H. Kurahashi

发表

Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion.

Y. Makita, M. Masuno, K. Maizumi, 1995, Journal of medical genetics.

Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation

Y. Cho, Y. Makita, H. Kurahashi, 2011, Journal of Human Genetics.

Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus

H. Kurahashi, S. Hirose, A. Kumakura, 2009, Brain and Development.

Acute encephalopathy in children with tuberous sclerosis complex

T. Shiihara, M. Kubota, H. Kurahashi, 2021, Orphanet Journal of Rare Diseases.

Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion

Y. Makita, M. Masuno, K. Tachibana, 1998, European Journal of Pediatrics.

Posterior reversible encephalopathy syndrome in a child with bronchial asthma

H. Kurahashi, A. Okumura, M. Magota, 2006, Brain and Development.

Clinical spectrum of SCN2A mutations

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

Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders

Katsuhiro Kobayashi, T. Akiyama, H. Kurahashi, 2019, Brain and Development.

Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

H. Kurahashi, S. Hirose, 2015 .

Administration of nusinersen via paramedian approach for spinal muscular atrophy

H. Kurahashi, A. Okumura, N. Wakao, 2020, Brain and Development.

Procalcitonin as a Biomarker of Unresponsiveness to Intravenous Immunoglobulin for Kawasaki Disease

H. Kurahashi, A. Okumura, Toshinori Hori, 2020, The Pediatric infectious disease journal.

On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation

H. Kurahashi, N. Higurashi, S. Hirose, 2012, Brain and Development.

Clinical spectrum of SCN 2 A mutations

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

An Analysis of Domestic Water Demand Structure and Water Recycling in Beijing

H. Kurahashi, K. Fujie, R. Qi, 2011 .

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

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

Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2.

H. Kurahashi, M. Shima, A. Yoshioka, 2000, American journal of medical genetics.

Focal epilepsy resulting from a de novo SCN1A mutation.

H. Kurahashi, A. Okumura, K. Watanabe, 2007, Neuropediatrics.

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

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

Increased fetal heart rate variability in periventricular leukomalacia

H. Kurahashi, A. Itakura, Kazuyoshi Watanabe, 2016, Brain and Development.

A trial of lacosamide for benign convulsions with gastroenteritis

H. Kurahashi, A. Okumura, Shingo Numoto, 2020, Brain and Development.

Long-term efficacy of nusinersen and its evaluation in adolescent and adult patients with spinal muscular atrophy types 1 and 2

H. Kurahashi, A. Okumura, Y. Azuma, 2022, Brain and Development.

HPeV3-associated acute encephalitis/encephalopathy among Japanese infants

H. Kurahashi, Y. Daimon, H. Matsumoto, 2021, Brain and Development.

A nationwide survey of norovirus-associated encephalitis/encephalopathy in Japan

H. Kurahashi, A. Okumura, Toshiaki Shimizu, 2019, Brain and Development.

Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders

A. Takata, N. Matsumoto, M. Shiina, 2018, Human molecular genetics.

The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy

N. Kurahashi, H. Kurahashi, S. Kojima, 2016, Brain and Development.

White Blood Cell and Neutrophil Counts and Response to Intravenous Immunoglobulin in Kawasaki Disease

H. Kurahashi, A. Okumura, Y. Shimomura, 2019, Global pediatric health.

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

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

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.

Epilepsies in Children with 2q24.3 Deletion/Duplication

H. Kurahashi, A. Okumura, Toshiyuki Yamamoto, 2015, Journal of Pediatric Epilepsy.

Splenial Lesions in Benign Convulsions With Gastroenteritis Associated With Rotavirus Infection.

S. Saitoh, H. Kurahashi, A. Okumura, 2019, Pediatric neurology.

Acute encephalopathy in children with tuberous sclerosis complex

T. Shiihara, M. Kubota, H. Kurahashi, 2020, Orphanet Journal of Rare Diseases.

Long‐term Follow‐up of Patients with Benign Partial Epilepsy in Infancy

H. Kurahashi, Kazuyoshi Watanabe, A. Okumura, 2006, Epilepsia.

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

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

CDKL5 deficiency causes epileptic seizures independent of cellular mosaicism

H. Kurahashi, Takayoshi Koike, R. Takeguchi, 2022, Journal of the Neurological Sciences.

Decreased platelet count in children with epilepsy treated with valproate and its relationship to the immature platelet fraction

H. Kurahashi, A. Okumura, K. Murotani, 2017, International Journal of Hematology.

MRI findings in children with congenital cytomegalovirus infection retrospectively diagnosed with dried umbilical cord

H. Kurahashi, A. Okumura, H. Kidokoro, 2020, Neuroradiology.

Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin

M. Mizuguchi, H. Kurahashi, M. Hosoya, 2009, Brain and Development.

Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes

H. Kurahashi, N. Higurashi, S. Hirose, 2016, Brain and Development.

Cumulative Contents to Volume 38

V. S. Gupta, Japan., F. Pidcock, 2016, Brain and Development.

MYRF is associated with encephalopathy with reversible myelin vacuolization

A. Masuda, K. Ohno, M. Mizuguchi, 2018, Annals of neurology.

Spinocerebellar ataxias type 27 derived from a disruption of the fibroblast growth factor 14 gene with mimicking phenotype of paroxysmal non-kinesigenic dyskinesia

