liver

1 reference

12 December 2020

Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes

1 reference

12 December 2020

Neuropathological findings of an autopsy case of adult beta-galactosidase and neuraminidase deficiency

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12 December 2020

Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.

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12 December 2020

Neuraminidase deficiency and accumulation of sialic acid in lymphocytes in adult type sialidosis with partial beta-galactosidase deficiency

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12 December 2020

Identifiers

DOI

10.1007/BF00296543

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1 November 2017

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