Results 131 to 140 of about 114,162 (186)

Tratamiento quirúrgico de la enfermedad poliquística hepática autosómica dominante, serie de casos

Revista Colombiana de Cirugía
Nowadays liver and biliary tract surgery are the most commonly performed procedures worldwide; refinement in surgical techniques, anesthetic care and liver transplantation have revolutionized the treatment of liver diseases that were previously incurable.
Andrés Ayala, Juan Carlos Aguilar, Fernando Jiménez, Frans Serpa   +3 more
doaj  

Screening for intracranial aneurysms in ADPKD [PDF]

, 2009
Ong, A.C.M.
core   +1 more source

Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment

International Journal of Nephrology and Renovascular Disease, 2010
Christian R Halvorson1, Matthew S Bremmer1, Stephen C Jacobs11Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, USAAbstract: Both autosomal dominant and recessive polycystic kidney disease are conditions with severe ...
Christian R Halvorson, Matthew S Bremmer, Stephen C Jacobs   +2 more
doaj  

Polycystin 2 is increased in disease to protect against stress-induced cell death [PDF]

, 2020
Brill, Allison L., Campbell, Stuart G., Cantley, Lloyd G., Chung, Hee Jung, Ehrlich, Barbara E., Fischer, Tom T., Johnson, Eric K., Marlier, Arnaud, Moeckel, Gilbert, Nerbonne, Jeanne M., Robert, Marie E., Sewanan, Lorenzo R., Walters, Jennifer M., Wilson, Parker C.   +13 more
core   +1 more source

A case report of atypical autosomal dominant polycystic kidney disease presenting as glomerulocystic kidney superimposed with thin basement membrane nephropathy. [PDF]

BMC Nephrol
Wang W, Chen L, Ding F, Li X.
europepmc   +1 more source

Pneumatocele Development after Deceased-Donor Liver Transplantation for Multiple Hepatic Cysts due to Autosomal Dominant Polycystic Kidney Disease: A Case Report. [PDF]

Surg Case Rep
Yoshiyama A, Kawashima M, Nagata S, Fukushima T, Aze K, Cong Y, Nakao K, Nakao M, Toyokawa G, Konoeda C, Hasegawa K, Sato M.   +11 more
europepmc   +1 more source

A Rare Coexisting Presentation of Autosomal Dominant Polycystic Kidney Disease With Rapid Deterioration of Renal Function and Neurofibromatosis Type 1. [PDF]

Cureus
Noishiki H, Yamauchi H, Komaki K, Kusaba T, Tamagaki K.   +4 more
europepmc   +1 more source

The prospect of novel orphan therapeutic protocol for TSC2/PKD1 contiguous gene syndrome: a case report. [PDF]

BMC Nephrol
Agavriloaei BD, Costache RC, Babici RG, Racoviță S, Dodi G, Covic AC, Mititiuc IL.   +6 more
europepmc   +1 more source

Antibiotic-driven pathogen replacement events in a kidney transplant recipient with ADPKD: a case report. [PDF]

BMC Infect Dis
Yan Z, Wang Y, Zeng W, Hui J, Yang B, Xu J, Miao Y, Xia R.   +7 more
europepmc   +1 more source

The pathophysiological significance between autosomal dominant polycystic kidney disease and neutrophil gelatinase-associated lipocalin. [PDF]

Kidney Res Clin Pract
Devapatla P, Jeng WY, Chiu WT, Hsieh-Li HM.   +3 more
europepmc   +1 more source