المؤلفون: Camila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, Priscila Nicolicht, João Bosco Pesquero, Anete Sevciovic Grumach

المصدر: Frontiers in Medicine, Vol 6 (2019)

مصطلحات موضوعية: hereditary angioedema, acute pancreatitis, abdominal swelling, C1-inhibitor deficiency, F12 mutation, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fmed.2019.00080/fullTest; https://doaj.org/toc/2296-858XTest

الوصول الحر: https://doaj.org/article/f15f112d33b245b584b2bae9abd391f7Test

المؤلفون: Camila Lopes Veronez, Anne Aabom, Renan Paulo Martin, Rafael Filippelli-Silva, Rozana Fátima Gonçalves, Priscila Nicolicht, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Anete Sevciovic Grumach, Eli Mansour, Anette Bygum, João Bosco Pesquero

المصدر: Frontiers in Medicine, Vol 6 (2019)

مصطلحات موضوعية: hereditary angioedema, Kallikrein-Kinin System, genetic variation, genotype-phenotype correlation, C1 inhibitor deficiency, F12 mutation, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fmed.2019.00028/fullTest; https://doaj.org/toc/2296-858XTest

الوصول الحر: https://doaj.org/article/11f2c8ef89a14a6c8e850219d5e9c290Test

المؤلفون: Veronez, Camila Lopes, Aabom, Anne, Martin, Renan Paulo, Filippelli-Silva, Rafael, Gonçalves, Rozana Fátima, Nicolicht, Priscila, Mendes, Agatha Ribeiro, Da Silva, Jane, Guilarte, Mar, Grumach, Anete Sevciovic, Mansour, Eli, Bygum, Anette, Pesquero, João Bosco

المصدر: Veronez , C L , Aabom , A , Martin , R P , Filippelli-Silva , R , Gonçalves , R F , Nicolicht , P , Mendes , A R , Da Silva , J , Guilarte , M , Grumach , A S , Mansour , E , Bygum , A & Pesquero , J B 2019 , ' Genetic variation of Kallikrein-Kinin system and related genes in patients with hereditary angioedema ' , Frontiers in Medicine , vol. 6 , no. FEB , 28 . https://doi.org/10.3389/fmed.2019.00028Test

مصطلحات موضوعية: C1 inhibitor deficiency, F12 mutation, Genetic variation, Genotype-phenotype correlation, Hereditary angioedema, Kallikrein-Kinin System

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/7ea00728-35e0-4159-8a35-d0843a77ed79Test

الإتاحة: https://doi.org/10.3389/fmed.2019.00028Test
https://portal.findresearcher.sdu.dk/da/publications/7ea00728-35e0-4159-8a35-d0843a77ed79Test
https://findresearcher.sdu.dk/ws/files/151671040/Genetic_variation_of_Kallikrein_Kinin_system_and_related_genes_in_patients_with_hereditary_angioedema.pdfTest

المؤلفون: Vatsiou S., Zamanakou M., Loules G., González-Quevedo T., Porȩbski G., Juchacz A., Bova M., Suffritti C., Firinu D., Csuka D., Manousakis E., Valerieva A., Staevska M., Magerl M., Farkas H., Germenis A. E.

المساهمون: Vatsiou, S., Zamanakou, M., Loules, G., González-Quevedo, T., Porȩbski, G., Juchacz, A., Bova, M., Suffritti, C., Firinu, D., Csuka, D., Manousakis, E., Valerieva, A., Staevska, M., Magerl, M., Farkas, H., Germenis, A. E.

مصطلحات موضوعية: Bradykinin, Histamine receptor, amino acid substitution, Amplicon, Angioneurotic edema, Article, Exon, F12 gene, Gene, Gene library, Gene mutation, Gene segregation, Genetic analysi, Genetic polymorphism, Genotype, Human, Major clinical study, Missense mutation, Next generation sequencing, Protein metabolism, Sanger sequencing, SERPING1 gene, Whole exome sequencing, F12 mutation, Hereditary angioedema, Next-generation sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000463193600007; volume:23; issue:4; firstpage:205; lastpage:210; numberofpages:6; journal:ALERGIA ASTMA IMMUNOLOGIA; http://hdl.handle.net/11584/282791Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85072814343

