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Page 1
Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa.
Kabuyi PL, Mbayabo G, Ngole M, Zola AL, Race V, Matthijs G, Van Geet C, Tshilobo PL, Devriendt K, Mikobi TM. Kabuyi PL, et al. Among authors: devriendt k. EJHaem. 2023 Jul 19;4(3):595-601. doi: 10.1002/jha2.735. eCollection 2023 Aug. EJHaem. 2023. PMID: 37601858 Free PMC article.
Genetic Modulators of Diversity in the Biological Expression of Sickle Cell Anemia in Patients from Democratic Republic of Congo: Role of βs-globin Haplotypes.
Ngole M, Mbayabo G, Lumbala P, Race V, Mvuama N, Deman S, Souche E, Lukusa PT, Van Geet C, Devriendt K, Matthijs G, Lumaka A, Cleynen I. Ngole M, et al. Among authors: devriendt k. Mediterr J Hematol Infect Dis. 2025 Jan 1;17(1):e2025001. doi: 10.4084/MJHID.2025.001. eCollection 2025. Mediterr J Hematol Infect Dis. 2025. PMID: 39830798 Free PMC article. No abstract available.
First Insights Into the Phenotype and Genotype of Inherited Retinal Disorders in the Democratic Republic of Congo (DRC).
Nsiangani Lusambo N, Fuanani P, Mubungu G, Makay P, Ngole M, Ngweme G, Kajingulu FP, Perry D, Kesari A, Calzetti G, Rivolta C, Devriendt K, Lukusa Tshilobo P, Thorpe E, Taft RJ, Lumaka A. Nsiangani Lusambo N, et al. Among authors: devriendt k. Ann Hum Genet. 2025 Jul;89(4):141-148. doi: 10.1111/ahg.12604. Epub 2025 May 16. Ann Hum Genet. 2025. PMID: 40377368
Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature.
Makay P, Fasquelle C, Mubungu G, Ekolo E, Mupuala A, Fuanani P, Sonet I, Charloteaux B, Palmeira L, Gatot JS, Lukusa Tshilobo P, Bours V, Devriendt K, Lumaka A. Makay P, et al. Among authors: devriendt k. Clin Dysmorphol. 2024 Dec 10:10.1097/MCD.0000000000000510. doi: 10.1097/MCD.0000000000000510. Online ahead of print. Clin Dysmorphol. 2024. PMID: 39807610 No abstract available.
Persistent Uninterpretable or Failed Prenatal Cell-Free DNA Screening Indicates a High-Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA-Analysis: A Prospective Cohort Study.
Lannoo L, Van Den Bogaert K, Belmans A, Brison N, Dehaspe L, De Langhe E, Vancoillie L, Parijs I, Vermeesch JR, Devriendt K, Van Calsteren K. Lannoo L, et al. Among authors: devriendt k. Prenat Diagn. 2025 May;45(5):581-590. doi: 10.1002/pd.6778. Epub 2025 Mar 20. Prenat Diagn. 2025. PMID: 40114366
A cross-country comparison of pregnant women's decision-making and perspectives when opting for non-invasive prenatal testing in the Netherlands and Belgium.
Lannoo L, van der Meij KRM, Bekker MN, De Catte L, Deckers S, Devriendt K, Roggen N, Galjaard RH, Gitsels-van der Wal J, Macville MVE, Martin L, Sistermans EA, Van Calsteren K, Van Keirsbilck J, Crombag N, Henneman L. Lannoo L, et al. Among authors: devriendt k. Prenat Diagn. 2023 Mar;43(3):294-303. doi: 10.1002/pd.6329. Epub 2023 Feb 17. Prenat Diagn. 2023. PMID: 36740754
Unexpected High Prevalence of Focal Facial Dermal Dysplasia (FFDD) Type IV Is Linked to a Founder Effect in the Belgian Population.
Beyens A, Van De Voorde S, Guerreiro Santano Ramos Da Silva M, De Meulemeester S, Devriendt K, Goeteyn M, Janssens S, Kooy RF, Rosseel T, Symoens S, Hes FJ, Keymolen K, Dimitrov B, Callewaert B. Beyens A, et al. Among authors: devriendt k. Clin Genet. 2025 May;107(5):579-581. doi: 10.1111/cge.14705. Epub 2025 Jan 19. Clin Genet. 2025. PMID: 39828664
606 results