K. Sugai

A. Takahashi, M. Iwasaki, M. Sasaki, 2019, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Two siblings with cortical dysplasia: Clinico‐electroencephalographic features

A. Kakita, Mitsuhiro Kato, Kazuyoshi Watanabe, 2015, Pediatrics international : official journal of the Japan Pediatric Society.

Abnormal maturation and differentiation of neocortical neurons in epileptogenic cortical malformation: Unique distribution of layer-specific marker cells of focal cortical dysplasia and hemimegalencephaly

A. Takahashi, S. Nabatame, M. Sasaki, 2012, Brain Research.

Behavioral Improvement Following Focal Resection in a Child with Frontal Lobe Epilepsy : A Case Report

M. Kaga, M. Sasaki, Hideyuki Nakama, 2009 .

Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy

M. Inagaki, M. Iwasaki, M. Sasaki, 2020, Brain and Development.

Behavioral disorder in people with an intellectual disability and epilepsy: A report of the Intellectual Disability Task Force of the Neuropsychiatric Commission of ILAE

Sarah J Wilson, K. Kanemoto, C. Brandt, 2016, Epilepsia open.

Postnatal evolution of cortical malformation in the “non-affected” hemisphere of hemimegalencephaly

M. Sasaki, T. Otsuki, E. Nakagawa, 2010, Brain and Development.

A case of alternating hemiplegia of childhood with cerebellar atrophy.

M. Sasaki, T. Hashimoto, K. Sugai, 1998, Pediatric neurology.

Pontine malformation, undecussated pyramidal tracts, and regional polymicrogyria: a new syndrome.

E. Engle, Y. Nakata, Toshiyuki Yamamoto, 2014, Pediatric neurology.

A severely brain-damaged case of 3-hydroxyisobutyric aciduria

M. Sasaki, M. Fukumizu, S. Yamaguchi, 2001, Brain and Development.

Eleven novel single nucleotide polymorphisms in the NR1I2 (PXR) gene, four of which induce non-synonymous amino acid alterations.

Y. Goto, Yoshiro Saito, S. Koyano, 2002, Drug metabolism and pharmacokinetics.

Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis

S. Tsujino, M. Kaga, M. Sasaki, 2001, Journal of Human Genetics.

Decreased resting energy expenditure in patients with Duchenne muscular dystrophy

H. Mochizuki, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population

Teruhiko Yoshida, N. Saijo, Y. Goto, 2004, Human mutation.

Variant in the neuronal vesicular SNARE VAMP2 (synaptobrevin-2): First report in Japan

K. Kosaki, K. Sugai, Y. Sunaga, 2020, Brain and Development.

Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophy

I. Nonaka, Y. Hayashi, I. Nishino, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing

T. Matsuishi, A. Fattal-Valevski, A. Takata, 2019, Journal of Medical Genetics.

Efficacy, safety, and pharmacokinetics of intravenous midazolam in Japanese children with status epilepticus

M. Ōsawa, K. Sugai, S. Hamano, 2019, Journal of the Neurological Sciences.

Extremely severe complicated spastic paraplegia 3A with neonatal onset.

T. Yonekawa, M. Sasaki, H. Takashima, 2014, Pediatric neurology.

A de novo missense mutation in SLC12A5 found in a compound heterozygote patient with epilepsy of infancy with migrating focal seizures

M. Sasaki, S. Hirose, K. Sugai, 2017, Clinical genetics.

Clinical and pedigree study on familial cases of West syndrome in Japan

S. Fujimoto, S. Hirano, Y. Fukuyama, 2001, Brain and Development.

Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination

Y. Matsubara, Y. Aoki, M. Sasaki, 2011, Brain and Development.

Mechanical ventilation care in severe childhood neurological disorders

M. Kaga, M. Sasaki, M. Fukumizu, 2001, Brain and Development.

Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding region

I. Nonaka, K. Hayasaka, K. Sugai, 1995, Journal of the Neurological Sciences.

Epilepsy surgery in children under 3 years of age: surgical and developmental outcomes.

