A genetic cause for neonatal encephalopathy: incontinentia pigmenti with NEMO mutation-Reference-Cited by-同舟云学术

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A genetic cause for neonatal encephalopathy: incontinentia pigmenti with NEMO mutation

Published:2008-01-31 Issue:3 Volume:97 Page:379-381
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Loh Ne-Ron,Jadresic Lyda P,Whitelaw Andrew

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2007.00630.x/fullpdf

Reference5 articles.

1. Clinical study of 40 cases of incontinentia pigmenti;Hadj-Rabia;Arch Dermatol,2003

2. Lines of Blaschko;Bolognia;J Am Acad Dermatol,1994

3. NFκB and inflammation in genetic disease;Sebban;Biochem Pharmacol,2006

4. Insights into the pathogenesis of cerebral lesions in incontinentia pigmenti;Hennel;Pediatr Neurol,2003

5. Lipopolysaccharide-induced inflammation and perinatal brain injury;Wang;Sem Fetal Neonatal Med,2006

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromes;European Journal of Paediatric Neurology;2021-07

2. INCONTINENTIA PIGMENTI;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

3. Incontinentia Pigmenti;Harper's Textbook of Pediatric Dermatology;2019-11-20

4. Cerebral Arteriopathy in a Newborn With Incontinentia Pigmenti;Pediatric Neurology;2016-01

5. Epilepsy Associated with Incontinentia Pigmenti;Journal of Pediatric Epilepsy;2015-12-08

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