Perioperative management of children with glycogen storage disease type II-Pompe disease-Reference-Cited by-同舟云学术

Perioperative management of children with glycogen storage disease type II-Pompe disease

Published:2018-03-25 Issue:5 Volume:28 Page:428-435
ISSN:1155-5645
Container-title:Pediatric Anesthesia
language:en
Short-container-title:Pediatr Anaesth

Author:

Bosman Linelot¹,Hoeks Sanne E.¹,González Candel Antonia²,van den Hout Hannerieke J. M.³,van der Ploeg Ans T.³,Staals Lonneke M.²^ORCID

Affiliation:

1. Department of Anesthesiology; Erasmus MC; University Medical Centre; Rotterdam The Netherlands

2. Department of Anesthesiology; Erasmus MC-Sophia Children's Hospital; University Medical Centre; Rotterdam The Netherlands

3. Division of Metabolic Diseases and Genetics; Department of Pediatrics; Erasmus MC-Sophia Children's Hospital; University Medical Centre; Rotterdam The Netherlands

Funder

Sectie Kinderanesthesiologie (Dutch Society for Pediatric Anesthesiology) of the Dutch Society for Anesthesiology

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pan.13361/fullpdf

Reference25 articles.

1. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

2. The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature;Van den Hout;Pediatrics,2003

3. A retrospective, multinational, multicenter study of the natural history of infantile-onset Pompe disease;Kishnani;J Pediatr,2006

4. Pompe disease diagnosis and management guideline;Kishnani;Genet Med,2006

5. Recombinant human alpha-glucosidase from rabbit milk in Pompe patients;Van den Hout;Lancet,2000

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