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Page 1
Meningocele in a congolese female with beckwith-wiedemann phenotype.
Mbuyi-Musanzayi S, Lubala Kasole T, Lumaka A, Kayembe Kitenge T, Kabamba Ngombe L, Kalenga Muenze P, Lukusa Tshilobo P, Tshilombo Katombe F, Banza Lubaba Nkulu C, Devriendt K. Mbuyi-Musanzayi S, et al. Case Rep Genet. 2014;2014:989425. doi: 10.1155/2014/989425. Epub 2014 Dec 28. Case Rep Genet. 2014. PMID: 25610673 Free PMC article.
Mirror-image gastroschisis in monochorionic female twins.
Lubala TK, Mbuyi-Musanzayi S, Lubala N, Luboya ON, Kalenga PM, Devriendt K, Lukusa-Tshilobo P. Lubala TK, et al. Eur J Med Genet. 2015 Apr;58(4):266-9. doi: 10.1016/j.ejmg.2015.03.001. Epub 2015 Mar 14. Eur J Med Genet. 2015. PMID: 25782636
Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the Congo.
Kayembe Kitenge T, Kasole Lubala T, Mbuyi-Musanzayi S, Kabamba Ngombe L, Katshiez Nawej C, Musa Obadia P, Banza Lubaba Nkulu C, Nemery B, Devriendt K. Kayembe Kitenge T, et al. Clin Dysmorphol. 2016 Oct;25(4):178-80. doi: 10.1097/MCD.0000000000000129. Clin Dysmorphol. 2016. PMID: 27088280 No abstract available.
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. Clin Genet. 2017 Aug;92(2):166-171. doi: 10.1111/cge.12948. Epub 2017 Jan 16. Clin Genet. 2017. PMID: 27925162
Anthropometric and aesthetic outcomes for the nasolabial region in 101 consecutive African children with unilateral cleft lip one year after repair using the anatomical subunit approximation technique.
Mbuyi-Musanzayi S, Tshilombo Katombe F, Lukusa Tshilobo P, Kalenga Mwenze Kayamba P, Devriendt K, Reychler H. Mbuyi-Musanzayi S, et al. Int J Oral Maxillofac Surg. 2017 Oct;46(10):1338-1345. doi: 10.1016/j.ijom.2017.05.022. Epub 2017 Jun 16. Int J Oral Maxillofac Surg. 2017. PMID: 28629945
Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo.
Van Brusselen D, Kayembe-Kitenge T, Mbuyi-Musanzayi S, Lubala Kasole T, Kabamba Ngombe L, Musa Obadia P, Kyanika Wa Mukoma D, Van Herck K, Avonts D, Devriendt K, Smolders E, Nkulu CBL, Nemery B. Van Brusselen D, et al. Among authors: mbuyi musanzayi s. Lancet Planet Health. 2020 Apr;4(4):e158-e167. doi: 10.1016/S2542-5196(20)30059-0. Lancet Planet Health. 2020. PMID: 32353296 Free article.
Fragile X syndrome with mosaic size mutation in a Bantu patient from Central Africa.
Lubala TK, Lumaka A, Mbuyi-Musanzayi S, Kayembe T, Shongo MYP, Mukuku O, Lubala N, Malamba-Lez D, Luboya ON, Lukusa-Tshilobo P. Lubala TK, et al. Among authors: mbuyi musanzayi s. Clin Dysmorphol. 2018 Apr;27(2):66-69. doi: 10.1097/MCD.0000000000000208. Clin Dysmorphol. 2018. PMID: 29319541 No abstract available.
Agnathia otocephaly: A case from the Katanga Copperbelt.
Kayembe-Kitenge T, Manyong'a Kadiamba V, de Luca C, Musa Obadia P, Kasamba Ilunga E, Mbuyi-Musanzayi S, Nawrot T, Lubaba Nkulu CB, Nemery B, Devriendt K. Kayembe-Kitenge T, et al. Among authors: mbuyi musanzayi s. Birth Defects Res. 2020 Oct;112(16):1287-1291. doi: 10.1002/bdr2.1758. Epub 2020 Jul 8. Birth Defects Res. 2020. PMID: 32639113
17 results