المؤلفون: Stepien, Karolina M, Kieć-Wilk, Beata, Lampe, Christina, Tangeraas, Trine, Cefalo, Graziella, Belmatoug, Nadia, Francisco, Rita, Del Toro, Mireia, Wagner, Leona, Lauridsen, Anne-Grethe, Sestini, Sylvia, Weinhold, Nathalie, Hahn, Andreas, Montanari, Chiara, Rovelli, Valentina, Bellettato, Cinzia M, Paneghetti, Laura, van Lingen, Corine, Scarpa, Maurizio

المساهمون: K.M. Stepien, B. Kieć-Wilk, C. Lampe, T. Tangeraa, G. Cefalo, N. Belmatoug, R. Francisco, M. Del Toro, L. Wagner, A. Lauridsen, S. Sestini, N. Weinhold, A. Hahn, C. Montanari, V. Rovelli, C.M. Bellettato, L. Paneghetti, C. van Lingen, M. Scarpa

مصطلحات موضوعية: adult metabolic patient, adulthood (18 years and older), challenge, continuity of care, inherited metabolic disease(s), rare disease, transition process, Settore MED/38 - Pediatria Generale e Specialistica

Relation: info:eu-repo/semantics/altIdentifier/pmid/33738294; info:eu-repo/semantics/altIdentifier/wos/WOS:000629292700001; volume:8; firstpage:1; lastpage:9; numberofpages:9; journal:FRONTIERS IN MEDICINE; https://hdl.handle.net/2434/988530; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85102786125

الاتاحة: https://hdl.handle.net/2434/988530
https://doi.org/10.3389/fmed.2021.652358

المؤلفون: Stepien, Karolina M., Kieć-Wilk, Beata, Lampe, Christina, Tangeraas, Trine, Cefalo, Graziella, Belmatoug, Nadia, Francisco, Rita, Del Toro, Mireia, Wagner, Leona, Lauridsen, Anne-Grethe, Sestini, Sylvia, Weinhold, Nathalie, Hahn, Andreas, Montanari, Chiara, Rovelli, Valentina, Bellettato, Cinzia M., Paneghetti, Laura, van Lingen, Corine, Scarpa, Maurizio, Universitat Autònoma de Barcelona

مصطلحات موضوعية: Rare disease, Inherited metabolic disease(s), Transition process, Challenge, Adulthood (18 years and older), Continuity of care, Adult metabolic patient

وصف الملف: application/pdf

Relation: Frontiers in Medicine; Vol. 8 (february 2021); https://ddd.uab.cat/record/237950; urn:10.3389/fmed.2021.652358; urn:oai:ddd.uab.cat:237950; urn:pmcid:PMC7962750; urn:pmid:33738294; urn:oai:pubmedcentral.nih.gov:7962750

الاتاحة: https://ddd.uab.cat/record/237950

المؤلفون: Karolina M. Stepien, Beata Kieć-Wilk, Christina Lampe, Trine Tangeraas, Graziella Cefalo, Nadia Belmatoug, Rita Francisco, Mireia del Toro, Leona Wagner, Anne-Grethe Lauridsen, Sylvia Sestini, Nathalie Weinhold, Andreas Hahn, Chiara Montanari, Valentina Rovelli, Cinzia M. Bellettato, Laura Paneghetti, Corine van Lingen, Maurizio Scarpa

المساهمون: Institut Català de la Salut, [Stepien KM] Adult Inherited Metabolic Diseases, Salford Royal NHS Foundation Trust, Salford, United Kingdom. [Kieć-Wilk B] Department of Metabolic Diseases and Diabetes, Krakow University Hospital, Krakow, Poland. Department of Metabolic Diseases, Medical College, Jagiellonian University, Krakow, Poland. [Lampe C] Department of Child Neurology, Center for Rare Diseases Giessen (ZSEGI), Justus-Liebig University, Giessen, Germany. [Tangeraas T] Norwegian National Unit for Newborn Screening, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway. [Cefalo G] Department of Maternal and Child Health, San Paolo Hospital, University of Milan, ASST Santi Paolo e Carlo, Milan, Italy. [Belmatoug N] Referral Center for Lysosomal Diseases, AP-HP Nord, Beaujon Hospital, Paris University, Clichy, France. [Del Toro M] Servei de Neurologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Recercat. Dipósit de la Recerca de Catalunya
instname
Frontiers in Medicine, Vol 8 (2021)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Medicine
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Scientia

مصطلحات موضوعية: medicine.medical_specialty, Medical staff, Adult metabolic patient, Genetic Phenomena::Genotype::Genetic Predisposition to Disease [PHENOMENA AND PROCESSES], Diàtesi, rare disease, transition process, Economic shortage, Adulthood (18 years and older), Metabolisme - Trastorns - Aspectes genètics, Eu countries, Unmet needs, Nutritional and Metabolic Diseases::Metabolic Diseases [DISEASES], continuity of care, adult metabolic patient, Health care, Other subheadings::Other subheadings::/genetics [Other subheadings], Medicine, Inherited metabolic disease(s), Challenge, fenómenos genéticos::genotipo::predisposición genética a la enfermedad [FENÓMENOS Y PROCESOS], Original Research, lcsh:R5-920, Otros calificadores::Otros calificadores::/genética [Otros calificadores], business.industry, Transition process, digestive, oral, and skin physiology, inherited metabolic disease(s), Emergency plan, General Medicine, enfermedades nutricionales y metabólicas::enfermedades metabólicas [ENFERMEDADES], Family medicine, adulthood (18 years and older), challenge, Life expectancy, Continuity of care, lcsh:Medicine (General), business, Rare disease

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e03234c458454d4e0ccbee5c1434228
http://hdl.handle.net/2072/447647

المؤلفون: Karolina M. Stepien (8845502), Beata Kieć-Wilk (5663302), Christina Lampe (426094), Trine Tangeraas (9104654), Graziella Cefalo (10192406), Nadia Belmatoug (437766), Rita Francisco (2377693), Mireia del Toro (10192409), Leona Wagner (10192412), Anne-Grethe Lauridsen (10192415), Sylvia Sestini (10192418), Nathalie Weinhold (10192421), Andreas Hahn (275151), Chiara Montanari (10192424), Valentina Rovelli (6017179), Cinzia M. Bellettato (10192427), Laura Paneghetti (10192430), Corine van Lingen (10192433), Maurizio Scarpa (3167829)

مصطلحات موضوعية: Dermatology, Emergency Medicine, Gastroenterology and Hepatology, Geriatrics and Gerontology, Intensive Care, Medical Genetics (excl. Cancer Genetics), Nephrology and Urology, Nuclear Medicine, Orthopaedics, Otorhinolaryngology, Pathology (excl. Oral Pathology), Radiology and Organ Imaging, Foetal Development and Medicine, Obstetrics and Gynaecology, Family Care, Primary Health Care, Medical and Health Sciences not elsewhere classified, rare disease, inherited metabolic disease(s), transition process, challenge, adulthood (18 years and older), continuity of care, adult metabolic patient

Relation: https://figshare.com/articles/dataset/Data_Sheet_1_Challenges_in_Transition_From_Childhood_to_Adulthood_Care_in_Rare_Metabolic_Diseases_Results_From_the_First_Multi-Center_European_Survey_PDF/14141498

الاتاحة: https://doi.org/10.3389/fmed.2021.652358.s001