Hirofumi Watanabe
Niigata, 9518510, Japan
Last Updated: 09/26/2026
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Found 19 publications
An extrarenal renin-producing tumor associated with a 3 cm mature cystic teratoma.
Journal: JCEM case reports
Published: February 19, 2026
Shared T -Cell Receptor Repertoire in the Tonsils of Patients with IgA Nephropathy.
Journal: Kidney360
Published: October 18, 2025
Dual Renal and Cardiac Phenotypes Associated with Rare Variants Inherited from Both Parents.
Journal: Internal medicine (Tokyo, Japan)
Published: October 01, 2025
Genetic and protein structure prediction analyses identify a rare pathogenic PKD1 variant causing autosomal dominant polycystic kidney disease.
Journal: CEN case reports
Published: December 10, 2024
Ectopic Production of Parathyroid Hormone and Production of Parathyroid Hormone-related Protein in Dedifferentiated Endometrial Carcinoma Induced Severe Hypercalcemia.
Journal: Internal medicine (Tokyo, Japan)
Published: September 04, 2024
CD38 ligation in sepsis promotes nicotinamide phosphoribosyltransferase-mediated IL-6 production in kidney stromal cells.
Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: March 21, 2024
Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP).
Journal: Clinical and experimental nephrology
Published: February 19, 2024
Nephrotic syndrome induces the upregulation of cell proliferation-related genes in tubular cells in mice.
Journal: Clinical and experimental nephrology
Published: December 06, 2023
Defective C3d caused by C3 p.W1034R in inherited atypical hemolytic uremic syndrome.
Journal: Molecular genetics & genomic medicine
Published: April 27, 2023
Assessing fluid volume and determining outcomes of acute heart failure using plasma human atrial natriuretic peptide.
Journal: Clinical and experimental nephrology
Published: December 08, 2022
Pathogenic variants of Alport syndrome and monogenic diabetes identified by exome sequencing in a family.
Journal: Human genome variation
Published: November 14, 2022
Last Updated: 09/26/2026