الإتاحة: http://hdl.handle.net/11584/282791Test

المؤلفون: Eli Mansour, Rozana Fátima Gonçalves, Anette Bygum, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Priscila Nicolicht, Camila Lopes Veronez, Rafael Filippelli-Silva, Anete Sevciovic Grumach, Renan Paulo Martin, Anne Aabom, João Bosco Pesquero

المساهمون: Institut Català de la Salut, [Veronez CL, Nicholicht P, Filippelli-Silva R] Department of Biophysics, Federal University of São Paulo, São Paulo, Brazil. [Aabom A] Department of Dermatology and Allergy Centre, Odense University Hospital, Odense, Denmark. [Martin RP] Department of Biophysics, Federal University of São Paulo, São Paulo, Brazil. Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, United States. [Gonçalves RF] Private Allergy and Immunology Clinic, Belo Horizonte, Brazil. [Guilarte M] Servei d'Al•lergologia, Servei de Medicina Interna, Hospital Universitari Vall d'Hebron, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Frontiers in Medicine, Vol 6 (2019)
Frontiers in Medicine
Veronez, C L, Aabom, A, Martin, R P, Filippelli-Silva, R, Gonçalves, R F, Nicolicht, P, Mendes, A R, Da Silva, J, Guilarte, M, Grumach, A S, Mansour, E, Bygum, A & Pesquero, J B 2019, ' Genetic variation of Kallikrein-Kinin system and related genes in patients with hereditary angioedema ', Frontiers in Medicine, vol. 6, no. FEB, 28 . https://doi.org/10.3389/fmed.2019.00028Test
Scientia

مصطلحات موضوعية: Genotype-phenotype correlation, Chemical Phenomena::Biochemical Phenomena::Osmoregulation::Water-Electrolyte Balance::Kallikrein-Kinin System [PHENOMENA AND PROCESSES], Kallikrein-Kinin System, fenómenos químicos::fenómenos bioquímicos::osmorregulación::equilibrio hidroelectrolítico::sistema calicreína-cinina [FENÓMENOS Y PROCESOS], genotype-phenotype correlation, Biology, Genotype-phenotype distinction, fenómenos genéticos::variación genética [FENÓMENOS Y PROCESOS], Genetic variation, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Epigenetics, Gene, Hereditary angioedema, Genetics, F12 mutation, lcsh:R5-920, Genetic diversity, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Mutació (Biologia), Autosomal dominant trait, General Medicine, Brief Research Report, medicine.disease, Phenotype, Cardiovascular Diseases::Vascular Diseases::Angioedema::Angioedemas, Hereditary [DISEASES], hereditary angioedema, Edema - Aspectes genètics, Genetic Phenomena::Genetic Variation [PHENOMENA AND PROCESSES], Proteïnes de la sang, genetic variation, Medicine, C1 inhibitor deficiency, lcsh:Medicine (General), enfermedades cardiovasculares::enfermedades vasculares::angioedema::angioedemas hereditarios [ENFERMEDADES]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adcf31bf8bd0f3a5b393761b29000948Test
https://doi.org/10.3389/fmed.2019.00028Test

المؤلفون: Camila Lopes Veronez, Anne Aabom, Renan Paulo Martin, Rafael Filippelli-Silva, Rozana Fátima Gonçalves, Priscila Nicolicht, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Anete Sevciovic Grumach, Eli Mansour, Anette Bygum, João Bosco Pesquero

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, hereditary angioedema, Kallikrein-Kinin System, genetic variation, genotype-phenotype correlation, C1 inhibitor deficiency, F12 mutation

العلاقة: https://figshare.com/articles/dataset/Table_2_Genetic_Variation_of_Kallikrein-Kinin_System_and_Related_Genes_in_Patients_With_Hereditary_Angioedema_xlsx/7750004Test

الإتاحة: https://doi.org/10.3389/fmed.2019.00028.s002Test
https://figshare.com/articles/dataset/Table_2_Genetic_Variation_of_Kallikrein-Kinin_System_and_Related_Genes_in_Patients_With_Hereditary_Angioedema_xlsx/7750004Test