K. Yokochi, H. Kurahashi, A. Okumura, 2012, Brain and Development.

A nationwide survey of human metapneumovirus-associated encephalitis/encephalopathy in Japan

H. Kurahashi, A. Okumura, Y. Kawano, 2023, Brain & development (Tokyo. 1979).

A One-Month-Old Boy With a Seizure During a Febrile Illness

H. Kurahashi, A. Okumura, H. Minagawa, 2018, Clinical pediatrics.

The magnetic resonance imaging spectrum of Pelizaeus–Merzbacher disease: A multicenter study of 19 patients

K. Yokochi, H. Matsuda, J. Takanashi, 2016, Brain and Development.

A rare case of fetal extensive intracranial hemorrhage and whole-cerebral hypoplasia due to latent maternal vitamin K deficiency.

H. Kurahashi, A. Okumura, H. Kakita, 2018, Journal of neonatal-perinatal medicine.

Delayed recognition of childhood arterial ischemic stroke

S. Saitoh, H. Kurahashi, T. Yoshikawa, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia

H. Kurahashi, T. Awaya, J. Tohyama, 2019, Seizure.

Attitudes of school teachers toward epilepsy in Nagoya, Japan

S. Saitoh, H. Kurahashi, A. Okumura, 2020, Epilepsy & Behavior.

The semiology of febrile seizures: Focal features are frequent

H. Kurahashi, Kazuyoshi Watanabe, A. Okumura, 2017, Epilepsy & Behavior.

Serum Free Carnitine Levels in Children with Kawasaki Disease.

H. Kurahashi, A. Okumura, H. Agata, 2021, Pediatrics International.

Elevated Serum Free Carnitine Levels in Children with Kawasaki Disease and Their Relation to Unresponsiveness to Intravenous Immunoglobulin: retrospective study

H. Kurahashi, A. Okumura, Toshinori Hori, 2020 .

Insulin-like growth factor-1 level is a poor diagnostic indicator of growth hormone deficiency

H. Kurahashi, A. Okumura, W. Ohashi, 2021, Scientific Reports.

Sodium channel blockers are effective for benign infantile epilepsy

H. Kurahashi, A. Okumura, Y. Azuma, 2021, Seizure.

Case report: Mild encephalitis with a reversible splenial lesion associated with SARS-CoV-2 infection in a patient with MYRF variant

H. Kurahashi, A. Okumura, Toshiaki Shimizu, 2022, Frontiers in Pediatrics.

Respiratory illness and acute flaccid myelitis in the Tokai district in 2018

S. Saitoh, H. Kurahashi, T. Yoshikawa, 2019, Pediatrics International.

Chromosome 22q11 deletion complicated by dissecting pulmonary arterial aneurysm and jejunal atresia in an infant.

H. Kurahashi, S. Yamanaka, Y. Tanaka, 2000, Archives of pathology & laboratory medicine.

Serum carnitine levels of children with epilepsy: Related factors including valproate

H. Kurahashi, A. Okumura, Shingo Numoto, 2019, Brain and Development.

Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy

H. Kurahashi, N. Higurashi, S. Hirose, 2012, Epilepsy Research.

Diagnostic accuracy of insulin-like growth factor-1 for screening growth hormone deficiency: a prospective, single-center, diagnostic accuracy study

H. Kurahashi, A. Okumura, T. Muto, 2021 .

Diagnostic accuracy of IGF-1 for screening growth hormone deficiency: a prospective, single-center, diagnostic accuracy study

H. Kurahashi, A. Okumura, W. Ohashi, 2021 .

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features

Mami Shibata, T. Kawai, Y. Okuno, 2018, Brain and Development.

Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion.

N. Kurahashi, S. Saitoh, H. Kurahashi, 2014, Pediatric neurology.

Phenytoin desensitization monitored by antigen specific T cell response using carboxyfluorescein succinimidyl ester dilution assay.

H. Kurahashi, Kazuyoshi Watanabe, A. Okumura, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Fournier’s gangrene during ACTH therapy

H. Kurahashi, A. Numaguchi, A. Okumura, 2017, Brain & development (Tokyo. 1979).

Effects of l-carnitine supplementation in patients with childhood-onset epilepsy prescribed valproate

H. Kurahashi, A. Okumura, Y. Azuma, 2021, Epilepsy & Behavior.

Yale Observation Scale for Predicting Serious Illness in Japanese Primary Care Settings

H. Kurahashi, A. Okumura, T. Kishino, 2019 .

The effects of antihistamines on the semiology of febrile seizures

H. Kurahashi, A. Okumura, T. Kubota, 2019, Brain and Development.

Clinical spectrum of SCN2A mutations

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

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features

Mami Shibata, T. Kawai, Y. Okuno, 2018, Brain and Development.