Naoya Morisada

Chuo, 6500047, Japan

Last Updated: 09/26/2026

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Found 135 publications

Clinical and genetic characteristics of hypoparathyroidism, deafness, and renal dysplasia syndrome in a chronic kidney disease cohort.

Clinical and genetic characteristics of hypoparathyroidism, deafness, and renal dysplasia syndrome in a chronic kidney disease cohort.

Journal: Pediatric nephrology (Berlin, Germany)

Published: May 30, 2026

Serial Kidney Biopsies Reveal Progressive Pathology in Townes-Brocks Syndrome: A Case Report.

Serial Kidney Biopsies Reveal Progressive Pathology in Townes-Brocks Syndrome: A Case Report.

Journal: Kidney medicine

Published: April 24, 2026

Functional characterization of a novel ZIP8 variant causing impaired manganese homeostasis and congenital disorders of glycosylation.

Functional characterization of a novel ZIP8 variant causing impaired manganese homeostasis and congenital disorders of glycosylation.

Journal: Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine

Published: April 17, 2026

A deep intronic IFT172 variant causing pseudoexon inclusion identified by whole-genome sequencing in nephronophthisis.

A deep intronic IFT172 variant causing pseudoexon inclusion identified by whole-genome sequencing in nephronophthisis.

Journal: CEN case reports

Published: March 15, 2026

A Novel MAF Variant Causing Aymé-Gripp Syndrome With Transient Anemia.

A Novel MAF Variant Causing Aymé-Gripp Syndrome With Transient Anemia.

Journal: Congenital anomalies

Published: October 02, 2025

Early-onset kidney failure in a girl with autosomal dominant tubulointerstitial kidney disease due to a de novo UMOD variant.

Early-onset kidney failure in a girl with autosomal dominant tubulointerstitial kidney disease due to a de novo UMOD variant.

Journal: CEN case reports

Published: September 14, 2025

A novel PKD1 variant in a patient with very-early-onset ADPKD.

A novel PKD1 variant in a patient with very-early-onset ADPKD.

Journal: Human genome variation

Published: July 29, 2025

Burosumab treatment for FGF23-related hypophosphatemia in a two-year-old girl with McCune-Albright syndrome.

Burosumab treatment for FGF23-related hypophosphatemia in a two-year-old girl with McCune-Albright syndrome.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: July 21, 2025

Cystic Fibrosis Detected on Abdominal Imaging: Pancreatic Atrophy With Fat Deposition in an 8-Year-Old Girl.

Cystic Fibrosis Detected on Abdominal Imaging: Pancreatic Atrophy With Fat Deposition in an 8-Year-Old Girl.

Journal: Journal of paediatrics and child health

Published: July 19, 2025

Hepatic Cyst Infection in a Hemodialysis Patient with Autosomal Dominant Polycystic Kidney Disease Complicated by Non-symptomatic Caroli Disease.

Hepatic Cyst Infection in a Hemodialysis Patient with Autosomal Dominant Polycystic Kidney Disease Complicated by Non-symptomatic Caroli Disease.

Journal: Internal medicine (Tokyo, Japan)

Published: July 16, 2025

Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation.

Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation.

Journal: Internal medicine (Tokyo, Japan)

Published: June 18, 2025

Clinical characteristics of patients with SALL1-related disorder.

Clinical characteristics of patients with SALL1-related disorder.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 25, 2025

Showing 1-12 of 135

Last Updated: 09/26/2026