Pregnancy in patients with mucopolysaccharidosis: a case series-Reference-Cited by-同舟云学术

Pregnancy in patients with mucopolysaccharidosis: a case series

Published:2016-09 Issue: Volume:8 Page:111-115
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Stewart Fiona J.,Bentley Andrew,Burton Barbara K.,Guffon Nathalie,Hale Susan L.,Harmatz Paul R.,Kircher Susanne G.,Kochhar Pavan K.,Mitchell John J.,Plöckinger Ursula,Graham Sue,Sande Stephen,Sisic Zlatko,Johnston Tracey A.

Funder

BioMarin Pharmaceutical Inc.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference25 articles.

1. Overview of the mucopolysaccharidoses;Muenzer;Rheumatology (Oxford),2011

2. Síndrome de morquio (mucopolisacaridosis tipo IV) y embarazo;Salinas;Rev. Chil. Obstet. Ginecol.,2005

3. Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutation;Hendriksz;J. Inherit. Metab. Dis.,2004

4. Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type I;Anbu;J. Inherit. Metab. Dis.,2006

5. Pregnancy complicated by myelopathy due to Maroteaux-Lamy syndrome;Bacchus;Am. J. Obstet. Gynecol.,1980

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