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Rhombencephalitis and Coxsackievirus A16.
Published in:
2009
By:
- Goto, Kazuna;
- Sanefuji, Masafumi;
- Kusuhara, Koichi;
- Nishimura, Yorihiro;
- Shimizu, Hiroyuki;
- Kira, Ryutaro;
- Torisu, Hiroyuki;
- Hara, Toshiro
Publication type:
Letter
Association of toll-like receptor 3 gene polymorphism with subacute sclerosing panencephalitis.
Published in:
Journal of NeuroVirology, 2008, v. 14, n. 6, p. 486, doi. 10.1080/13550280802298120
By:
- Ishizaki, Yoshito;
- Takemoto, Megumi;
- Kira, Ryutaro;
- Kusuhara, Koichi;
- Torisu, Hiroyuki;
- Sakai, Yasunari;
- Sanefuji, Masafumi;
- Yukaya, Naoko;
- Hara, Toshiro
Publication type:
Article
Interleukin-10 is associated with resistance to febrile seizures: Genetic association and experimental animal studies.
Published in:
Epilepsia (Series 4), 2009, v. 50, n. 4, p. 761, doi. 10.1111/j.1528-1167.2008.01861.x
By:
- Ishizaki, Yoshito;
- Kira, Ryutaro;
- Fukuda, Mitsumasa;
- Torisu, Hiroyuki;
- Sakai, Yasunari;
- Sanefuji, Masafumi;
- Yukaya, Naoko;
- Hara, Toshiro
Publication type:
Article
Parental age and child growth and development: Child health check-up data.
Published in:
Pediatrics International, 2011, v. 53, n. 5, p. 709, doi. 10.1111/j.1442-200X.2011.03331.x
By:
- Iwayama, Mariko;
- Kira, Ryutaro;
- Kinukawa, Naoko;
- Sakai, Yasunari;
- Torisu, Hiroyuki;
- Sanefuji, Masafumi;
- Ishizaki, Yoshito;
- Nose, Yoshiaki;
- Matsumoto, Toshimichi;
- Hara, Toshiro
Publication type:
Article
An N‐terminal and ankyrin repeat domain interactome of Shank3 identifies the protein complex with the splicing regulator Nono in mice.
Published in:
Genes to Cells, 2024, v. 29, n. 9, p. 746, doi. 10.1111/gtc.13142
By:
- Okuzono, Sayaka;
- Fujii, Fumihiko;
- Setoyama, Daiki;
- Taira, Ryoji;
- Shinmyo, Yohei;
- Kato, Hiroki;
- Masuda, Keiji;
- Yonemoto, Kousuke;
- Akamine, Satoshi;
- Matsushita, Yuki;
- Motomura, Yoshitomo;
- Sakurai, Takeshi;
- Kawasaki, Hiroshi;
- Han, Kihoon;
- Kato, Takahiro A.;
- Torisu, Hiroyuki;
- Kang, Dongchon;
- Nakabeppu, Yusaku;
- Ohga, Shouichi;
- Sakai, Yasunari
Publication type:
Article
Gene expression profiles in peripheral blood mononuclear cells from patients with subacute sclerosing panencephalitis using oligonucleotide microarrays.
Published in:
Journal of NeuroVirology, 2005, v. 11, n. 3, p. 299, doi. 10.1080/13550280590953825
By:
- Takemoto, Megumi;
- Kira, Ryutaro;
- Kusuhara, Koichi;
- Torisu, Hiroyuki;
- Sakai, Yasunari;
- Hara, Toshiro
Publication type:
Article
Long-lasting pain and somatosensory disturbances in children with myelin oligodendrocyte glycoprotein antibody-associated disease.
Published in:
European Journal of Pediatrics, 2023, v. 182, n. 7, p. 3175, doi. 10.1007/s00431-023-04989-z
By:
- Ichimiya, Yuko;
- Chong, Pin Fee;
- Sonoda, Yuri;
- Tocan, Vlad;
- Watanabe, Mitsuru;
- Torisu, Hiroyuki;
- Kira, Ryutaro;
- Takahashi, Toshiyuki;
- Kira, Jun-Ichi;
- Isobe, Noriko;
- Sakai, Yasunari;
- Ohga, Shouichi
Publication type:
Article
Sustained endocrine profiles of a girl with WAGR syndrome.
Published in:
2017
By:
- Yui Takada;
- Yasunari Sakai;
- Yuki Matsushita;
- Kazuhiro Ohkubo;
- Yuhki Koga;
- Satoshi Akamine;
- Michiko Torio;
- Yoshito Ishizaki;
- Masafumi Sanefuji;
- Hiroyuki Torisu;
- Shaw, Chad A.;
- Masayo Kagami;
- Toshiro Hara;
- Shouichi Ohga
Publication type:
Case Study
Corrigendum: Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice.
