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RANBP2 Mutation in Clinically Undiagnosed Acute Necrotizing Encephalopathy.

作者信息

Işıkay Sedat, Şahin Yavuz

机构信息

Department of Physiotherapy and Rehabilitation, School of Health Sciences, Hasan Kalyoncu University, Gaziantep, Turkey.

Department of Pediatric Neurology, Medical Park Hospital, 52063 Street, Şehitkamil, Gaziantep, Turkey.

出版信息

Indian J Pediatr. 2018 Sep;85(9):820-821. doi: 10.1007/s12098-018-2678-0. Epub 2018 Apr 24.

DOI:10.1007/s12098-018-2678-0
PMID:29687329
Abstract
摘要

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本文引用的文献

1
Acute necrotizing encephalopathy: an underrecognized clinicoradiologic disorder.急性坏死性脑病：一种未被充分认识的临床放射学疾病。
Mediators Inflamm. 2015;2015:792578. doi: 10.1155/2015/792578. Epub 2015 Mar 22.
2
The interplay of infection and genetics in acute necrotizing encephalopathy.感染与遗传在急性坏死性脑病中的相互作用。
Curr Opin Pediatr. 2010 Dec;22(6):751-7. doi: 10.1097/MOP.0b013e3283402bfe.
3
Acute necrotizing encephalopathy of childhood: a novel form of acute encephalopathy prevalent in Japan and Taiwan.儿童急性坏死性脑病：一种在日本和台湾地区流行的新型急性脑病。
急性甲型流感脑炎致具有遗传易感性患儿的神经眼科并发症
BMJ Case Rep. 2020 Sep 14;13(9):e235636. doi: 10.1136/bcr-2020-235636.
4
susceptibility to infection-induced encephalopathy: Clinicoradiologic and molecular description in a Malaysian family.感染性脑病易感性：马来西亚一个家族的临床放射学和分子描述
Mol Genet Metab Rep. 2020 Jul 27;24:100627. doi: 10.1016/j.ymgmr.2020.100627. eCollection 2020 Sep.
5
Acute Necrotizing Encephalopathy of Childhood with H1N1 Infection.儿童感染甲型H1N1流感病毒所致急性坏死性脑病
J Pediatr Intensive Care. 2020 Sep;9(3):222-224. doi: 10.1055/s-0040-1705182. Epub 2020 Mar 6.
6
Genetic Acute Necrotizing Encephalopathy Associated with RANBP2: Clinical and Therapeutic Implications in Pediatrics.与RANBP2相关的遗传性急性坏死性脑病：儿科临床及治疗意义
Mult Scler Relat Disord. 2020 Aug;43:102194. doi: 10.1016/j.msard.2020.102194. Epub 2020 May 15.
Brain Dev. 1997 Mar;19(2):81-92. doi: 10.1016/s0387-7604(96)00063-0.