Detalhe da pesquisa
1.
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.
J Am Soc Nephrol
; 34(6): 1105-1119, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36995132
2.
Sleep-disordered breathing and heart failure: a vicious cycle of cardiovascular risk.
Monaldi Arch Chest Dis
; 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37667884
3.
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations.
Nephrol Dial Transplant
; 37(12): 2351-2362, 2022 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35772019
4.
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.
Pediatr Nephrol
; 37(9): 2185-2207, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35713730
5.
Multiple, random spot urine sampling for estimating urinary sodium excretion.
Eur J Pediatr
; 181(1): 83-90, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34196792
6.
Single, Dual, and Triple Antithrombotic Therapy in Cancer Patients with Coronary Artery Disease: Searching for Evidence and Personalized Approaches.
Semin Thromb Hemost
; 47(8): 950-961, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34261150
7.
Bloody Diarrhea and Shiga Toxin-Producing Escherichia coli Hemolytic Uremic Syndrome in Children: Data from the ItalKid-HUS Network.
J Pediatr
; 237: 34-40.e1, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34197890
8.
Fenoldopam and renal hemodynamics in shiga toxin-related hemolytic uremic syndrome.
Pediatr Nephrol
; 36(9): 2891-2894, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002291
9.
Hemoglobinuria for the early identification of STEC-HUS in high-risk children: data from the ItalKid-HUS Network.
Eur J Pediatr
; 180(9): 2791-2795, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33759020
10.
Successful surgical repair of left ventricular pseudoaneurysm in a patient with subacute ST-elevation myocardial infarction.
Monaldi Arch Chest Dis
; 92(2)2021 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34579519
11.
Cardiac teleconsulting in the time of COVID-19 global pandemic: The "Antonio Cardarelli" Hospital project.
Monaldi Arch Chest Dis
; 91(2)2021 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33849264
12.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(5): 789-802, 2017 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29100090
13.
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
N Engl J Med
; 376(8): 742-754, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28121514
14.
Is Shigatoxin 1 protective for the development of Shigatoxin 2-related hemolytic uremic syndrome in children? Data from the ItalKid-HUS Network.
Pediatr Nephrol
; 35(10): 1997-2001, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32734345
15.
77 Routine outpatients visits during SARS-CoV2 global pandemic.
Eur Heart J Suppl
; 22(Suppl N): N135-N137, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38626258
16.
Cardiopulmonary exercise testing and echocardiographic exam: an useful interaction.
Cardiovasc Ultrasound
; 17(1): 29, 2019 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31796047
17.
Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.
Int J Mol Sci
; 18(4)2017 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28398236
18.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(6): 1034, 2017 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220675
19.
Outcome of atypical hemolytic uremic syndrome: role of triggers and complement abnormalities in the response to C5 inhibition.
J Nephrol
; 2024 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38280096
20.
[Role of vitamin D in the pathogenesis of chronic kidney disease]. / Ruolo della vitamina D nei pazienti con malattia renale cronica.
Recenti Prog Med
; 104(1): 33-40, 2013 Jan.
Artigo
em Italiano
| MEDLINE | ID: mdl-23439539