Published in:
Scientific Reports, 2016, p. 27164, doi. 10.1038/srep27164
By:
- Matsushita, Yuki;
- Sakai, Yasunari;
- Shimmura, Mitsunori;
- Shigeto, Hiroshi;
- Nishio, Miki;
- Akamine, Satoshi;
- Sanefuji, Masafumi;
- Ishizaki, Yoshito;
- Torisu, Hiroyuki;
- Nakabeppu, Yusaku;
- Suzuki, Akira;
- Takada, Hidetoshi;
- Hara, Toshiro
Publication type:
Article
Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice.
Published in:
Scientific Reports, 2016, p. 22991, doi. 10.1038/srep22991
By:
- Matsushita, Yuki;
- Sakai, Yasunari;
- Shimmura, Mitsunori;
- Shigeto, Hiroshi;
- Nishio, Miki;
- Akamine, Satoshi;
- Sanefuji, Masafumi;
- Ishizaki, Yoshito;
- Torisu, Hiroyuki;
- Nakabeppu, Yusaku;
- Suzuki, Akira;
- Takada, Hidetoshi;
- Hara, Toshiro
Publication type:
Article
De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis.
Published in:
2016
By:
- Hikaru Kanemasa;
- Ryoko Fukai;
- Yasunari Sakai;
- Michiko Torio;
- Noriko Miyake;
- Sooyoung Lee;
- Hiroaki Ono;
- Satoshi Akamine;
- Kei Nishiyama;
- Masafumi Sanefuji;
- Yoshito Ishizaki;
- Hiroyuki Torisu;
- Hirotomo Saitsu;
- Naomichi Matsumoto;
- Toshiro Hara;
- Kanemasa, Hikaru;
- Fukai, Ryoko;
- Sakai, Yasunari;
- Torio, Michiko;
- Miyake, Noriko
Publication type:
journal article
PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis.
Published in:
Human Genetics, 2010, v. 127, n. 4, p. 411, doi. 10.1007/s00439-009-0781-z
By:
- Ishizaki, Yoshito;
- Yukaya, Naoko;
- Kusuhara, Koichi;
- Kira, Ryutaro;
- Torisu, Hiroyuki;
- Ihara, Kenji;
- Sakai, Yasunari;
- Sanefuji, Masafumi;
- Pipo-Deveza, Judy R.;
- Silao, Catherine Lynn T.;
- Sanchez, Benilda C.;
- Lukban, Marissa B.;
- Salonga, Aida M.;
- Hara, Toshiro
Publication type:
Article
Founder effect of the C9 R95X mutation in Orientals.
Published in:
Human Genetics, 2003, v. 112, n. 3, p. 244, doi. 10.1007/s00439-002-0870-8
By:
- Khajoee, Vahid;
- Ihara, Kenji;
- Kira, Ryutaro;
- Takemoto, Megumi;
- Torisu, Hiroyuki;
- Sakai, Yasunari;
- Guanjun, Jia;
- Hee, Park Myoung;
- Tokunaga, Katsushi;
- Hara, Toshiro
Publication type:
Article
Early‐onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2.
Published in:
Epilepsia Open, 2018, v. 3, n. 1, p. 81, doi. 10.1002/epi4.12085
By:
- Akamine, Satoshi;
- Sagata, Noriaki;
- Sakai, Yasunari;
- Kato, Takahiro A.;
- Nakahara, Takeshi;
- Matsushita, Yuki;
- Togao, Osamu;
- Hiwatashi, Akio;
- Sanefuji, Masafumi;
- Ishizaki, Yoshito;
- Torisu, Hiroyuki;
- Saitsu, Hirotomo;
- Matsumoto, Naomichi;
- Hara, Toshiro;
- Sawa, Akira;
- Kano, Shinichi;
- Furue, Masutaka;
- Kanba, Shigenobu;
- Shaw, Chad A.;
- Ohga, Shouichi
Publication type:
Article
Systemic vascular phenotypes of Loeys-Dietz syndrome in a child carrying a de novo R381P mutation in TGFBR2: a case report.
Published in:
2013
By:
- Kiyoshi Uike;
- Yuki Matsushita;
- Yasunari Sakai;
- Osamu Togao;
- Michinobu Nagao;
- Yoshito Ishizaki;
- Hazumu Nagata;
- Kenichiro Yamamura;
- Hiroyuki Torisu;
- Toshiro Hara
Publication type:
Case Study
Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome.
