Detalhe da pesquisa
1.
Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance.
Am J Kidney Dis
; 82(5): 581-596.e0, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37301502
2.
Rituximab or Cyclophosphamide in the Treatment of Membranous Nephropathy: The RI-CYCLO Randomized Trial.
J Am Soc Nephrol
; 32(4): 972-982, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33649098
3.
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes.
Kidney Int
; 98(6): 1589-1604, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32750457
4.
Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?
Am J Nephrol
; 53(8-9): 624-627, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36349760
5.
Bortezomib-based therapy combined with high cut-off hemodialysis is highly effective in newly diagnosed multiple myeloma patients with severe renal impairment.
Am J Hematol
; 90(7): 647-52, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25858483
6.
[IgA nephropathy and granulomatosis with polyangiitis-overlap: a rare coexistence of two glomerular nephropathies with remission after steroids and rituximab].
G Ital Nefrol
; 40(1)2023 Feb 27.
Artigo
em Italiano
| MEDLINE | ID: mdl-36883919
7.
The Role of Rituximab in Primary Focal Segmental Glomerular Sclerosis of the Adult.
Kidney Int Rep
; 7(8): 1878-1886, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35967114
8.
Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathy.
Heart
; 108(1): 54-60, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33563631
9.
Circulating miR-184 is a potential predictive biomarker of cardiac damage in Anderson-Fabry disease.
Cell Death Dis
; 12(12): 1150, 2021 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34897278
10.
Diagnostic accuracy of anti-phospholipase A2 receptor (PLA2R) antibodies in idiopathic membranous nephropathy: an Italian experience.
J Nephrol
; 34(2): 573-579, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33123964
11.
Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: protocol of a pilot randomised controlled trial.
BMJ Open
; 9(12): e029232, 2019 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31806605
12.
The challenge of diagnosing atheroembolic renal disease: clinical features and prognostic factors.
Circulation
; 116(3): 298-304, 2007 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-17606842
13.
Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome.
Am J Kidney Dis
; 49(1): 91-8, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17185149
14.
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy.
PLoS One
; 12(7): e0180581, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28672034
15.
The ultrastructural basis of renal pathology in monoclonal gammopathies.
J Nephrol
; 18(6): 659-75, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16358223
16.
Adult nondiarrhea hemolytic uremic syndrome associated with Shiga toxin Escherichia coli O157:H7 bacteremia and urinary tract infection.
Am J Kidney Dis
; 41(1): e4.1 - e4.4, 2003 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12500215
17.
Lack of association between dialysis modality and outcomes in atheroembolic renal disease.
Clin J Am Soc Nephrol
; 5(3): 454-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20019115
18.
Renal involvement in systemic amyloidosis--an Italian retrospective study on epidemiological and clinical data at diagnosis.
Nephrol Dial Transplant
; 22(6): 1608-18, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17395661