Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

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 6
2009 5
2010 10
2011 13
2012 7
2013 8
2014 11
2015 15
2016 8
2017 8
2018 19
2019 8
2020 10
2021 6
2022 9
2023 4
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

385 results

Results by year

Filters applied: . Clear all
Page 1
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.
The Evolution of the Journal Club: From Osler to Twitter.
Topf JM, Sparks MA, Phelan PJ, Shah N, Lerma EV, Graham-Brown MPM, Madariaga H, Iannuzzella F, Rheault MN, Oates T, Jhaveri KD, Hiremath S. Topf JM, et al. Among authors: phelan pj. Am J Kidney Dis. 2017 Jun;69(6):827-836. doi: 10.1053/j.ajkd.2016.12.012. Epub 2017 Feb 21. Am J Kidney Dis. 2017. PMID: 28233653 Review.
A Janeway Lesson.
Phelan PS. Phelan PS. Int J Dermatol. 2018 Sep;57(9):1145-1146. doi: 10.1111/ijd.14149. Epub 2018 Jul 9. Int J Dermatol. 2018. PMID: 29984410 No abstract available.
Using omics to explore complications of kidney transplantation.
Stapleton CP, Conlon PJ, Phelan PJ. Stapleton CP, et al. Among authors: phelan pj. Transpl Int. 2018 Mar;31(3):251-262. doi: 10.1111/tri.13067. Epub 2017 Oct 12. Transpl Int. 2018. PMID: 28892567 Free article. Review.
Vesiculopustular Rash in a Neonate.
McKinnon AT, Phelan PS, Evans MS. McKinnon AT, et al. Among authors: phelan ps. J Pediatr. 2022 Jun;245:240-242. doi: 10.1016/j.jpeds.2022.03.025. Epub 2022 Mar 18. J Pediatr. 2022. PMID: 35314151 No abstract available.
Innexins get into the gap.
Phelan P, Starich TA. Phelan P, et al. Bioessays. 2001 May;23(5):388-96. doi: 10.1002/bies.1057. Bioessays. 2001. PMID: 11340620 Review.
Offspring of incest.
Phelan P. Phelan P. Med J Aust. 1978 Apr 8;1(7):388. doi: 10.5694/j.1326-5377.1978.tb107918.x. Med J Aust. 1978. PMID: 566844 No abstract available.
385 results