(Q36050607)

11 August 2017

Morquio-Ullrich's Disease: An Inborn Error of Metabolism? (English)

1 reference

11 August 2017

Dyggve HV

1

1 reference

11 August 2017

Melchior JC

series ordinal

2

1 reference

11 August 2017

Clausen J

series ordinal

3

1 reference

11 August 2017

language of work or name

English

0 references

publication date

1 October 1962

1 reference

Archives of Disease in Childhood

11 August 2017

1 reference

11 August 2017

37

1 reference

11 August 2017

195

1 reference

11 August 2017

525-534

1 reference

A Rare Disease in Two Brothers

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2012915

A report of seven cases of chondro-osteo-dystrophy (Morquio's disease)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2012915

Morquio's disease; a review of the literature with a description of four cases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2012915

Gargoylism; a mucopolysaccharidosis.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2012915

Osteochondrodystrophy (Morquio-Brailsford type); occurrence in three siblings.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2012915

[On differentiating dysostosis Morquio from gargoylism as an independent disease]

23 September 2018

1 reference

12 December 2020

Some recent methods for fractionation of proteins employed in diagnostic examination of cerebrospinal fluid. Agar-gel micro-electrophoresis and immuno-electrophoresis

1 reference

12 December 2020

[Extensive and generally hereditary development and growth defects of the skeleton]

1 reference

12 December 2020

[Polytope hereditary enchondral dysostosis]

1 reference

12 December 2020

1 reference

12 December 2020

Studies on the biochemistry of connective tissue

1 reference

12 December 2020

[Corneal opacities and metabolic disorders in Morquio's disease]

1 reference

12 December 2020

A paper spot test useful in study of Hurler's syndrome

1 reference

12 December 2020

Morquio-Ullrich's disease. Report of 2 cases

1 reference

12 December 2020

Gargoylism (lipochondrodystrophy); a study of 10 cases, with emphasis on the formes frustes of the disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.37.195.525

1 reference

11 August 2017

1 reference

11 August 2017

1 reference