نتائج البحث - "Elena Bresin"

المساهمون: Noris, Marina, Galbusera, Miriam, Gastoldi, Sara, Macor, Paolo, Banterla, Federica, Bresin, Elena, Tripodo, Claudio, Bettoni, Serena, Donadelli, Roberta, Valoti, Elisabetta, Tedesco, Francesco, Amore, Alessandro, Coppo, Rosanna, Ruggenenti, Piero, Gotti, Eliana, Remuzzi, Giuseppe, Noris, M, Galbusera, M, Gastoldi, S, Macor, P, Banterla, F, Bresin, E, Tripodo, C, Bettoni, S, Donadelli, R, Valoti, E, Tedesco, F, Amore, A, Coppo, R, Ruggenenti, P, Gotti, E, Remuzzi, G.

المصدر: Blood. 124(11)

مصطلحات موضوعية: Male, Time Factors, Clinical Trials and Observations, Complement Membrane Attack Complex, urologic and male genital diseases, Biochemistry, Glomerulonephritis, Inside BLOOD Commentary, hemic and lymphatic diseases, Membranoproliferative glomerulonephritis, Monoclonal, Humanized, Complement Activation, Atypical Hemolytic Uremic Syndrome, Endothelial Cell, Hematology, Remission Induction, food and beverages, Complement C3, Eculizumab, medicine.anatomical_structure, Factor H, Female, complement,aHUS, eculizumab, medicine.drug, Membranoproliferative, Human, medicine.medical_specialty, Endothelium, Monitoring, Time Factor, Glomerulonephritis, Membranoproliferative, Immunology, Biology, Antibodies, Monoclonal, Humanized, Antibodies, Internal medicine, Atypical hemolytic uremic syndrome, medicine, Humans, Physiologic, Monitoring, Physiologic, Adenosine Diphosphate Ribose, Endothelial Cells, Cell Biology, medicine.disease, Complement system, Hemolytic-Uremic Syndrome, Complement membrane attack complex

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1ca50529aab218f11ea491c9858de98Test
https://pubmed.ncbi.nlm.nih.gov/25214194Test

10

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

المؤلفون: Elena Bresin, Edward M. Conway, Irene van der Meer, Chiara Mossali, Peter F. Zipfel, Sara Gamba, Timothy H.J. Goodship, Marina Noris, Jessica Caprioli, Roberta Donadelli, Erica Daina, Annalisa Sorosina, Federica Castelletti, Gaia Pianetti, Rossella Piras, Giuseppe Remuzzi, Chiara Fenili, Ramona Maranta

مصطلحات موضوعية: Male, Time Factors, Epidemiology, Thrombomodulin, DNA Mutational Analysis, Kaplan-Meier Estimate, Gene mutation, Critical Care and Intensive Care Medicine, urologic and male genital diseases, Gene Frequency, Recurrence, Risk Factors, hemic and lymphatic diseases, Registries, Aged, 80 and over, medicine.diagnostic_test, Microangiopathic hemolytic anemia, Complement C3, Eculizumab, Pedigree, Phenotype, Treatment Outcome, Nephrology, Factor H, Complement Factor H, Female, medicine.drug, Adult, Adolescent, Complement factor I, Risk Assessment, Disease-Free Survival, Membrane Cofactor Protein, Young Adult, Atypical hemolytic uremic syndrome, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Genetic Testing, Genetic testing, Autoantibodies, Proportional Hazards Models, Transplantation, Chi-Square Distribution, Polymorphism, Genetic, business.industry, Infant, Newborn, Infant, Original Articles, Complement System Proteins, medicine.disease, Kidney Transplantation, Immunology, Hemolytic-Uremic Syndrome, Mutation, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::966cb92f0f80e0492ccd275e4be7312bTest
https://europepmc.org/articles/PMC2974386Test/

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