Results 241 to 250 of about 56,242 (306)

FK 506 in the management of nephrotic syndrome after renal transplantation [PDF]

, 1993
Jensen, C, Jordan, M, McCauley, J, Scantlebury, V, Shapiro, R, Starzl, TE, Vivas, C   +6 more
core  

Ciliary G-Protein Coupled Receptor Signaling in Polycystic Kidney Disease. [PDF]

Int J Mol Sci
Buqaileh R, Alshriem LA, AbouAlaiwi W.
europepmc   +1 more source

Dual-faced guardians: SGLT2 inhibitors' kidney protection and health challenges: a position statement by Kasralainy nephrology group (KANG). [PDF]

Diabetol Metab Syndr
Soliman AR, Elkhatib M, El-Khashab S, Darwish RA, Fayed A, Abdelaziz TS, Hammad H, Ahmed RM, Maamoun HA.   +8 more
europepmc   +1 more source

Functional Defects in Lysosomal Enzymes in Autosomal Dominant Polycystic Kidney Disease (ADPKD): Abnormalities in Synthesis, Molecular Processing, Polarity, and Secretion

, 1997
Patricia A. Hartz, Patricia D. Wilson
openalex   +1 more source

Identification of ETFDH gene c. 487 + 2 T > A pathogenic variant and mechanisms for polycystic kidney in neonatal onset MADD. [PDF]

Orphanet J Rare Dis
Zhang B, Zhang D, Sun F, Si X, Luan M, He R.   +5 more
europepmc   +1 more source

Estimating Lifetime Risk of Autosomal Recessive Kidney Diseases Using Population-Based Genotypic Data. [PDF]

Kidney Int Rep
Braunisch MC, Großewinkelmann CM, Menke M, Hannane N, Berutti R, Ćomić J, Günthner R, Renders L, Schmaderer C, Heemann U, Riedhammer KM, Wagner M, Hoefele J.   +12 more
europepmc   +1 more source

Collagen Type IV Variants and Kidney Cysts: Decoding the COL4A Puzzle. [PDF]

Genes (Basel)
Rigato M, Caprara C, Cabrera-Aguilar JS, Marzano N, Giuliani A, Mancini B, Gastaldon F, Ronco C, Zanella M, Zuccarello D, Corradi V.   +10 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

Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease

, 1997
Alberto Turco, Sandro Rossetti, Elena Bresin, Sabine Englisch, Stefano Corrà, Pier Franco Pignatti   +5 more
openalex   +1 more source

Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet). [PDF]

Pediatr Nephrol
van Eerde AM, Teixeira A, Galletti F, Maternik M, Capone V, Westland R, Mulder J, Halbritter J, Osterholt T, Neukel V, Weber LT, Liebau MC, Schaefer F, Kohl S.   +13 more
europepmc   +1 more source