Treatment of neuroblastoma in congenital central hypoventilation syndrome with a PHOX2B polyalanine repeat expansion mutation: New twist on a neurocristopathy syndrome-Reference-Cited by-同舟云学术

Treatment of neuroblastoma in congenital central hypoventilation syndrome with a PHOX2B polyalanine repeat expansion mutation: New twist on a neurocristopathy syndrome

Published:2015-05-22 Issue:11 Volume:62 Page:2007-2010
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Armstrong Amy E.¹,Weese-Mayer Debra E.²,Mian Amir³,Maris John M.⁴,Batra Vandana⁴,Gosiengfiao Yasmin⁵,Reichek Jennifer⁵,Madonna Mary Beth⁶,Bush Jonathan W.⁷,Shore Richard M.⁸,Walterhouse David O.⁵

Affiliation:

1. Department of Pediatrics; Ann & Robert H. Lurie Children's Hospital of Chicago; Chicago Illinois

2. Ann & Robert H. Lurie Children's Hospital of Chicago; Center for Autonomic Medicine in Pediatrics (CAMP); Northwestern University of Feinberg School of Medicine and Stanley Manne Children's Research Institute; Chicago Illinois

3. Department of Pediatric Hematology-Oncology; College of Medicine; Arkansas Children's Hospital; University of Arkansas Medical Sciences; Little Rock Arkansas

4. Division of Hematology; Oncology & Transplantation; Children's Hospital of Philadelphia; University of Pennsylvania School of Medicine and Abramson Family Center Research Institute; Philadelphia Pennsylvania

5. Division of Hematology; Oncology & Transplantation; Robert Lurie Comprehensive Cancer Center; Ann & Robert H. Lurie Children's Hospital of Chicago; Northwestern University Feinberg School of Medicine; Chicago Illinois

6. Department of Pediatric Surgery; Ann & Robert H. Lurie Children's Hospital of Chicago; Northwestern University Feinberg School of Medicine; Chicago Illinois

7. Department of Pathology; Ann & Robert H. Lurie Children's Hospital of Chicago; Northwestern University Feinberg School of Medicine; Chicago Illinois

8. Department of Medical Imaging; Ann & Robert H. Lurie Children's Hospital of Chicago; Northwestern University Feinberg School of Medicine; Chicago Illinois

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.25572/fullpdf

Reference20 articles.

1. New aspects of neuroblastoma treatment: ASPHO 2011 symposium review;Zage;Pediatr Blood Cancer,2012

2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet,2003

3. Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2B;Weese-Mayer;Am J Med Genet A,2003

4. Germline PHOX2B mutation in hereditary neuroblastoma;Mosse;Am J Hum Genet,2004

5. Distinct neuroblastoma-associated alterations of PHOX2B impair sympathetic neuronal differentiation in zebrafish models;Pei;PLoS Genet,2013

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