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Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2017-09, Vol.20 (5), p.764-771

2017

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IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation

Journal of clinical immunology, 2021-01, Vol.41 (1), p.125-135

2021

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A case of pulmonary pleomorphic carcinoma difficult to distinguish from pulmonary hematoma

The Journal of the Japanese Association for Chest Surgery, 2022/09/15, Vol.36(6), pp.688-693

2022

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A case of alpha-fetoprotein-positive thymic small cell carcinoma: a case report

Surgical case reports, 2023-09, Vol.9 (1), p.165-165, Article 165

2023

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Factors Associated with Overlap between Functional Dyspepsia and Nonerosive Reflux Disease in Endoscopy-based Helicobacter pylori-uninfected Japanese Health Checkup Participants: A Prospective, Multicenter Cross-sectional Study

Internal Medicine, 2024/03/01, Vol.63(5), pp.639-647

2024

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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings

Journal of clinical immunology, 2021-07, Vol.41 (5), p.975-986

2021

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Human granulocytes undergo cell death via autophagy

Cell death discovery, 2018-12, Vol.4 (1), p.111-6, Article 111

2018

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Perceived Parenting Mediates Serotonin Transporter Gene (5-HTTLPR) and Neural System Function during Facial Recognition: A Pilot Study

PloS one, 2015-09, Vol.10 (9), p.e0134685-e0134685

2015

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Prevalence of and risk factors for non-alcoholic fatty liver disease in a non-obese Japanese population, 2011–2012

Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

Human gain-of-function STAT1 mutation disturbs IL-17 immunity in mice

NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations

The Impact of PNPLA3 rs738409 Genetic Polymorphism and Weight Gain ≥10 kg after Age 20 on Non-Alcoholic Fatty Liver Disease in Non-Obese Japanese Individuals

Impact of graft-versus-host disease on the clinical outcome of allogeneic hematopoietic stem cell transplantation for non-malignant diseases

Downregulation of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in a co-culture system with human stimulated X-linked CGD neutrophils

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

Bone marrow transplantation from a human leukocyte antigen-mismatched unrelated donor in a case with C1q deficiency associated with refractory systemic lupus erythematosus

Molecular mechanism and structural basis of gain-of-function of STAT1 caused by pathogenic R274Q mutation

Effects of idursulfase enzyme replacement therapy for Mucopolysaccharidosis type II when started in early infancy: Comparison in two siblings

Prospective validation of the provisional entity of refractory cytopenia of childhood, proposed by the World Health Organization

Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations

Phosphatase and tensin homolog ( PTEN ) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency

Examination time as a quality indicator of screening upper gastrointestinal endoscopy for asymptomatic examinees

NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia

Characteristics of gastric cancer in negative test of serum anti-Helicobacter pylori antibody and pepsinogen test: a multicenter study

IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation

A case of pulmonary pleomorphic carcinoma difficult to distinguish from pulmonary hematoma

A case of alpha-fetoprotein-positive thymic small cell carcinoma: a case report

Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

Factors Associated with Overlap between Functional Dyspepsia and Nonerosive Reflux Disease in Endoscopy-based Helicobacter pylori-uninfected Japanese Health Checkup Participants: A Prospective, Multicenter Cross-sectional Study

Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings

Human granulocytes undergo cell death via autophagy

Perceived Parenting Mediates Serotonin Transporter Gene (5-HTTLPR) and Neural System Function during Facial Recognition: A Pilot Study

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