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Fingerprint Dive into the research topics where Marina Noris is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 20 Similar Profiles
Hemolytic-Uremic Syndrome Medicine & Life Sciences
Kidney Medicine & Life Sciences
Complement Factor H Medicine & Life Sciences
Mutation Medicine & Life Sciences
Thrombotic Thrombocytopenic Purpura Medicine & Life Sciences
Transplants Medicine & Life Sciences
Thrombotic Microangiopathies Medicine & Life Sciences
Complement Activation Medicine & Life Sciences

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Research Output 1989 2019

  • 12985 Citations
  • 60 h-Index
  • 189 Article
  • 5 Chapter
  • 1 Editorial
  • 1 Review article

An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome

Galbusera, M., Noris, M., Gastoldi, S., Bresin, E., Mele, C., Breno, M., Cuccarolo, P., Alberti, M., Valoti, E., Piras, R., Donadelli, R., Vivarelli, M., Murer, L., Pecoraro, C., Ferrari, E., Perna, A., Benigni, A., Portalupi, V. & Remuzzi, G., Mar 6 2019, In : American Journal of Kidney Diseases.

Research output: Contribution to journalArticle

Complement Membrane Attack Complex
Hemolytic-Uremic Syndrome
Complement Activation
Endothelium
Serum

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN

Registry of Membranoproliferative Glomerulonephritis/C3 Glomerulopathy, Jan 2018, In : Journal of the American Society of Nephrology : JASN. 29, 1, p. 283-294 12 p.

Research output: Contribution to journalArticle

Antigen-Antibody Complex
Cluster Analysis
Complement Activation
Serum
Complement C3-C5 Convertases

Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome

Goicoechea de Jorge, E., Tortajada, A., García, S. P., Gastoldi, S., Merinero, H. M., García-Fernández, J., Arjona, E., Cao, M., Remuzzi, G., Noris, M. & Rodríguez de Córdoba, S., Jan 2018, In : Journal of the American Society of Nephrology : JASN. 29, 1, p. 240-249 10 p.

Research output: Contribution to journalArticle

Complement Factor H
Gene Conversion
Genes
Chromosomes
Thrombotic Microangiopathies

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

Osborne, A. J., Breno, M., Borsa, N. G., Bu, F., Frémeaux-Bacchi, V., Gale, D. P., van den Heuvel, L. P., Kavanagh, D., Noris, M., Pinto, S., Rallapalli, P. M., Remuzzi, G., Rodríguez de Cordoba, S., Ruiz, A., Smith, R. J. H., Vieira-Martins, P., Volokhina, E., Wilson, V., Goodship, T. H. J. & Perkins, S. J., Apr 1 2018, In : Journal of Immunology. 200, 7, p. 2464-2478 15 p.

Research output: Contribution to journalArticle

Genes
Exome
Gene Frequency
Alternative Complement Pathway
Atypical Hemolytic Uremic Syndrome

Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN

Donadelli, R., Pulieri, P., Piras, R., Iatropoulos, P., Valoti, E., Benigni, A., Remuzzi, G. & Noris, M., 2018, In : Frontiers in Immunology. 9, p. 2329

Research output: Contribution to journalArticle

Complement C3 Nephritic Factor
Membranoproliferative Glomerulonephritis
Antigen-Antibody Complex
Properdin
Complement C3-C5 Convertases