Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1990 2
1991 1
1997 3
1999 3
2000 2
2002 2
2003 2
2004 3
2005 1
2006 4
2007 5
2008 3
2009 4
2010 6
2011 6
2012 8
2013 6
2014 10
2015 7
2016 6
2017 8
2018 6
2019 4
2020 7
2021 10
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

108 results
Results by year
Filters applied: . Clear all
Page 1
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Loeys BL, et al. Among authors: coucke pj. N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695. N Engl J Med. 2006. PMID: 16928994 Free article.
Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.
Tonelli F, Bek JW, Besio R, De Clercq A, Leoni L, Salmon P, Coucke PJ, Willaert A, Forlino A. Tonelli F, et al. Among authors: coucke pj. Front Endocrinol (Lausanne). 2020 Jul 31;11:489. doi: 10.3389/fendo.2020.00489. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32849280 Free PMC article. Review.
The corneoscleral shape in Marfan syndrome.
Vanhonsebrouck E, Consejo A, Coucke PJ, Leroy BP, Kreps EO. Vanhonsebrouck E, et al. Among authors: coucke pj. Acta Ophthalmol. 2021 Jun;99(4):405-410. doi: 10.1111/aos.14636. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996688
DFNA 2, 5, 8, 12.
Van Camp G, Coucke PJ, Van Hauwe P, Van Laer L, Verhoeven K, Wuyts F, Smith RJ. Van Camp G, et al. Among authors: coucke pj. Adv Otorhinolaryngol. 2000;56:68-77. doi: 10.1159/000059084. Adv Otorhinolaryngol. 2000. PMID: 10868216 Review. No abstract available.
Arterial tortuosity syndrome: 40 new families and literature review.
Beyens A, Albuisson J, Boel A, Al-Essa M, Al-Manea W, Bonnet D, Bostan O, Boute O, Busa T, Canham N, Cil E, Coucke PJ, Cousin MA, Dasouki M, De Backer J, De Paepe A, De Schepper S, De Silva D, Devriendt K, De Wandele I, Deyle DR, Dietz H, Dupuis-Girod S, Fontenot E, Fischer-Zirnsak B, Gezdirici A, Ghoumid J, Giuliano F, Diéz NB, Haider MZ, Hardin JS, Jeunemaitre X, Klee EW, Kornak U, Landecho MF, Legrand A, Loeys B, Lyonnet S, Michael H, Moceri P, Mohammed S, Muiño-Mosquera L, Nampoothiri S, Pichler K, Prescott K, Rajeb A, Ramos-Arroyo M, Rossi M, Salih M, Seidahmed MZ, Schaefer E, Steichen-Gersdorf E, Temel S, Uysal F, Vanhomwegen M, Van Laer L, Van Maldergem L, Warner D, Willaert A, Collins TR, Taylor A, Davis EC, Zarate Y, Callewaert B. Beyens A, et al. Among authors: coucke pj. Genet Med. 2018 Oct;20(10):1236-1245. doi: 10.1038/gim.2017.253. Epub 2018 Jan 11. Genet Med. 2018. PMID: 29323665
108 results