S. Yasumoto

发表

Altered automatic face processing in individuals with high-functioning autism spectrum disorders: Evidence from visual evoked potentials

S. Tobimatsu, Y. Kamio, T. Yamasaki, 2013 .

Mutations of Neuronal Voltage‐gated Na+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

H. Oguni, Kazuyoshi Watanabe, A. Mitsudome, 2004, Epilepsia.

Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus–Merzbacher disease patient with a partial PLP1 duplication

Toshiyuki Yamamoto, T. Fujita, S. Yasumoto, 2012, Journal of Human Genetics.

The effectiveness of clonazepam on the rolandic discharges

Thoru Yamada, A. Mitsudome, S. Yasumoto, 1997, Brain and Development.

Clinical spectrum of SCN2A mutations

H. Kurahashi, E. Nakagawa, S. Yasumoto, 2012, Brain and Development.

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis

Masahiro Ito, Wang-Tso Lee, T. Fujita, 2013, Brain and Development.

Diagnosing nocturnal frontal lobe epilepsy: A case study of two children

A. Mitsudome, T. Fujita, S. Yasumoto, 2011, Seizure.

Clinical spectrum of SCN 2 A mutations

H. Kurahashi, E. Nakagawa, S. Yasumoto, 2012 .

Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

E. Nakagawa, S. Yasumoto, S. Hirose, 2009, Brain and Development.

Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies

T. Kojima, M. Okada, S. Kaneko, 2010, Journal of Human Genetics.

Early onset and focal spike discharges as indicators of poor prognosis for myoclonic-astatic epilepsy

T. Fujita, S. Yasumoto, S. Hirose, 2014, Brain and Development.

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

T. Hara, T. Matsuishi, M. Sanefuji, 2010, Brain & development (Tokyo. 1979).

Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis.

H. Mori, Kenichi Tanaka, Eriko Kikuchi, 2020, Pediatric Neurology.

Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan

H. Mori, A. Okumura, H. Shimizu, 2019, Brain and Development.

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

T. Shiihara, H. Mori, S. Kusunoki, 2017, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Survival and late effects on development of patients with infantile brain tumor

T. Fukushima, S. Yasumoto, S. Hirose, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy

A. Konagaya, H. Kurahashi, T. Kojima, 2008, Epilepsia.

Valproate therapy does not deplete carnitine levels in otherwise healthy children.

Y. Tomoda, A. Mitsudome, S. Yasumoto, 1998, Pediatrics.

KCNQ2 abnormality in BECTS: Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2

H. Kurahashi, S. Yasumoto, S. Hirose, 2012, Epilepsy Research.

Benign convulsion with mild gastroenteritis and benign familial infantile seizure

T. Hara, Y. Sakai, R. Kira, 2006, Epilepsy Research.

FULL-LENGTH ORIGINAL RESEARCH Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy

A. Konagaya, H. Kurahashi, T. Kojima, 2008 .

A case of hemiplegic migraine in childhood: transient unilateral hyperperfusion revealed by perfusion MR imaging and MR angiography.

A. Mitsudome, S. Yasumoto, H. Utsunomiya, 2001, AJNR. American journal of neuroradiology.

A Case of West Syndrome Associated with Neonatal Hypoglycemic Brain Injury

T. Fujita, S. Yasumoto, S. Hirose, 2010 .

Favorable Seizure Outcome in Kabuki Make-up Syndrome Associated With Epilepsy

Y. Kuroki, Y. Tomoda, A. Mitsudome, 2003, Journal of child neurology.

Kabuki make‐up syndrome associated with West syndrome

A. Mitsudome, S. Yasumoto, A. Ogawa, 1997, Acta paediatrica Japonica : Overseas edition.

[Wernicke encephalopathy in a chronic peritoneal dialysis patient--correlation between diffusion MR and pathological findings].

S. Yasumoto, H. Utsunomiya, T. Kanaumi, 2007, No to hattatsu = Brain and development.

Rhythmic Slow Activity in Benign Childhood Epilepsy with Centrotemporal Spikes

A. Mitsudome, S. Yasumoto, A. Ogawa, 1997, Clinical EEG.

PCDH19 mutation in Japanese females with epilepsy

H. Shiraishi, Y. Makita, N. Higurashi, 2012, Epilepsy Research.

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions

Y. Makita, A. Mitsudome, M. Okada, 2009, Brain and Development.

Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study

H. Mori, S. Ohga, R. Kira, 2021, Clinical Neurophysiology.

Japanese monozygotic twins with Rett syndrome

A. Mitsudome, S. Yasumoto, A. Ogawa, 1997, Brain & development (Tokyo. 1979).

Pseudotumor cerebri associated with Yersinia pseudotuberculosis infection

A. Mitsudome, S. Yasumoto, M. Ohfu, 1994, Acta paediatrica.

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

T. Hara, T. Matsuishi, M. Sanefuji, 2010, Brain and Development.

Nosocomial meningitis due to Campylobacter fetus subspecies fetus in a neonatal intensive care unit

S. Yasumoto, T. Morooka, T. Oda, 1992, Acta paediatrica Japonica : Overseas edition.

Clinical spectrum of SCN2A mutations

H. Kurahashi, E. Nakagawa, S. Yasumoto, 2012, Brain and Development.

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures

T. Inoue, H. Kurahashi, T. Kojima, 2009, Neurology.

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis

Wang-Tso Lee, T. Fujita, S. Yasumoto, 2013, Brain and Development.

Scalp EEG-recorded high-frequency oscillations can predict seizure activity in Panayiotopoulos syndrome

T. Fujita, S. Yasumoto, Takahito Inoue, 2023, Clinical Neurophysiology.

Magnetic resonance imaging volumetry and clinical analysis of epilepsy patients with unilateral hippocampal abnormality

S. Takashima, A. Mitsudome, S. Yasumoto, 2012, Pediatrics international : official journal of the Japan Pediatric Society.