المؤلفون: Magerl, Markus, Sala Cunill, Anna, Weber-Chrysochoou, Christina, Trainotti, Susanne, Mormile, Ilaria, SPADARO, Giuseppe

المساهمون: Institut Català de la Salut, Magerl M Institute of Allergology IFA, Charité – Universitätsmedizin Berlin, Berlin, Germany. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Allergology and Immunology, Berlin, Germany. Sala-Cunill A Servei d’Al·lergologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Weber-Chrysochoou C Allergy Unit, Dermatology Department, University Hospital of Zurich, Zurich, Switzerland. Trainotti S Department of Otorhinolaryngology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany. Mormile I, Spadaro G Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Inflamació, Pell - Malalties - Diagnòstic, Pell - Malalties - Aspectes genètics, Malalties rares, DISEASES::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Angioedemas, Other subheadings::Other subheadings::/diagnosis, ENFERMEDADES::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::angioedemas hereditarios, Otros calificadores::Otros calificadores::/diagnóstico

وصف الملف: application/pdf

العلاقة: Clinical and Translational Allergy;13(9); https://doi.org/10.1002/clt2.12297Test; Magerl M, Sala-Cunill A, Weber-Chrysochoou C, Trainotti S, Mormile I, Spadaro G. Could it be hereditary angioedema?—Perspectives from different medical specialties. Clin Transl Allergy. 2023 Sep 19;13(9):e12297.; https://hdl.handle.net/11351/10389Test

الإتاحة: https://doi.org/10.1002/clt2.12297Test
https://hdl.handle.net/11351/10389Test

المؤلفون: Navarro, S., Murillo-Sanjuán, Laura, Rodriguez-Vigil Iturrate, Carmen, Blazquez Goñi, Cristina, Uria Oficialdegui, Maria Luz, Benitez Carabante, Maria Isabel, Diaz de Heredia, Cristina

المساهمون: Institut Català de la Salut, Uria-Oficialdegui ML, Murillo-Sanjuan L, Benitez-Carbante MI, Diaz-de-Heredia C Servei d'Hematologia i Oncologia Pediàtriques, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Navarro S Pediatric Division, Hospital Universitario SonEspases, Palma de Mallorca, Spain. Rodriguez-Vigil C Pediatric Oncohaematology Unit, Paediatric Division, Hospital Universitario Miguel Servet, Zaragoza, Spain. Blazquez-Goñi C Hematology Division, Hospital Virgen del Rocío, Sevilla, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Malalties rares, Pell - Malalties - Aspectes genètics, Pell - Malalties - Diagnòstic, Telòmer, DISEASES::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Congenital Abnormalities::Skin Abnormalities::Dyskeratosis Congenita, Other subheadings::Other subheadings::/diagnosis, PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Structures::Chromosome Structures::Telomere, ENFERMEDADES::enfermedades y anomalías neonatales congénitas y hereditarias::anomalías congénitas::anomalías cutáneas::disqueratosis congénita, Otros calificadores::Otros calificadores::/diagnóstico, FENÓMENOS Y PROCESOS::fenómenos genéticos::estructuras genéticas::estructuras cromosómicas::telómero

وصف الملف: application/pdf

العلاقة: Frontiers in Pediatrics;11; https://doi.org/10.3389/fped.2023.1182476Test; Uria-Oficialdegui ML, Navarro S, Murillo-Sanjuan L, Rodriguez-Vigil C, Benitez-Carbante MI, Blazquez-Goñi C, et al. Dyskeratosis congenita: natural history of the disease through the study of a cohort of patients diagnosed in childhood. Front Pediatr. 2023 Aug 1;11:1182476.; https://hdl.handle.net/11351/10207Test; 001048089400001

الإتاحة: https://doi.org/10.3389/fped.2023.1182476Test
https://hdl.handle.net/11351/10207Test