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

Year Number of Results
2000 1
2002 2
2003 1
2004 1
2005 1
2006 1
2007 2
2008 4
2009 2
2010 3
2012 1
2013 3
2014 2
2015 6
2016 5
2017 5
2018 6
2019 2
2020 7
2021 3
2022 3
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56 results
Results by year
Filters applied: . Clear all The following term was not found in PubMed: Marjakoski
Page 1
Primary lymphoedema.
Brouillard P, Witte MH, Erickson RP, Damstra RJ, Becker C, Quéré I, Vikkula M. Brouillard P, et al. Nat Rev Dis Primers. 2021 Oct 21;7(1):77. doi: 10.1038/s41572-021-00309-7. Nat Rev Dis Primers. 2021. PMID: 34675250 Review.
Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.
Amyere M, Revencu N, Helaers R, Pairet E, Baselga E, Cordisco M, Chung W, Dubois J, Lacour JP, Martorell L, Mazereeuw-Hautier J, Pyeritz RE, Amor DJ, Bisdorff A, Blei F, Bombei H, Dompmartin A, Brooks D, Dupont J, González-Enseñat MA, Frieden I, Gérard M, Kvarnung M, Hanson-Kahn AK, Hudgins L, Léauté-Labrèze C, McCuaig C, Metry D, Parent P, Paul C, Petit F, Phan A, Quere I, Salhi A, Turner A, Vabres P, Vicente A, Wargon O, Watanabe S, Weibel L, Wilson A, Willing M, Mulliken JB, Boon LM, Vikkula M. Amyere M, et al. Circulation. 2017 Sep 12;136(11):1037-1048. doi: 10.1161/CIRCULATIONAHA.116.026886. Epub 2017 Jul 7. Circulation. 2017. PMID: 28687708 Free article.
Genetics of vascular anomalies.
Nguyen HL, Boon LM, Vikkula M. Nguyen HL, et al. Semin Pediatr Surg. 2020 Oct;29(5):150967. doi: 10.1016/j.sempedsurg.2020.150967. Epub 2020 Sep 16. Semin Pediatr Surg. 2020. PMID: 33069286 Review.
Theranostic Advances in Vascular Malformations.
Dekeuleneer V, Seront E, Van Damme A, Boon LM, Vikkula M. Dekeuleneer V, et al. J Invest Dermatol. 2020 Apr;140(4):756-763. doi: 10.1016/j.jid.2019.10.001. J Invest Dermatol. 2020. PMID: 32200879 Free article. Review.
Genomics of Fibromuscular Dysplasia.
Di Monaco S, Georges A, Lengelé JP, Vikkula M, Persu A. Di Monaco S, et al. Int J Mol Sci. 2018 May 21;19(5):1526. doi: 10.3390/ijms19051526. Int J Mol Sci. 2018. PMID: 29883369 Free PMC article. Review.
Venous Malformations of the Head and Neck.
Seront E, Vikkula M, Boon LM. Seront E, et al. Otolaryngol Clin North Am. 2018 Feb;51(1):173-184. doi: 10.1016/j.otc.2017.09.003. Otolaryngol Clin North Am. 2018. PMID: 29217061 Review.
Etiology and Genetics of Congenital Vascular Lesions.
Queisser A, Boon LM, Vikkula M. Queisser A, et al. Otolaryngol Clin North Am. 2018 Feb;51(1):41-53. doi: 10.1016/j.otc.2017.09.006. Otolaryngol Clin North Am. 2018. PMID: 29217067 Review.
Characterization of ANGPT2 mutations associated with primary lymphedema.
Leppänen VM, Brouillard P, Korhonen EA, Sipilä T, Jha SK, Revencu N, Labarque V, Fastré E, Schlögel M, Ravoet M, Singer A, Luzzatto C, Angelone D, Crichiutti G, D'Elia A, Kuurne J, Elamaa H, Koh GY, Saharinen P, Vikkula M, Alitalo K. Leppänen VM, et al. Sci Transl Med. 2020 Sep 9;12(560):eaax8013. doi: 10.1126/scitranslmed.aax8013. Sci Transl Med. 2020. PMID: 32908006
Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
Brouillard P, Schlögel MJ, Homayun Sepehr N, Helaers R, Queisser A, Fastré E, Boutry S, Schmitz S, Clapuyt P, Hammer F, Dompmartin A, Weitz-Tuoretmaa A, Laranne J, Pasquesoone L, Vilain C, Boon LM, Vikkula M. Brouillard P, et al. Orphanet J Rare Dis. 2021 Jun 10;16(1):267. doi: 10.1186/s13023-021-01898-y. Orphanet J Rare Dis. 2021. PMID: 34112235 Free PMC article.
56 results