M. Morimoto

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Aliases
M Morimoto, M. Morimoto, Masafumi Morimoto
Publication record
80 papers · 2,984 citations · H-index 26

PAPERS

CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate
202211 citationsauthor #14
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
20223 citationsauthor #32
Low‐grade IVH in preterm infants causes cerebellar damage, motor, and cognitive impairment
202110 citationsauthor #8
Impaired neuronal activity and differential gene expression in STXBP1 encephalopathy patient iPSC-derived GABAergic neurons.
202119 citationsauthor #10
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate
20214 citationsauthor #14
A novel Drosophila model for neurodevelopmental disorders associated with Shwachman-Diamond syndrome.
20209 citationsauthor #7
Prenatal clinical manifestations in individuals with COL4A1/2 variants
202035 citationsauthor #7
Gender differences in occurrence of behavioral and emotional problems at the lower grades of elementary school: Association with developmental and behavioral characteristics at 5 years.
20196 citationsauthor #5
Plasma neurofilament light chain: A potential prognostic biomarker of dementia in adult Down syndrome patients
201928 citationsauthor #6
UBAP 1 mutations cause juvenile-onset hereditary spastic paraplegias ( SPG 80 ) and impair UBAP 1 targeting to endosomes
20190 citationsauthor #8
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
201922 citationsauthor #8
High-fat diet accelerates extreme obesity with hyperphagia in female heterozygous Mecp2-null mice
201919 citationsauthor #11
Frequency and risk factors for subsyndromal delirium in an intensive care unit.
201835 citationsauthor #5
Cerebellar peduncle injury predicts motor impairments in preterm infants: A quantitative tractography study at term-equivalent age.
20188 citationsauthor #8
A 5-Year Follow-Up of Triple-Seronegative Myasthenia Gravis Successfully Treated with Tacrolimus Therapy
20185 citationsauthor #7
Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum
201830 citationsauthor #7
DHA Mitigates Autistic Behaviors Accompanied by Dopaminergic Change in a Gene/Prenatal Stress Mouse Model.
201826 citationsauthor #5
Detection of copy number variations in epilepsy using exome data
201843 citationsauthor #11
Increased levels of plasma total tau in adult Down syndrome
201739 citationsauthor #7
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
201743 citationsauthor #11
Luteolin attenuates interleukin-6-mediated astrogliosis in human iPSC-derived neural aggregates: A candidate preventive substance for maternal immune activation-induced abnormalities.
201725 citationsauthor #12
Longitudinal change in white matter in preterm infants without magnetic resonance imaging abnormalities: Assessment of serial diffusion tensor imaging and their relationship to neurodevelopmental outcomes.
201711 citationsauthor #2
[Meet the experts: therapy of myasthenia gravis in childhood].
20160 citationsauthor #1
A Video Report of Brain–Lung–Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene
20163 citationsauthor #8
Mislocalization of syntaxin‐1 and impaired neurite growth observed in a human iPSC model for STXBP1‐related epileptic encephalopathy
201642 citationsauthor #8
The Collapse of the BDNF/POMC System in the Hypothalamus is Responsible for the Extreme Obesity with Hyperphagia Observed in Female Heterozygous MeCP2 Null Mice
20160 citationsauthor #10
Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome
201626 citationsauthor #9
Modeling the Early Phenotype at the Neuromuscular Junction of Spinal Muscular Atrophy Using Patient-Derived iPSCs
201595 citationsauthor #9
Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
201515 citationsauthor #13
Low-grade intraventricular hemorrhage disrupts cerebellar white matter in preterm infants: evidence from diffusion tensor imaging
201548 citationsauthor #2
IgA nephropathy in a girl with mitochondrial disease
20155 citationsauthor #2
Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies
201452 citationsauthor #8
Effects of chemotherapy on the brain in childhood: diffusion tensor imaging of subtle white matter damage
201335 citationsauthor #2
Glycosylphosphatidylinositol (GPI) anchor deficiency caused by mutations in PIGW is associated with West syndrome and hyperphosphatasia with mental retardation syndrome
2013104 citationsauthor #3
Altered somatosensory barrel cortex refinement in the developing brain of Mecp2-null mice.
20138 citationsauthor #3
[Successful treatment with levetiracetam in a case of Ohtahara syndrome caused by STXBP1 mutation].
20137 citationsauthor #9
[A case with recurrent asystole due to breath-holding spells: successful treatment with levetiracetam].
20122 citationsauthor #9
Fatal varicella with multi‐organ failure associated with low‐dose adrenocorticotropic hormone therapy
20121 citationsauthor #7
Development of Corpus Callosum in Preterm Infants Is Affected by the Prematurity: In Vivo Assessment of Diffusion Tensor Imaging at Term-Equivalent Age
201166 citationsauthor #3
P25.4 Cerebellar peduncles injury in preterm infants with cerebral palsy as detected by quantitative tractography
