المؤلفون: Giovanni Maria Rossi, Caterina Mele, Lucio Manenti, Federico Ricco, Francesco Fontana, Isabella Pisani, Enrico Fiaccadori, Renzo Mignani, Micaela Gentile, Elena Bresin, Francesco Paolo Pilato, Marco Delsante

المصدر: Journal of Nephrology. 35:1091-1100

مصطلحات موضوعية: Adult, Male, Nephrology, medicine.medical_specialty, Thrombotic microangiopathy, urologic and male genital diseases, Gastroenterology, Nephropathy, hemic and lymphatic diseases, Internal medicine, Atypical hemolytic uremic syndrome, Humans, Medicine, Atypical Hemolytic Uremic Syndrome, Retrospective Studies, Proteinuria, medicine.diagnostic_test, business.industry, Glomerulonephritis, IGA, Retrospective cohort study, Complement System Proteins, medicine.disease, Kidney Failure, Chronic, Female, Renal biopsy, medicine.symptom, business, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae817e44b3c06f0afb5718ffd8fd1f7Test
https://doi.org/10.1007/s40620-021-01189-6Test

المؤلفون: Giuseppe Remuzzi, Elena Bresin, Alexandra Bruel, Marina Noris, Chantal Loirat, François Provôt, Edwin K.S. Wong, Vicky Brocklebank, Yahsou Delmas, Fadi Fakhouri, Caterina Mele, David J. Kavanagh, Véronique Frémeaux-Bacchi

المصدر: Clinical Journal of the American Society of Nephrology. 12:1237-1247

مصطلحات موضوعية: Pediatrics, Time Factors, Epidemiology, medicine.medical_treatment, 030232 urology & nephrology, 030204 cardiovascular system & hematology, Critical Care and Intensive Care Medicine, Gastroenterology, 0302 clinical medicine, Pregnancy, Recurrence, Complement Activation, Plasma Exchange, Postpartum Period, Middle Aged, Eculizumab, Europe, Phenotype, Treatment Outcome, Complement Factor I, Nephrology, Complement Factor H, Disease Progression, Female, medicine.drug, Adult, medicine.medical_specialty, Thrombotic microangiopathy, Adolescent, Complement factor I, Antibodies, Monoclonal, Humanized, Young Adult, 03 medical and health sciences, Renal Dialysis, Internal medicine, Atypical hemolytic uremic syndrome, medicine, Humans, Genetic Predisposition to Disease, Renal Insufficiency, Chronic, Dialysis, Retrospective Studies, Transplantation, business.industry, Genetic Variation, Original Articles, medicine.disease, Complement system, Pregnancy Complications, Complement Inactivating Agents, Hemolytic-Uremic Syndrome, Kidney Failure, Chronic, business, Postpartum period

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd3483cbe4272106c13449b6b761b50eTest
https://doi.org/10.2215/cjn.00280117Test

المؤلفون: Rossella Piras, Annalisa Perna, Ariela Benigni, Luisa Murer, Paola Cuccarolo, Elisa Ferrari, Elisabetta Valoti, Roberta Donadelli, Valentina Portalupi, Matteo Breno, Caterina Mele, Miriam Galbusera, Marta Alberti, Sara Gastoldi, Giuseppe Remuzzi, Marina Vivarelli, Carmine Pecoraro, Elena Bresin, Marina Noris

المصدر: American journal of kidney diseases : the official journal of the National Kidney Foundation. 74(1)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Endothelium, 030232 urology & nephrology, Complement Membrane Attack Complex, In Vitro Techniques, Antibodies, Monoclonal, Humanized, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Atypical hemolytic uremic syndrome, Secondary Prevention, Medicine, Humans, 030212 general & internal medicine, Complement Activation, Atypical Hemolytic Uremic Syndrome, biology, Dose-Response Relationship, Drug, business.industry, Reproducibility of Results, Eculizumab, medicine.disease, Discontinuation, Complement system, medicine.anatomical_structure, Complement Inactivating Agents, Nephrology, Factor H, Complement Factor H, biology.protein, Female, Endothelium, Vascular, Antibody, Drug Monitoring, business, Ex vivo, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74eff3cace7878cdaf159b08fc704b05Test
https://pubmed.ncbi.nlm.nih.gov/30851964Test

المؤلفون: Sonia Pasquali, Marina Noris, Carlo Buzio, Elena Bresin, Francesco Paolo Pilato, Lucio Manenti, Augusto Vaglio, Elisa Gnappi, Elisabetta Valoti, Landino Allegri

