Results 171 to 180 of about 98,685 (336)

Knowledge and Adherence to Lifestyle Habits to Prevent Complications Associated With Immunosuppression in Kidney Transplant Recipients: A Single‐Center Survey

Transplant Infectious Disease, EarlyView.
We performed a survey on lifestyle habits aimed at reducing the risks associated with immunosuppression in kidney transplant recipients. We found gaps in dental hygiene, sunscreen use, vaccination, and consumption of high‐risk foods. Cultural and economic factors influenced adherence.
Tamara Ruiz‐Merlo, Isabel Rodríguez‐Goncer, Francisco López‐Medrano, Natalia Polanco, Esther González, Hernando Trujillo, Marina Fayos, Natalia Redondo, Rafael San Juan, Amado Andrés, José María Aguado, Mario Fernández‐Ruiz   +11 more
wiley   +1 more source

Autosomal dominant polycystic kidney disease. [PDF]

, 1993
John C. Lieske, F. Gary Toback
openalex   +1 more source

A Novel Inhibitor of Methyltransferase SMYD2, AZ505 Protects Against Peritoneal Fibrosis in Mice

Clinical and Experimental Pharmacology and Physiology, Volume 52, Issue 7, July 2025.
AZ505, a highly selective inhibitor of SMYD2, may exhibit an antifibrotic effect in peritoneal fibrosis. ABSTRACT AZ505, a highly selective inhibitor of SMYD2, exhibits an antifibrotic effect in renal fibrosis. Its effect on peritoneal fibrosis remains unexplored.
Taijing Xu, Binbin Cui, Feng Liu, Mengjun Liu, Xiying Hou, Xuan Hong, Hualin Qi   +6 more
wiley   +1 more source

Rare Combination of Phenotypes of Karyomegalic Interstitial Nephritis and Autosomal Recessive Polycystic Kidney Disease in an Omani Child

Oman Medical Journal
Autosomal recessive polycystic kidney disease is one of the most prevalent inherited cystic kidney diseases in infants and children, common in highly consanguineous societies such as Oman. Karyomegalic interstitial nephritis is a rare cause of hereditary
Intisar Al Alawi, Maryam Al Shehhi, Naifain Al Kalbani, Aliya Al Hosni, Ashwaq Al Mimani, Issa Al Salmi, John A. Sayer   +6 more
doaj   +1 more source

Prenatal diagnosis by ultrasound in pregnancies at risk for autosomal recessive polycystic kidney disease [PDF]

, 1990
A. Reuss, J. W. Wladimiroff, P. A. Stewart, Martinus F. Niermeijer   +3 more
openalex   +1 more source

The Vertebrate Breed Ontology: Toward Effective Breed Data Standardization

Journal of Veterinary Internal Medicine, Volume 39, Issue 4, July/August 2025.
ABSTRACT Background Limited universally‐adopted data standards in veterinary medicine hinder data interoperability and therefore integration and comparison; this ultimately impedes the application of existing information‐based tools to support advancement in diagnostics, treatments, and precision medicine.
Kathleen R. Mullen, Imke Tammen, Nicolas A. Matentzoglu, Marius Mather, James P. Balhoff, Elizabeth Esdaile, Gregoire Leroy, Carissa A. Park, Halie M. Rando, Nadia T. Saklou, Tracy L. Webb, Nicole A. Vasilevsky, Christopher J. Mungall, Melissa A. Haendel, Frank W. Nicholas, Sabrina Toro   +15 more
wiley   +1 more source

NOTES ON THE POLYCYSTIC KIDNEY DISEASE IN THE GOLDFISH, WITH DESCRIPTION OF SOME OF THE ENDOCRINE GLANDS

, 1963
Yoshiharu Honma
openalex   +2 more sources

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. [PDF]

, 1990
M.H. Breuning, F.G.M. Snijdewint, Johannes G. Dauwerse, Jasper J. Saris, Egbert Bakker, P. Pearson, Gjb Vanommen   +6 more
openalex   +1 more source

Apoptosis Inhibitor of Macrophages in Cats: A Potential Link Between an Exon 3 Variant Allele and Progression of Naturally Occurring Chronic Kidney Disease

Journal of Veterinary Internal Medicine, Volume 39, Issue 4, July/August 2025.
ABSTRACT Background The protein apoptosis inhibitor of macrophages (AIM) is involved in kidney repair. An AIM (fAIM) genetic variant in cats resulting in a domain duplication might abrogate fAIM's protective effect on kidney function. Objectives To confirm that the domain duplication previously described in fAIM results from an exon duplication at the ...
Gabriela C. L. Evangelista, Julianne K. Hwang, Liam E. Broughton‐Neiswanger, Emily C. Carlo Reis, Michael H. Court, Katrina A. Mealey, Nicolas F. Villarino   +6 more
wiley   +1 more source

Intrafamilial Variability of ADPKD

Kidney International Reports, 2019
Introduction: Discordance in kidney disease severity between affected relatives is a recognized feature of autosomal dominant polycystic kidney disease (ADPKD). Here, we report a systematic study of a large cohort of families to define the prevalence and
Matthew B. Lanktree, Elsa Guiard, Weili Li, Pedram Akbari, Amirreza Haghighi, Ioan-Andrei Iliuta, Belili Shi, Chen Chen, Ning He, Xuewen Song, Peter J. Margetts, Alistair J. Ingram, Korosh Khalili, Andrew D. Paterson, York Pei   +14 more
doaj