20110 citationsauthor #1
T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake.
201116 citationsauthor #2
P07.16 Radionuclide cisternographic findings of children with spontaneous cerebrospinal fluid leaks
20110 citationsauthor #3
Effects of stress of postnatal development on corticosterone, serotonin and behavioral changes.
20107 citationsauthor #2
[Recurrence of transient splenial lesions in a child with "benign convulsions with gastroenteritis"].
20106 citationsauthor #7
Postnatal changes in serotonergic innervation to the hippocampus of methyl-CpG-binding protein 2-null mice.
201027 citationsauthor #2
Successful Treatment with Chloramphenicol in an Infantile Case of Bacterial Meningitis with Subdural Abscess
20090 citationsauthor #3
Wernicke’s encephalopathy in a patient with nephrotic syndrome
200916 citationsauthor #4
Treatment for Leigh syndrome by monitoring dichloroacetate concentration
20092 citationsauthor #2
An age-dependent change in serotonin innervation to the forebrain of Mecp2-null mice
20090 citationsauthor #8
Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy.
200832 citationsauthor #9
Bone marrow transplantation for Rasmussen Syndrome
20080 citationsauthor #2
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
2008125 citationsauthor #12
Fiber-Tracking Techniques Can Predict the Degree of Neurologic Impairment for Periventricular Leukomalacia
200887 citationsauthor #2
Alternative psychosis and dysgraphia accompanied by forced normalization in a girl with occipital lobe epilepsy.
20088 citationsauthor #2
Partial tandem duplication of GRIA3 in a male with mental retardation
200739 citationsauthor #4
SERIAL MRI IN A BOY WITH RASMUSSEN SYNDROME: THE EFFICACY OF IMMUNOGLOBULIN THERAPY
20060 citationsauthor #2
Effects of edaravone on N‐methyl‐d‐aspartate (NMDA)‐mediated cytochrome c release and apoptosis in neonatal rat cerebrocortical slices
20068 citationsauthor #5
SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy
200675 citationsauthor #1
Infantile bilateral striatal necrosis associated with human herpes virus-6 (HHV-6) infection.
200522 citationsauthor #2
Imaging analysis of mineralocorticoid receptor and importins in single living cells by using GFP color variants
200525 citationsauthor #3
Blood flow deficits due to perivascular nerve degeneration: a novel mechanism of ALS
20050 citationsauthor #8
VEGF is a modifier gene of amyotrophic lateral sclerosis in humans
20030 citationsauthor #3
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
2003902 citationsauthor #3
Ring Chromosome 14 with Localization‐related Epilepsy: Three Cases
200324 citationsauthor #1
Yellow fluorescent protein-tagged and cyan fluorescent protein-tagged imaging analysis of glucocorticoid receptor and importins in single living cells.
200338 citationsauthor #3
Infantile Spasms in a Patient with Williams Syndrome and Craniosynostosis
200335 citationsauthor #1
73 A CASE OF INFANTILE GRAVE'S DISEASE WITH UNUSUAL SYMPTOMS LIKE PARAPLEGIA
20020 citationsauthor #5
I D4 Anti-histaminergic/allergic drug-induced seizures in children of our out-patient clinic
20020 citationsauthor #2
Chronic Loss of Glucocorticoids Following Adrenalectomy Down‐regulates the Expression of Glucocorticoid Receptor mRNA in the Rat Forebrain
19979 citationsauthor #3
Distribution of glucocorticoid receptor immunoreactivity and mRNA in the rat brain: an immunohistochemical and in situ hybridization study.
1996464 citationsauthor #1
315 Cellular and subcellular distributions pattern of glucocorticoid receptors in the rat brain
19960 citationsauthor #2
1113 Glucocorticoid receptor expression during cerebellar development
19960 citationsauthor #4
The alteration of glucocorticoid receptor-immunoreactivity in the rat forebrain following short-term and long-term adrenalectomy.
199628 citationsauthor #4
1351 The effect of glucocorticoid on cell birth and death in adult rat hippocampal dentate gyrus
19960 citationsauthor #3
Phenotypic alterations of neuropeptide Y, vasoactive intestinal peptide and choline acetyltransferase in rat cultured chromaffin cells as effected by nerve growth factor and glucocorticoid.
19960 citationsauthor #1
The effects of NGF and glucocorticoid on the cytological features of rat chromaffin cells in vitro.
19949 citationsauthor #1
Steroid hormone effects on gene expression, neuronal structure, and differentiation.
199433 citationsauthor #3
1237 Effects of NGF and glucocorticoid on rat chromaffin cells in vitro
19930 citationsauthor #1
Neurenteric cysts with meningomyelocele or meningocele
199010 citationsauthor #6

TIMELINE

1990 10 citations

1993 0 citations

1994 42 citations

1996 492 citations

1997 9 citations

2002 0 citations

2003 999 citations

2005 47 citations

2006 83 citations

2007 39 citations

2008 252 citations

2009 18 citations

2010 40 citations

2011 82 citations

2012 3 citations

2013 154 citations

2014 52 citations

2015 163 citations

2016 71 citations

2017 118 citations

2018 147 citations

2019 75 citations

2020 44 citations

2021 33 citations

2022 14 citations

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