Encefalopatía aguda necrosante familiar o recurrente desencadenada por infecciones
- 30 September 2009
- journal article
- case report
- Published by Elsevier BV in Anales de Pediatría
- Vol. 71 (3), 235-239
- https://doi.org/10.1016/j.anpedi.2009.05.020
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2American Journal of Human Genetics, 2008
- The nucleoporin Nup358 associates with and regulates interphase microtubulesFEBS Letters, 2007
- Association of the Kinesin‐Binding Domain of RanBP2 to KIF5B and KIF5C Determines Mitochondria Localization and FunctionTraffic, 2007
- RanBP2 Modulates Cox11 and Hexokinase I Activities and Haploinsufficiency of RanBP2 Causes Deficits in Glucose MetabolismPLoS Genetics, 2006
- Acute Necrotizing Encephalopathy of Childhood in Non-Asian Patients: Report of Three Cases and Literature ReviewJournal of Child Neurology, 2006
- Nuclear Envelope Breakdown Is Coordinated by Both Nup358/RanBP2 and Nup153, Two Nucleoporins with Zinc Finger ModulesMolecular Biology of the Cell, 2006
- Autosomal dominant acute necrotizing encephalopathy maps to 2q12.1‐2q13Annals of Neurology, 2004
- Autosomal dominant acute necrotizing encephalopathyNeurology, 2003
- Acute necrotizing encephalopathy of childhood (infantile bilateral thalamic necrosis): two non‐Japanese casesDevelopmental Medicine and Child Neurology, 1998
- Acute necrotizing encephalopathy of childhood: a novel form of acute encephalopathy prevalent in Japan and TaiwanBrain & Development, 1997