A. Takahashi, M. Iwasaki, T. Otsuki, 2021, Journal of neurosurgery. Pediatrics.

Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome

M. Kubota, M. Sasaki, K. Kurosawa, 2011, Brain and Development.

A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement

I. Nonaka, Y. Hayashi, I. Nishino, 2012, Neuromuscular Disorders.

A nationwide survey on Marinesco-Sjögren syndrome in Japan

I. Nonaka, Y. Hayashi, I. Nishino, 2014, Orphanet Journal of Rare Diseases.

Hemiconvulsion–hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy

H. Kurahashi, M. Sasaki, E. Nakagawa, 2009, Epilepsia.

MECP2 Duplication Syndrome in Male Patients with Severe Mental Retardation and Intractable Epilepsy

J. Inazawa, Y. Goto, J. Tohyama, 2010 .

Nationwide survey (incidence, clinical course, prognosis) of Rasmussen’s encephalitis

H. Osaka, S. Nabatame, H. Oguni, 2010, Brain and Development.

Pathologic Active mTOR Mutation in Brain Malformation with Intractable Epilepsy Leads to Cell-Autonomous Migration Delay.

A. Takahashi, S. Koizumi, M. Hoshino, 2017, The American journal of pathology.

A pediatric patient with myopathy associated with antibodies to a signal recognition particle

Y. Hayashi, I. Nishino, M. Sasaki, 2012, Brain and Development.

Progressive Leukoencephalopathy Associated With Aluminum Deposits in Myelin Sheath

T. Otsuki, K. Sugai, M. Itoh, 2008, Journal of child neurology.

Urinary prostaglandin metabolites as Duchenne muscular dystrophy progression markers

M. Sasaki, H. Tachimori, E. Nakagawa, 2018, Brain and Development.

The effect of the guidelines for management of febrile seizures 2015 on clinical practices: Nationwide survey in Japan

H. Yoshinaga, M. Kubota, Y. Maegaki, 2019, Brain and Development.

A family of distal arthrogryposis type 5 due to a novel PIEZO2 mutation

N. Matsumoto, N. Miyake, M. Sasaki, 2015, American journal of medical genetics. Part A.

Acute nonparaneoplastic limbic encephalitis in childhood: a case series in Japan.

M. Sasaki, K. Sugai, H. Sakuma, 2010, Pediatric neurology.

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation

Y. Goto, M. Sasaki, E. Nakagawa, 2011, Journal of the Neurological Sciences.

Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood

H. Oguni, Y. Inoue, T. Fujiwara, 2013, Brain and Development.

Three Cases of Myoclonic Encephalopathy in Non-progressive Disorders

M. Sasaki, E. Nakagawa, K. Sugai, 2017 .

Treatment of epilepsy in severely disabled children with bilateral brain malformations

Y. Maegaki, M. Sasaki, T. Otsuki, 2009, Journal of Neurological Sciences.

Duane retraction syndrome associated with Chiari I malformation.

K. Sugai, H. Yamanouchi, K. Mukuno, 1993, Pediatric neurology.

Treatable renal failure found in non-ambulatory Duchenne muscular dystrophy patients

M. Sasaki, M. Murata, K. Sugai, 2015, Neuromuscular Disorders.

Episodic tremors representing cortical myoclonus are characteristic in Angelman syndrome due to UBE3A mutations

K. Kikuchi, S. Saitoh, M. Sasaki, 2015, Brain and Development.

Seizures with Clonazepam: Discontinuation and Suggestions for Safe Discontinuation Rates in Children

K. Sugai, 1993, Epilepsia.

Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms

M. Sasaki, E. Nakagawa, K. Sugai, 2010, Brain and Development.

Characteristic EEG findings in ring 20 syndrome as a diagnostic clue.

K. Kobayashi, M. Sasaki, T. Hashimoto, 1998, Electroencephalography and clinical neurophysiology.

Twenty-six novel single nucleotide polymorphisms and their frequencies of the NR1I3 (CAR) gene in a Japanese population.

Teruhiko Yoshida, N. Saijo, Y. Goto, 2003, Drug metabolism and pharmacokinetics.

