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Page 1
Variations in antenatal management and outcomes in haemolytic disease of the fetus and newborn: an international, retrospective, observational cohort study.
de Winter DP, Lopriore E, Thorup E, Petersen OB, Dziegiel MH, Sundberg K, Devlieger R, de Catte L, Lewi L, Debeer A, Houfflin-Debarge V, Ghesquiere L, Garabedian C, Le Duc K, Antolin E, Mendez N, Castleman J, Tse WT, Jouannic JM, Maurice P, Currie J, Mullen E, Geerts L, Rademan K, Khalil A, Poljak B, Prasad S, Tiblad E, Bohlin K, Geipel A, Rath J, Malone F, Mackin D, Yinon Y, Cohen S, Ryan G, Vlachodimitropoulou E, Gloning KP, Verlohren S, Mayer B, Lanna M, Faiola S, Sršen TP, Cerar LK, Snowise S, Sun L, Otaño L, Meller CH, Connors NK, Saxonhouse M, Wolter A, Bedei I, Klaritsch P, Jauch S, da Silva Ribeiro ET, Filho FMP, Martinez-Portilla RJ, Matias A, Abad OA, Roca JP, Grisi ÁGA, Navarro EJJC, van der Bom JG, de Haas M, Verweij EJ; DIONYSUS investigators. de Winter DP, et al. Among authors: antolin e. Lancet Haematol. 2024 Dec;11(12):e927-e937. doi: 10.1016/S2352-3026(24)00314-4. Epub 2024 Nov 8. Lancet Haematol. 2024. PMID: 39527958
Fetal Anemia: Determinants and Perinatal Outcomes according to the Method of Intrauterine Blood Transfusion.
Donepudi R, Jouannic JM, Maisonneuve E, Sananes N, Muller C, Sánchez-Durán MA, Molina F, Carretero P, Antolin E, Duyos I, Fabietti I, Khalil A, Coutinho CM, Sangi-Haghpeykar H, Sanz Cortes M. Donepudi R, et al. Among authors: antolin e. Fetal Diagn Ther. 2024;51(1):76-84. doi: 10.1159/000534523. Epub 2023 Oct 9. Fetal Diagn Ther. 2024. PMID: 37812923
Variations and Opportunities in Postnatal Management of Hemolytic Disease of the Fetus and Newborn.
de Winter DP, Verweij EJTJ, Debeer A, Devlieger R, Lewi L, Verbeeck S, Maurice P, Jouannic JM, Guillemin MG, Mailloux A, Pessoa Dos Santos MC, Amaral de Moura Sá Pacheco C, Lopes Moreira ME, Martins de Vasconcelos Vaena M, Bohlin K, Tiblad E, Thorup E, Petersen OB, Sanchez-Holgado M, Viejo Llorente A, Poljak B, Khalil A, Le Duc K, Ghesquiere L, Lozar Krivec J, Soltirovska-Šalamon A, Dame C, Blank JD, Hohnecker A, Saxonhouse M, Connors NK, Geipel A, Rath J, Prasad S, van Wyk L, Geerts L, Schuler R, Thon N, Leibovitch L, Cohen S, Canul-Euan AA, Kelly E, Raghuram K, Cavigioli F, Colombo SFG, Elanjikal Z, Brayley J, Pfurtscheller D, Pichler G, Alcázar Grisi ÁG, Chávez Navarro EJJ, Pereira-Nunes J, Soares H, Zhou M, Garcia Borau MJ, Moliner Calderón E, Galletti MF, Mariani GL, Mackin D, Malone F, Lampland A, Tse WT, Castleman J, van der Bom JG, de Haas M, Lopriore E; Worldwide Collaboration for Hemolytic Disease of the Fetus and Newborn (DIONYSUS) Investigators. de Winter DP, et al. JAMA Netw Open. 2025 Jan 2;8(1):e2454330. doi: 10.1001/jamanetworkopen.2024.54330. JAMA Netw Open. 2025. PMID: 39792381 Free PMC article.
Prenatal Management and Perinatal Outcome in a Large Series of Hydrops Fetalis.
Sebastián de Lucas LM, Ordás Álvarez P, de Castro Marzo L, Illescas Molina T, Herrero B, Bartha JL, Antolín E. Sebastián de Lucas LM, et al. Among authors: antolin e. Fetal Diagn Ther. 2024;51(4):335-342. doi: 10.1159/000538857. Epub 2024 Apr 20. Fetal Diagn Ther. 2024. PMID: 38643756
Prevalence of contrast intravasation in HyCoSy/HyFoSy. Results of a multicenter study and systematic review of the literature with meta-analysis.
Alcazar JL, Peñate L, Casanova V, Piera C, Engels V, Medina M, Ros C, Sotillo L, Antolín E, Pelayo I, Bermejo C, Pascual MÁ, Graupera B, Barreche I, Orozco R, Ajossa S, Guerriero S. Alcazar JL, et al. Among authors: antolin e. Eur J Obstet Gynecol Reprod Biol. 2024 Dec 9;305:100-106. doi: 10.1016/j.ejogrb.2024.12.004. Online ahead of print. Eur J Obstet Gynecol Reprod Biol. 2024. PMID: 39673914
Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene.
Tenorio-Castano J, Mansilla Aparicio E, García Santiago FA, Klotz CM, Regojo RM, Anguita E, Ryan E, Juusola J, Herrero B, Arias P, Parra A, Pascual P, Gallego N, Cazalla M, Rodriguez-González R, Antolín E, Nevado J, Ruiz-Perez VL, Lapunzina P. Tenorio-Castano J, et al. Among authors: antolin e. Clin Genet. 2024 Dec;106(6):713-720. doi: 10.1111/cge.14601. Epub 2024 Aug 27. Clin Genet. 2024. PMID: 39191491
Identification of copy-number variants in patients with overgrowth disorders.
Parra A, Tenorio-Castano J, Nevado J, Cazalla M, Miranda-Alcaraz L, Gallego-Zazo N, Silván C, Arias P, Pozo-Román J, Ballesta-Martínez MJ, Guillén-Navarro E, Arroyo I, Lotersztein V, Cosentino V, González-Meneses A, Galán E, Rosell J, Ramos F; Spanish OverGrowth Registry Initiative; Lapunzina P. Parra A, et al. Clin Genet. 2024 Nov;106(5):614-624. doi: 10.1111/cge.14596. Epub 2024 Aug 1. Clin Genet. 2024. PMID: 39091142
Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis.
Abulí A, Antolín E, Borrell A, Garcia-Hoyos M, García Santiago F, Gómez Manjón I, Maíz N, González González C, Rodríguez-Revenga L, Valenzuena Palafoll I, Suela J. Abulí A, et al. Among authors: antolin e. J Med Genet. 2024 Jul 19;61(8):727-733. doi: 10.1136/jmg-2024-109878. J Med Genet. 2024. PMID: 38834294 Free article.
76 results