Torio M - Search Results

1

Neurodevelopmental Outcomes of High-Risk Preterm Infants: A Prospective Study in Japan.

Torio M, Iwayama M, Sawano T, Inoue H, Ochiai M, Taira R, Yonemoto K, Ichimiya Y, Sonoda Y, Sasazuki M, Ishizaki Y, Sanefuji M, Yamane K, Yamashita H, Torisu H, Kira R, Hara T, Kanba S, Sakai Y, Ohga S. Torio M, et al. Neurol Clin Pract. 2021 Oct;11(5):398-405. doi: 10.1212/CPJ.0000000000000920. Neurol Clin Pract. 2021. PMID: 34840866 Free PMC article.

2

Nephrolithiasis as an extra-intestinal presentation of pediatric inflammatory bowel disease unclassified.

Torio M, Ishimura M, Ohga S, Doi T, Utsunomiya R, Ohkubo K, Suga N, Tatsugami K, Matsumoto T, Takada H, Hara T. Torio M, et al. J Crohns Colitis. 2010 Dec;4(6):674-8. doi: 10.1016/j.crohns.2010.05.012. Epub 2010 Jun 30. J Crohns Colitis. 2010. PMID: 21122580

3

[A one-year-old male infant with sleep-associated febrile myoclonus].

Torio M, Sanefuji M, Hara T. Torio M, et al. No To Hattatsu. 2013 Jul;45(4):314-7. No To Hattatsu. 2013. PMID: 23951945 Review. Japanese.

4

A case of pontine tegmental cap dysplasia with comorbidity of oculoauriculovertebral spectrum.

Chong PF, Haraguchi K, Torio M, Kirino M, Ogata R, Matsukura M, Sakai Y, Ishizaki Y, Yamamoto T, Kira R. Chong PF, et al. Among authors: torio m. Brain Dev. 2015 Jan;37(1):171-4. doi: 10.1016/j.braindev.2014.02.007. Epub 2014 Mar 17. Brain Dev. 2015. PMID: 24650581

5

Periodic Epileptiform Discharges in Children With Advanced Stages of Progressive Myoclonic Epilepsy.

Isobe N, Sakai Y, Kira R, Sanefuji M, Ishizaki Y, Sakata A, Sasazuki M, Torio M, Akamine S, Torisu H, Hara T. Isobe N, et al. Among authors: torio m. Clin EEG Neurosci. 2016 Oct;47(4):317-323. doi: 10.1177/1550059415579767. Epub 2015 Mar 30. Clin EEG Neurosci. 2016. PMID: 25828483

6

Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency.

Ichiyama M, Ohga S, Ochiai M, Fukushima K, Ishimura M, Torio M, Urata M, Hotta T, Kang D, Hara T. Ichiyama M, et al. Among authors: torio m. Brain Dev. 2016 Feb;38(2):253-6. doi: 10.1016/j.braindev.2015.07.004. Epub 2015 Aug 4. Brain Dev. 2016. PMID: 26250584

7

De Novo Truncating Mutation of TRIM8 Causes Early-Onset Epileptic Encephalopathy.

Sakai Y, Fukai R, Matsushita Y, Miyake N, Saitsu H, Akamine S, Torio M, Sasazuki M, Ishizaki Y, Sanefuji M, Torisu H, Shaw CA, Matsumoto N, Hara T. Sakai Y, et al. Among authors: torio m. Ann Hum Genet. 2016 Jul;80(4):235-40. doi: 10.1111/ahg.12157. Ann Hum Genet. 2016. PMID: 27346735

8

De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis.

Kanemasa H, Fukai R, Sakai Y, Torio M, Miyake N, Lee S, Ono H, Akamine S, Nishiyama K, Sanefuji M, Ishizaki Y, Torisu H, Saitsu H, Matsumoto N, Hara T. Kanemasa H, et al. Among authors: torio m. BMC Neurol. 2016 Sep 15;16:174. doi: 10.1186/s12883-016-0680-6. BMC Neurol. 2016. PMID: 27634470 Free PMC article.

9

Involuntary movements and coma as the prognostic marker for acute encephalopathy with biphasic seizures and late reduced diffusion.

Lee S, Sanefuji M, Torio M, Kaku N, Ichimiya Y, Mizuguchi S, Baba H, Sakai Y, Ishizaki Y, Torisu H, Kira R, Hara T, Ohga S. Lee S, et al. Among authors: torio m. J Neurol Sci. 2016 Nov 15;370:39-43. doi: 10.1016/j.jns.2016.09.018. Epub 2016 Sep 10. J Neurol Sci. 2016. PMID: 27772782

10

Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion.

Ichimiya Y, Kaku N, Sakai Y, Yamashita F, Matsuoka W, Muraoka M, Akamine S, Mizuguchi S, Torio M, Motomura Y, Hirata Y, Ishizaki Y, Sanefuji M, Torisu H, Takada H, Maehara Y, Ohga S. Ichimiya Y, et al. Among authors: torio m. Brain Dev. 2017 Aug;39(7):621-624. doi: 10.1016/j.braindev.2017.03.023. Epub 2017 Apr 13. Brain Dev. 2017. PMID: 28413125

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