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A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy

Neurological sciences, 2012-12, Vol.33 (6), p.1389-1392

2012

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Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (8), p.3117-3122

2008

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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

PloS one, 2012-12, Vol.7 (12), p.e51155

2012

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Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2794, p.1

Momoi, Mariko Y

2024

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LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

PloS one, 2014-03, Vol.9 (3), p.e92695

2014

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Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Clinical neurophysiology, 2012-06, Vol.123 (6), p.1147-1157

2012

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Impairment of social and emotional behaviors in Cadm1-knockout mice

Biochemical and biophysical research communications, 2010-06, Vol.396 (3), p.703-708

2010

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Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

PloS one, 2012-01, Vol.7 (1), p.e30151-e30151

2012

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Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Journal of neurochemistry, 2016-10, Vol.139 (2), p.245-255

2016

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Cytokine profiles of seventeen cytokines, growth factors and chemokines in cord blood and its relation to perinatal clinical findings

Cytokine (Philadelphia, Pa.), 2010-03, Vol.49 (3), p.331-337

2010

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Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Journal of neurochemistry, 2015-01, Vol.132 (1), p.61-69

2015

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Association of moderately abnormal behavior and administered neuraminidase inhibitors

Drug Discoveries & Therapeutics, 2020/02/29, Vol.14(1), pp.50-53

2020

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MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus

Brain & development (Tokyo. 1979), 2014-01, Vol.36 (1), p.64-69

2014

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Inquiry into some gap among oseltamivir use and severe abnormal behavior in Japanese children and adolescents with influenza

Drug Discoveries & Therapeutics, 2018/12/31, Vol.12(6), pp.381-383

2018

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Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

Neuropathology, 2013-06, Vol.33 (3), p.292-298

2013

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Th2 cells predominate in idiopathic steroid-sensitive nephrotic syndrome

Clinical and experimental nephrology, 2010-12, Vol.14 (6), p.578-583

2010

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Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: a fNIRS study

NeuroImage clinical, 2014-01, Vol.6 (C), p.192-201

2014

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Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

NeuroImage clinical, 2012-01, Vol.1 (1), p.131-140

2012

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Expression analysis and mutation detection of DLX5 and DLX6 in autism

Brain & development (Tokyo. 1979), 2010-02, Vol.32 (2), p.98-104

2010

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Utility of non‐enhanced magnetic resonance imaging to detect acute pyelonephritis

Pediatrics international, 2014-06, Vol.56 (3), p.e4-e6

2014

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A marked decrease in CD4-positive lymphocytes at the onset of hepatitis in a patient with hepatitis-associated aplastic anemia

Journal of pediatric hematology/oncology, 2012-07, Vol.34 (5), p.375-377

2012

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Identification and characterization of a natural inter-genotypic (2b/1b) recombinant hepatitis C virus in Japan

Archives of virology, 2011-09, Vol.156 (9), p.1591-1601

2011

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Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers

Brain & development (Tokyo. 1979), 2013-06, Vol.35 (6), p.582-585

2013

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Comment on: Risk of neuropsychiatric adverse events associated with the use of oseltamivir: a nationwide population-based case-crossover study

Journal of antimicrobial chemotherapy, 2019-06, Vol.74 (6), p.1762-1764

2019

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Mutation analysis of methyl-CpG binding protein family genes in autistic patients

Brain & development (Tokyo. 1979), 2005-08, Vol.27 (5), p.321-325

2005

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A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases

LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Impairment of social and emotional behaviors in Cadm1-knockout mice

Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Cytokine profiles of seventeen cytokines, growth factors and chemokines in cord blood and its relation to perinatal clinical findings

Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Association of moderately abnormal behavior and administered neuraminidase inhibitors

MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus

Inquiry into some gap among oseltamivir use and severe abnormal behavior in Japanese children and adolescents with influenza

Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

Th2 cells predominate in idiopathic steroid-sensitive nephrotic syndrome

Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: a fNIRS study

Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

Expression analysis and mutation detection of DLX5 and DLX6 in autism

Utility of non‐enhanced magnetic resonance imaging to detect acute pyelonephritis

A marked decrease in CD4-positive lymphocytes at the onset of hepatitis in a patient with hepatitis-associated aplastic anemia

Identification and characterization of a natural inter-genotypic (2b/1b) recombinant hepatitis C virus in Japan

Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers

Comment on: Risk of neuropsychiatric adverse events associated with the use of oseltamivir: a nationwide population-based case-crossover study

Mutation analysis of methyl-CpG binding protein family genes in autistic patients

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