418 related articles for article (PubMed ID: 19118815)
1. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
Neilson DE; Adams MD; Orr CM; Schelling DK; Eiben RM; Kerr DS; Anderson J; Bassuk AG; Bye AM; Childs AM; Clarke A; Crow YJ; Di Rocco M; Dohna-Schwake C; Dueckers G; Fasano AE; Gika AD; Gionnis D; Gorman MP; Grattan-Smith PJ; Hackenberg A; Kuster A; Lentschig MG; Lopez-Laso E; Marco EJ; Mastroyianni S; Perrier J; Schmitt-Mechelke T; Servidei S; Skardoutsou A; Uldall P; van der Knaap MS; Goglin KC; Tefft DL; Aubin C; de Jager P; Hafler D; Warman ML
Am J Hum Genet; 2009 Jan; 84(1):44-51. PubMed ID: 19118815
[TBL] [Abstract][Full Text] [Related]
2. Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation.
Sell K; Storch K; Hahn G; Lee-Kirsch MA; Ramantani G; Jackson S; Neilson D; von der Hagen M; Hehr U; Smitka M
Brain Dev; 2016 Sep; 38(8):777-80. PubMed ID: 26923722
[TBL] [Abstract][Full Text] [Related]
3. Recurrent acute necrotizing encephalopathy in a boy with RANBP2 mutation and thermolabile CPT2 variant: The first case of ANE1 in Japan.
Ohashi E; Hayakawa I; Murofushi Y; Kawai M; Suzuki-Muromoto S; Abe Y; Yoshida M; Kono N; Kosaki R; Hoshino A; Mizuguchi M; Kubota M
Brain Dev; 2021 Sep; 43(8):873-878. PubMed ID: 34059398
[TBL] [Abstract][Full Text] [Related]
4. Familial acute necrotizing encephalopathy with RANBP2 mutation: The first report in Northeast Asia.
Lee YJ; Hwang SK; Lee SM; Kwon S
Brain Dev; 2017 Aug; 39(7):625-628. PubMed ID: 28336122
[TBL] [Abstract][Full Text] [Related]
5. RANBP2 mutation and acute necrotizing encephalopathy: 2 cases and a literature review of the expanding clinico-radiological phenotype.
Singh RR; Sedani S; Lim M; Wassmer E; Absoud M
Eur J Paediatr Neurol; 2015 Mar; 19(2):106-13. PubMed ID: 25522933
[TBL] [Abstract][Full Text] [Related]
6. Radiological manifestation of familial acute necrotizing encephalopathy with RANBP2 mutation in a Far-East Asian family: Case report.
Park YJ; Hwang JY; Kim YW; Lee YJ; Ko A
Medicine (Baltimore); 2021 Mar; 100(12):e25171. PubMed ID: 33761695
[TBL] [Abstract][Full Text] [Related]
7. A novel variation in RANBP2 associated with infection-triggered familial acute necrotizing encephalopathy.
Hu Y; Tian Z; Zhao B; Dong C; Cao L
Neurol Sci; 2022 Jun; 43(6):3973-3977. PubMed ID: 35348941
[TBL] [Abstract][Full Text] [Related]
8. Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family.
Gika AD; Rich P; Gupta S; Neilson DE; Clarke A
Dev Med Child Neurol; 2010 Jan; 52(1):99-102. PubMed ID: 19811512
[TBL] [Abstract][Full Text] [Related]
9. Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene.
Denier C; Balu L; Husson B; Nasser G; Burglen L; Rodriguez D; Labauge P; Chevret L
J Neurol Sci; 2014 Oct; 345(1-2):236-8. PubMed ID: 25128471
[TBL] [Abstract][Full Text] [Related]
10. [Infection-triggered familial or recurrent acute necrotizing encephalopathy].
López-Laso E; Mateos-González ME; Pérez-Navero JL; Camino-León R; Briones P; Neilson DE
An Pediatr (Barc); 2009 Sep; 71(3):235-9. PubMed ID: 19643689
[TBL] [Abstract][Full Text] [Related]
11. The interplay of infection and genetics in acute necrotizing encephalopathy.
Neilson DE
Curr Opin Pediatr; 2010 Dec; 22(6):751-7. PubMed ID: 21610332
[TBL] [Abstract][Full Text] [Related]
12. H1N1 triggered recurrent acute necrotizing encephalopathy in a family with a T653I mutation in the RANBP2 gene.
Anand G; Visagan R; Chandratre S; Segal S; Nemeth AH; Squier W; Sheerin F; Neilson D; Jayawant S
Pediatr Infect Dis J; 2015 Mar; 34(3):318-20. PubMed ID: 25170550
[TBL] [Abstract][Full Text] [Related]
13. Familial acute necrotizing encephalopathy without RANBP2 mutation: Poor outcome.
Nishimura N; Higuchi Y; Kimura N; Nozaki F; Kumada T; Hoshino A; Saitoh M; Mizuguchi M
Pediatr Int; 2016 Nov; 58(11):1215-1218. PubMed ID: 27882739
[TBL] [Abstract][Full Text] [Related]
14. Influenza-Associated Acute Necrotizing Encephalopathy in Siblings.
Howard A; Uyeki TM; Fergie J
J Pediatric Infect Dis Soc; 2018 Aug; 7(3):e172-e177. PubMed ID: 29741717
[TBL] [Abstract][Full Text] [Related]
15. COVID-19 related acute necrotizing encephalopathy with extremely high interleukin-6 and RANBP2 mutation in a patient with recently immunized inactivated virus vaccine and no pulmonary involvement.
Pongpitakmetha T; Hemachudha P; Rattanawong W; Thanapornsangsuth P; Viswanathan A; Hemachudha T
BMC Infect Dis; 2022 Jul; 22(1):640. PubMed ID: 35870896
[TBL] [Abstract][Full Text] [Related]
16. First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype.
Ayaz A; Doğru Z; Kılıç B; Süzek BE
Clin Neurol Neurosurg; 2022 Oct; 221():107418. PubMed ID: 36029610
[TBL] [Abstract][Full Text] [Related]
17. RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathy.
Sondhi V; Chakrabarty B; Kumar A; Kohli S; Saxena R; Verma IC; Gulati S
Brain Dev; 2016 Nov; 38(10):937-942. PubMed ID: 27591117
[TBL] [Abstract][Full Text] [Related]
18. Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy.
Loh NR; Appleton DB
Eur J Pediatr; 2010 Oct; 169(10):1299-302. PubMed ID: 20473521
[TBL] [Abstract][Full Text] [Related]
19. Acute encephalopathy and encephalitis caused by influenza virus infection.
Wang GF; Li W; Li K
Curr Opin Neurol; 2010 Jun; 23(3):305-11. PubMed ID: 20455276
[TBL] [Abstract][Full Text] [Related]
20. [Postinfectious family case of acute necrotizing encephalopathy caused by RANBP2 gene mutation].
Di Meglio C; Cano A; Milh M; Girard N; Burglen L; Chabrol B
Arch Pediatr; 2014 Jan; 21(1):73-7. PubMed ID: 24321870
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
