Results 121 to 130 of about 16,655 (259)

Generation of an induced pluripotent stem cell line (ZSPHARi002-A) from a patient with autosomal dominant polycystic kidney disease carrying a heterozygous PKD1 mutation

Stem Cell Research
Autosomal dominant polycystic kidney disease (ADPKD), a single-gene-inherited kidney disease, is a common cause of end-stage kidney disease (ESKD). The PKD1 gene mutation is the most common cause of ADPKD, accounting for approximately 78% of cases. ADPKD
Yeye Zhang, Ye Chen, Jun Fan, Guangzhao Lu, Qianzhou Lv, Donghui Lao, Xiaoyu Li   +6 more
doaj   +1 more source

End-stage renal disease in autosomal dominant polycystic kidney disease: a comparison of dialysis-related utilization and costs with other chronic kidney diseases

ClinicoEconomics and Outcomes Research, 2015
Steven M Brunelli,1 Christopher M Blanchette,2,3 Ami J Claxton,1 Debosree Roy,2 Sandro Rossetti,3 Benjamin Gutierrez31DaVita Clinical Research, Minneapolis, MN, USA; 2University of North Carolina, Charlotte, NC, USA; 3Otsuka America Pharmaceutical, Inc.,
Brunelli SM, Blanchette CM, Claxton AJ, Roy D, Rossetti S, Gutierrez B   +5 more
doaj  

Type of PKD1 Mutation Influences Renal Outcome in ADPKD [PDF]

, 2013
Émilie Cornec-Le Gall, Marie‐Pierre Audrézet, Jian‐Min Chen, Maryvonne Hourmant, Marie-Pascale Morin, Régine Perrichot, Christophe Charasse, B. Whebe, E. Renaudineau, Philippe Jousset, Marie-Paule Guillodo, Anne Grall-Jézéquel, Philippe Saliou, Claude Férec, Yannick Le Meur   +14 more
openalex   +1 more source

Diagnosis of cyst infection in patients with autosomal dominant polycystic kidney disease: attributes and limitations of the current modalities [PDF]

, 2017
Cyst infection is a diagnostic challenge in patients with autosomal dominant polycystic kidney disease (ADPKD) because of the lack of specific manifestations and limitations of conventional imaging procedures.
Annet, Laurence, Devuyst, Olivier, Hassoun, Ziad, Jouret, François, Kanaan, Nada, Lhommel, Renaud, Pirson, Yves   +6 more
core  

#5783 REAL-LIFE USE OF TOLVAPTAN IN ADPKD: A RETROSPECTIVE ANALYSIS OF A LARGE CANADIAN COHORT [PDF]

, 2023
Luca Calvaruso, Kevin Yau, Pedram Akbari, Fatemeh Nasri, Shirley Xiaoxuan Deng, Saima Khowaja, Ning He, Amirreza Haghighi, Korosh Khalili, York Pei   +9 more
openalex   +1 more source

Estudo de ligação molecular do rim policístico do adulto (ADPKD) com primers do cromossomo 16 (PKD1) e 4 (PKD2). [PDF]

, 1998
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Ferreira, Fernando Romariz
core  

Decision letter for "Characterization of Primary Cilia in Osteoblasts Isolated from ADPKD and CKD Patients"

, 2020

openalex   +1 more source

SO054CYTOKINE TWEAK AS AN INTERMEDIARY IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD) [PDF]

, 2016
Olaya Lamas-González, Ana B. Sanz, María Dolores Sánchez-Niño, Ana Barcia de la Iglesia, Adrian Cordido Eijo, Patricia Viaño, Alberto Ortíz, Miguel A. García-González   +7 more
openalex   +1 more source

No relationship between total kindey volume class or genotype and 24h blood pressure control in adult ADPKD patients [PDF]

, 2018
Allamani, Mandelina, Devos, Hannes, Schots, Lisa, Tonnelier, Annelies, Van der Niepen, Patricia   +4 more
core   +2 more sources

ADPKD

, 2019
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inheritable kidney disease. It is characterized by progressive kidney cyst formation throughout life, which can lead to kidney failure. However, only 70% of patients will develop kidney failure and the age at which patients develop kidney failure shows a large interindividual ...
openaire   +1 more source