Mutesa L - Search Results

1

An Assessment of the Knowledge and Perceptions of Precision Medicine (PM) in the Rwandan Healthcare Setting.

Musanabaganwa C, Ruton H, Ruhangaza D, Nsabimana N, Kayitare E, Muvunyi TZ, Semakula M, Ntirenganya F, Musoni E, Ndoli J, Hategekimana E, Nassir A, Makokha F, Uwimana A, Gasana J, Munezero PC, Uwinkindi F, Muvunyi CM, Nyirazinyoye L, Mazarati JB, Mutesa L. Musanabaganwa C, et al. Among authors: mutesa l. J Pers Med. 2023 Dec 14;13(12):1707. doi: 10.3390/jpm13121707. J Pers Med. 2023. PMID: 38138934 Free PMC article.

2

Prediction and validation of the structural features of Ov58GPCR, an immunogenic determinant of Onchocerca volvulus.

Shey RA, Ghogomu SM, Njume FN, Gainkam LOT, Poelvoorde P, Mutesa L, Robert A, Humblet P, Munyampundu JP, Kamgno J, Lelubre C, Vanhamme L, Souopgui J. Shey RA, et al. Among authors: mutesa l. PLoS One. 2018 Sep 26;13(9):e0202915. doi: 10.1371/journal.pone.0202915. eCollection 2018. PLoS One. 2018. PMID: 30256790 Free PMC article.

3

VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report.

Uwineza A, Caberg JH, Hitayezu J, Wenric S, Mutesa L, Vial Y, Drunat S, Passemard S, Verloes A, El Ghouzzi V, Bours V. Uwineza A, et al. Among authors: mutesa l. Eur J Med Genet. 2019 Aug;62(8):103704. doi: 10.1016/j.ejmg.2019.103704. Epub 2019 Jun 14. Eur J Med Genet. 2019. PMID: 31207318 Free article.

4

[Hutchinson-Gilford progeria syndrome: clinical and molecular analysis in an African patient].

Mutesa L, Pierquin G, Cwiny-Ay N, Buzizi P, Bours V. Mutesa L, et al. Rev Med Liege. 2007 Mar;62(3):155-8. Rev Med Liege. 2007. PMID: 17511383 Free article. French.

5

Diagnostic challenges of cystic fibrosis in patients of African origin.

Mutesa L, Bours V. Mutesa L, et al. J Trop Pediatr. 2009 Oct;55(5):281-6. doi: 10.1093/tropej/fmp064. Epub 2009 Jul 22. J Trop Pediatr. 2009. PMID: 19625487 Review. No abstract available.

6

22q11.2 deletion syndrome in diverse populations.

Kruszka P, Addissie YA, McGinn DE, Porras AR, Biggs E, Share M, Crowley TB, Chung BH, Mok GT, Mak CC, Muthukumarasamy P, Thong MK, Sirisena ND, Dissanayake VH, Paththinige CS, Prabodha LB, Mishra R, Shotelersuk V, Ekure EN, Sokunbi OJ, Kalu N, Ferreira CR, Duncan JM, Patil SJ, Jones KL, Kaplan JD, Abdul-Rahman OA, Uwineza A, Mutesa L, Moresco A, Obregon MG, Richieri-Costa A, Gil-da-Silva-Lopes VL, Adeyemo AA, Summar M, Zackai EH, McDonald-McGinn DM, Linguraru MG, Muenke M. Kruszka P, et al. Among authors: mutesa l. Am J Med Genet A. 2017 Apr;173(4):879-888. doi: 10.1002/ajmg.a.38199. Am J Med Genet A. 2017. PMID: 28328118 Free PMC article.

7

Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutation.

Mutesa L, Muganga N, Lissens W, Boemer F, Schoos R, Pierquin G, Bours V. Mutesa L, et al. J Trop Pediatr. 2007 Dec;53(6):434-7. doi: 10.1093/tropej/fmm056. Epub 2007 Jul 5. J Trop Pediatr. 2007. PMID: 17616540

8

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.

Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, Mbuyi-Musanzayi S, Breckpot J, Holvoet M, de Ravel T, Van Buggenhout G, Peeters H, Donnai D, Mutesa L, Verloes A, Lukusa Tshilobo P, Devriendt K. Lumaka A, et al. Among authors: mutesa l. Clin Genet. 2017 Aug;92(2):166-171. doi: 10.1111/cge.12948. Epub 2017 Jan 16. Clin Genet. 2017. PMID: 27925162

9

Precocious puberty associated with partial trisomy 18q and monosomy 11q.

Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A. Mutesa L, et al. Genet Couns. 2007;18(2):201-7. Genet Couns. 2007. PMID: 17710872

10

Malaria parasite carriage and risk determinants in a rural population: a malariometric survey in Rwanda.

Kateera F, Mens PF, Hakizimana E, Ingabire CM, Muragijemariya L, Karinda P, Grobusch MP, Mutesa L, van Vugt M. Kateera F, et al. Among authors: mutesa l. Malar J. 2015 Jan 21;14:16. doi: 10.1186/s12936-014-0534-x. Malar J. 2015. PMID: 25604040 Free PMC article.

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