Zobrazeno 1 - 10
of 7 942
pro vyhledávání: '"Autosomal dominant polycystic kidney"'
Autor:
Shunsuke Takayanagi, Keita P. Mori, Shigeto Kubo, Natsumi Mishima, Tomoka Watanabe, Mea Asou, Misaki Taniguchi, Miho Miyauchi, Yoshiaki Higashi, Takaya Handa, Tomomi Endo, Takeshi Matsubara, Tatsuo Tsukamoto
Publikováno v:
Renal Replacement Therapy, Vol 10, Iss 1, Pp 1-15 (2024)
Abstract Background In patients with autosomal dominant polycystic kidney disease (ADPKD), renal and hepatic cystic infections are common complications, sometimes frequent and refractory. Hemorrhagic complications are often present in these cases. Ow
Externí odkaz:
https://doaj.org/article/ca75a2288a57420e8839b7ee58e17a3d
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-4 (2024)
Abstract Background Tuberous sclerosis complex (TSC) is a multisystem genetic disorder characterized by the development of benign tumors in various organs, including the brain, kidneys, heart, lungs, skin, and eyes. Herein, an infant who was followed
Externí odkaz:
https://doaj.org/article/3711a030592f420db6ed50bb0ca784dd
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract This retrospective study investigated the incidence, medication use, and outcomes in pediatric autosomal-dominant polycystic kidney disease (ADPKD) using Taiwan's National Health Insurance Research Database (NHIRD). A 1:4 matched control gro
Externí odkaz:
https://doaj.org/article/4c17ec6ae8e74c508b73c4cd9636d9d1
Autor:
Liliana Italia De Rosa, Martina Catania, Francesca Tunesi, Marta Vespa, Romina Bucci, Kristiana Kola, Giuseppe Vezzoli, Maria Teresa Sciarrone Alibrandi
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 116-121 (2024)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease and the 4th leading cause of renal replacement therapy in the world. ADPKD is a systemic disorder as cysts may develop in several organs. Liv
Externí odkaz:
https://doaj.org/article/377331f6c1344cb5b74345e91fce0f8c
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 104-109 (2024)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, which is mainly caused by pathogenic variants in two particular genes: PKD1 and PKD2. ADPKD caused by variants in other genes (GANAB or I
Externí odkaz:
https://doaj.org/article/1e348d8228474ea885b6928b6d0fa88b
Autor:
Marie C. Hogan, Christopher J. Ward
Publikováno v:
Extracellular Vesicle, Vol 4, Iss , Pp 100048- (2024)
Autosomal dominant polycystic kidney (ADPKD) disease is the commonest genetic cause of kidney failure (affecting 1:800 individuals) and is due to heterozygous germline mutations in either of two genes, PKD1 and PKD2. Homozygous germline mutations in
Externí odkaz:
https://doaj.org/article/5bb8d547eb204f1ebab4f4f9be7b7af8
Publikováno v:
Renal Failure, Vol 46, Iss 2 (2024)
Background and hypothesis Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a major genetic contributor to end-stage kidney disease (ESKD). Current evidence on tolvaptan primarily focuses on slowing estimated glomerular filtration rate (eGFR) d
Externí odkaz:
https://doaj.org/article/5db091d713cd444eba556294f6164013
Autor:
Daniela Maria Allmer, Diego Parada Rodriguez, Christof Aigner, Franco Laccone, Mato Nagel, Sylvia Metz-Schimmerl, Gere Sunder-Plassmann
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Autosomal-dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease and fourth leading cause for renal replacement therapy worldwide. Disease progression is tightly linked to genotype, however, factors like genetic modifi
Externí odkaz:
https://doaj.org/article/4e0c897339694106b97ae9ccbff20d3a
Publikováno v:
Vascular Specialist International, Vol 40 (2024)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary kidney diseases. In addition to renal involvement, vascular complications including intracranial arterial, aortic aneurysms and dissections are common in these
Externí odkaz:
https://doaj.org/article/1644fe7d53b14077b0a65b0f49a689ff
Publikováno v:
Zeitschrift für Medizinische Physik, Vol 34, Iss 2, Pp 330-342 (2024)
An accurate prognosis of renal function decline in Autosomal Dominant Polycystic Kidney Disease (ADPKD) is crucial for early intervention. Current biomarkers used are height-adjusted total kidney volume (HtTKV), estimated glomerular filtration rate (
Externí odkaz:
https://doaj.org/article/e2beb9d4004049fc8e788818a1a8d872