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The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies: A European Register-Based Cohort Study.
Heino A, Morris JK, Garne E, Baldacci S, Barisic I, Cavero-Carbonell C, García-Villodre L, Given J, Jordan S, Loane M, Lutke LR, Neville AJ, Santoro M, Scanlon I, Tan J, de Walle HEK, Kiuru-Kuhlefelt S, Gissler M. Heino A, et al. Among authors: cavero carbonell c. Matern Child Health J. 2024 Jun;28(6):1020-1030. doi: 10.1007/s10995-024-03911-9. Epub 2024 Mar 4. Matern Child Health J. 2024. PMID: 38438690 Free PMC article.
Hospital care in the first 10 years of life of children with congenital anomalies in six European countries: data from the EUROlinkCAT cohort linkage study.
Morris JK, Loane M, Wahlich C, Tan J, Baldacci S, Ballardini E, Cavero-Carbonell C, Damkjær M, García-Villodre L, Gissler M, Given J, Gorini F, Heino A, Limb E, Lutke R, Neville A, Rissmann A, Scanlon L, Tucker DF, Urhoj SK, de Walle HE, Garne E. Morris JK, et al. Among authors: cavero carbonell c. Arch Dis Child. 2024 Apr 18;109(5):402-408. doi: 10.1136/archdischild-2023-326557. Arch Dis Child. 2024. PMID: 38373775 Free PMC article.
Higher risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study.
Urhoj SK, Morris J, Loane M, Ballardini E, Barrachina-Bonet L, Cavero-Carbonell C, Coi A, Gissler M, Given J, Heino A, Jordan S, Neville A, Santoro M, Tan J, Tucker D, Wellesley D, Garne E, Damkjaer M. Urhoj SK, et al. Among authors: cavero carbonell c. Acta Paediatr. 2024 May;113(5):1024-1031. doi: 10.1111/apa.17136. Epub 2024 Feb 7. Acta Paediatr. 2024. PMID: 38324400
Timing of Cardiac Surgical Interventions and Postoperative Mortality in Children With Severe Congenital Heart Defects Across Europe: Data From the EUROlinkCAT Study.
Damkjær M, Garne E, Loane M, Urhoj SK, Ballardini E, Cavero-Carbonell C, Coi A, García-Villodre L, Given J, Gissler M, Heino A, Jordan S, Limb E, Neville AJ, Pierini A, Rissmann A, Tan J, Scanlon I, Morris JK. Damkjær M, et al. Among authors: cavero carbonell c. J Am Heart Assoc. 2023 Dec 19;12(24):e029871. doi: 10.1161/JAHA.122.029871. Epub 2023 Dec 18. J Am Heart Assoc. 2023. PMID: 38108249 Free PMC article.
Surveillance of multiple congenital anomalies; searching for new associations.
Morris JK, Bergman JEH, Barisic I, Wellesley D, Tucker D, Limb E, Addor MC, Cavero-Carbonell C, Matias Dias C, Draper ES, Echevarría-González-de-Garibay LJ, Gatt M, Klungsøyr K, Lelong N, Luyt K, Materna-Kiryluk A, Nelen V, Neville A, Perthus I, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Rouget F, Sayers G, Wertelecki W, Kinsner-Ovaskainen A, Garne E. Morris JK, et al. Among authors: cavero carbonell c. Eur J Hum Genet. 2024 Apr;32(4):407-412. doi: 10.1038/s41431-023-01502-w. Epub 2023 Dec 5. Eur J Hum Genet. 2024. PMID: 38052905 Free PMC article. Review.
Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study.
Divin N, Given JE, Tan J, Astolfi G, Ballardini E, Barrachina-Bonet L, Cavero-Carbonell C, Coi A, Garne E, Gissler M, Heino A, Jordan S, Pierini A, Scanlon I, Urhøj SK, Morris JK, Loane M. Divin N, et al. Among authors: cavero carbonell c. BMJ Open. 2023 Oct 13;13(10):e068885. doi: 10.1136/bmjopen-2022-068885. BMJ Open. 2023. PMID: 37832979 Free PMC article.
Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study.
Tan J, Glinianaia SV, Rankin J, Pierini A, Santoro M, Coi A, Garne E, Loane M, Given JE, Brigden J, Ballardini E, Cavero-Carbonell C, de Walle HEK, García-Villodre L, Gatt M, Gissler M, Heino A, Jordan S, Khoshnood B, Klungsoyr K, Lelong N, Lutke RL, Neville AJ, Tucker D, Urhoj SK, Wellesley D, Morris JK. Tan J, et al. Among authors: cavero carbonell c. Paediatr Perinat Epidemiol. 2023 Nov;37(8):679-690. doi: 10.1111/ppe.13010. Epub 2023 Oct 10. Paediatr Perinat Epidemiol. 2023. PMID: 37817457
ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability.
Mazzucato M, Pozza LVD, Facchin P, Angin C, Agius F, Cavero-Carbonell C, Corrochano V, Hanusova K, Kirch K, Lambert D, Lucano C, Maiella S, Panzaru M, Rusu C, Weber S, Zurriaga O, Zvolsky M, Rath A. Mazzucato M, et al. Among authors: cavero carbonell c. Orphanet J Rare Dis. 2023 Sep 4;18(1):267. doi: 10.1186/s13023-023-02864-6. Orphanet J Rare Dis. 2023. PMID: 37667299 Free PMC article.
68 results