(Q48848951)

16 February 2018

title

Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms (English)

1 reference

2 September 2023

1 reference

2 September 2023

1 reference

B. Kustermann-Kuhn

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6228513

2 September 2023

K. Harzer

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6228513

2 September 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6228513

2 September 2023

publication date

1 January 1983

1 reference

16 February 2018

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00286657.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00286657/fulltext.html

2 September 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00286657

2 September 2023

1 reference

2 September 2023

1 reference

16 February 2018

volume

65

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16 February 2018

issue

2

1 reference

16 February 2018

page(s)

172-175

1 reference

16 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00286657

exact match

0 references

cites work

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: Prenatal Diagnosis

1 reference

12 December 2020

Letter: Prenatal diagnosis of Tay-Sachs disease

1 reference

12 December 2020

PRENATAL DIAGNOSIS OF TAY-SACHS DISEASE

1 reference

12 December 2020

The biochemical genetics of the hexosaminidase system in man

1 reference

12 December 2020

Hexosaminidase C in Tay-Sachs and sandhoff disease

1 reference

12 December 2020

Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).

1 reference

12 December 2020

Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)

1 reference

12 December 2020

Subunit structure of human hexosaminidase verified: interconvertibility of hexosaminidase isozymes

1 reference

12 December 2020

Characterization and tissue distribution of N-acetyl hexosaminidase C: suggestive evidence for a separate hexosaminidase locus

1 reference

12 December 2020

Pitfalls in the prenatal diagnosis of Tay-Sachs disease

1 reference

12 December 2020

N-acetyl-β-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses

1 reference

12 December 2020

Electrophoretic separation of -N-acetylhexosaminidases of human and bovine brain and liver and of Tay-Sachs brain tissue

1 reference

12 December 2020

Hexosaminidase C in brain affected by Tay-Sachs disease

1 reference

12 December 2020

Prenatal diagnosis of Tay-Sachs disease

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Caveats of antenatal diagnosis of Tay-Sachs disease

1 reference

12 December 2020

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

1 reference

12 December 2020

Studies on human N-acetyl-Beta-d-hexosaminidase C separated from neonatal brain

1 reference

12 December 2020

Characterization of Hex S, the major residual beta hexosaminidase activity in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease)

1 reference

12 December 2020

Australian paediatric journal

13

10

23

CA Michael

1974

1 reference

2 September 2023

Identifiers

DOI

10.1007/BF00286657

1 reference

16 February 2018

1 reference

16 February 2018