(Q52087763)

English

Early diagnosis of Maroteaux-Lamy syndrome in two patients with accelerated growth and advanced bone maturation.

scientific article published in June 2004

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scholarly article

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

Early diagnosis of Maroteaux-Lamy syndrome in two patients with accelerated growth and advanced bone maturation. (English)

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

Delphine Héron

1

object named as

Delphine Heron

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

Clarisse Baumann

2

object named as

Clarisse Baumann

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

author name string

Jean Jacques Benichou

3

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

Jean Paul Harpey

4

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

Martine Le Merrer

5

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

publication date

1 June 2004

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

European Journal of Pediatrics

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

163

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

6

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

323-326

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

https://scigraph.springernature.com/pub.10.1007/s00431-004-1428-7

0 references

Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical definition of the Hurler-Hunter phenotypes. A review of 50 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucopolysaccharidosis VI (Maroteaux-Lamy's disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone-Marrow Transplantation in the Maroteaux–Lamy Syndrome (Mucopolysaccharidosis Type VI)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation in a patient with Maroteaux-Lamy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A NEW DYSOSTOSIS WITH URINARY ELIMINATION OF CHONDROITIN SULFATE B

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Valvular heart disease in four patients with Maroteaux-Lamy syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An N-acetylgalactosamine-4-sulfatase mutation (delta G238) results in a severe Maroteaux-Lamy phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hematopoietic cell transplantation for inherited metabolic diseases: an overview of outcomes and practice guidelines

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of Maroteaux-Lamy syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15346915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-004-1428-7

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/15346915

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