(Q70441519)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6409799%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Morquio-B disease, spondyloepiphyseal dysplasia associated with acid beta-galactosidase deficiency. Report of three cases in one family (English)

1 reference

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11 October 2019

author name string

J J van Gemund

1

1 reference

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11 October 2019

M A Giesberts

2

1 reference

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11 October 2019

R F Eerdmans

3

1 reference

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11 October 2019

W Blom

4

1 reference

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11 October 2019

W J Kleijer

5

1 reference

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11 October 2019

publication date

1 January 1983

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11 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6409799%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

volume

64

1 reference

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11 October 2019

issue

1

1 reference

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11 October 2019

page(s)

50-54

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https://scigraph.springernature.com/pub.10.1007/bf00289478

11 October 2019

exact match

0 references

cites work

Two-dimensional electrophoresis of urinary mucopolysaccharides on cellulose acetate after N-cetylpyridiniumchloride (CPC) precipitation: a method suitable for the routine laboratory

1 reference

12 December 2020

Adult GM1 gangliosidosis: clinical and biochemical studies on two patients and comparison to other patients called variant or adult GM1 gangliosidosis

1 reference

12 December 2020

The mucopolysaccharide of normal human urine

1 reference

12 December 2020

[Column chromatographic fractionation of acid mucopolysaccharides in the urine]

1 reference

12 December 2020

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

12 December 2020

Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency.

1 reference

12 December 2020

Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiency

1 reference

12 December 2020

The use of alpha-L-iduronidase activity determinations in leucocytes for the detection of Hurler and Scheie syndromes

1 reference

12 December 2020

The systemic mucopolysaccharidoses.

1 reference

12 December 2020

A modified uronic acid carbazole reaction

1 reference

12 December 2020

Morquio-like syndrome (MPS IV B) associated with deficiency of a beta-galactosidase

1 reference

12 December 2020

Rapid prenatal diagnosis of GM1-gangliosidosis using microchemical methods

1 reference

12 December 2020

Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB

1 reference

12 December 2020

Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography

1 reference

12 December 2020

Beta galactosidase and the Morquio syndrome

1 reference

12 December 2020

Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Pericellular glycosaminoglycans in cultured human cells. A possible source of error in prenatal diagnosis of Mucopolysaccharidoses

1 reference

12 December 2020

Morquio syndrome (mucopolysaccharidosis IV B) associated with beta-galactosidase deficiency. Report of two cases.

1 reference

12 December 2020

Morquio syndrome: clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVB.

1 reference

12 December 2020

N-acetylgalactosamine-6-sulfate sulfatase in man. Absence of the enzyme in Morquio disease

1 reference

12 December 2020

Heterogeneity of formes frustes of Morquio's disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00289478

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6409799%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference