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

Year Number of Results
1953 1
1976 1
1978 1
1979 5
1980 1
1981 5
1982 1
1983 6
1984 6
1985 3
1986 9
1987 11
1988 11
1989 5
1990 7
1991 11
1992 10
1993 8
1994 10
1995 6
1996 10
1997 8
1998 9
1999 14
2000 8
2001 11
2002 8
2003 2
2004 6
2005 14
2006 8
2007 7
2008 5
2009 3
2010 3
2011 1
2012 1
2013 1
2014 1
2015 1
2016 1
2018 1
2019 3
2020 2
2021 5
2022 1
2024 1

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248 results

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Page 1
Peutz-Jeghers syndrome: a systematic review and recommendations for management.
Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV. Beggs AD, et al. Among authors: friedl w. Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499. Gut. 2010. PMID: 20581245
Nailing of lower extremity fractures.
Friedl W, Gradl G. Friedl W, et al. Injury. 2019 Aug;50 Suppl 3:1-3. doi: 10.1016/j.injury.2019.07.007. Epub 2019 Aug 1. Injury. 2019. PMID: 31378547 No abstract available.
[Hereditary gastrointestinal tumors].
Jungck M, Friedl W, Propping P. Jungck M, et al. Among authors: friedl w. Internist (Berl). 1999 May;40(5):502-12. doi: 10.1007/s001080050364. Internist (Berl). 1999. PMID: 10407760 Review. German. No abstract available.
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
Mangold E, Pagenstecher C, Friedl W, Mathiak M, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Müller-Koch Y, Keller G, Schackert HK, Krüger S, Goecke T, Moeslein G, Kloor M, Gebert J, Kunstmann E, Schulmann K, Rüschoff J, Propping P. Mangold E, et al. Among authors: friedl w. Int J Cancer. 2005 Sep 20;116(5):692-702. doi: 10.1002/ijc.20863. Int J Cancer. 2005. PMID: 15849733
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).
Vasen HF, Möslein G, Alonso A, Bernstein I, Bertario L, Blanco I, Burn J, Capella G, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Mecklin JP, Møller P, Nagengast F, Parc Y, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Wijnen J. Vasen HF, et al. Among authors: friedl w. J Med Genet. 2007 Jun;44(6):353-62. doi: 10.1136/jmg.2007.048991. Epub 2007 Feb 27. J Med Genet. 2007. PMID: 17327285 Free PMC article. Review.
CLCN2 variants in idiopathic generalized epilepsy.
Kleefuss-Lie A, Friedl W, Cichon S, Haug K, Warnstedt M, Alekov A, Sander T, Ramirez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H. Kleefuss-Lie A, et al. Among authors: friedl w. Nat Genet. 2009 Sep;41(9):954-5. doi: 10.1038/ng0909-954. Nat Genet. 2009. PMID: 19710712 No abstract available.
248 results