Published in:
BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-19
By:
- Yasunari Sakai;
- Ryota Souzaki;
- Hidetaka Yamamoto;
- Yuki Matsushita;
- Hazumu Nagata;
- Yoshito Ishizaki;
- Hiroyuki Torisu;
- Yoshinao Oda;
- Tomoaki Taguchi;
- Shaw, Chad A.;
- Toshiro Hara
Publication type:
Article
De Novo Truncating Mutation of TRIM8 Causes Early-Onset Epileptic Encephalopathy.
Published in:
Annals of Human Genetics, 2016, v. 80, n. 4, p. 235, doi. 10.1111/ahg.12157
By:
- Sakai, Yasunari;
- Fukai, Ryoko;
- Matsushita, Yuki;
- Miyake, Noriko;
- Saitsu, Hirotomo;
- Akamine, Satoshi;
- Torio, Michiko;
- Sasazuki, Momoko;
- Ishizaki, Yoshito;
- Sanefuji, Masafumi;
- Torisu, Hiroyuki;
- Shaw, Chad A;
- Matsumoto, Naomichi;
- Hara, Toshiro
Publication type:
Article
Nationwide Survey of Pediatric-onset Japanese Encephalitis in Japan.
Published in:
Clinical Infectious Diseases, 2019, v. 68, n. 12, p. 2099, doi. 10.1093/cid/ciy816
By:
- Nanishi, Etsuro;
- Hoshina, Takayuki;
- Sanefuji, Masafumi;
- Kadoya, Ryo;
- Kitazawa, Katsuhiko;
- Arahata, Yukie;
- Sato, Tetsuya;
- Hirayama, Yoshimichi;
- Hirai, Katsuki;
- Yanai, Masaaki;
- Nikaido, Kaori;
- Maeda, Akihiko;
- Torisu, Hiroyuki;
- Okada, Kenji;
- Sakai, Yasunari;
- Ohga, Shouichi
Publication type:
Article
Clinical Features of Acute Flaccid Myelitis Temporally Associated With an Enterovirus D68 Outbreak: Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August-December 2015.
Published in:
Clinical Infectious Diseases, 2018, v. 66, n. 5, p. 653, doi. 10.1093/cid/cix860
By:
- Chong, Pin Fee;
- Kira, Ryutaro;
- Mori, Harushi;
- Okumura, Akihisa;
- Torisu, Hiroyuki;
- Yasumoto, Sawa;
- Shimizu, Hiroyuki;
- Fujimoto, Tsuguto;
- Hanaoka, Nozomu;
- Kusunoki, Susumu
Publication type:
Article
Moyamoya disease susceptibility gene RNF213 links inflammatory and angiogenic signals in endothelial cells.
Published in:
Scientific Reports, 2015, p. 13191, doi. 10.1038/srep13191
By:
- Ohkubo, Kazuhiro;
- Sakai, Yasunari;
- Inoue, Hirosuke;
- Akamine, Satoshi;
- Ishizaki, Yoshito;
- Matsushita, Yuki;
- Sanefuji, Masafumi;
- Torisu, Hiroyuki;
- Ihara, Kenji;
- Sardiello, Marco;
- Hara, Toshiro
Publication type:
Article
Autopsy Case of Later-Onset Pontocerebellar Hypoplasia Type 1: Pontine Atrophy and Pyramidal Tract Involvement.
Published in:
2010
By:
- Sanefuji, Masafumi;
- Kira, Ryutaro;
- Matsumoto, Kenichi;
- Gondo, Kenjiro;
- Torisu, Hiroyuki;
- Kawakami, Hideshi;
- Iwaki, Toru;
- Hara, Toshiro
Publication type:
Case Study
Epstein-Barr Virus-Associated Meningoencephalomyelitis: Intrathecal Reactivation of the Virus in an Immunocompetent Child.
Published in:
Journal of Child Neurology, 2008, v. 23, n. 9, p. 1072, doi. 10.1177/0883073808315414
By:
- Sanefuji, Masafumi;
- Ohga, Shouichi;
- Kira, Ryutaro;
- Nomura, Akihiko;
- Torisu, Hiroyuki;
- Takada, Hidetoshi;
- Kusuhara, Koichi;
- Hara, Toshiro
Publication type:
Article
Moyamoya Syndrome in a Splenectomized Patient With β-Thalassemia Intermedia.
Published in:
Journal of Child Neurology, 2006, v. 21, n. 1, p. 75, doi. 10.1177/08830738060210010501
By:
- Sanefuji, Masafumi;
- Ohga, Shouichi;
- Kira, Ryutaro;
- Yoshiura, Takashi;
- Torisu, Hiroyuki;
- Hara, Toshiro
Publication type:
Article

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