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Results by year

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

Year Number of Results
1945 2
1946 3
1948 4
1949 1
1950 6
1951 2
1952 8
1954 2
1955 2
1956 4
1957 1
1958 4
1959 1
1960 1
1961 3
1962 1
1963 4
1965 1
1966 1
1967 1
1968 4
1969 6
1970 4
1971 3
1972 5
1973 5
1974 4
1975 4
1976 8
1977 7
1978 3
1979 7
1980 11
1981 12
1982 13
1983 16
1984 26
1985 24
1986 21
1987 27
1988 21
1989 28
1990 23
1991 25
1992 26
1993 20
1994 22
1995 22
1996 32
1997 32
1998 38
1999 37
2000 37
2001 42
2002 42
2003 47
2004 41
2005 52
2006 60
2007 64
2008 65
2009 50
2010 56
2011 57
2012 73
2013 63
2014 69
2015 62
2016 54
2017 56
2018 62
2019 81
2020 71
2021 86
2022 49
2023 8
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Article attribute
Article type
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Search Results

1,772 results
Results by year
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Page 1
[Gallstones - review].
Hjaltadottir K, Haraldsdottir KH, Moller PH. Hjaltadottir K, et al. Among authors: moller ph. Laeknabladid. 2020 Oct;106(10):464-472. doi: 10.17992/lbl.2020.10.602. Laeknabladid. 2020. PMID: 32991309 Free article. Review. Icelandic.
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Dominguez-Valentin M, Sampson JR, Seppälä TT, Ten Broeke SW, Plazzer JP, Nakken S, Engel C, Aretz S, Jenkins MA, Sunde L, Bernstein I, Capella G, Balaguer F, Thomas H, Evans DG, Burn J, Greenblatt M, Hovig E, de Vos Tot Nederveen Cappel WH, Sijmons RH, Bertario L, Tibiletti MG, Cavestro GM, Lindblom A, Della Valle A, Lopez-Köstner F, Gluck N, Katz LH, Heinimann K, Vaccaro CA, Büttner R, Görgens H, Holinski-Feder E, Morak M, Holzapfel S, Hüneburg R, Knebel Doeberitz MV, Loeffler M, Rahner N, Schackert HK, Steinke-Lange V, Schmiegel W, Vangala D, Pylvänäinen K, Renkonen-Sinisalo L, Hopper JL, Win AK, Haile RW, Lindor NM, Gallinger S, Le Marchand L, Newcomb PA, Figueiredo JC, Thibodeau SN, Wadt K, Therkildsen C, Okkels H, Ketabi Z, Moreira L, Sánchez A, Serra-Burriel M, Pineda M, Navarro M, Blanco I, Green K, Lalloo F, Crosbie EJ, Hill J, Denton OG, Frayling IM, Rødland EA, Vasen H, Mints M, Neffa F, Esperon P, Alvarez K, Kariv R, Rosner G, Pinero TA, Gonzalez ML, Kalfayan P, Tjandra D, Winship IM, Macrae F, Möslein G, Mecklin JP, Nielsen M, Møller P. Dominguez-Valentin M, et al. Among authors: moller p. Genet Med. 2020 Jan;22(1):15-25. doi: 10.1038/s41436-019-0596-9. Epub 2019 Jul 24. Genet Med. 2020. PMID: 31337882 Free PMC article.
Single-cell-resolved differentiation of human induced pluripotent stem cells into pancreatic duct-like organoids on a microwell chip.
Wiedenmann S, Breunig M, Merkle J, von Toerne C, Georgiev T, Moussus M, Schulte L, Seufferlein T, Sterr M, Lickert H, Weissinger SE, Möller P, Hauck SM, Hohwieler M, Kleger A, Meier M. Wiedenmann S, et al. Among authors: moller p. Nat Biomed Eng. 2021 Aug;5(8):897-913. doi: 10.1038/s41551-021-00757-2. Epub 2021 Jul 8. Nat Biomed Eng. 2021. PMID: 34239116 Free PMC article.
[Chordoma-An update].
Mellert K, Seeling C, Möller P, Barth TFE. Mellert K, et al. Among authors: moller p. Pathologie (Heidelb). 2022 Aug;43(Suppl 1):50-55. doi: 10.1007/s00292-022-01118-9. Epub 2022 Sep 29. Pathologie (Heidelb). 2022. PMID: 36175666 Review. German.
Cancer Risks for PMS2-Associated Lynch Syndrome.
Ten Broeke SW, van der Klift HM, Tops CMJ, Aretz S, Bernstein I, Buchanan DD, de la Chapelle A, Capella G, Clendenning M, Engel C, Gallinger S, Gomez Garcia E, Figueiredo JC, Haile R, Hampel HL, Hopper JL, Hoogerbrugge N, von Knebel Doeberitz M, Le Marchand L, Letteboer TGW, Jenkins MA, Lindblom A, Lindor NM, Mensenkamp AR, Møller P, Newcomb PA, van Os TAM, Pearlman R, Pineda M, Rahner N, Redeker EJW, Olderode-Berends MJW, Rosty C, Schackert HK, Scott R, Senter L, Spruijt L, Steinke-Lange V, Suerink M, Thibodeau S, Vos YJ, Wagner A, Winship I, Hes FJ, Vasen HFA, Wijnen JT, Nielsen M, Win AK. Ten Broeke SW, et al. Among authors: moller p. J Clin Oncol. 2018 Oct 10;36(29):2961-2968. doi: 10.1200/JCO.2018.78.4777. Epub 2018 Aug 30. J Clin Oncol. 2018. PMID: 30161022 Free PMC article.
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
Seppälä TT, Latchford A, Negoi I, Sampaio Soares A, Jimenez-Rodriguez R, Sánchez-Guillén L, Evans DG, Ryan N, Crosbie EJ, Dominguez-Valentin M, Burn J, Kloor M, Knebel Doeberitz MV, Duijnhoven FJBV, Quirke P, Sampson JR, Møller P, Möslein G; European Hereditary Tumour Group (EHTG) and European Society of Coloproctology (ESCP). Seppälä TT, et al. Among authors: moller p. Br J Surg. 2021 May 27;108(5):484-498. doi: 10.1002/bjs.11902. Br J Surg. 2021. PMID: 34043773
Use of non-invasive stimulation in movement disorders: a critical review.
Godeiro C, França C, Carra RB, Saba F, Saba R, Maia D, Brandão P, Allam N, Rieder CRM, Freitas FC, Capato T, Spitz M, Faria DD, Cordellini M, Veiga BAAG, Rocha MSG, Maciel R, Melo LB, Möller PDS, R R Júnior M, Fornari LHT, Mantese CE, Barbosa ER, Munhoz RP, Coletta MVD, Cury RG. Godeiro C, et al. Among authors: moller pds. Arq Neuropsiquiatr. 2021 Jul;79(7):630-646. doi: 10.1590/0004-282X-ANP-2020-0381. Arq Neuropsiquiatr. 2021. PMID: 34468499 Free article. Review.
1,772 results