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Results by year

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

Year Number of Results
1947 2
1948 1
1949 2
1951 3
1952 1
1953 4
1955 1
1961 1
1962 1
1966 3
1967 2
1968 4
1969 2
1970 5
1971 6
1973 2
1974 1
1975 1
1976 1
1977 1
1978 2
1979 1
1980 1
1981 1
1982 1
1984 2
1985 1
1987 2
1988 3
1989 3
1991 3
1992 4
1993 1
1994 3
1995 4
1996 1
1997 2
1998 2
1999 4
2000 4
2001 6
2002 4
2003 5
2004 4
2005 9
2006 6
2007 9
2008 6
2009 4
2010 6
2011 10
2012 6
2013 4
2014 6
2015 2
2016 12
2017 8
2018 11
2019 4
2020 6
2021 5
2022 5
2023 9
2024 9

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231 results

Results by year

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Page 1
Syncytin-1, syncytin-2 and suppressyn in human health and disease.
Priščáková P, Svoboda M, Feketová Z, Hutník J, Repiská V, Gbelcová H, Gergely L. Priščáková P, et al. Among authors: gergely l. J Mol Med (Berl). 2023 Dec;101(12):1527-1542. doi: 10.1007/s00109-023-02385-6. Epub 2023 Oct 19. J Mol Med (Berl). 2023. PMID: 37855856 Free PMC article. Review.
[Drug therapy of lymphomas].
Gergely L. Gergely L. Magy Onkol. 2017 Mar 8;61(1):89-96. Epub 2016 Jun 15. Magy Onkol. 2017. PMID: 28273193 Free article. Review. Hungarian.
[Waldenström macroglobulinemia].
Telek B, Batár P, Váróczy L, Gergely L, Rejtő L, Szász R, Miltényi Z, Simon Z, Udvardy M, Illés A. Telek B, et al. Among authors: gergely l. Orv Hetil. 2013 Dec 1;154(50):1970-4. doi: 10.1556/OH.2013.29776. Orv Hetil. 2013. PMID: 24317355 Hungarian.
Post-mortem rapid aneuploidy testing for holoprosencephaly.
Gergely L, Repiská V, Böhmer D, Korbeľ M, Václavová Z, McCullough L, Melišová K, Priščáková P. Gergely L, et al. Birth Defects Res. 2024 Apr;116(4):e2342. doi: 10.1002/bdr2.2342. Birth Defects Res. 2024. PMID: 38632851
Tests of General Relativity with GW170817.
Abbott BP, Abbott R, Abbott TD, Acernese F, Ackley K, Adams C, Adams T, Addesso P, Adhikari RX, Adya VB, Affeldt C, Agarwal B, Agathos M, Agatsuma K, Aggarwal N, Aguiar OD, Aiello L, Ain A, Ajith P, Allen B, Allen G, Allocca A, Aloy MA, Altin PA, Amato A, Ananyeva A, Anderson SB, Anderson WG, Angelova SV, Antier S, Appert S, Arai K, Araya MC, Areeda JS, Arène M, Arnaud N, Arun KG, Ascenzi S, Ashton G, Ast M, Aston SM, Astone P, Atallah DV, Aubin F, Aufmuth P, Aulbert C, AultONeal K, Austin C, Avila-Alvarez A, Babak S, Bacon P, Badaracco F, Bader MKM, Bae S, Baker PT, Baldaccini F, Ballardin G, Ballmer SW, Banagiri S, Barayoga JC, Barclay SE, Barish BC, Barker D, Barkett K, Barnum S, Barone F, Barr B, Barsotti L, Barsuglia M, Barta D, Bartlett J, Bartos I, Bassiri R, Basti A, Batch JC, Bawaj M, Bayley JC, Bazzan M, Bécsy B, Beer C, Bejger M, Belahcene I, Bell AS, Beniwal D, Bensch M, Berger BK, Bergmann G, Bernuzzi S, Bero JJ, Berry CPL, Bersanetti D, Bertolini A, Betzwieser J, Bhandare R, Bilenko IA, Bilgili SA, Billingsley G, Billman CR, Birch J, Birney R, Birnholtz O, Biscans S, Biscoveanu S, Bisht A, Bitossi M, Bizouard MA, Blackburn JK, Blackman J, Blair CD, Blair DG, Blair RM… See abstract for full author list ➔ Abbott BP, et al. Among authors: gergely l. Phys Rev Lett. 2019 Jul 3;123(1):011102. doi: 10.1103/PhysRevLett.123.011102. Phys Rev Lett. 2019. PMID: 31386391 Free article.
Low-burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation.
László T, Kotmayer L, Fésüs V, Hegyi L, Gróf S, Nagy Á, Kajtár B, Balogh A, Weisinger J, Masszi T, Nagy Z, Farkas P, Demeter J, Istenes I, Szász R, Gergely L, Sulák A, Borbényi Z, Lévai D, Schneider T, Pettendi P, Bodai E, Szerafin L, Rejtő L, Bátai Á, Dömötör MÁ, Sánta H, Plander M, Szendrei T, Hamed A, Lázár Z, Pauker Z, Radványi G, Kiss A, Körösmezey G, Jakucs J, Dombi PJ, Simon Z, Klucsik Z, Gurzó M, Tiboly M, Vidra T, Ilonczai P, Bors A, Andrikovics H, Egyed M, Székely T, Masszi A, Alpár D, Matolcsy A, Bödör C. László T, et al. Among authors: gergely l. J Pathol Clin Res. 2024 Jan;10(1):e351. doi: 10.1002/cjp2.351. Epub 2023 Nov 21. J Pathol Clin Res. 2024. PMID: 37987115 Free PMC article.
231 results