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Results by year

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

Year Number of Results
1948 1
1955 1
1963 1
1965 1
1968 1
1969 5
1971 2
1972 5
1973 9
1974 3
1975 4
1976 4
1977 4
1978 8
1979 11
1980 7
1981 9
1982 5
1983 4
1984 5
1985 10
1986 5
1987 7
1988 6
1989 9
1990 9
1991 12
1992 7
1993 8
1994 10
1995 12
1996 5
1997 12
1998 15
1999 3
2000 2
2001 7
2002 7
2003 3
2004 4
2005 11
2006 8
2007 5
2008 7
2009 7
2010 10
2011 13
2012 7
2013 8
2014 12
2015 15
2016 8
2017 8
2018 20
2019 8
2020 12
2021 11
2022 13
2023 9
2024 4

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Article attribute

Article type

Publication date

Search Results

405 results

Results by year

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Page 1
Empagliflozin in Patients with Chronic Kidney Disease.
The EMPA-KIDNEY Collaborative Group; Herrington WG, Staplin N, Wanner C, Green JB, Hauske SJ, Emberson JR, Preiss D, Judge P, Mayne KJ, Ng SYA, Sammons E, Zhu D, Hill M, Stevens W, Wallendszus K, Brenner S, Cheung AK, Liu ZH, Li J, Hooi LS, Liu W, Kadowaki T, Nangaku M, Levin A, Cherney D, Maggioni AP, Pontremoli R, Deo R, Goto S, Rossello X, Tuttle KR, Steubl D, Petrini M, Massey D, Eilbracht J, Brueckmann M, Landray MJ, Baigent C, Haynes R. The EMPA-KIDNEY Collaborative Group, et al. N Engl J Med. 2023 Jan 12;388(2):117-127. doi: 10.1056/NEJMoa2204233. Epub 2022 Nov 4. N Engl J Med. 2023. PMID: 36331190 Free PMC article. Clinical Trial.
Dexamethasone in Hospitalized Patients with Covid-19.
RECOVERY Collaborative Group; Horby P, Lim WS, Emberson JR, Mafham M, Bell JL, Linsell L, Staplin N, Brightling C, Ustianowski A, Elmahi E, Prudon B, Green C, Felton T, Chadwick D, Rege K, Fegan C, Chappell LC, Faust SN, Jaki T, Jeffery K, Montgomery A, Rowan K, Juszczak E, Baillie JK, Haynes R, Landray MJ. RECOVERY Collaborative Group, et al. N Engl J Med. 2021 Feb 25;384(8):693-704. doi: 10.1056/NEJMoa2021436. Epub 2020 Jul 17. N Engl J Med. 2021. PMID: 32678530 Free PMC article. Clinical Trial.
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype.
Senum SR, Li YSM, Benson KA, Joli G, Olinger E, Lavu S, Madsen CD, Gregory AV, Neatu R, Kline TL, Audrézet MP, Outeda P, Nau CB, Meijer E, Ali H, Steinman TI, Mrug M, Phelan PJ, Watnick TJ, Peters DJM, Ong ACM, Conlon PJ, Perrone RD, Cornec-Le Gall E, Hogan MC, Torres VE, Sayer JA; Genomics England Research Consortium, the HALT PKD, CRISP, DIPAK, ADPKD Modifier, and TAME PKD studies; Harris PC. Senum SR, et al. Among authors: phelan pj. Am J Hum Genet. 2022 Jan 6;109(1):136-156. doi: 10.1016/j.ajhg.2021.11.016. Epub 2021 Dec 9. Am J Hum Genet. 2022. PMID: 34890546 Free PMC article.
Unilateral alar ulceration.
Phelan PS, Nahmias ZP, Gordon SL, Mann CM. Phelan PS, et al. Cutis. 2020 Dec;106(6):E9-E10. doi: 10.12788/cutis.0150. Cutis. 2020. PMID: 33471888 No abstract available.
Hearing loss and renal syndromes.
Phelan PJ, Rheault MN. Phelan PJ, et al. Pediatr Nephrol. 2018 Oct;33(10):1671-1683. doi: 10.1007/s00467-017-3835-9. Epub 2017 Nov 12. Pediatr Nephrol. 2018. PMID: 29130116 Review.
Chopin's illnesses.
Phelan PD. Phelan PD. J R Soc Med. 1995 Aug;88(8):483-4. J R Soc Med. 1995. PMID: 7562840 Free PMC article. No abstract available.
405 results