(Q50441368)

English

Progression of organ manifestations upon enzyme replacement therapy in a patient with mucopolysaccharidosis type I/Hurler.

scientific article published on 13 November 2009

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scholarly article

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

Progression of organ manifestations upon enzyme replacement therapy in a patient with mucopolysaccharidosis type I/Hurler. (English)

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

enzyme replacement therapy

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mucopolysaccharidosis I

1 reference

based on heuristic

inferred from title

Saadet Mercimek-Mahmutoglu

1

object named as

Saadet Mercimek-Mahmutoglu

1 reference

Europe PubMed Central

14 March 2018

author name string

Christopher Reilly

2

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

Derek Human

3

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

Paula J Waters

4

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

Sylvia Stoeckler-Ipsiroglu

5

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

publication date

13 November 2009

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

World Journal of Pediatrics

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

5

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

4

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

319-321

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

https://scigraph.springernature.com/pub.10.1007/s12519-009-0062-x

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alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Outcome after three years of laronidase enzyme replacement therapy in a patient with Hurler syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Safety and efficacy of enzyme replacement therapy in combination with hematopoietic stem cell transplantation in Hurler syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme-replacement therapy in mucopolysaccharidosis I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19911152

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12519-009-0062-X

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/19911152

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