Mutesa L - Search Results

1

Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.

Uwineza A, Hitayezu J, Jamar M, Caberg JH, Murorunkwere S, Janvier N, Bours V, Mutesa L. Uwineza A, et al. Among authors: mutesa l. J Trop Pediatr. 2016 Feb;62(1):38-45. doi: 10.1093/tropej/fmv065. Epub 2015 Oct 27. J Trop Pediatr. 2016. PMID: 26507407 Free PMC article.

2

The Evolution of Post-Vaccine G8P[4] Group a Rotavirus Strains in Rwanda; Notable Variance at the Neutralization Epitope Sites.

Mwangi PN, Potgieter RL, Uwimana J, Mutesa L, Muganga N, Murenzi D, Tusiyenge L, Mwenda JM, Mogotsi MT, Rakau K, Esona MD, Steele AD, Seheri ML, Nyaga MM. Mwangi PN, et al. Among authors: mutesa l. Pathogens. 2023 Apr 28;12(5):658. doi: 10.3390/pathogens12050658. Pathogens. 2023. PMID: 37242329 Free PMC article.

3

Agreement between Xpert and AmpFire tests for high-risk human papillomavirus among HIV-positive women in Rwanda.

Murangwa A, Desai KT, Gage JC, Murenzi G, Tuyisenge P, Kanyabwisha F, Musafili A, Kubwimana G, Mutesa L, Anastos K, Kim HY, Castle PE. Murangwa A, et al. Among authors: mutesa l. Afr J Lab Med. 2022 Oct 19;11(1):1827. doi: 10.4102/ajlm.v11i1.1827. eCollection 2022. Afr J Lab Med. 2022. PMID: 36353194 Free PMC 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

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

6

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

7

Neonatal screening for sickle cell disease in Central Africa: a study of 1825 newborns with a new enzyme-linked immunosorbent assay test.

Mutesa L, Boemer F, Ngendahayo L, Rulisa S, Rusingiza EK, Cwinya-Ay N, Mazina D, Kariyo PC, Bours V, Schoos R. Mutesa L, et al. J Med Screen. 2007;14(3):113-6. doi: 10.1258/096914107782066211. J Med Screen. 2007. PMID: 17925082

8

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. 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.

9

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. 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.

10

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. Chest. 2009 May;135(5):1233-1242. doi: 10.1378/chest.08-2246. Epub 2008 Nov 18. Chest. 2009. PMID: 19017867 Free article.

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