Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Alessio Coi(Istituto di Fisiologia Clinica), Joan K. Morris(St George's, University of London), Laura García‐Villodre(Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana), Maria Loane(University of Ulster), Joanne Given(University of Ulster), Diana Wellesley(University Hospital Southampton NHS Foundation Trust), Clara Cavero‐Carbonell(Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana), Abigail-Kate Reid(St George's, University of London), Makan Rahshenas(Inserm), Ester Garne(University of Southern Denmark), Ieuan Scanlon(Swansea University), Kari Klungsøyr(Norwegian Institute of Public Health), Mika Gissler(Finnish Institute for Health and Welfare), Anna Pierini(Istituto di Fisiologia Clinica), Stine Kjær Urhøj(Lillebaelt Hospital), Michele Santoro(Agostino Gemelli University Polyclinic), Sonja Kiuru‐Kuhlefelt(Finnish Institute for Health and Welfare), Judith Rankin(Cumbria Northumberland Tyne and Wear NHS Foundation Trust), Sue Jordan(Swansea University), Elisa Ballardini(University of Ferrara), L. Renée Lutke(University Medical Center Groningen), Miriam Gatt(Ministry for Health), Joachim Tan(St George's, University of London), Nathalie Lelong(Inserm), Hermien E. K. de Walle(University of Groningen), Amanda J. Neville(University of Ferrara), Svetlana V. Glinianaia(Newcastle University)
Orphanet Journal of Rare Diseases
March 29, 2022
Cited by 19


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