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

Year Number of Results
2002 1
2004 1
2007 1
2010 1
2011 1
2012 1
2013 2
2014 1
2015 1
2017 3
2018 1
2019 2
2020 7
2021 6
2022 1
2023 4
2024 2

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33 results

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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.
Genetics of lymphatic anomalies.
Brouillard P, Boon L, Vikkula M. Brouillard P, et al. J Clin Invest. 2014 Mar;124(3):898-904. doi: 10.1172/JCI71614. Epub 2014 Mar 3. J Clin Invest. 2014. PMID: 24590274 Free PMC article. Review.
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema.
Byrne AB, Brouillard P, Sutton DL, Kazenwadel J, Montazaribarforoushi S, Secker GA, Oszmiana A, Babic M, Betterman KL, Brautigan PJ, White M, Piltz SG, Thomas PQ, Hahn CN, Rath M, Felbor U, Korenke GC, Smith CL, Wood KH, Sheppard SE, Adams DM, Kariminejad A, Helaers R, Boon LM, Revencu N, Moore L, Barnett C, Haan E, Arts P, Vikkula M, Scott HS, Harvey NL. Byrne AB, et al. Among authors: brouillard p. Sci Transl Med. 2022 Mar 2;14(634):eabm4869. doi: 10.1126/scitranslmed.abm4869. Epub 2022 Mar 2. Sci Transl Med. 2022. PMID: 35235341
Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations.
Seront E, Van Damme A, Legrand C, Bisdorff-Bresson A, Orcel P, Funck-Brentano T, Sevestre MA, Dompmartin A, Quere I, Brouillard P, Revencu N, De Bortoli M, Hammer F, Clapuyt P, Dumitriu D, Vikkula M, Boon LM. Seront E, et al. Among authors: brouillard p. JCI Insight. 2023 Nov 8;8(21):e173095. doi: 10.1172/jci.insight.173095. JCI Insight. 2023. PMID: 37937645 Free PMC article. Clinical Trial.
Genetic causes of vascular malformations.
Brouillard P, Vikkula M. Brouillard P, et al. Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R140-9. doi: 10.1093/hmg/ddm211. Epub 2007 Jul 31. Hum Mol Genet. 2007. PMID: 17670762 Review.
Angiosarcoma arising from congenital primary lymphedema.
Janssens P, Dekeuleneer V, Van Damme A, Brouillard P, Revencu N, Clapuyt P, Ferreira I, Ballieux F, Vikkula M, Marot L, Baeck M, Boon LM. Janssens P, et al. Among authors: brouillard p. Pediatr Dermatol. 2018 Nov;35(6):e382-e388. doi: 10.1111/pde.13664. Epub 2018 Sep 14. Pediatr Dermatol. 2018. PMID: 30216524
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. Among authors: brouillard p. Sci Transl Med. 2020 Sep 9;12(560):eaax8013. doi: 10.1126/scitranslmed.aax8013. Sci Transl Med. 2020. PMID: 32908006
KRAS-driven model of Gorham-Stout disease effectively treated with trametinib.
Homayun-Sepehr N, McCarter AL, Helaers R, Galant C, Boon LM, Brouillard P, Vikkula M, Dellinger MT. Homayun-Sepehr N, et al. Among authors: brouillard p. JCI Insight. 2021 Aug 9;6(15):e149831. doi: 10.1172/jci.insight.149831. JCI Insight. 2021. PMID: 34156985 Free PMC article.
EPHB4 mutation causes adult and adolescent-onset primary lymphedema.
Greene AK, Brouillard P, Sudduth CL, Smits PJ, Konczyk DJ, Vikkula M. Greene AK, et al. Among authors: brouillard p. Am J Med Genet A. 2021 Dec;185(12):3810-3813. doi: 10.1002/ajmg.a.62416. Epub 2021 Jul 7. Am J Med Genet A. 2021. PMID: 34231312
33 results