Early onset distal muscular dystrophy

I. Nonaka, K. Sugai, H. Kinoshita, 1995, Brain and Development.

Effect of selenium deficiency on cardiac function of individuals with severe disabilities under long‐term tube feeding

M. Sasaki, T. Hashimoto, K. Sugai, 1998, Developmental medicine and child neurology.

Clinical Aspects of Hemimegalencephaly by Means of a Nationwide Survey

M. Sasaki, T. Hashimoto, K. Sugai, 2004, Journal of child neurology.

Reassessment of phenytoin for treatment of late stage progressive myoclonus epilepsy complicated with status epilepticus

M. Sasaki, E. Nakagawa, K. Sugai, 2009, Epilepsy Research.

Positron emission tomography using pyruvate-l-11C in two cases of mytochondrial encephalomyopathy

M. Iio, T. Hara, K. Sugai, 1989 .

Congenital monomelic neurogenic disorder with calf muscle hypertrophy

I. Nonaka, M. Sasaki, M. Fukumizu, 2003, Brain and Development.

Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification

S. Robertson, I. Nonaka, I. Nishino, 2009, Neuromuscular Disorders.

De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood

N. Matsumoto, Taki Nishimura, N. Miyake, 2013, Nature Genetics.

A mild case of giant axonal neuropathy without central nervous system manifestation

T. Shiihara, M. Sasaki, H. Takashima, 2016, Brain and Development.

Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation

S. Weiss, D. Chitayat, H. Arai, 2013, Epilepsia.

Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay

H. Shiraishi, N. Matsumoto, S. Saitoh, 2016, Scientific Reports.

Clinical and immunohistochemical studies of subependymal giant cell astrocytomas associated with tuberous sclerosis

S. Takashima, M. Sasaki, K. Sugai, 1990, Brain & development (Tokyo. 1979).

Clinical and imaging characteristics of localized megalencephaly: a retrospective comparison of diffuse hemimegalencephaly and multilobar cortical dysplasia

M. Ota, Y. Tsushima, M. Sasaki, 2009, Neuroradiology.

[Severely retarded children in a defined area of Japan--prevalence rate, associated disabilities and causes].

M. Aihara, K. Sugai, H. Suzuki, 1991, No to hattatsu = Brain and development.

Clobazam as a New Antiepileptic Drug and Clorazepate Dipotassium as an Alternative Antiepileptic Drug in Japan

K. Sugai, 2004, Epilepsia.

Apneustic breathing in children with brainstem damage due to hypoxic–ischemic encephalopathy

M. Sasaki, T. Hashimoto, M. Fukumizu, 1999, Developmental medicine and child neurology.

Muscle histochemistry in myotubular (centronuclear) myopathy

I. Nonaka, K. Sugai, K. Kumagai, 1989, Brain and Development.

Effectiveness of lidocaine infusion for status epilepticus in childhood: A retrospective multi-institutional study in Japan

Takao Takahashi, K. Haginoya, M. Ōsawa, 2008, Brain and Development.

Characteristic clinical features in a case of fulminant subacute sclerosing panencephalitis

S. Takashima, K. Sugai, Yuji Iwasaki, 1994, Brain and Development.

Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease

K. Hayasaka, M. Shimohata, K. Sugai, 2006, Journal of Human Genetics.

[Three cases of benign myoclonus of early infancy].

K. Sugai, Yuji Iwasaki, Y. Fujikawa, 2003, No to hattatsu = Brain and development.

Cerebro-Oculo-Hepato-Renal Syndrome (Arima's Syndrome): A Distinct Clinocopathological Entity

T. Matsuzaka, K. Sugai, N. Sakuragawa, 1986, Journal of child neurology.

Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability: Coexistence of auditory neuropathy and cochlear hearing loss

M. Kaga, M. Sasaki, M. Fukumizu, 2006, Brain and Development.

Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children

M. Sasaki, E. Nakagawa, K. Sugai, 2010, Brain and Development.

Transient seizure disappearance due to bilateral striatal necrosis in a patient with intractable epilepsy

H. Matsuda, M. Sasaki, T. Hashimoto, 2000, Brain and Development.

Case report CD4 + CD25 high regulatory T cell in childhood ocular myasthenia gravis

M. Sasaki, E. Nakagawa, K. Sugai, 2011 .

Effective immunoglobulin therapy for brief tonic seizures in methylmalonic acidemia

M. Sasaki, K. Sugai, N. Sakuragawa, 1997, Brain and Development.

Somatosensory Evoked Potentials With a Unilateral Migration Disorder of the Cerebrum

H. Ozawa, M. Kaga, M. Inagaki, 1998, Journal of child neurology.

Asymmetrical interhemispheric fiber tracts in patients with hemimegalencephaly on diffusion tensor magnetic resonance imaging.

