Publications (922)
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Prescriptions for insulin and insulin analogues in children with and without major congenital anomalies: a data linkage cohort study across six European regions
Prescriptions for insulin and insulin analogues in children with and without major congenital anomalies: a data linkage cohort study across six European regions
Given J, Morris JK, Garne E, Ballardini E, Barrachina-Bonet L, Cavero-Carbonell C, Gissler M, Gorini F, Heino A, Jordan S, Neville AJ, Pierini A, Scanlon I, Tan J, Urhoj SK, Loane M
Eur J Pediatr 2023
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Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions
Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions
Damkjaer M, Loane M, Urhøj SK, Ballardini E, Cavero- Carbonell C, Coi A, García-Villodre L, Given JE, Gissler M, Heino A, Jordan S, Neville AJ, Pierini A, Tan J, Scanlon I, Garne E, Morris JK
BMJ Open 2022;12(10):e061746
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Survival of children with rare structural congenital anomalies: a multi-registry cohort study
Survival of children with rare structural congenital anomalies: a multi-registry cohort study
Coi A, Santoro M, Pierini A, Rankin J, Glinianaia SV, Tan J, Reid AK, Garne E, Loane M, Given J, Ballardini A, Cavero-Carbonell C, de Walle HEK, Gatt M, García-Villodre L, Gissler M, Jordan S, Kiuru-Kuhlefelt S, Kjaer Urhoj S, Klungsøyr K, Lelong N, Lutke LR, Neville AJ, Rahshenas M, Scanlon I, Wellesley D, Morris JK
Orphanet Journal of Rare Diseases 2022;17(1):142
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Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study
Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study
Santoro M, Garne E, Coi A, Tan J, Loane M, Ballardini E, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Jordan S, Klungsøyr K, Lelong N, Urhoj SK, Wellesley DG, Morris JK
Arch Dis Child 2023;108(7):550-55
Anomalies: Pierre Robin Sequence -
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study
Santoro M, Coi A, Pierini A, Rankin J, Glinianaia SV, Tan J, Reid A, Garne E, Loane M, Given J, Aizpurua A, Astolfi G, Barisic I, Cavero‐Carbonell C, de Walle HEK, Den Hond E, García‐Villodre L, Gatt M, Gissler M, Jordan S, Khoshnood B, Kiuru‐Kuhlefelt S, Klungsøyr K, Lelong N, Lutke R, Mokoroa O, Nelen V, Neville AJ, Odak L, Rissmann A, Scanlon I, Urhoj SK, Wellesley D, Wertelecki W, Yevtushok L, Morris JK
Paediatric and Perinatal Epidemiology 2022;36(6):792-803
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Ten-Year Survival of Children With Congenital Anomalies: A European Cohort Study
Ten-Year Survival of Children With Congenital Anomalies: A European Cohort Study
Glinianaia SV, Rankin J, Pierini A, Coi A, Santoro M, Tan J, Reid A, Garne E, Loane M, Given J, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Heino A, Khoshnood B, Klungsøyr K, Lelong N, Neville AJ, Thayer DS, Tucker D, Urhøj SK, Wellesley D, Zurriaga O, Morris JK
Pediatrics 2022;149(3)
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Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study.
Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study.
Glinianaia SV, Rankin J, Tan J, Loane M, Garne E, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Klungsøyr K, Lelong N, Neville A, Pierini A, Tucker DF, Urhoj SK, Wellesley DG, Morris JK
Arch Dis Child 2023
Anomalies: Trisomy 13, Trisomy 18 -
The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies: A European Register-Based Cohort Study
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
Maternal and Child Health Journal 2024;28(6):1020-30
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The burden of disease for children born alive with Turner syndrome—A European cohort study
The burden of disease for children born alive with Turner syndrome—A European cohort study
Andersen A-LR, Urhoj SK, Tan J, Cavero-Carbonell C, Gatt M, Gissler M, Klungsoyr K, Khoshnood B, Morris J, Neville AJ, Pierini A, Scanlon I, de Walle HAK, Wellesley D, Garne E, Loane M
Birth Defects Research 2023;115(16):1459-68
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The quality and the accuracy of codes for terminations of pregnancy for fetal anomalies recorded in hospital databases in three countries in northern Europe.
The quality and the accuracy of codes for terminations of pregnancy for fetal anomalies recorded in hospital databases in three countries in northern Europe.
Garne E, Urhoj SK, Bakker M, Gissler M, Given J, Heino A, Limb E, Loane M, de Walle HEK, Morris J
Birth Defects Res 2023;115(3):405-12