المصدر: Nephrology Dialysis Transplantation. 28:2246-2259

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, C3 Glomerulonephritis, urologic and male genital diseases, Gastroenterology, Young Adult, Glomerulonephritis, Focal segmental glomerulosclerosis, Glomerulopathy, hemic and lymphatic diseases, Internal medicine, Membranoproliferative glomerulonephritis, Atypical hemolytic uremic syndrome, medicine, Humans, Aged, Atypical Hemolytic Uremic Syndrome, Transplantation, business.industry, Complement System Proteins, Middle Aged, medicine.disease, Review Literature as Topic, Nephrology, Hemolytic-Uremic Syndrome, Immunology, Female, business, Granulomatosis with polyangiitis, Nephrotic syndrome, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71245d020400262fefce3559e05203dcTest
https://doi.org/10.1093/ndt/gft220Test

المؤلفون: Elena Bresin, Timothy H.J. Goodship, Marina Noris, Erica Rurali, Elisabetta Valoti, Marta Alberti, Santiago Rodríguez de Córdoba, Sheila Pinto, Véronique Frémeaux-Bacchi, Pilar Sánchez-Corral, Giuseppe Remuzzi, Jessica Caprioli, David Ribes

المصدر: Journal of the American Society of Nephrology; Vol 24

مصطلحات موضوعية: Adult, Male, 030232 urology & nephrology, Penetrance, Disease, Biology, Gene mutation, medicine.disease_cause, Membrane Cofactor Protein, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Clinical Research, Risk Factors, Atypical hemolytic uremic syndrome, medicine, Humans, Child, Gene, Genotyping, Genetic Association Studies, Atypical Hemolytic Uremic Syndrome, 030304 developmental biology, 0303 health sciences, Mutation, Haplotype, Fibrinogen, Infant, Complement C3, Complement System Proteins, General Medicine, Middle Aged, medicine.disease, Pedigree, 3. Good health, Haplotypes, Nephrology, Child, Preschool, Complement Factor H, Hemolytic-Uremic Syndrome, Immunology, Female, Complement Factor B

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edbc36e8dae2bc7c979d1cccb177c7fdTest
https://doi.org/10.1681/asn.2012090884Test

المؤلفون: Miriam Galbusera, Marina Noris, Friedrich Thaiss, Claudio Tripodo, Elena Bresin, Elisabetta Valoti, Marta Alberti, Rossella Piras, Giuseppe Remuzzi

المساهمون: Alberti, M., Valoti, E., Piras, R., Bresin, E., Galbusera, M., Tripodo, C., Thaiss, F., Remuzzi, G., Noris, M.

المصدر: American Journal of Transplantation; Vol 13

مصطلحات موضوعية: Shiga-toxin, Graft Rejection, Male, DNA Primer, 030232 urology & nephrology, Escherichia coli Infection, Gene mutation, urologic and male genital diseases, Gastroenterology, 0302 clinical medicine, Recurrence, Risk Factors, hemic and lymphatic diseases, Immunology and Allergy, Pharmacology (medical), gene mutation, Kidney transplantation, Escherichia coli Infections, 0303 health sciences, Kidney, medicine.diagnostic_test, Shiga-Toxigenic Escherichia coli, Antigens, CD46, Microangiopathic hemolytic anemia, Middle Aged, Prognosis, female genital diseases and pregnancy complications, 3. Good health, Pedigree, medicine.anatomical_structure, Complement Factor I, Complement factor I, hemolytic uremic syndrome, kidney transplantation, membrane cofactor protein, Adult, Case-Control Studies, DNA Primers, Female, Genetic Testing, Hemolytic-Uremic Syndrome, Heterozygote, Humans, Kidney Failure, Chronic, Kidney Transplantation, Mutation, Thrombocytopenia, Young Adult, Transplantation, Case-Control Studie, Human, medicine.medical_specialty, Prognosi, Membrane Cofactor Protein, 03 medical and health sciences, Internal medicine, medicine, 030304 developmental biology, Genetic testing, business.industry, CD46, Risk Factor, medicine.disease, Immunology, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92a235562de7ebc5fbc798f5597defbbTest

المؤلفون: Giuseppe Remuzzi, Serena Bettoni, Miriam Galbusera, Chiara Tentori, Hugo Yebenes, Giuseppina Spartà, Sara Gastoldi, Caterina Mele, Agustín Tortajada, Roberta Donadelli, Marta Alberti, Elena Bresin, Marina Noris