T. Asada, F. Yamashita, M. Ota, 2009, Journal of neuroradiology. Journal de neuroradiologie.

Aberrant Midsagittal Fiber Tracts in Patients with Hemimegalencephaly

M. Ota, T. Takahashi, Y. Nakata, 2008, American Journal of Neuroradiology.

8p deletion and 9p duplication in two children with electrical status epilepticus in sleep syndrome

S. Nabatame, Toshiyuki Yamamoto, M. Sasaki, 2012, Seizure.

Hemifacial seizures due to ganglioglioma of cerebellum

M. Sasaki, T. Otsuki, E. Nakagawa, 2010, Brain and Development.

Multiple band frequency analysis in a child of medial temporal lobe ganglioglioma

Yoshiaki Saito, Taisuke Otsuki, Hirofumi Komaki, 2011, Child's Nervous System.

Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly

H. Matsuda, M. Ota, M. Iwasaki, 2019, Brain and Development.

Electrophysiological evidence of cerebral dysfunction in childhood opsoclonus‐myoclonus syndrome

M. Kaga, M. Inagaki, M. Sasaki, 2010, Movement disorders : official journal of the Movement Disorder Society.

[Nineteen cases of school-aged children with degenerative or metabolic neurological disorders initially presenting with learning difficulty and/or behavior disturbance].

M. Sasaki, E. Nakagawa, K. Sugai, 2012, No to hattatsu = Brain and development.

A study of ring 20 chromosome karyotype with epilepsy

K. Kobayashi, K. Sugai, H. Yamadera, 1998, Psychiatry and clinical neurosciences.

KCNT1-positive epilepsy of infancy with migrating focal seizures successfully treated with nonnarcotic antitussive drugs after treatment failure with quinidine: A case report

Tomohiro Watanabe, N. Matsumoto, T. Mizuguchi, 2020, Brain & development (Tokyo. 1979).

Bromoderma in a patient with migrating partial seizures in infancy

S. Nabatame, M. Sasaki, E. Nakagawa, 2010, Epilepsy Research.

Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation

N. Matsumoto, H. Saitsu, M. Sasaki, 2015, Brain and Development.

Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies

M. Sasaki, K. Sugai, A. Ishiyama, 2012, Brain and Development.

Medical treatment in infants and young children with epilepsy: Off‐label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in Children

L. Lagae, S. Auvin, A. Arzimanoglou, 2022, Epilepsia open.

Five novel single nucleotide polymorphisms in the EPHX1 gene encoding microsomal epoxide hydrolase.

Y. Goto, Yoshiro Saito, S. Ozawa, 2003, Drug Metabolism and Pharmacokinetics.

Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan

I. Nonaka, M. Sasaki, K. Sugai, 2016, Brain and Development.

New guidelines for management of febrile seizures in Japan

H. Yoshinaga, M. Kubota, Y. Maegaki, 2017, Brain and Development.

[A case of Möbius syndrome presenting with symptoms of severe infantile form of congenital muscular disorder].

M. Sasaki, E. Nakagawa, N. Sato, 2007, No to hattatsu = Brain and development.

A case of bulbar type cerebral palsy: Representative symptoms of dorsal brainstem syndrome

Toshiyuki Yamamoto, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

Evaluation of FDG-PET and ECD-SPECT in patients with subcortical band heterotopia

H. Matsuda, K. Kamiya, Masako Watanabe, 2014, Brain and Development.

Efficacy of intravenous midazolam for status epilepticus in childhood.

Takao Takahashi, K. Haginoya, M. Ōsawa, 2007, Pediatric neurology.

