Proceedings of the 14th International Newborn Brain Conference: Fetal and/or neonatal brain development, both normal and abnormal.

Autor: Abdi K, Adams E, Agarwal S, Ergun MA, Altamimi T, Aral A, Arfi H, Armour E, Armstrong L, Mulkey SB, Bambi J, Baxter L, Benner E, Bhattacharya S, Biselele T, Bolay H, Mayorga PC, Carrasco M, Carter E, Chao A, Cooke A, Corsi-Cabrera M, Cubero-Rego L, Cuddyer D, Gano DD, Cubero-Rego MLA, de Ribaupierre S, Drobyshevsky A, El-Dib M, Elmazoglu Z, Emrick L, Epstein A, Erdei C, Flynn P, Duerden EG, Gibson K, Gregory S, Topa EGA, Aliyu MH, Harmony T, Harshbarger J, Hartley C, Hayakawa M, Kazan HH, Inder T, Ito Y, Jain V, Jurkiewicz M, Kapoor B, Kebaya L, Keles Gulnerman E, Kidokoro H, Kling E, Kumai S, Lebane D, Lemmon M, Salihu HM, Marchant S, Maxfield C, Mbayabo G, Meyerink P, Millman R, Mitsumatsu T, Nakata T, Narita H, Natsume J, Pacheco J, Pagano L, Pardo A, Peyton C, Pineda R, Reddy S, Ricardo-Garcell J, Rikard B, Roychaudhuri S, Nichols ES, Sadowska-Krawczenko I, Sato Y, Sawamura F, Scher M, Sharon D, Sheldon Y, Shiraki A, Singh E, Steele T, Suzui R, Tady BP, Taga G, Tarui T, Trapp N, Tristao L, Tuka D, Ushida T, Usman F, Venkatesan C, Watanabe H, Witulska-Alagöz A, Yamamoto H, Yarnykh V, Younge N

Publikováno v: Journal of neonatal-perinatal medicine [J Neonatal Perinatal Med] 2023; Vol. 16 (s1), pp. S1-S19.

Dysmorphism and major anomalies are a main predictor of survival in newborns admitted to the neonatal intensive care unit in the Democratic Republic of Congo.

Autor: Mubungu G; Faculty of Medicine, Center for Human Genetics, University of Kinshasa, Kinshasa, Congo.; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo.; Center for Human Genetics, University Hospital, University of Leuven, Leuven, Belgium., Makay P; Faculty of Medicine, Center for Human Genetics, University of Kinshasa, Kinshasa, Congo.; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo., Lumaka A; Faculty of Medicine, Center for Human Genetics, University of Kinshasa, Kinshasa, Congo.; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo.; Département des Sciences Biomédicales et Précliniques, GIGA-R, Laboratoire de Génétique Humaine, University of Liège, Liège, Belgium.; Institut National de Recherche Biomédicale, Kinshasa, Kinshasa, Congo., Mvuama N; Faculty of Medicine, Kinshasa School of Public Health, University of Kinshasa, Kinshasa, Congo., Tshika D; Faculty of Medicine, Center for Human Genetics, University of Kinshasa, Kinshasa, Congo.; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo., Tady BP; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo., Biselele T; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo., Roelants M; Department of Public Health and Primary Care, Environment and Health, KU Leuven-University of Leuven, Leuven, Belgium., Tshilobo PL; Faculty of Medicine, Center for Human Genetics, University of Kinshasa, Kinshasa, Congo.; Faculty of Medicine, Department of Pediatrics, University of Kinshasa, Kinshasa, Congo.; Center for Human Genetics, University Hospital, University of Leuven, Leuven, Belgium.; Institut National de Recherche Biomédicale, Kinshasa, Kinshasa, Congo., Devriendt K; Center for Human Genetics, University Hospital, University of Leuven, Leuven, Belgium.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Feb; Vol. 185 (2), pp. 453-460. Date of Electronic Publication: 2020 Nov 27.

A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family.

Autor: Lumaka A; Centre for Human Genetics, University Hospitals, University of Leuven, P.O. Box 602, 3000 Leuven, Belgium; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; Department of Pediatrics, University Hospitals, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; INRB, Institut National de Recherche Biomedicale, P.O. Box, Kin I, Kinshasa, The Democratic Republic of the Congo., Mubungu G; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; Department of Pediatrics, University Hospitals, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; INRB, Institut National de Recherche Biomedicale, P.O. Box, Kin I, Kinshasa, The Democratic Republic of the Congo., Mukaba P; Department of Surgery, University Hospitals, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo., Mutantu P; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; INRB, Institut National de Recherche Biomedicale, P.O. Box, Kin I, Kinshasa, The Democratic Republic of the Congo., Luyeye G; Department of Medical Imaging, Provincial General Hospital of Kinshasa, P.O. Box, Kin I, Kinshasa, The Democratic Republic of the Congo., Corveleyn A; Centre for Human Genetics, University Hospitals, University of Leuven, P.O. Box 602, 3000 Leuven, Belgium., Tady BP; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; Department of Pediatrics, University Hospitals, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo., Lukusa Tshilobo P; Centre for Human Genetics, University Hospitals, University of Leuven, P.O. Box 602, 3000 Leuven, Belgium; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; Department of Pediatrics, University Hospitals, University of Kinshasa, P.O. Box 123, Kin XI, Kinshasa, The Democratic Republic of the Congo; INRB, Institut National de Recherche Biomedicale, P.O. Box, Kin I, Kinshasa, The Democratic Republic of the Congo., Devriendt K; Centre for Human Genetics, University Hospitals, University of Leuven, P.O. Box 602, 3000 Leuven, Belgium. Electronic address: koenraad.devriendt@uzleuven.be.

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2014 Mar; Vol. 57 (4), pp. 169-73. Date of Electronic Publication: 2014 Jan 28.