Detalhe da pesquisa
1.
Screening for intracranial aneurysms in autosomal dominant polycystic kidney disease is cost-effective.
Kidney Int
; 93(3): 716-726, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29061331
2.
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
; 33(3): 473-483, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29058154
3.
Rare inherited disorders with renal involvement-approach to the patient.
Kidney Int
; 87(5): 901-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25651365
4.
3-Nitrotyrosine as a biomarker for vascular involvement in Fabry disease.
Kidney Int
; 86(1): 5-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24978372
5.
Increased risk of solid renal tumors in lithium-treated patients.
Kidney Int
; 86(1): 184-90, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24451323
6.
Kidney failure: aims for the next 10 years and barriers to success.
Lancet
; 382(9889): 353-62, 2013 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-23727164
7.
Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations.
Kidney Int
; 81(8): 779-83, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22237748
8.
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.
Kidney Int
; 82(4): 454-64, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22456601
9.
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.
Kidney Int
; 81(5): 494-501, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22166847
10.
Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.
J Am Soc Nephrol
; 22(2): 239-45, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21258034
11.
Progress in nephron sparing therapy for renal cell carcinoma and von Hippel-Lindau disease.
J Urol
; 185(6): 2056-60, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21496837
12.
Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome.
Blood
; 112(12): 4542-5, 2008 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18658028
13.
Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN).
Nephrol Dial Transplant
; 25(7): 2168-77, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19833663
14.
The authors reply.
Kidney Int
; 86(4): 857-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25265956
15.
Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
Kidney Int
; 75(7): 727-35, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19145239
16.
Hemolysis: a fatal complication of alkaptonuria in a severe renal failure patient.
Clin Nephrol
; 81(5): 374-6, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24691015
17.
Monitoring of glomerular filtration rate in lithium-treated outpatients--an ambulatory laboratory database surveillance.
Nephrol Dial Transplant
; 23(2): 562-5, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17999992
18.
Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
J Med Genet
; 44(3): 193-9, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17018561
19.
[3rd cancer plan]. / Le 3e plan cancer.
Rev Prat
; 63(9): 1197-8, 2013 Nov.
Artigo
em Francês
| MEDLINE | ID: mdl-24422284
20.
Exonic duplication of the hepatocyte nuclear factor-1beta gene (transcription factor 2, hepatic) as a cause of maturity onset diabetes of the young type 5.
J Clin Endocrinol Metab
; 92(7): 2844-7, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17440011