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Kidney International Reports|September 18, 2024
Importance of <i>IFT140</i> in Patients with Polycystic Kidney Disease Without a Family HistoryTakuya Fujimaru, Takayasu Mori, Akinari Sekine, et al.
American Journal of Nephrology|August 14, 2020
Genetics May Predict Effectiveness of Tolvaptan in Autosomal Dominant Polycystic Kidney DiseaseAkinari Sekine, Junichi Hoshino, Takuya Fujimaru, et al.
Kidney International Reports|May 20, 2024
Genetic Diagnosis of Adult Hemodialysis Patients With Unknown EtiologyTakuya Fujimaru, Takayasu Mori, Motoko Chiga, et al.
Case Reports in Nephrology and Dialysis|June 1, 2018
Transcatheter Arterial Embolization Therapy for Huge Renal Cysts: Two Case ReportsNaoya Toriu, Junichi Hoshino, Saeko Kobori, et al.
CEN Case Reports|April 18, 2026
A case of giant renal angiomyolipoma and diabetic nephropathy with abnormalities in the genes TSC2 and HNF1BHisashi Sugimoto, Naoki Sawa, Yuki Oba, et al.
American Journal of Nephrology|March 2, 2019
Genotype-Clinical Correlations in Polycystic Kidney Disease with No Apparent Family HistoryAkinari Sekine, Takuya Fujimaru, Junichi Hoshino, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
<i>CFAP47</i> is a novel causative gene implicated in X-linked polycystic kidney diseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
Kidney International Reports|December 19, 2024
CFAP47 is Implicated in X-Linked Polycystic Kidney DiseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
Clinical and Experimental Nephrology|May 11, 2024
Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP)Shinya Nakatani, Haruna Kawano, Mai Sato, et al.
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