Suchergebnisse - (Person:"Fakhouri, Fadi")

PubPharm (6)

1

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

2

Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome

enthalten in: Kidney international | 2018

von Schaefer, F. | Ardissino, G. | Ariceta, G. | +29

3

C5 nephritic factors drive the biological phenotype of C3 glomerulopathies

enthalten in: Kidney international | 2017

von Marinozzi, M. | Chauvet, S. | Le Quintrec, M. | +13

CommentIn: Nat Rev Nephrol. 2017 Oct;13(10):597. - PMID 28757638

4

C3 glomerulopathy : consensus report

enthalten in: Kidney international | 2013

von Pickering, M. | D'Agati, V. | Nester, C. | +32

5

Treatment with human complement factor H rapidly reverses renal complement deposition in factor H-deficient mice

enthalten in: Kidney international | 2010

von Fakhouri, F. | de Jorge, E. | Brune, F. | +3

6

Lithium-induced nephropathy : Rate of progression and prognostic factors

enthalten in: Kidney international | 2003

von Presne, C. | Fakhouri, F. | Noël, L. | +5

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