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CEN Case Reports|April 8, 2020
Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutationsNaoya Morisada, Riku Hamada, Kenichiro Miura, et al.
Human Genome Variation|March 29, 2024
End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapyHiroaki Hanafusa, Hiroshi Yamaguchi, Naoya Morisada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 9, 2026
Burosumab treatment for FGF23-related hypophosphatemia in a two-year-old girl with McCune-Albright syndromeTomoki Saito, Kana Hiromoto, Naoya Morisada, et al.
Internal Medicine (Tokyo, Japan)|April 3, 2020
Medullary Cystic Kidney Disease and Focal Segmental Glomerulosclerosis Caused by a Compound Heterozygous Mutation in TTC21BSatoshi Hibino, Naoya Morisada, Asami Takeda, et al.
Case Reports in Nephrology and Dialysis|May 27, 2016
Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2Yoichi Iwafuchi, Tetsuo Morioka, Takashi Morita, et al.
Human Genome Variation|September 23, 2016
A 12p13 GRIN2B deletion is associated with developmental delay and macrocephalyNaoya Morisada, Tomoaki Ioroi, Mariko Taniguchi-Ikeda, et al.
Human Genome Variation|September 1, 2020
A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathyAyumi Shishido, Naoya Morisada, Kenta Tominaga, et al.
CEN Case Reports|October 13, 2020
A woman with a dual genetic diagnosis of autosomal dominant tubulointerstitial kidney disease and KBG syndromeYu Tanaka, Naoya Morisada, Tomohiro Suzuki, et al.
The Kobe Journal of Medical Sciences|June 13, 2013
SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutationsShingo Ishimori, Hiroshi Kaito, Natsuki Matsunoshita, et al.
CEN Case Reports|September 21, 2019
A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney diseaseKen Saida, Koichi Kamei, Naoya Morisada, et al.
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