Search Results - Lukusa, Prosper
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Homozygous Deletion Alpha-Thalassemia and Hereditary Persistence of Fetal Hemoglobin, Two Genetic Factors Predictive the Reduction of Morbidity and Mortality During Pregnancy in Si... by Mikobi, Tite Minga, Lukusa, Prosper Tshilobo, Muamba, Jean-Marie Mbuyi, Rhama, Tozin
Published 2019Text -
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DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo by Ngole, Mamy, Race, Valerie, Mbayabo, Gloire, Lumbala, Paul, Songo, Cathy, Lukusa, Prosper Tshilobo, Devriendt, Koenraad, Matthijs, Gert, Lumaka, Aimé
Published 2022Text -
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Clinical presentation and evolution of Xia-Gibbs syndrome due to p.Gly375ArgfsTer3 variant in a patient from DR Congo (Central Africa) by Mubungu, Gerrye, Makay, Prince, Boujemla, Bouchra, Yanda, Stephane, Posey, Jennifer E., Lupski, James R., Bours, Vincent, Lukusa, Prosper, Devriendt, Koenraad, Lumaka, Aimé
Published 2021Text -
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Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α(3.7) triplication in congolese patients than in worldwide series by Mikobi, Tite Minga, Lukusa, Prosper Tshilobo, Aloni, Michel Ntetani, Lumaka, Aimé, Akilimali, Pierre Zalagile, Devriendt, Koenraad, Matthijs, Gert, Mbuyi Muamba, Jean‐Marie, Race, Valerie
Published 2017Text -
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Protective BCL11A and HBS1L‐MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia by Mikobi, Tite Minga, Tshilobo Lukusa, Prosper, Aloni, Michel Ntetani, Lumaka, Aimé Zola, Kaba, Didine Kinkodi, Devriendt, Koenraad, Matthijs, Gert, Mbuyi Muamba, Jean Marie, Race, Valérie
Published 2017Text -
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A COMPREHENSIVE CLINICAL AND GENETIC STUDY IN 127 PATIENTS WITH ID IN KINSHASA, DR CONGO by Lumaka, Aimé, Race, Valerie, Peeters, Hilde, Corveleyn, Anniek, Coban-Akdemir, Zeynep, Jhangiani, Shalini N., Xiaofei, Song, Mubungu, Gerrye, Posey, Jennifer, Lupski, James R, Vermeesch, Joris R, Lukusa, Prosper, Devriendt, Koenraad
Published 2018Text -
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Exploring association between MBL2 gene polymorphisms and the occurrence of clinical blackwater fever through a case–control study in Congolese children by Bodi, Joseph M., Nsibu, Célestin N., Longenge, Roland L., Aloni, Michel N., Akilimali, Pierre Z., Kayembe, Patrick K., Omar, Ahmeddin H., Verhaegen, Jan, Tshibassu, Pierre M., Lukusa, Prosper T., Lumaka, Aimé, Hirayama, Kenji
Published 2020Text -
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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity by Cheng, Hanyin, Capponi, Simona, Wakeling, Emma, Marchi, Elaine, Li, Quan, Zhao, Mengge, Weng, Chunhua, Piatek, Stefan G., Ahlfors, Helena, Kleyner, Robert, Rope, Alan, Lumaka, Aimé, Lukusa, Prosper, Devriendt, Koenraad, Vermeesch, Joris, Posey, Jennifer E., Palmer, Elizabeth E., Murray, Lucinda, Leon, Eyby, Diaz, Jullianne, Worgan, Lisa, Mallawaarachchi, Amali, Vogt, Julie, de Munnik, Sonja A., Dreyer, Lauren, Baynam, Gareth, Ewans, Lisa, Stark, Zornitza, Lunke, Sebastian, Gonçalves, Ana R., Soares, Gabriela, Oliveira, Jorge, Fassi, Emily, Willing, Marcia, Waugh, Jeff L., Faivre, Laurence, Riviere, Jean-Baptiste, Moutton, Sebastien, Mohammed, Shehla, Payne, Katelyn, Walsh, Laurence, Begtrup, Amber, Sacoto, Maria J. Guillen, Douglas, Ganka, Alexander, Nora, Buckley, Michael F., Mark, Paul R., Adès, Lesley C., Sandaradura, Sarah A., Lupski, James R., Roscioli, Tony, Agrawal, Pankaj B., Kline, Antonie D., Wang, Kai, Timmers, H. T. Marc, Lyon, Gholson J.
Published 2019Text