المصدر: Journal of immunology (Baltimore, Md. : 1950). 199(3)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Endothelium, Adolescent, Immunology, Complement Pathway, Alternative, ADAMTS13 Protein, Complement C5a, Complement C3-C5 Convertases, Complement Membrane Attack Complex, 030204 cardiovascular system & hematology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, medicine, Immunology and Allergy, Humans, Child, biology, Purpura, Thrombotic Thrombocytopenic, Chemistry, Infant, Newborn, Endothelial Cells, Thrombosis, ADAMTS13, Complement system, Cell biology, 030104 developmental biology, medicine.anatomical_structure, Child, Preschool, Complement C3b, Microvessels, Alternative complement pathway, biology.protein, Female, Complement membrane attack complex, circulatory and respiratory physiology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52237ad8913b64b99e294e66c8f7d3f2Test
https://pubmed.ncbi.nlm.nih.gov/28652401Test

المؤلفون: Marina Noris, Friedhelm Hildebrandt, Federica Banterla, Peter F. Zipfel, Marta Todeschini, Federica Castelletti, Christine Skerka, Edgar A. Otto, Jessica Caprioli, Roberta Donadelli, Giuseppe Remuzzi, Elena Bresin, Rosangela Artuso, Rosa Maria Caruso, Alessandra Renieri

المصدر: Proceedings of the National Academy of Sciences. 105:2538-2543

مصطلحات موضوعية: Adult, Male, Models, Molecular, Pathology, medicine.medical_specialty, Adolescent, Glomerular deposits, Kidney Glomerulus, Lupus nephritis, Biology, Nephropathy, Pathogenesis, Glomerulopathy, medicine, Humans, Missense mutation, Genetic Predisposition to Disease, Child, Genetics, Multidisciplinary, Autosomal dominant trait, Middle Aged, Biological Sciences, medicine.disease, Penetrance, Recombinant Proteins, Fibronectins, Pedigree, Protein Structure, Tertiary, Gene Expression Regulation, Mutation, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b83a0fbe4dc0af0ae06232525149ffTest
https://doi.org/10.1073/pnas.0707730105Test

المؤلفون: Erica Rurali, Federica Banterla, Miriam Galbusera, Marina Noris, Mary Underwood, Flora Peyvandi, Sara Gastoldi, Roberta Donadelli, Giuseppe Remuzzi, Elena Bresin

المصدر: Clinical journal of the American Society of Nephrology : CJASN. 10(11)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Epidemiology, ADAMTS13 Protein, Congenital Thrombotic Thrombocytopenic Purpura, Critical Care and Intensive Care Medicine, Young Adult, Von Willebrand factor, In vivo, hemic and lymphatic diseases, Internal medicine, medicine, Humans, Renal Insufficiency, Young adult, Child, Transplantation, Metalloproteinase, Thrombospondin, biology, Purpura, Thrombotic Thrombocytopenic, business.industry, Infant, Newborn, Infant, Original Articles, Middle Aged, ADAMTS13, In vitro, ADAM Proteins, Endocrinology, Nephrology, Child, Preschool, Mutation, biology.protein, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5411b8dadee7cd6fd54d9d08ac6c4e6eTest
https://pubmed.ncbi.nlm.nih.gov/26342041Test

المؤلفون: Alessandra Renieri, Elena Bresin, Francesca Mari, Chiara Pescucci, Marco Seri, Rosanna Gusmano, Nunzia Miglietti, Cataldo Abaterusso, Paraskevi Vogiatzi, Elisa Scala, Rossella Caselli, Ilaria Longo

المساهمون: Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, Abaterusso C, Gusmano R, Seri M, Miglietti N, Bresin E, Renieri A

المصدر: Università degli Studi di Siena-IRIS

مصطلحات موضوعية: Adult, Collagen Type IV, Male, Genetic counseling, COL4A3, Nephritis, Hereditary, ALPORT SYNDROME, Kidney, urologic and male genital diseases, Asymptomatic, Autoantigens, medicine, Humans, COL4A4, Alport syndrome, Microhematuria, collagen IV genes, Child, COL4A3 gene, Aged, Genes, Dominant, Genetics, Aged, 80 and over, incomplete penetrance, Genetic heterogeneity, business.industry, COL4A4 gene, Glomerulonephritis, Middle Aged, medicine.disease, Penetrance, medicine.icd_9_cm_classification, Pedigree, Phenotype, inherited nephropathy, Nephrology, Mutation (genetic algorithm), Mutation, phenotypic variability, Female, autosomal-dominant Alport syndrome, medicine.symptom, business

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba4241beeae5010042e58d8f284c5d24Test