Taketsugu Hama

Wakayama, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 20 publications

A case of membranous nephropathy secondary to asymptomatic Graves' disease.

A case of membranous nephropathy secondary to asymptomatic Graves' disease.

Journal: CEN case reports

Published: August 02, 2021

A digest from evidence-based Clinical Practice Guideline for Polycystic Kidney Disease 2020.

A digest from evidence-based Clinical Practice Guideline for Polycystic Kidney Disease 2020.

Journal: Clinical and experimental nephrology

Published: June 09, 2021

DNA damage is overcome by TRIP13 overexpression during cisplatin nephrotoxicity.

DNA damage is overcome by TRIP13 overexpression during cisplatin nephrotoxicity.

Journal: JCI insight

Published: April 13, 2020

Crescentic IgA nephropathy in children.

Crescentic IgA nephropathy in children.

Journal: Pediatric nephrology (Berlin, Germany)

Published: July 30, 2019

Serum high mobility group box protein 1 (HMGB1) levels reflect clinical features of childhood hemophagocytic lymphohistiocytosis.

Serum high mobility group box protein 1 (HMGB1) levels reflect clinical features of childhood hemophagocytic lymphohistiocytosis.

Journal: Journal of blood medicine

Published: May 17, 2019

Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial).

Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial).

Journal: BMC nephrology

Published: June 21, 2018

Serine Protease Inhibitor Kazal Type I (SPINK1) Mutation: A Risk Factor for Early-onset Chronic Pancreatitis?

Serine Protease Inhibitor Kazal Type I (SPINK1) Mutation: A Risk Factor for Early-onset Chronic Pancreatitis?

Journal: Journal of pediatric gastroenterology and nutrition

Published: May 11, 2018

A review of clinical characteristics and genetic backgrounds in Alport syndrome.

A review of clinical characteristics and genetic backgrounds in Alport syndrome.

Journal: Clinical and experimental nephrology

Published: April 12, 2018

Aberrant Smad3 phosphoisoforms in cyst-lining epithelial cells in the cpk mouse, a model of autosomal recessive polycystic kidney disease.

Aberrant Smad3 phosphoisoforms in cyst-lining epithelial cells in the cpk mouse, a model of autosomal recessive polycystic kidney disease.

Journal: American journal of physiology. Renal physiology

Published: December 27, 2016

IgA nephropathy with presentation of nephrotic syndrome at onset in children.

IgA nephropathy with presentation of nephrotic syndrome at onset in children.

Journal: Pediatric nephrology (Berlin, Germany)

Published: July 21, 2016

Heterotrimeric G protein signaling in polycystic kidney disease.

Heterotrimeric G protein signaling in polycystic kidney disease.

Journal: Physiological genomics

Published: May 21, 2016

TRIP13-deficient tubular epithelial cells are susceptible to apoptosis following acute kidney injury.

TRIP13-deficient tubular epithelial cells are susceptible to apoptosis following acute kidney injury.

Journal: Scientific reports

Published: February 01, 2016

Showing 1-12 of 20

Last Updated: 09/26/2026