(Q48382693)

11 February 2018

title

Adult-onset lysosomal storage disease in a Schipperke dog: clinical, morphological and biochemical studies (English)

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11 February 2018

lysosomal storage disease

main subject

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K Knowles

1

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11 February 2018

J Alroy

2

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11 February 2018

M Castagnaro

3

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11 February 2018

S S Raghavan

4

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11 February 2018

R M Jakowski

5

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11 February 2018

G O Freden

6

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11 February 2018

publication date

1 January 1993

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11 February 2018

published in

Acta Neuropathologica

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11 February 2018

volume

86

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11 February 2018

issue

3

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11 February 2018

page(s)

306-312

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11 February 2018

Reconsideration of the classification of the neuronal ceroid-lipofuscinoses.

cites work

1 reference

12 December 2020

Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosis

1 reference

12 December 2020

Human lysosomal protective protein. Glycosylation, intracellular transport, and association with beta-galactosidase in the endoplasmic reticulum

1 reference

12 December 2020

Gangliosides: structure, isolation, and analysis

1 reference

12 December 2020

Lectin histochemistry of glycolipid storage diseases on frozen and paraffin-embedded tissue sections

1 reference

12 December 2020

Biochemical basis of type AB GM2 gangliosidosis in a Japanese spaniel

1 reference

12 December 2020

Deficient lysosomal carboxypeptidase activity in galactosialidosis

1 reference

12 December 2020

Gangliosides in the nervous system

1 reference

12 December 2020

Trafficking of lysosomal enzymes in normal and disease states

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12 December 2020

Lysosomal storage diseases

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12 December 2020

Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency.

1 reference

12 December 2020

GM2 gangliosidosis in a Japanese spaniel

1 reference

12 December 2020

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

1 reference

12 December 2020

Different ceramide compositions of gangliosides between human motor and sensory nerves

1 reference

12 December 2020

Saposin proteins: structure, function, and role in human lysosomal storage disorders

1 reference

12 December 2020

Lysosphingolipids inhibit protein kinase C: implications for the sphingolipidoses

1 reference

12 December 2020

Modulation of carbohydrate residues in regenerative nodules and neoplasms of canine and feline pancreas

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Animal models for lysosomal storage diseases: their past and future contribution

1 reference

12 December 2020

Galactosialidosis: simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00304147

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11 February 2018

1 reference

11 February 2018