Treatment of convulsive status epilepticus in infants and young children in Japan

K. Sugai, 2007, Acta neurologica Scandinavica.

Adaptive behavior and its related factors in children with focal epilepsy

M. Inagaki, M. Iwasaki, M. Sasaki, 2020, Epilepsy & Behavior.

Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations

N. Matsumoto, Tomomi Tanaka, T. Kinoshita, 2018, Brain and Development.

A case of congenital axonal neuropathy associated with West syndrome

I. Nonaka, M. Sasaki, E. Nakagawa, 2011, Brain and Development.

Current management of febrile seizures in Japan: An overview

K. Sugai, 2010, Brain and Development.

Effects of acetazolamide on epileptic apnea in migrating partial seizures in infancy

S. Nabatame, M. Sasaki, E. Nakagawa, 2011, Epilepsy Research.

Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria

M. Sasaki, M. Fukumizu, K. Sugai, 2006, Brain and Development.

Renal disease in Arima syndrome is nephronophthisis as in other Joubert‐related Cerebello–oculo–renal syndromes

K. Arima, M. Nagata, M. Sasaki, 2004, American journal of medical genetics. Part A.

Near-infrared Spectroscopy-based Assessment of Ictal Cerebral Hemodynamics of a Frontal Area in Startle Epilepsy

M. Sasaki, E. Nakagawa, K. Sugai, 2012 .

Startle epilepsy associated with gait‐induced seizures: Pathomechanism analysis using EEG, MEG, and PET studies

M. Sasaki, E. Nakagawa, Y. Kaneko, 2009, Epilepsia.

Six Novel Nonsynonymous CYP1A2 Gene Polymorphisms: Catalytic Activities of the Naturally Occurring Variant Enzymes

Kazuo Komamura, Yoshiro Saito, Shiro Kamakura, 2004, Journal of Pharmacology and Experimental Therapeutics.

Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection

N. Higurashi, M. Sasaki, E. Nakagawa, 2011, Brain and Development.

Norie Murayama, Akiko Soyama, Yoshiro Saito, Yukiko Nakajima, Kazuo

Y. Goto, M. Kitakaze, S. Ozawa, 2003 .

MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene

Y. Goto, I. Nishino, M. Sasaki, 2014, Brain and Development.

Hemimegalencephaly: a study of abnormalities occurring outside the involved hemisphere.

Y. Miki, F. Yamashita, K. Nemoto, 2007, AJNR. American journal of neuroradiology.

Imbalance of interneuron distribution between neocortex and basal ganglia: Consideration of epileptogenesis of focal cortical dysplasia

T. Otsuki, A. Takahashi, M. Sasaki, 2012, Journal of the Neurological Sciences.

Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophy

A. Takahashi, K. Arima, M. Mizuguchi, 2009, Journal of the Neurological Sciences.

Periodic cycles of seizure clustering and suppression in children with epilepsy strongly suggest focal cortical dysplasia

A. Kakita, M. Iwasaki, M. Atobe, 2022, Developmental medicine and child neurology.

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L

S. Tsujino, M. Kaga, A. Imamura, 2003, Brain and Development.

Severe Central Nervous System Involvement in a Patient With Congenital Fiber-Type Disproportion Myopathy

I. Nonaka, E. Nakagawa, K. Sugai, 1996, Journal of child neurology.

Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings

I. Nonaka, H. Ozawa, M. Sasaki, 2000, Brain and Development.

Correlation of augmented startle reflex with brainstem electrophysiological responses in Tay–Sachs disease

M. Inagaki, M. Sasaki, K. Sugai, 2015, Brain and Development.

Tremor and seizures associated with chronic manganese intoxication

T. Hashimoto, K. Sugai, H. Komaki, 1999, Brain and Development.

Two Japanese cases of epileptic encephalopathy associated with an FGF12 mutation

N. Matsumoto, H. Saitsu, M. Nakashima, 2018, Brain and Development.

Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy.

A. Takahashi, S. Koizumi, S. Nabatame, 2014, Journal of neuropathology and experimental neurology.

Therapeutic effect and [123I]IMP SPECT findings of sodium dichloroacetate in a patient with MELAS

Hiroshi Matsuda, Akira Sudo, Masayuki Sasaki, 2004, Neurology.

Surgical management of cortical dysplasia in infancy and early childhood

A. Takahashi, M. Sasaki, T. Otsuki, 2013, Brain and Development.

Delayed Maturation and Differentiation of Neurons in Focal Cortical Dysplasia With the Transmantle Sign: Analysis of Layer-Specific Marker Expression

A. Takahashi, M. Sasaki, T. Otsuki, 2012, Journal of neuropathology and experimental neurology.

CYP2C8 haplotype structures and their influence on pharmacokinetics of paclitaxel in a Japanese population

Teruhiko Yoshida, N. Saijo, Y. Ohe, 2007, Pharmacogenetics and genomics.

