High Sustained Antibody Titers in Patients with Classic Infantile Pompe Disease Following Immunomodulation at Start of Enzyme Replacement Therapy-Reference-Cited by-同舟云学术

High Sustained Antibody Titers in Patients with Classic Infantile Pompe Disease Following Immunomodulation at Start of Enzyme Replacement Therapy

Published:2018-04 Issue: Volume:195 Page:236-243.e3
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Poelman Esther,Hoogeveen-Westerveld Marianne,Kroos-de Haan Marian A.,van den Hout Johanna M.P.,Bronsema Kees J.,van de Merbel Nico C.,van der Ploeg Ans T.,Pijnappel W.W.M. Pim^ORCID

Funder

Prinses Beatrix Spierfonds

Tex Net

Sophia Foundation for Medical Research (SSWO)

Metakids

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Colciencias and Sanofi Genzyme

TKI-programme Life Sciences & Health

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference32 articles.

1. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency;Hirschhorn,2001

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. Pompe's disease;van der Ploeg;Lancet,2008

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

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

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