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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1975 1
1981 3
1982 1
1983 2
1984 1
1985 1
1987 3
1988 1
1989 1
1990 3
1991 5
1992 1
1993 3
1997 2
1998 5
1999 1
2000 2
2001 2
2002 3
2003 5
2004 5
2005 3
2006 3
2007 5
2008 2
2010 5
2011 8
2012 6
2013 3
2014 4
2015 6
2016 3
2017 11
2018 10
2019 5
2020 6
2021 9
2022 12
2023 9
2024 4

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151 results

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Page 1
Acute Kidney Injury: Biomarker-Guided Diagnosis and Management.
Yoon SY, Kim JS, Jeong KH, Kim SK. Yoon SY, et al. Medicina (Kaunas). 2022 Feb 23;58(3):340. doi: 10.3390/medicina58030340. Medicina (Kaunas). 2022. PMID: 35334515 Free PMC article. Review.
Acute kidney injury (AKI) is a common clinical syndrome that is characterized by abnormal renal function and structure. The Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference in 2019 reviewed the stages of AKI and the definition …
Acute kidney injury (AKI) is a common clinical syndrome that is characterized by abnormal renal function and structure. The …
Swiss consensus recommendations on urinary tract infections in children.
Buettcher M, Trueck J, Niederer-Loher A, Heininger U, Agyeman P, Asner S, Berger C, Bielicki J, Kahlert C, Kottanattu L, Meyer Sauteur PM, Paioni P, Posfay-Barbe K, Relly C, Ritz N, Zimmermann P, Zucol F, Gobet R, Shavit S, Rudin C, Laube G, von Vigier R, Neuhaus TJ. Buettcher M, et al. Eur J Pediatr. 2021 Mar;180(3):663-674. doi: 10.1007/s00431-020-03714-4. Epub 2020 Jul 3. Eur J Pediatr. 2021. PMID: 32621135 Free PMC article. Review.
The main risk factors for sequelae after urinary tract infections (UTI) are congenital anomalies of the kidney and urinary tract (CAKUT) and bladder-bowel dysfunction. ...What is New: Vesicoureteric reflux (VUR) remains a risk factor for UTI but per se is nei …
The main risk factors for sequelae after urinary tract infections (UTI) are congenital anomalies of the kidney and urin …
A Practical Guide for Treatment of Rapidly Progressive ADPKD with Tolvaptan.
Chebib FT, Perrone RD, Chapman AB, Dahl NK, Harris PC, Mrug M, Mustafa RA, Rastogi A, Watnick T, Yu ASL, Torres VE. Chebib FT, et al. J Am Soc Nephrol. 2018 Oct;29(10):2458-2470. doi: 10.1681/ASN.2018060590. Epub 2018 Sep 18. J Am Soc Nephrol. 2018. PMID: 30228150 Free PMC article. Review.
In the past, the treatment of autosomal dominant polycystic kidney disease (ADPKD) has been limited to the management of its symptoms and complications. Recently, the US Food and Drug Administration (FDA) approved tolvaptan as the first drug treatment to slow kidney …
In the past, the treatment of autosomal dominant polycystic kidney disease (ADPKD) has been limited to the management of its symptoms …
Management of antenatal hydronephrosis.
Yalçınkaya F, Özçakar ZB. Yalçınkaya F, et al. Pediatr Nephrol. 2020 Dec;35(12):2231-2239. doi: 10.1007/s00467-019-04420-6. Epub 2019 Dec 6. Pediatr Nephrol. 2020. PMID: 31811536 Review.
Antenatal hydronephrosis (AHN) is the most frequently detected abnormality by prenatal ultrasonography. Differential diagnosis of AHN includes a wide variety of congenital abnormalities of the kidney and urinary tract ranging from mild abnorm …
Antenatal hydronephrosis (AHN) is the most frequently detected abnormality by prenatal ultrasonography. Differential diagnosis of AHN …
Clinical presentation & management of glomerular diseases: hematuria, nephritic & nephrotic syndrome.
Khanna R. Khanna R. Mo Med. 2011 Jan-Feb;108(1):33-6. Mo Med. 2011. PMID: 21462608 Free PMC article. Review.
The etiology of glomerulonephritis can be classified by their clinical presentation (nephrotic, nephritic, rapidly progressive GN, chronic GN) or by histopathology. GN may be restricted to the kidney (primary glomerulonephritis) or be a secondary to a systemic disea …
The etiology of glomerulonephritis can be classified by their clinical presentation (nephrotic, nephritic, rapidly progressive GN, chronic G …
Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players.
