Hoshino A - Search Results

1

Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes.

Hoshino A, Saitoh M, Oka A, Okumura A, Kubota M, Saito Y, Takanashi J, Hirose S, Yamagata T, Yamanouchi H, Mizuguchi M. Hoshino A, et al. Brain Dev. 2012 May;34(5):337-43. doi: 10.1016/j.braindev.2011.07.012. Epub 2011 Sep 15. Brain Dev. 2012. PMID: 21924570

2

Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.

Shimojima K, Inoue T, Hoshino A, Kakiuchi S, Watanabe Y, Sasaki M, Nishimura A, Takeshita-Yanagisawa A, Tajima G, Ozawa H, Kubota M, Tohyama J, Sasaki M, Oka A, Saito K, Osawa M, Yamamoto T. Shimojima K, et al. Among authors: hoshino a. Brain Dev. 2010 Mar;32(3):171-9. doi: 10.1016/j.braindev.2009.02.011. Epub 2009 Mar 27. Brain Dev. 2010. PMID: 19328639

3

High-dose lorazepam for convulsive status epilepticus in an infant with holoprosencephaly.

Okazaki K, Kondo M, Kubota M, Kakinuma R, Hoshino A, Kimura H, Itoh S. Okazaki K, et al. Among authors: hoshino a. Pediatr Int. 2010 Aug;52(4):664-7. doi: 10.1111/j.1442-200X.2010.03077.x. Pediatr Int. 2010. PMID: 20958878 No abstract available.

4

Thermolabile CPT II variants and low blood ATP levels are closely related to severity of acute encephalopathy in Japanese children.

Kubota M, Chida J, Hoshino H, Ozawa H, Koide A, Kashii H, Koyama A, Mizuno Y, Hoshino A, Yamaguchi M, Yao D, Yao M, Kido H. Kubota M, et al. Among authors: hoshino a, hoshino h. Brain Dev. 2012 Jan;34(1):20-7. doi: 10.1016/j.braindev.2010.12.012. Epub 2011 Jan 28. Brain Dev. 2012. PMID: 21277129

5

Autoimmune neurological disorders associated with group-A beta-hemolytic streptococcal infection.

Hachiya Y, Miyata R, Tanuma N, Hongou K, Tanaka K, Shimoda K, Kanda S, Hoshino A, Hanafusa Y, Kumada S, Kurihara E, Hayashi M. Hachiya Y, et al. Among authors: hoshino a. Brain Dev. 2013 Aug;35(7):670-4. doi: 10.1016/j.braindev.2012.10.003. Epub 2012 Nov 9. Brain Dev. 2013. PMID: 23142103

6

Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.

Shimada S, Shimojima K, Sangu N, Hoshino A, Hachiya Y, Ohto T, Hashi Y, Nishida K, Mitani M, Kinjo S, Tsurusaki Y, Matsumoto N, Morimoto M, Yamamoto T. Shimada S, et al. Among authors: hoshino a. Brain Dev. 2015 Nov;37(10):960-6. doi: 10.1016/j.braindev.2015.03.003. Epub 2015 Apr 3. Brain Dev. 2015. PMID: 25843247

7

Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.

Saitoh M, Ishii A, Ihara Y, Hoshino A, Terashima H, Kubota M, Kikuchi K, Yamanaka G, Amemiya K, Hirose S, Mizuguchi M. Saitoh M, et al. Among authors: hoshino a. Epilepsy Res. 2015 Nov;117:1-6. doi: 10.1016/j.eplepsyres.2015.08.001. Epub 2015 Aug 6. Epilepsy Res. 2015. PMID: 26311622

8

Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy.

Hoshino A, Saitoh M, Miyagawa T, Kubota M, Takanashi JI, Miyamoto A, Tokunaga K, Oka A, Mizuguchi M. Hoshino A, et al. Genes Immun. 2016 Sep;17(6):367-9. doi: 10.1038/gene.2016.32. Epub 2016 Jul 28. Genes Immun. 2016. PMID: 27467284

9

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. Nishimura N, et al. Among authors: hoshino a. Pediatr Int. 2016 Nov;58(11):1215-1218. doi: 10.1111/ped.13119. Pediatr Int. 2016. PMID: 27882739

10

Acute necrotizing encephalopathy and a carnitine palmitoyltransferase 2 variant in an adult.

Kobayashi Y, Kanazawa H, Hoshino A, Takamatsu R, Watanabe R, Hoshi K, Ishii W, Yahikozawa H, Mizuguchi M, Sato S. Kobayashi Y, et al. Among authors: hoshino a. J Clin Neurosci. 2019 Mar;61:264-266. doi: 10.1016/j.jocn.2018.11.045. Epub 2018 Nov 22. J Clin Neurosci. 2019. PMID: 30470651

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