Koji Nagatani

Uwajima, Japan

Last Updated: 09/26/2026

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Found 12 publications

Genetic Screening of Patients With Inherited Fanconi Syndrome.

Genetic Screening of Patients With Inherited Fanconi Syndrome.

Journal: Kidney international reports
Published: February 17, 2026

A Case of Neonatal Lupus Presenting with Fever and Rash in Early Infancy with Anti-dsDNA Antibodies, Born to an Asymptomatic Mother Negative for Anti-dsDNA Antibodies.

A Case of Neonatal Lupus Presenting with Fever and Rash in Early Infancy with Anti-dsDNA Antibodies, Born to an Asymptomatic Mother Negative for Anti-dsDNA Antibodies.

Journal: Modern rheumatology case reports
Published: February 06, 2026

Elevated salivary amylase levels in paediatric acute recurrent pancreatitis: possible involvement of CFTR mutations.

Elevated salivary amylase levels in paediatric acute recurrent pancreatitis: possible involvement of CFTR mutations.

Journal: BMJ case reports
Published: January 27, 2026

Epidemiology conduction of paediatric rheumatic diseases based on the registry database of the Pediatric Rheumatology Association of Japan.

Epidemiology conduction of paediatric rheumatic diseases based on the registry database of the Pediatric Rheumatology Association of Japan.

Journal: Modern rheumatology
Published: July 05, 2022

Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome.

Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: June 18, 2021

BCS1L mutations produce Fanconi syndrome with developmental disability.

BCS1L mutations produce Fanconi syndrome with developmental disability.

Journal: Journal of human genetics
Published: April 04, 2021

Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophy.

Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophy.

Journal: Muscle & nerve
Published: June 05, 2019

Combination therapy improves pathology indices in diffuse mesangial sclerosis.

Combination therapy improves pathology indices in diffuse mesangial sclerosis.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: October 22, 2018

Clinical spectrum of male patients with OFD1 mutations.

Clinical spectrum of male patients with OFD1 mutations.

Journal: Journal of human genetics
Published: October 01, 2018

Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.

Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.

Journal: Journal of human genetics
Published: December 04, 2017

Involvement of CD5+CD19+Cell in steroid-dependent nephrotic syndrome treated with B-cell targeting therapy.

Involvement of CD5+CD19+Cell in steroid-dependent nephrotic syndrome treated with B-cell targeting therapy.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: February 16, 2013

Life-threatening acute renal failure due to imperforate hymen in an infant.

Life-threatening acute renal failure due to imperforate hymen in an infant.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 18, 2012
Showing 1-12 of 12

Last Updated: 09/26/2026