(Q44770850)

6 December 2017

title

Laboratory diagnosis of canine GM2-gangliosidosis using blood and cerebrospinal fluid (English)

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6 December 2017

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Osamu Yamato

1

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6 December 2017

Hiroyuki Satoh

2

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6 December 2017

Naoaki Matsuki

3

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6 December 2017

Kenichiro Ono

4

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6 December 2017

Masahiro Yamasaki

5

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6 December 2017

Yoshimitsu Maede

6

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6 December 2017

publication date

1 January 2004

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Journal of Veterinary Diagnostic Investigation

6 December 2017

published in

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6 December 2017

volume

16

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6 December 2017

issue

1

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6 December 2017

page(s)

39-44

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Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypes.

6 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

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https://api.crossref.org/works/10.1177%2F104063870401600107

GM 2 Ganglioside Lysosomal Storage Disease in Cats with α-Hexosaminidase Deficiency

21 January 2018

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https://api.crossref.org/works/10.1177%2F104063870401600107

GM2 gangliosidosis in a Japanese spaniel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Partial deficiency of beta-hexosaminidase activity in canine GM2-gangliosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Naturally occurring GM2 gangliosidosis in two Muntjak deer with pathological and biochemical features of human classical Tay-Sachs disease (type B GM2 gangliosidosis).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Biochemical basis of type AB GM2 gangliosidosis in a Japanese spaniel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Normal developmental profiles of CSF gangliotetraose-series gangliosides from neonatal period to adolescence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Clinical and Biochemical Abnormalities in Porcine GM2-Gangliosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Biochemical consequences of mutations causing the GM2 gangliosidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats

21 January 2018

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https://api.crossref.org/works/10.1177%2F104063870401600107

Recognition and diagnosis of lysosomal storage diseases in the cat and dog.

21 January 2018

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https://api.crossref.org/works/10.1177%2F104063870401600107

47 Enzymic diagnosis of sphingolipidoses

21 January 2018

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https://api.crossref.org/works/10.1177%2F104063870401600107

Partial deficiency of hexosaminidase component A in juvenile GM2-gangliosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Morphological, biochemical and molecular biology approaches for the diagnosis of lysosomal storage diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F104063870401600107

Separation of three isoenzymes of N-acetyl-beta-D-hexosaminidase from human tissues by cellulose acetate membrane electrophoresis

21 January 2018

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10.1177/104063870401600107

21 January 2018

Identifiers

DOI

1 reference

6 December 2017

1 reference