「Involvement of brain structures in childhood epilepsy with centrotemporal spikes」の関連論文
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Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy
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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Lipoteichoic acid is involved in the ability of the immunobiotic strain Lactobacillus plantarum CRL1506 to modulate the intestinal antiviral innate immunity triggered by TLR3 activation
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思春期早発症の9歳女児に急性発症した上腸間膜動脈症候群の1例
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Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
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Association of Socio-Demographic and Climatic Factors with the Duration of Hospital Stay of Under-Five Children with Severe Pneumonia in Urban Bangladesh: An Observational Study.
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Association of Socio-Demographic and Climatic Factors with the Duration of Hospital Stay of Under-Five Children with Severe Pneumonia in Urban Bangladesh: An Observational Study.
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HLA-B*51:01 and CYP2C9*3 are risk factors for phenytoin-induced eruption in the Japanese population: analysis of data from the Biobank Japan Project
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The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
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Differentiation of Hypertrophic Chondrocytes from Human iPSCs for the In Vitro Modeling of Chondrodysplasias
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Reasons for Undergoing CT During Childhood : Can CT-Exposed and CT-Naïve Populations Be Compared?
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Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
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Development of highly efficient methods for comprehensive pathogen detection using next generation sequencing
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Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort
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Potential roles of gastroesophageal reflux in patients with superficial esophageal squamous cell carcinoma without major causative risk factors
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An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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Clinical characteristics and outcomes of the right congenital diaphragmatic hernia compared to the left: a 10-year single-center experience
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The Natural History of Spontaneously Occurred Endometriosis in Cynomolgus Monkeys by Monthly Follow-Up Laparoscopy for Two Years.
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Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism
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Prevalence and associated factors of orphan symptoms in advanced cancer patients: a multicenter observational study
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α-Synuclein BAC transgenic mice exhibit RBD-like behaviour and hyposmia: a prodromal Parkinson’s disease model
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Prevalence of incidental meningiomas and gliomas on MRI : a meta-analysis and meta-regression analysis.
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Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants
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Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial)
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A case of paroxysmal kinesigenic dyskinesia suspected to be reflex epilepsy
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Analysis of immunologic comorbidities in ulcerative colitis patients: a tool to prevent exacerbations in ulcerative colitis cases
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A case of Cockayne syndrome with unusually mild clinical manifestations
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Studies on Peripheral Blood mMDSC Based-Biomarker Exploration and a Novel Therapeutic Agent for Cancer Immunotherapy
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Long-term Effect of Regular Physical Activity and Exercise Habits in Patients With Early Parkinson Disease
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Pilot Study of a Video-Based Educational Program to Reduce Family Violence for Parents of Adult Children with Schizophrenia
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Negative impact of behavior restriction amidst a clustered COVID-19 infection on immobility syndrome in older patients negative for COVID-19: report from a chronic care hospital in Japan
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Labyrinthine calcification in ears with otitis media and antineutrophil cytoplasmic antibody-associated vasculitis (OMAAV): A report of two cases
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Study profile of The Tohoku Medical Megabank Community-Based Cohort Study.
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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
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Usefulness of interleukin-18 as a diagnostic biomarker to differentiate adult-onset Still’s disease with/without macrophage activation syndrome from other secondary hemophagocytic lymphohistiocytosis in adults
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
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Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
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The prevalence and characteristics of hypouricemia: a descriptive study of medical check-up and administrative claims data
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TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum
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Nationwide survey of refractory asthma with bronchiectasis by inflammatory subtypes
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Comment to our article; Effects of varicocelectomy on testis volume and semen parameters in adolescents: a randomized prospective study
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Active role of the central amygdala in widespread mechanical sensitization in rats with facial inflammatory pain
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Incidence of Cranial Adjacent Segment Disease after Posterior Lumbar Interbody Fusion Using the Cortical Bone Trajectory Technique for the Treatment of Single-Level Degenerative Lumbar Spondylolisthesis; More than a 2-Year Follow-Up.
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Feasibility of targeting Traf2-and-Nck-Interacting kinase in synovial sarcoma (本文)
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Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
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Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
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Genetic and Epigenetic Pathogenesis of Acromegaly
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Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease