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

Year Number of Results
1949 1
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1957 6
1958 5
1959 8
1960 12
1961 11
1962 12
1963 14
1964 10
1965 12
1966 13
1967 3
1968 10
1969 8
1970 7
1971 4
1972 5
1973 3
1974 6
1975 7
1976 6
1977 4
1978 4
1979 1
1980 1
1983 1
1984 2
1985 10
1986 1
1987 8
1988 3
1989 1
1990 4
1991 4
1992 5
1993 4
1994 3
1995 4
1996 1
1997 4
1998 7
1999 9
2000 10
2001 13
2002 15
2003 15
2004 12
2005 13
2006 8
2007 23
2008 13
2009 14
2010 19
2011 7
2012 20
2013 22
2014 19
2015 24
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2017 18
2018 16
2019 18
2020 35
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Page 1
Showing results for perrin a
Search for Perrein A instead (3 results)
Chromoanasynthesis.
Pellestor F, Gaillard JB, Ganne B, Perrin A, Morel F, Gatinois V. Pellestor F, et al. Among authors: perrin a. Methods Mol Biol. 2025;2968:35-51. doi: 10.1007/978-1-0716-4750-9_2. Methods Mol Biol. 2025. PMID: 40884636
Positron Emission Tomography Imaging With [18F]flortaucipir and Postmortem Assessment of Alzheimer Disease Neuropathologic Changes.
Fleisher AS, Pontecorvo MJ, Devous MD Sr, Lu M, Arora AK, Truocchio SP, Aldea P, Flitter M, Locascio T, Devine M, Siderowf A, Beach TG, Montine TJ, Serrano GE, Curtis C, Perrin A, Salloway S, Daniel M, Wellman C, Joshi AD, Irwin DJ, Lowe VJ, Seeley WW, Ikonomovic MD, Masdeu JC, Kennedy I, Harris T, Navitsky M, Southekal S, Mintun MA; A16 Study Investigators. Fleisher AS, et al. Among authors: perrin a. JAMA Neurol. 2020 Jul 1;77(7):829-839. doi: 10.1001/jamaneurol.2020.0528. JAMA Neurol. 2020. PMID: 32338734 Free PMC article.
Was the Last Bacterial Common Ancestor a Monoderm after All?
Léonard RR, Sauvage E, Lupo V, Perrin A, Sirjacobs D, Charlier P, Kerff F, Baurain D. Léonard RR, et al. Among authors: perrin a. Genes (Basel). 2022 Feb 18;13(2):376. doi: 10.3390/genes13020376. Genes (Basel). 2022. PMID: 35205421 Free PMC article. Review.
A positive influence on stoma care practice.
Perrin A, White M. Perrin A, et al. Br J Nurs. 2023 Sep 7;32(16):S3. doi: 10.12968/bjon.2023.32.16.S3. Br J Nurs. 2023. PMID: 37682769 No abstract available.
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.
Ramakrishna NB, Mohamad Sahari UB, Johmura Y, Ali NA, Alghamdi M, Bauer P, Khan S, Ordoñez N, Ferreira M, Pinto Basto J, Alkuraya FS, Faqeih EA, Mori M, Almontashiri NAM, Al Shamsi A, ElGhazali G, Abu Subieh H, Al Ojaimi M, El-Hattab AW, Said Al-Kindi SA, Alhashmi N, Alhabshan F, Al Saman A, Tfayli H, Arabi M, Khalifeh S, Taylor A, Alfadhel M, Jain R, Sinha S, Shenbagam S, Ramachandran R, Altunoğlu U, Jacob A, Thalange N, El Bejjani M, Perrin A, Shin JW, Al-Maawali A, Al-Shidhani A, Al-Futaisi A, Rabea F, Chekroun I, Almarri MA, Ohta T, Nakanishi M, Alsheikh-Ali A, Ali FR, Bertoli-Avella AM, Reversade B, Abou Tayoun A. Ramakrishna NB, et al. Among authors: perrin a. Am J Hum Genet. 2025 May 1;112(5):1233-1246. doi: 10.1016/j.ajhg.2025.03.013. Epub 2025 Apr 10. Am J Hum Genet. 2025. PMID: 40215970
BioConvert: a comprehensive format converter for life sciences.
Caro H, Dollin S, Biton A, Brancotte B, Desvillechabrol D, Dufresne Y, Li B, Kornobis E, Lemoine F, Maillet N, Perrin A, Traut N, Néron B, Cokelaer T. Caro H, et al. Among authors: perrin a. NAR Genom Bioinform. 2023 Aug 21;5(3):lqad074. doi: 10.1093/nargab/lqad074. eCollection 2023 Sep. NAR Genom Bioinform. 2023. PMID: 37608802 Free PMC article.
741 results