Single-photon emission computed tomography of the brain in autism: effect of the developmental level.

H Matsuda, H. Matsuda, M. Sasaki, 2000, Pediatric neurology.

[Migrating partial seizures in infancy].

J. Takahashi, K. Sugai, 2020, Ryoikibetsu shokogun shirizu.

Brain perfusion SPECT and EEG findings in children with autism spectrum disorders and medically intractable epilepsy

M. Sasaki, E. Nakagawa, N. Sato, 2010, Brain and Development.

Anterior striatum with dysmorphic neurons associated with the epileptogenesis of focal cortical dysplasia

A. Takahashi, A. Kakita, Hitoshi Takahashi, 2010, Seizure.

Intractable epilepsy due to a rosette‐forming glioneuronal tumor with a dysembryoplastic neuroepithelial background

A. Takahashi, A. Kakita, M. Sasaki, 2018, Neuropathology : official journal of the Japanese Society of Neuropathology.

CD4+CD25high regulatory T cell in childhood ocular myasthenia gravis

M. Sasaki, E. Nakagawa, K. Sugai, 2011, Brain & development (Tokyo. 1979).

Characteristic expression of p57/Kip2 in balloon cells in focal cortical dysplasia

H. Kitaura, A. Kakita, S. Kameyama, 2015, Neuropathology (Kyoto. 1993).

Peripheral nerve abnormalities in pediatric patients with spinal muscular atrophy

T. Yonekawa, M. Sasaki, K. Sugai, 2013, Brain and Development.

Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosis

I. Takamisawa, M. Sasaki, E. Nakagawa, 2012, Developmental medicine and child neurology.

A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked Adrenoleukodystrophy: Analysis of the Stability and Function of the Mutant ABCD1 Protein.

N. Shimozawa, M. Morita, R. Koide, 2013, JIMD reports.

Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study

A. Takahashi, M. Sasaki, E. Nakagawa, 2013, Brain and Development.

Characterization of ictal slow waves in epileptic spasms.

A. Okumura, M. Sasaki, E. Nakagawa, 2015, Epileptic disorders : international epilepsy journal with videotape.

Undetectable levels of CSF hypocretin-1 (orexin-A) in two prepubertal boys with narcolepsy.

M. Fukumizu, K. Sugai, T. Kanbayashi, 2002, Neuropediatrics.

IBA57 mutations abrogate iron-sulfur cluster assembly leading to cavitating leukoencephalopathy

Y. Goto, I. Nonaka, Y. Hayashi, 2017, Neurology: Genetics.

Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report

Y. Goto, M. Sasaki, E. Nakagawa, 2019, Neuropediatrics.

Focal cortical myoclonus in rolandic cortical dysplasia presenting as hemifacial twitching

A. Gunji, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

SISCOM technique with a variable Z score improves detectability of focal cortical dysplasia: a comparative study with MRI

H. Matsuda, K. Kamiya, H. Sugimoto, 2012, Annals of Nuclear Medicine.

Transient water-electrolyte disturbance after hemispherotomy in young infants with epileptic encephalopathy

A. Takahashi, M. Iwasaki, M. Sasaki, 2019, Child's Nervous System.

Novel pathological abnormalities of deep brain structures including dysplastic neurons in anterior striatum associated with focal cortical dysplasia in epilepsy.

A. Takahashi, A. Kakita, Hitoshi Takahashi, 2012, Journal of neurosurgery. Pediatrics.

Oral high-dose phenobarbital therapy for early infantile epileptic encephalopathy.

H. Ozawa, K. Sugai, S. Noma, 2002, Pediatric neurology.

[Hereditary spastic paraplegia associated with congenital cataracts, mental retardation and peripheral neuropathy].

