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

Year Number of Results
1934 1
1957 1
1959 1
1962 1
1963 1
1965 1
1969 3
1970 1
1977 1
1981 1
1982 1
1983 1
1984 4
1985 3
1986 2
1988 1
1989 1
1990 2
1991 1
1992 4
1993 1
1994 1
1995 1
1996 1
1997 3
1998 4
1999 4
2000 4
2001 10
2002 8
2003 5
2004 7
2005 4
2006 9
2007 10
2008 11
2009 20
2010 27
2011 24
2012 26
2013 29
2014 33
2015 27
2016 30
2017 46
2018 41
2019 57
2020 62
2021 59
2022 63
2023 39
2024 64

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675 results

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Page 1
Post-stroke dementia - a comprehensive review.
Mijajlović MD, Pavlović A, Brainin M, Heiss WD, Quinn TJ, Ihle-Hansen HB, Hermann DM, Assayag EB, Richard E, Thiel A, Kliper E, Shin YI, Kim YH, Choi S, Jung S, Lee YB, Sinanović O, Levine DA, Schlesinger I, Mead G, Milošević V, Leys D, Hagberg G, Ursin MH, Teuschl Y, Prokopenko S, Mozheyko E, Bezdenezhnykh A, Matz K, Aleksić V, Muresanu D, Korczyn AD, Bornstein NM. Mijajlović MD, et al. Among authors: richard e. BMC Med. 2017 Jan 18;15(1):11. doi: 10.1186/s12916-017-0779-7. BMC Med. 2017. PMID: 28095900 Free PMC article. Review.
Lecanemab for Alzheimer's disease.
Walsh S, Merrick R, Richard E, Nurock S, Brayne C. Walsh S, et al. Among authors: richard e. BMJ. 2022 Dec 19;379:o3010. doi: 10.1136/bmj.o3010. BMJ. 2022. PMID: 36535691 No abstract available.
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
Richard EM, Santos-Cortez RLP, Faridi R, Rehman AU, Lee K, Shahzad M, Acharya A, Khan AA, Imtiaz A, Chakchouk I, Takla C, Abbe I, Rafeeq M, Liaqat K, Chaudhry T, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics; Schrauwen I, Khan SN, Morell RJ, Zafar S, Ansar M, Ahmed ZM, Ahmad W, Riazuddin S, Friedman TB, Leal SM, Riazuddin S. Richard EM, et al. Hum Mutat. 2019 Jan;40(1):53-72. doi: 10.1002/humu.23666. Epub 2018 Nov 18. Hum Mutat. 2019. PMID: 30303587 Free PMC article.
[Forgetfulness].
Moll van Charante EP, Richard E, Perry M. Moll van Charante EP, et al. Among authors: richard e. Ned Tijdschr Geneeskd. 2022 Mar 3;166:D6366. Ned Tijdschr Geneeskd. 2022. PMID: 35499584 Dutch.
Framework for Clinical Trials in Cerebral Small Vessel Disease (FINESSE): A Review.
Markus HS, van Der Flier WM, Smith EE, Bath P, Biessels GJ, Briceno E, Brodtman A, Chabriat H, Chen C, de Leeuw FE, Egle M, Ganesh A, Georgakis MK, Gottesman RF, Kwon S, Launer L, Mok V, O'Brien J, Ottenhoff L, Pendlebury S, Richard E, Sachdev P, Schmidt R, Springer M, Tiedt S, Wardlaw JM, Verdelho A, Webb A, Werring D, Duering M, Levine D, Dichgans M. Markus HS, et al. Among authors: richard e. JAMA Neurol. 2022 Nov 1;79(11):1187-1198. doi: 10.1001/jamaneurol.2022.2262. JAMA Neurol. 2022. PMID: 35969390 Free PMC article. Review.
Action Plan for Stroke in Europe 2018-2030.
Norrving B, Barrick J, Davalos A, Dichgans M, Cordonnier C, Guekht A, Kutluk K, Mikulik R, Wardlaw J, Richard E, Nabavi D, Molina C, Bath PM, Stibrant Sunnerhagen K, Rudd A, Drummond A, Planas A, Caso V. Norrving B, et al. Among authors: richard e. Eur Stroke J. 2018 Dec;3(4):309-336. doi: 10.1177/2396987318808719. Epub 2018 Oct 29. Eur Stroke J. 2018. PMID: 31236480 Free PMC article.
Poststroke apathy.
van Dalen JW, Moll van Charante EP, Nederkoorn PJ, van Gool WA, Richard E. van Dalen JW, et al. Among authors: richard e. Stroke. 2013 Mar;44(3):851-60. doi: 10.1161/STROKEAHA.112.674614. Epub 2013 Jan 29. Stroke. 2013. PMID: 23362076 Review. No abstract available.
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
Richard EM, Bakhtiari S, Marsh APL, Kaiyrzhanov R, Wagner M, Shetty S, Pagnozzi A, Nordlie SM, Guida BS, Cornejo P, Magee H, Liu J, Norton BY, Webster RI, Worgan L, Hakonarson H, Li J, Guo Y, Jain M, Blesson A, Rodan LH, Abbott MA, Comi A, Cohen JS, Alhaddad B, Meitinger T, Lenz D, Ziegler A, Kotzaeridou U, Brunet T, Chassevent A, Smith-Hicks C, Ekstein J, Weiden T, Hahn A, Zharkinbekova N, Turnpenny P, Tucci A, Yelton M, Horvath R, Gungor S, Hiz S, Oktay Y, Lochmuller H, Zollino M, Morleo M, Marangi G, Nigro V, Torella A, Pinelli M, Amenta S, Husain RA, Grossmann B, Rapp M, Steen C, Marquardt I, Grimmel M, Grasshoff U, Korenke GC, Owczarek-Lipska M, Neidhardt J, Radio FC, Mancini C, Claps Sepulveda DJ, McWalter K, Begtrup A, Crunk A, Guillen Sacoto MJ, Person R, Schnur RE, Mancardi MM, Kreuder F, Striano P, Zara F, Chung WK, Marks WA, van Eyk CL, Webber DL, Corbett MA, Harper K, Berry JG, MacLennan AH, Gecz J, Tartaglia M, Salpietro V, Christodoulou J, Kaslin J, Padilla-Lopez S, Bilguvar K, Munchau A, Ahmed ZM, Hufnagel RB, Fahey MC, Maroofian R, Houlden H, Sticht H, Mane SM, Rad A, Vona B, Jin SC, Haack TB, Makowski C, Hirsch Y, Riazuddin S, Kruer MC. Richard EM, et al. Am J Hum Genet. 2021 Oct 7;108(10):2006-2016. doi: 10.1016/j.ajhg.2021.08.003. Am J Hum Genet. 2021. PMID: 34626583 Free PMC article.
675 results