S. Takeshita

发表

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.

T. Hara, T. Matsuishi, A. Takata, 2018, Cell reports.

De novo GABRA1 mutations in Ohtahara and West syndromes

Naomichi Matsumoto, Mitsuhiro Kato, Akihiko Ishiyama, 2016, Epilepsia.

An MRI and MRS study of Pelizaeus-Merzbacher disease.

H. Osaka, S. Takeshita, A. Nezu, 1998, Pediatric neurology.

Safety and efficacy of canakinumab in Japanese patients with phenotypes of cryopyrin-associated periodic syndrome as established in the first open-label, phase-3 pivotal study (24-week results).

H. Takada, T. Hara, T. Heike, 2013, Clinical and experimental rheumatology.

Characteristic response to transcranial magnetic stimulation in Rett syndrome.

S. Takeshita, S. Kimura, A. Nezu, 1998, Electroencephalography and clinical neurophysiology.

Two cases of essential myoclonus, epilepsy, mental retardation and anxiety disorders

S. Takeshita, Miyabi Tanaka, A. Nezu, 1997, Brain and Development.

Two cases of essential myoclonus, epilepsy, mental and anxiety disorders retardation

S. Takeshita, Miyabi Tanaka, S. Kimura, 1997 .

Clinical and radiologic improvements in mitochondrial encephalomyelopathy following sodium dichloroacetate therapy

S. Takeshita, Miyabi Tanaka, A. Nezu, 1997, Brain and Development.

Effect of total callosotomy on KCNQ2-related intractable epilepsy

N. Matsumoto, S. Miyatake, S. Takeshita, 2020, Brain and Development.

Rasmussen syndrome combined with IgA deficiency and membranous nephropathy.

S. Ito, S. Takeshita, A. Nezu, 2009, Pediatric neurology.

Clinicopathological features of acute autonomic and sensory neuropathy.

Kazumasa Kuniyoshi, G. Sobue, K. Nakashima, 2010, Brain : a journal of neurology.

Cyclosporine for acute encephalopathy with biphasic seizures and late reduced diffusion

S. Takeshita, Hirotaka Motoi, M. Mori, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

MRI findings in pediatric neuromyelitis optica spectrum disorder with MOG antibody: Four cases and review of the literature

S. Takeshita, K. Kaneko, Toshiyuki Takahashi, 2019, Brain and Development.

Fulminant form of acute disseminated encephalomyelitis in a child treated with mild hypothermia

S. Takeshita, Hirotaka Motoi, Yoshihiro Watanabe, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

A case of chronic recurrent cerebellar ataxia responding to steroid therapy

S. Takeshita, M. Kikuchi, A. Nezu, 2009, Brain and Development.

PLPBP mutations cause variable phenotypes of developmental and epileptic encephalopathy

N. Matsumoto, S. Kanai, T. Okanishi, 2018, Epilepsia open.

Clinical and radiological variability of influenza‐related encephalopathy or encephalitis

S. Takeshita, Miyabi Tanaka, A. Nezu, 1998, Acta paediatrica Japonica : Overseas edition.

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

D. Lev, D. Chitayat, N. Matsumoto, 2013, Neurology.

Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy

K. Yokochi, T. Shiihara, A. Takata, 2019, Nature Communications.

Norovirus-associated encephalopathy.

S. Ito, S. Takeshita, S. Usuku, 2006, The Pediatric infectious disease journal.

Infection-associated decrease of serum creatine kinase levels in Fukuyama congenital muscular dystrophy

Takatoshi Sato, S. Takeshita, Yoshiaki Saito, 2020, Brain and Development.

A Pleuroperitoneal Shunt for Interactive Pleural Effusions With Yellow Nail Syndrome

S. Takeshita, M. Masuda, T. Kaneko, 2011 .

Usefulness of ketogenic diet in a girl with migrating partial seizures in infancy

N. Matsumoto, S. Takeshita, H. Saitsu, 2016, Brain and Development.

Molecular diagnosis of 405 individuals with autism spectrum disorder

T. Hara, T. Matsuishi, A. Fattal-Valevski, 2023, European journal of human genetics : EJHG.

Acute encephalopathy of Bacillus cereus mimicking Reye syndrome

S. Takeshita, M. Mori, N. Kikuchi, 2010, Brain and Development.

Magnetic stimulation of the corticospinal tracts in Pelizaeus-Merzbacher disease.

H. Osaka, S. Takeshita, S. Kimura, 1998, Electroencephalography and clinical neurophysiology.

Functional recovery in hemiplegic cerebral palsy: ipsilateral electromyographic responses to focal transcranial magnetic stimulation

S. Takeshita, Miyabi Tanaka, A. Nezu, 1999, Brain and Development.

Salmonella encephalopathy successfully treated with high-dose methylpredonisolone therapy

S. Takeshita, K. Ichikawa, Akiko Tsutsumi, 2009, Brain and Development.

[Clinical study in 28 patients with infection-related acute onset encephalitis].

S. Takeshita, A. Nezu, S. Kimura, 1999, No to hattatsu = Brain and development.

Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate.

Katsuhiro Kobayashi, T. Akiyama, M. Kubota, 2020, Pediatric neurology.

Novel mutations in SH3TC2 in a young Japanese girl with Charcot‐Marie‐Tooth disease type 4C

S. Takeshita, H. Takashima, A. Hashiguchi, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy

K. Yokochi, T. Shiihara, A. Takata, 2019, Nature Communications.

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

D. Lev, D. Chitayat, N. Matsumoto, 2013, Neurology.

Rasmussen syndrome combined with IgA deficiency and membranous nephropathy.

S. Ito, S. Takeshita, A. Nezu, 2009, Pediatric neurology.

Topographical differences in the developmental profile of central motor conduction time

S. Takeshita, A. Nezu, S. Kimura, 1999, Clinical Neurophysiology.

Case report: Evolution of catatonic mutism and psychotic symptoms in an adolescent with Down syndrome: transition from Down syndrome disintegrative disorder to anti-N-methyl-D-aspartate receptor encephalitis

S. Takeshita, Yukitoshi Takahashi, Yoshiaki Saito, 2023, Frontiers in Neurology.