Detalhe da pesquisa
1.
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Kidney Int;
103(5): 962-972, 2023 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36898413
2.
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
J Am Soc Nephrol;
33(4): 732-745, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35149593
3.
Efficacy and safety of nerinetide for the treatment of acute ischaemic stroke (ESCAPE-NA1): a multicentre, double-blind, randomised controlled trial.
Lancet;
395(10227): 878-887, 2020 03 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32087818
4.
ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.
Am J Med Genet A;
185(12): 3740-3753, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34331327
5.
Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic review.
Pediatr Nephrol;
36(6): 1353-1364, 2021 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32651716
6.
High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
Kidney Int;
96(6): 1408-1416, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31672324
7.
Corrigendum to "A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants." Kidney Int. 2023;103:962-972.
Kidney Int;
105(1): 213-214, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38182294
8.
Transplantation of a Gitelman Syndrome Kidney Ameliorates Hypertension: A Case Report.
Am J Kidney Dis;
73(3): 421-424, 2019 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30201548
9.
Management of children with congenital nephrotic syndrome: challenging treatment paradigms.
Nephrol Dial Transplant;
34(8): 1369-1377, 2019 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30215773
10.
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
J Am Soc Nephrol;
29(7): 1849-1858, 2018 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29654216
11.
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Kidney Int;
93(4): 961-967, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29398133
12.
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.
J Am Soc Nephrol;
28(8): 2529-2539, 2017 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28373276
13.
Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration.
Rheumatology (Oxford);
56(2): 209-213, 2017 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27150194
14.
Surgical clipping or endovascular coiling for unruptured intracranial aneurysms: a pragmatic randomised trial.
J Neurol Neurosurg Psychiatry;
88(8): 663-668, 2017 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28634280
15.
Quantitative non-contrast measurements improve diagnosing dural venous sinus thrombosis.
Neuroradiology;
58(7): 657-63, 2016 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27040817
16.
Dynamic CT angiography for cyberknife radiosurgery planning of intracranial arteriovenous malformations: a technical/feasibility report.
Radiol Oncol;
49(2): 192-9, 2015 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26029032
17.
Computed tomographic angiography and cerebral blood volume can predict final infarct volume and outcome after recanalization.
Stroke;
45(9): 2683-8, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25104844
18.
Navigation of Stents across Communicating Arteries for Aneurysm Embolization.
Can J Neurol Sci;
41(2): 193-9, 2014 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24534030
19.
Acute stroke patients treated with stent retrievers in carotid "T" occlusions have improved recanalization and outcome.
Can J Neurol Sci;
41(6): 709-13, 2014 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25410249
20.
Endovascular treatment for cerebral septic embolic stroke.
J Stroke Cerebrovasc Dis;
23(5): e375-7, 2014.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24529601