A mild case of Cockayne syndrome (日本研究皮膚科学会第41回年次学術大会・総会 2016)
A child case of xeroderma pigmentosum complementation group C (4th Eastern Asia Dermatology Congress 2016)
当院で実施した色素性乾皮症(XP)の遺伝子変異検査について (第65回日本医学検査学会 2016)
Xeroderma pigmentosum (XP) genetic screening in Kobe University Hospital (第32回世界医学検査学会 2016)
Xerodermapigmentosum as the model of photoaging-The present features of XP in Japan (第17回光老化研究会 2016)
The effects of Cxcl1 antagonist on UVB-induced skin inflammation in Xeroderma pigmentosum type A deficient mice (16th World Congress on Cancers of the Skin 2016)
Usefulness of flow-cytometry based nucleotide excision repair assay for diagnosis of xeroderma pigmentosum variant type (日本研究皮膚科学会第40回年次学術大会・総会 2015)
New-Onset Diabetes After Transplantation in a Pediatric Patient with Congenital Anomalies of the Kidney and Urinary Tract: The Role of Hepatocyte Nuclear Factor 1β. (Kidney Week 2015 2015)
Genital Organ Anomalies in Female Pediatric Patients with End-Stage Renal Disease. (Kidney Week 2015 2015)
A Family Case of Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome with a Novel Mutation of GATA3. (Kidney Week 2015 2015)