M. Sasaki, E. Nakagawa, K. Sugai, 2010, No to hattatsu = Brain and development.

Severe infantile dentatorubral pallidoluysian atrophy with extreme expansion of CAG repeats

M. Sasaki, M. Fukumizu, K. Sugai, 2001, Neurology.

Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgery

A. Takahashi, Y. Nakata, M. Sasaki, 2014, Brain and Development.

Alteration of the anatomical covariance network after corpus callosotomy in pediatric intractable epilepsy

H. Matsuda, M. Inagaki, M. Iwasaki, 2019, PloS one.

Augmented startle responses in opsoclonus-myoclonus syndrome

T. Yonekawa, M. Inagaki, M. Sasaki, 2011, Brain & development (Tokyo. 1979).

Case report Augmented startle responses in opsoclonus-myoclonus syndrome

T. Yonekawa, M. Inagaki, M. Sasaki, 2011 .

Single-photon emission CT and MR findings in Klüver-Bucy syndrome after Reye syndrome.

H. Matsuda, H. Ozawa, M. Sasaki, 1997, AJNR. American journal of neuroradiology.

Hemimegalencephaly: a study of abnormalities occurring outside the involved hemisphere.

Y. Miki, F. Yamashita, Y. Nakata, 2007, AJNR. American journal of neuroradiology.

Case Report Complex behavioral automatism arising from insular cortex

Hideyuki Nakama, T. Otsuki, Y. Kubota, 2006 .

Hyperkinetic movement disorder in a child treated by globus pallidus stimulation

M. Sasaki, Hideyuki Nakama, T. Otsuki, 2009, Brain & development (Tokyo. 1979).

Importance of CAG repeat length in childhood-onset dentatorubral–pallidoluysian atrophy

Y. Goto, M. Sasaki, Hajime Tanaka, 2012, Journal of Neurology.

Hypoalbuminemia in early onset dentatorubral−pallidoluysian atrophy due to leakage of albumin in multiple organs

Y. Goto, S. Ito, K. Matsuoka, 2013, Journal of Neurology.

Exacerbation of Epileptic Seizures after Japanese Encephalitis Vaccination: A Case Report

M. Sasaki, E. Nakagawa, K. Sugai, 2015 .

Improved detection of cortical and subcortical tubers in tuberous sclerosis by fluid-attenuated inversion recovery MRI

T. Kato, K. Sugai, H. Yamanouchi, 1997, Neuroradiology.

De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood

N. Matsumoto, Taki Nishimura, N. Miyake, 2013, Nature Genetics.

Focal cortical myoclonus in rolandic cortical dysplasia presenting as hemifacial twitching

A. Gunji, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

Pathologic Active mTOR Mutation in Brain Malformation with Intractable Epilepsy Leads to Cell-Autonomous Migration Delay.

A. Takahashi, S. Koizumi, M. Hoshino, 2017, The American journal of pathology.

Five novel single nucleotide polymorphisms in the EPHX1 gene encoding microsomal epoxide hydrolase.

Y. Goto, Yoshiro Saito, S. Ozawa, 2003, Drug metabolism and pharmacokinetics.

[A case of congenital hypomyelination neuropathy with type I Chiari malformation and mental retardation].

I. Nonaka, S. Hirano, M. Sasaki, 1997, No to hattatsu = Brain and development.

New guidelines for management of febrile seizures in Japan

H. Yoshinaga, M. Kubota, Y. Maegaki, 2017, Brain and Development.

Urinary prostaglandin metabolites as Duchenne muscular dystrophy progression markers

M. Sasaki, H. Tachimori, E. Nakagawa, 2018, Brain and Development.

3-Hydroxyisobutyric aciduria in two brothers.

M. Sasaki, T. Hashimoto, K. Sugai, 1998, Pediatric neurology.

Effects of low-dose hydrochlorothiazide on urolithiasis and bone metabolism in severely disabled individuals: A pilot study

M. Sasaki, K. Sugai, Yoshiaki Saito, 2011, Brain and Development.

Characteristic expression of p57/Kip2 in balloon cells in focal cortical dysplasia

H. Kitaura, A. Kakita, S. Kameyama, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

Surgical versus medical treatment for children with epileptic encephalopathy in infancy and early childhood: Results of an international multicenter cohort study in Far-East Asia (the FACE study)

Katsuhiro Kobayashi, Seung-Chyul Hong, S. Kameyama, 2016, Brain and Development.

Ictal deafness in drug-resistant MRI-negative epilepsy.

M. Iwasaki, M. Sasaki, E. Nakagawa, 2019, Epileptic disorders : international epilepsy journal with videotape.

MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene

Y. Goto, I. Nishino, M. Sasaki, 2014, Brain and Development.