Results 111 to 120 of about 16,655 (259)

Overview of ADPKD in Pregnancy

Kidney International Reports
Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder that often affects patients in their third to fifth decades of life and is characterized by kidney cysts, chronic kidney disease (CKD), hypertension, and hepatic cysts. The development of clinical symptoms often coincides with childbearing years. Consequently, there are several
Ruth E. Campbell, Charles L. Edelstein, Michel Chonchol   +2 more
openaire   +3 more sources

ADPedKD: A Global Online Platform on the Management of Children With ADPKD [PDF]

, 2019
Stéphanie De Rechter, Detlef Böckenhauer, Lisa M. Guay‐Woodford, Isaac Liu, Andrew J. Mallett, Neveen A. Soliman, Lucimary C. Sylvestre, Franz Schaefer, Max C. Liebau, Djalila Mekahli, Piotr Adamczyk, Nurver Akıncı, Harika Alpay, Carmen Ardelean, Nadia Ayasreh, Zeki Aydın, A. Bael, Véronique Baudouin, US Bayrakci, A Bensman, Hanna Bialkevich, A. Biebuyck, Omar Bjanid, Olivia Boyer, A. Bryłka, Salim Çalışkan, Alexandra Cambier, A. Camelio, Vincenza Carbone, Marina Charbit, Benedetta Chiodini, A. Chirita, Neslihan Çiçek, Rimantė Čerkauskienė, Laure Collard, Magda S. da Conceição, Ileana Constantinescu, Anne‐Laure Couderc, B. Crapella, Mirjana Cvetković, B. Dima, F. Diomeda, M. Docx, Nancy C. Dolan, Claire Dossier, Dorota Drożdż, Jens Drube, Oliver Dunand, Dušan Paripović, Loai Eid, Francesco Emma, M. Espino Hernández, Marc Fila, Mónica Furlano, Mihai Gafencu, M.S. Ghuysen, Mauro Giani, Mario Giordano, I. Girisgen, Nathalie Godefroid, Astrid Godron-Dubrasquet, I. Gojkovic, Elizabeth M. Gonzalez, İbrahim Gökçe, Jaap W. Groothoff, Stefano Guarino, Anne Guffens, P. R. Hansen, Jérôme Harambat, Sara Kretzschmar Haumann, Guanheng He, Laurence Heidet, Remon Helmy, F. Hémery, Nakysa Hooman, Brigitte Llanas, Augustina Jankauskienė, Peter Janssens, S. Karamaria, I. A. Kazyra, Julian Koenig, Saoussen Krid, Penny Krug, V. Kwon, Angela La Manna, V. Leroy, Mieczysław Litwin, Jacques Lombet, Germana Longo, Adrian Lungu, Amali Mallawaarachchi, Anna Marín, P. Marzuillo, Laura Massella, Antonio Mastrangelo, Helen McCarthy, Monika Miklaszewska, Anna Moczulska, Giovanni Montini, Aurelia Morawiec‐Knysak   +99 more
openalex   +1 more source

Phosphorylation, protein kinases and ADPKD

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2011
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disease characterized by renal cyst formation and caused by mutations in the PKD1 and PKD2 genes, which encode polycystin-1(PC-1) and -2 (PC-2) proteins, respectively. PC-1 is a large plasma membrane receptor involved in the regulation of several biological functions and signaling ...
openaire   +2 more sources

Fluoroquinolone-Associated Tendinopathy: An Important Complication of Cyst Infection Management in Polycystic Kidney Disease

International Medical Case Reports Journal
Miwa Kaneko, Tetsu Akimoto, Daisuke Nagata Division of Nephrology, Department of Internal Medicine, Jichi Medical University, Tochigi, JapanCorrespondence: Tetsu Akimoto, Division of Nephrology, Department of Internal Medicine, Jichi Medical University ...
Kaneko M, Akimoto T, Nagata D
doaj  

A rare cardiac manifestation in autosomal-dominant polycystic kidney disease

Saudi Journal of Kidney Diseases and Transplantation, 2017
Autosomal-dominant polycystic kidney disease (ADPKD) is a systemic disorder associated with various extrarenal complications. There is little information regarding the occurrence and distribution of cardiovascular abnormalities during the course of ADPKD.
Meriam Hajji, Hela Jebali, Khadija Mzoughi, Ihssen Zairi, Rania Kheder, Lilia Ben Fatma, Lamia Rais, Rokaya Kadouri, Sinda Kraiem, Wided Smaoui, Madiha Krid, Soumaya Beji, Karim Zouaghi   +12 more
doaj   +1 more source

Profiling of miRNAs and target genes related to cystogenesis in ADPKD mouse models [PDF]

, 2017
Yu Mi Woo, Do Yeon Kim, Nam Jin Koo, Yong‐Min Kim, Sun‐Young Lee, Je Yeong Ko, Yubin Shin, Bo Hye Kim, Hyowon Mun, Seonju Choi, Eun Ji Lee, Jeong-Oh Shin, Eun Young Park, Jinwoong Bok, Jong Hoon Park   +14 more
openalex   +1 more source

Immediate drop of urine osmolality upon tolvaptan initiation predicts impact on renal prognosis in patients with ADPKD [PDF]

, 2023
Taro Akihisa, Hiroshi Kataoka, Shiho Makabe, Shun Manabe, Rie Yoshida, Yusuke Ushio, Masayo Sato, Aiji Yajima, Norio Hanafusa, Ken Tsuchiya, Kosaku Nitta, Junichi Hoshino, Toshio Mochizuki   +12 more
openalex   +1 more source

The Relationship of Renalase with Diurnal Blood Pressure Rhythm, Left Ventricular Mass Index and Carotid Intima–media Thickness in Autosomal Dominant Polycystic Kidney Disease

Saudi Journal of Kidney Diseases and Transplantation
This study investigated the relationship between renalase and diurnal blood pressure (BP) rhythm, left ventricular mass index (LVMI) and carotid intima-media thickness (IMT) in autosomal dominant polycstic kidney disease (ADPKD) patients.
Veysel Erol, Mevlüt Çeri, Mehmet Mert, Oğuz Kılıç, İsmail Doğu Kılıç, İbrahim Hasbey, Nuran Sabır, Süleyman Demir, Ayşen Kardeşler, Belda Dursun   +9 more
doaj   +1 more source

ISEV2025 Abstract Book

Journal of Extracellular Vesicles, Volume 14, Issue S1, October 2025.
wiley   +1 more source

Unusual familial cystic kidney disease: combining fine radiologic and genetic evaluation to solve the case

BMC Nephrology
Background Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent hereditary kidney disease, characterized by enlarged kidneys with numerous cysts, high blood pressure, and a variety of extrarenal complications.
Sylvain Bodard, Rim Nabbout, Olivier Hélénon, Bertrand Knebelmann   +3 more
doaj   +1 more source