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Progress in searching for the febrile seizure susceptibility genes

Brain & development (Tokyo. 1979), 2009-05, Vol.31 (5), p.359-365

Nakayama, Junko

2009

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Anesthetic management of super-elderly patients with remimazolam: a report of two cases

JA clinical reports, 2021-09, Vol.7 (1), p.71-71, Article 71

2021

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Robot-assisted training using Hybrid Assistive Limb® for cerebral palsy

Brain & development (Tokyo. 1979), 2018-09, Vol.40 (8), p.642-648

2018

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Longitudinal, prospective study of head impacts in male high school football players

PloS one, 2023-09, Vol.18 (9), p.e0291374-e0291374

2023

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Benefits of a Wearable Cyborg HAL (Hybrid Assistive Limb) in Patients with Childhood-Onset Motor Disabilities: A 1-Year Follow-Up Study

Pediatric reports, 2023-03, Vol.15 (1), p.215-226

2023

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Task-specific enhancement of hippocampus-dependent learning in mice deficient in monoacylglycerol lipase, the major hydrolyzing enzyme of the endocannabinoid 2-arachidonoylglycerol

Frontiers in behavioral neuroscience, 2015-06, Vol.9, p.134-134

2015

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Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination

Brain & development (Tokyo. 1979), 2012-03, Vol.34 (3), p.234-237

2012

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A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation

Journal of human genetics, 2011-03, Vol.56 (3), p.250-252

2011

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Molecular genetics of febrile seizures

Epilepsy research, 2006-08, Vol.70, p.190-198

2006

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Inhibition of fatty achid amide hydrolase accelerates acquisition of cerebellum-dependent eyeblink conditioning

Neuroscience research, 2009, Vol.65, p.S126-S127

2009

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Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene ( GABRA1) and mood disorders

Biological psychiatry (1969), 2004, Vol.55 (1), p.40-45

2004

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Voluntary-assisted Upper Limb Training for Severe Cerebral Palsy Using Robotics Devices and Neuromuscular Electrical Stimulation: Three Case Reports

Progress in Rehabilitation Medicine, 2022, Vol.7, pp.20220050

2022

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Crosslinking of near responses in healthy young subjects

Acta ophthalmologica (Oxford, England), 2020-09, Vol.98 (6), p.e791-e793

2020

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A Patient with Rett Syndrome Maintained Motor Function by Periodic Rehabilitation Therapy and Proactive Daily Activities

Progress in Rehabilitation Medicine, 2020, Vol.5, pp.20200014

2020

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Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-11, Vol.123B (1), p.27-32

2003

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Failure to find causal mutations in the GABAA-receptor γ2 subunit (GABRG2) gene in Japanese febrile seizure patients

Neuroscience letters, 2003-06, Vol.343 (2), p.117-120

2003

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Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans

Neuroscience letters, 2002-08, Vol.329 (2), p.249-251

2002

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Family-based association study of the NOTCH4 gene in schizophrenia using Japanese and Chinese samples

Biological psychiatry (1969), 2003-07, Vol.54 (2), p.129-135

2003

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A novel homozygous mutation of GJC2 derived from maternal uniparental disomy in a female patient with Pelizaeus–Merzbacher-like disease

Journal of the neurological sciences, 2013-07, Vol.330 (1), p.123-126

2013

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Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia

The Journal of clinical investigation, 2012-02, Vol.122 (2), p.507-518

2012

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Molecular genetics of febrile seizures: Epileptic syndromes in infancy and early childhood: Proceedings of the International Symposium on Epileptic Syndromes in Infancy and Early Childhood - Evidence-based Toxonomy and its Implications in the ILAE Classification, 8th Annual Meeting of the Infantile Seizure Society, Tokyo, Japan, April 29-May 1, 2005

Epilepsy research, 2006, Vol.70

2006

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A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures

Annals of neurology, 2002-11, Vol.52 (5), p.654-657

2002

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Energy expenditure measured by the flow-through indirect calorimetry in children with severe motor and intellectual disabilities

No to hattatsu, 2015-01, Vol.47 (1), p.53

2015

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Application of flow cytometry for rapid determination of cell number of viable bacteria

Fisheries science, 1997, Vol.63 (6), p.1024-1029

1997

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A quantitative study of the progress of myelination in the rat central nervous system, using the immunohistochemical method for proteolipid protein

Brain research. Developmental brain research, 1998-06, Vol.108 (1), p.287-293

1998

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Progress in searching for the febrile seizure susceptibility genes

Anesthetic management of super-elderly patients with remimazolam: a report of two cases

Robot-assisted training using Hybrid Assistive Limb® for cerebral palsy

Longitudinal, prospective study of head impacts in male high school football players

Benefits of a Wearable Cyborg HAL (Hybrid Assistive Limb) in Patients with Childhood-Onset Motor Disabilities: A 1-Year Follow-Up Study

Task-specific enhancement of hippocampus-dependent learning in mice deficient in monoacylglycerol lipase, the major hydrolyzing enzyme of the endocannabinoid 2-arachidonoylglycerol

Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination

A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation

Molecular genetics of febrile seizures

Inhibition of fatty achid amide hydrolase accelerates acquisition of cerebellum-dependent eyeblink conditioning

Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene ( GABRA1) and mood disorders

Voluntary-assisted Upper Limb Training for Severe Cerebral Palsy Using Robotics Devices and Neuromuscular Electrical Stimulation: Three Case Reports

Crosslinking of near responses in healthy young subjects

A Patient with Rett Syndrome Maintained Motor Function by Periodic Rehabilitation Therapy and Proactive Daily Activities

Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia

Failure to find causal mutations in the GABAA-receptor γ2 subunit (GABRG2) gene in Japanese febrile seizure patients

Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans

Family-based association study of the NOTCH4 gene in schizophrenia using Japanese and Chinese samples

A novel homozygous mutation of GJC2 derived from maternal uniparental disomy in a female patient with Pelizaeus–Merzbacher-like disease

Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures

Energy expenditure measured by the flow-through indirect calorimetry in children with severe motor and intellectual disabilities

Application of flow cytometry for rapid determination of cell number of viable bacteria

A quantitative study of the progress of myelination in the rat central nervous system, using the immunohistochemical method for proteolipid protein

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