Segers K - Search Results

1

Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors.

Mutesa L, Pierquin G, Janin N, Segers K, Thomée C, Provenzi M, Bours V. Mutesa L, et al. Among authors: segers k. Cancer Genet Cytogenet. 2008 Apr 1;182(1):40-2. doi: 10.1016/j.cancergencyto.2007.12.005. Cancer Genet Cytogenet. 2008. PMID: 18328949 Free article.

2

Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis.

Mutesa L, Pierquin G, Segers K, Vanbellinghen JF, Gahimbare L, Bours V. Mutesa L, et al. Among authors: segers k. J Trop Pediatr. 2008 Oct;54(5):350-2. doi: 10.1093/tropej/fmn034. Epub 2008 May 22. J Trop Pediatr. 2008. PMID: 18499737 Free article.

3

Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants.

Mutesa L, Azad AK, Verhaeghe C, Segers K, Vanbellinghen JF, Ngendahayo L, Rusingiza EK, Mutwa PR, Rulisa S, Koulischer L, Cassiman JJ, Cuppens H, Bours V. Mutesa L, et al. Among authors: segers k. Chest. 2009 May;135(5):1233-1242. doi: 10.1378/chest.08-2246. Epub 2008 Nov 18. Chest. 2009. PMID: 19017867 Free article.

4

Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.

Mutesa L, Vanbellinghen JF, Hellin AC, Segers K, Jamar M, Pierquin G, Bours V. Mutesa L, et al. Among authors: segers k. Genet Couns. 2009;20(1):9-17. Genet Couns. 2009. PMID: 19400538

5

3-years experience review of neonatal screening for hemoglobin disorders using tandem mass spectrometry.

Boemer F, Cornet Y, Libioulle C, Segers K, Bours V, Schoos R. Boemer F, et al. Among authors: segers k. Clin Chim Acta. 2011 Jul 15;412(15-16):1476-9. doi: 10.1016/j.cca.2011.04.031. Epub 2011 May 4. Clin Chim Acta. 2011. PMID: 21569767

6

BRCA1 germline mutation and glioblastoma development: report of cases.

Boukerroucha M, Josse C, Segers K, El-Guendi S, Frères P, Jerusalem G, Bours V. Boukerroucha M, et al. Among authors: segers k. BMC Cancer. 2015 Mar 26;15:181. doi: 10.1186/s12885-015-1205-1. BMC Cancer. 2015. PMID: 25880076 Free PMC article.

7

Evaluation of BRCA1-related molecular features and microRNAs as prognostic factors for triple negative breast cancers.

Boukerroucha M, Josse C, ElGuendi S, Boujemla B, Frères P, Marée R, Wenric S, Segers K, Collignon J, Jerusalem G, Bours V. Boukerroucha M, et al. Among authors: segers k. BMC Cancer. 2015 Oct 21;15:755. doi: 10.1186/s12885-015-1740-9. BMC Cancer. 2015. PMID: 26490435 Free PMC article.

8

Breast cancer in a male-to-female transsexual patient with a BRCA2 mutation.

Corman V, Potorac I, Manto F, Dassy S, Segers K, Thiry A, Bours V, Daly AF, Beckers A. Corman V, et al. Among authors: segers k. Endocr Relat Cancer. 2016 May;23(5):391-7. doi: 10.1530/ERC-16-0057. Epub 2016 Mar 21. Endocr Relat Cancer. 2016. PMID: 27000661 Free article.

9

A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases.

Boemer F, Fasquelle C, d'Otreppe S, Josse C, Dideberg V, Segers K, Guissard V, Capraro V, Debray FG, Bours V. Boemer F, et al. Among authors: segers k. Sci Rep. 2017 Dec 15;7(1):17641. doi: 10.1038/s41598-017-18038-x. Sci Rep. 2017. PMID: 29247206 Free PMC article.

10

Innovative methodology for the identification of soluble biomarkers in fresh tissues.

Costanza B, Turtoi A, Bellahcène A, Hirano T, Peulen O, Blomme A, Hennequière V, Mutijima E, Boniver J, Meuwis MA, Josse C, Koopmansch B, Segers K, Yokobori T, Fahmy K, Thiry M, Coimbra C, Garbacki N, Colige A, Baiwir D, Bours V, Louis E, Detry O, Delvenne P, Nishiyama M, Castronovo V. Costanza B, et al. Among authors: segers k. Oncotarget. 2018 Jan 31;9(12):10665-10680. doi: 10.18632/oncotarget.24366. eCollection 2018 Feb 13. Oncotarget. 2018. PMID: 29535834 Free PMC article.

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