Results 381 to 390 of about 10,805,577 (430)

Deep learning-based histopathological assessment of tubulo-interstitial injury in chronic kidney diseases. [PDF]

Commun Med (Lond)
Suzuki N, Kojima K, Malvica S, Yamasaki K, Chikamatsu Y, Oe Y, Nagasawa T, Kondo E, Sanada S, Aiba S, Sato H, Miyazaki M, Ito S, Sato M, Tanaka T, Kinoshita K, Asano Y, Rosenberg AZ, Okamoto K, Shido K.   +19 more
europepmc   +1 more source

SGLT2 Inhibitors in Kidney Diseases-A Narrative Review. [PDF]

Int J Mol Sci
Gajewska A, Wasiak J, Sapeda N, Młynarska E, Rysz J, Franczyk B.   +5 more
europepmc   +1 more source

Dietary index for gut microbiota, a novel protective factor for the prevalence of chronic kidney diseases in the adults: insight from NHANES 2007-2018. [PDF]

Front Nutr
Xiao Y, Yang Y, Gao S, Zhang H, Wang J, Lin T, Bai Y.   +6 more
europepmc   +1 more source

Regulatory cell therapy for kidney transplantation and autoimmune kidney diseases. [PDF]

Pediatr Nephrol
Ho QY, Hester J, Issa F.
europepmc   +1 more source

Methyltransferase-like 3 represents a prospective target for the diagnosis and treatment of kidney diseases. [PDF]

Hum Genomics
Song B, Wu X, Zeng Y.
europepmc   +1 more source

Targeting cellular senescence in kidney diseases and aging: A focus on mesenchymal stem cells and their paracrine factors. [PDF]

Cell Commun Signal
Hejazian SM, Hejazian SS, Mostafavi SM, Hosseiniyan SM, Montazersaheb S, Ardalan M, Zununi Vahed S, Barzegari A.   +7 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Acute Kidney Disease to Chronic Kidney Disease

Critical Care Clinics, 2021
Acute kidney injury (AKI) and chronic kidney disease are common interconnected syndromes that represent a public health problem. Acute kidney disease (AKD) is defined as the post-AKI status of acute or subacute kidney damage/dysfunction manifested by persistence of AKI beyond 7 to 90 days after the initial AKI diagnosis.
Javier A. Neyra, Lakhmir S. Chawla
openaire   +3 more sources

The kidney in Fabry's disease

Clinical Genetics, 2014
Fabry disease (FD) is an X‐linked disease in which mutations of the GLA gene result in a deficiency of the enzyme α‐galactosidase A and subsequent progressive, intralysosomal deposition of undegraded glycosphingolipid products, primarily globotriaosylceramide, in multiple organs.
PISANI, ANTONIO, Visciano B, IMBRIACO, MASSIMO, Di Nuzzi A, Mancini A, Marchetiello C, Riccio E.   +6 more
openaire   +5 more sources