「Prenatal diagnosis of severe mitochondrial disease caused by nuclear gene defects: a study in Japan」の関連論文
-
Enhanced hospital-wide communication and interaction by team training to improve patient safety
-
Recurrent palmoplantar pustulosis at the site of insertion of therapeutic titanium
-
Association of Local Intrapulmonary Production of Antibodies Specific to Donor Major Histocompatibility Complex Class I With the Progression of Chronic Rejection of Lung Allografts
-
The effect of liraglutide on insulin allergy in a patient with glucocorticoid-induced diabetes and multiple sclerosis
-
Health education improves referral compliance of persons with probable Diabetic Retinopathy: A randomized controlled trial.
-
Health education improves referral compliance of persons with probable Diabetic Retinopathy: A randomized controlled trial.
-
Applicability and eligibility of the International Study of Comparative Health Effectiveness with Medical and Invasive Approaches (ISCHEMIA) for patients who underwent revascularization with percutaneous coronary intervention (本文)
-
In silico study of RNA-seq and H3 Trimethylation ChIP-seq analysis in combination with laser-microdissection on human lung cancer cells
-
Relationship between Intraocular Pressure and Coffee Consumption in a Japanese Population without Glaucoma: The Nagahama Study
-
Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation
-
Successful treatment of tetanus with magnesium in a dialysis patient
-
The association between early rehabilitation and ambulatory ability at discharge in patients with hip fractures at acute-phase rehabilitation wards: a survey of the Japan Association of Rehabilitation Database
-
生後18か月の幼児及びその両親の口腔細菌叢の比較
-
Genomic analysis for the prediction of prognosis in small-bowel cancer
-
Genomic analysis for the prediction of prognosis in small-bowel cancer
-
肝芽腫に対する二施設間連携による集学的治療
-
一般住民における多疾患重積は脆弱性骨折のリスクである
-
Safety comparisons among monoamine oxidase inhibitors against Parkinson’s disease using FDA adverse event reporting system
-
Hyperspectral and multispectral image processing for gross-level tumor detection in skin lesions: a systematic review
-
Comprehensive Detection of Candidate Pathogens in the Lower Respiratory Tract of Pediatric Patients With Unexpected Cardiopulmonary Deterioration Using Next-Generation Sequencing
-
Incidence of central serous chorioretinopathy (2011–2018): a nationwide population-based cohort study of Japan
-
Relationship between presarcopenia and event occurrence in patients with primary hepatocellular carcinoma
-
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
-
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
-
Study on the effect of S-allyl cysteine on testosterone production and neuroprotection
-
Spontaneous regression of hidroacanthoma simplex after skin biopsy
-
Iinfluence of plasma cytokine levels on the conversion risk from MCI to dementia in the Alzheimer's disease neuroimaging initiative database
-
The Estimated Absolute Risk of Coronary Artery Disease and Subclinical Atherosclerosis.
-
Case report : Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion
-
Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
-
Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
-
Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
-
MicroRNA profiling in adults with high-functioning autism spectrum disorder
-
Repurposing bromocriptine for Aβ metabolism in Alzheimer’s disease (REBRAnD) study: randomised placebo-controlled double-blind comparative trial and open-label extension trial to investigate the safety and efficacy of bromocriptine in Alzheimer’s disease with presenilin 1 (PSEN1) mutations
-
Vertical Transmission of Coxsackievirus A6 with Severe Congenital Pneumonia/Sepsis
-
Development of a home-visit nursing scale for helping spousal caregivers of terminal cancer patients develop positive perspectives of their caregiving experiences: A cross-sectional study
-
Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
-
Gender with marital status, cultural differences, and vulnerability to hypertension: Findings from the national survey for noncommunicable disease risk factors and mental health using WHO STEPS in Bhutan
-
Evaluation of Kidney Histological Images Using Unsupervised Deep Learning
-
Evolutionary genetics of socioemotional behavior in humans and other mammals
-
Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis
-
Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
-
Increasing hepatitis virus screening uptake at worksites in Japan using nudge theory and full subsidies (本文)
-
Current Overview of Osteogenesis Imperfecta.
-
Pathogenic mutation of TDP-43 impairs RNA processing in a cell type-specific manner : implications for the pathogenesis of ALS/FTLD (本文)
-
Study on the control of high pathogenicity and low pathogenicity avian influenza in Vietnam [an abstract of entire text]
-
Multidisciplinary diagnostic approach for fulminant myocarditis related to coronavirus disease 2019 messenger RNA vaccines: a case report
-
Prognostication of Ovarian Function after Ovarian Torsion Using Intraoperative Indocyanine Green Angiography
-
Exploring Hidden Atrial Fibrillation in Patients with Type 2 Diabetes Mellitus Admitted to Shinshu University Hospital
-
Interventions to improve locomotive syndrome: a systematic review and meta-analysis of randomized controlled trials