Godfraind C - Search Results

1

A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment.

Renard L, Godfraind C, Boon LM, Vikkula M. Renard L, et al. Among authors: godfraind c. Head Neck. 2003 Feb;25(2):146-51. doi: 10.1002/hed.10220. Head Neck. 2003. PMID: 12509798

2

Reconstructive surgery in the management of a patient with CLOVES syndrome.

Ballieux F, Modarressi A, Hammer F, Clapuyt P, Docquier PL, Godfraind C, Feyaerts A, Brouillard P, Vikkula M, Boon LM. Ballieux F, et al. Among authors: godfraind c. J Plast Reconstr Aesthet Surg. 2013 Dec;66(12):1813-5. doi: 10.1016/j.bjps.2013.06.045. Epub 2013 Jul 16. J Plast Reconstr Aesthet Surg. 2013. PMID: 23867238 No abstract available.

3

Common somatic alterations identified in maffucci syndrome by molecular karyotyping.

Amyere M, Dompmartin A, Wouters V, Enjolras O, Kaitila I, Docquier PL, Godfraind C, Mulliken JB, Boon LM, Vikkula M. Amyere M, et al. Among authors: godfraind c. Mol Syndromol. 2014 Dec;5(6):259-67. doi: 10.1159/000365898. Epub 2014 Aug 26. Mol Syndromol. 2014. PMID: 25565925 Free PMC article.

4

Somatic Activating PIK3CA Mutations Cause Venous Malformation.

Limaye N, Kangas J, Mendola A, Godfraind C, Schlögel MJ, Helaers R, Eklund L, Boon LM, Vikkula M. Limaye N, et al. Among authors: godfraind c. Am J Hum Genet. 2015 Dec 3;97(6):914-21. doi: 10.1016/j.ajhg.2015.11.011. Am J Hum Genet. 2015. PMID: 26637981 Free PMC article.

5

Primary orbital melanoma treated with iodine-125 plaque radiotherapy.

De Potter P, Levecq L, Godfraind C, Renard L. De Potter P, et al. Among authors: godfraind c. Am J Ophthalmol. 2006 Nov;142(5):864-6. doi: 10.1016/j.ajo.2006.05.050. Am J Ophthalmol. 2006. PMID: 17056373

6

Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB.

Uebelhoer M, Nätynki M, Kangas J, Mendola A, Nguyen HL, Soblet J, Godfraind C, Boon LM, Eklund L, Limaye N, Vikkula M. Uebelhoer M, et al. Among authors: godfraind c. Hum Mol Genet. 2013 Sep 1;22(17):3438-48. doi: 10.1093/hmg/ddt198. Epub 2013 Apr 30. Hum Mol Genet. 2013. PMID: 23633549 Free PMC article.

7

Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma.

Rousseau E, Palm T, Scaravilli F, Ruchoux MM, Figarella-Branger D, Salmon I, Ellison D, Lacroix C, Chapon F, Mikol J, Vikkula M, Godfraind C. Rousseau E, et al. Among authors: godfraind c. Mol Cancer. 2007 Jul 12;6:47. doi: 10.1186/1476-4598-6-47. Mol Cancer. 2007. PMID: 17626628 Free PMC article.

8

Expression profiling of ependymomas unravels localization and tumor grade-specific tumorigenesis.

Palm T, Figarella-Branger D, Chapon F, Lacroix C, Gray F, Scaravilli F, Ellison DW, Salmon I, Vikkula M, Godfraind C. Palm T, et al. Among authors: godfraind c. Cancer. 2009 Sep 1;115(17):3955-68. doi: 10.1002/cncr.24476. Cancer. 2009. PMID: 19536879 Free article.

9

DNA alteration-based classification of uveal melanoma gives better prognostic stratification than immune infiltration, which has a neutral effect in high-risk group.

Narasimhaiah D, Legrand C, Damotte D, Remark R, Munda M, De Potter P, Coulie PG, Vikkula M, Godfraind C. Narasimhaiah D, et al. Among authors: godfraind c. Cancer Med. 2019 Jun;8(6):3036-3046. doi: 10.1002/cam4.2122. Epub 2019 Apr 25. Cancer Med. 2019. PMID: 31025552 Free PMC article.

10

Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomas.

Godfraind C, Rousseau E, Ruchoux MM, Scaravilli F, Vikkula M. Godfraind C, et al. Neuropathol Appl Neurobiol. 2003 Oct;29(5):462-71. doi: 10.1046/j.1365-2990.2003.00484.x. Neuropathol Appl Neurobiol. 2003. PMID: 14507338

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