Suchergebnisse - "Vieira-Martins, Paula"

PubPharm (21)

1

Usefulness and analytical performances of complement multiplex assay for measuring complement biomarkers in plasma

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2024

von Meuleman, M. | Duval, A. | Grunenwald, A. | +13

2

Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GN

enthalten in: Clinical journal of the American Society of Nephrology : CJASN | 2023

von Meuleman, M. | Vieira-Martins, P. | El Sissy, C. | +23

3

C3 Glomerulopathy With Concurrent Thrombotic Microangiopathy : Clinical and Immunological Features

enthalten in: American journal of kidney diseases : the official journal of the National Kidney Foundation | 2023

von Chabannes, M. | Rabant, M. | El Sissy, C. | +18

4

Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria

enthalten in: Blood | 2023

von Prata, P. | Galimard, J. | Sicre de Fontbrune, F. | +12

CommentIn: Blood. 2023 Apr 13;141(15):1780-1782. - PMID 37052944

5

Complement activation in sickle cell disease : Dependence on cell density, hemolysis and modulation by hydroxyurea therapy

enthalten in: American journal of hematology | 2020

von Roumenina, L. | Chadebech, P. | Bodivit, G. | +12

6

Anti-Factor B Antibodies and Acute Postinfectious GN in Children

enthalten in: Journal of the American Society of Nephrology : JASN | 2020

von Chauvet, S. | Berthaud, R. | Devriese, M. | +17

CommentIn: Nat Rev Nephrol. 2020 May;16(5):252. - PMID 32099192

7

Complement activation in sickle cell disease : Dependence on cell density, hemolysis and modulation by hydroxyurea therapy

enthalten in: American Journal of Hematology | 2020

von Roumenina, L. | Chadebech, P. | Bodivit, G. | +12

8

Impact of hypertensive emergency and rare complement variants on the presentation and outcome of atypical hemolytic uremic syndrome

enthalten in: Haematologica | 2019

von El Karoui, K. | Boudhabhay, I. | Petitprez, F. | +9

9

Atypical and secondary hemolytic uremic syndromes have a distinct presentation and no common genetic risk factors

enthalten in: Kidney international | 2019

von Le Clech, A. | Simon-Tillaux, N. | Provôt, F. | +13

CommentIn: Kidney Int. 2019 Jun;95(6):1298-1300. - PMID 31122707

10

Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome : Retrospective Genetic and Clinical Study

enthalten in: Clinical journal of the American Society of Nephrology : CJASN | 2019

von Frémeaux-Bacchi, V. | Sellier-Leclerc, A. | Vieira-Martins, P. | +14