Domingo-Gallego A, Pybus M, Bullich G, Furlano M, Ejarque-Vila L, Lorente-Grandoso L, Ruiz P, Fraga G, López González M, Piñero-Fernández JA, Rodríguez-Peña L, Llano-Rivas I, Sáez R, Bujons-Tur A, Ariceta G, Guirado L, Torra R, Ars E. Domingo-Gallego A, et al. Nephrol Dial Transplant. 2022 Mar 25;37(4):687-696. doi: 10.1093/ndt/gfab019. Nephrol Dial Transplant. 2022. PMID: 33532864
BACKGROUND: Inherited kidney diseases are one of the leading causes of chronic kidney disease (CKD) that manifests before the age of 30 years. ...RESULTS: We achieved a global diagnostic yield of 65% (300/460), which varied depending on the clinical diagnostic group …
BACKGROUND: Inherited kidney diseases are one of the leading causes of chronic kidney disease (CKD) that manifests before the …
Secondary Hyperparathyroidism: Pathogenesis and Latest Treatment.
Mizobuchi M, Ogata H, Koiwa F. Mizobuchi M, et al. Ther Apher Dial. 2019 Aug;23(4):309-318. doi: 10.1111/1744-9987.12772. Epub 2018 Dec 18. Ther Apher Dial. 2019. PMID: 30411503 Review.
In dialysis patients with failed renal function, physiological mineral balance control by parathyroid hormone through the kidney fails and hyperparathyroidism progresses. In this process, many significant genetic findings have been established. Abnormalities …
In dialysis patients with failed renal function, physiological mineral balance control by parathyroid hormone through the kidney …
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.
La Scola C, Ammenti A, Bertulli C, Bodria M, Brugnara M, Camilla R, Capone V, Casadio L, Chimenz R, Conte ML, Conversano E, Corrado C, Guarino S, Luongo I, Marsciani M, Marzuillo P, Meneghesso D, Pennesi M, Pugliese F, Pusceddu S, Ravaioli E, Taroni F, Vergine G, Peruzzi L, Montini G. La Scola C, et al. Pediatr Nephrol. 2022 Sep;37(9):2185-2207. doi: 10.1007/s00467-022-05528-y. Epub 2022 Jun 17. Pediatr Nephrol. 2022. PMID: 35713730 Free PMC article. Review.
In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), with controversial results, and a worldwide consensus on management and follow-up is lacking. ...We recommend that any antenatal suspicion/diagno …
In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), with …
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference.
Levey AS, Eckardt KU, Dorman NM, Christiansen SL, Hoorn EJ, Ingelfinger JR, Inker LA, Levin A, Mehrotra R, Palevsky PM, Perazella MA, Tong A, Allison SJ, Bockenhauer D, Briggs JP, Bromberg JS, Davenport A, Feldman HI, Fouque D, Gansevoort RT, Gill JS, Greene EL, Hemmelgarn BR, Kretzler M, Lambie M, Lane PH, Laycock J, Leventhal SE, Mittelman M, Morrissey P, Ostermann M, Rees L, Ronco P, Schaefer F, St Clair Russell J, Vinck C, Walsh SB, Weiner DE, Cheung M, Jadoul M, Winkelmayer WC. Levey AS, et al. Kidney Int. 2020 Jun;97(6):1117-1129. doi: 10.1016/j.kint.2020.02.010. Epub 2020 Mar 9. Kidney Int. 2020. PMID: 32409237 Free article.
The worldwide burden of kidney disease is rising, but public awareness remains limited, underscoring the need for more effective communication by stakeholders in the kidney health community. ...Conference attendees reached general consensus on the following r …
The worldwide burden of kidney disease is rising, but public awareness remains limited, underscoring the need for more effective comm …
Differential diagnosis of familial diabetes insipidus.
Robertson GL. Robertson GL. Handb Clin Neurol. 2021;181:239-248. doi: 10.1016/B978-0-12-820683-6.00017-8. Handb Clin Neurol. 2021. PMID: 34238460 Review.
Hypothalamic and nephrogenic DI can also be caused by mutation of the gene that encodes the AVP prohormone, the AVP-2 receptors in the kidney, or the aquaporin-2 water channels that mediate antidiuresis. ...Thus the determination of plasma AVP and/or the response to …
Hypothalamic and nephrogenic DI can also be caused by mutation of the gene that encodes the AVP prohormone, the AVP-2 receptors in the …
151 results