Search details
1.
The number of risk factors not at target is associated with cardiovascular risk in a type 2 diabetic population with albuminuria in primary cardiovascular prevention. Post-hoc analysis of the NID-2 trial.
Cardiovasc Diabetol
; 21(1): 235, 2022 11 07.
Article
in English
| MEDLINE | ID: mdl-36344978
2.
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.
Blood
; 124(6): e4-e10, 2014 Aug 07.
Article
in English
| MEDLINE | ID: mdl-24990887
3.
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.
Haematologica
; 101(11): 1333-1342, 2016 11.
Article
in English
| MEDLINE | ID: mdl-27365488
4.
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Hum Mutat
; 35(2): 236-47, 2014 Feb.
Article
in English
| MEDLINE | ID: mdl-24186861
5.
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.
Am J Hum Genet
; 88(1): 115-20, 2011 Jan 07.
Article
in English
| MEDLINE | ID: mdl-21211618
6.
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.
Haematologica
; 99(8): 1387-94, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24763399
7.
Impact of liver fibrosis on COVID-19 in-hospital mortality in Southern Italy.
PLoS One
; 19(5): e0296495, 2024.
Article
in English
| MEDLINE | ID: mdl-38713731
8.
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.
Br J Haematol
; 181(5): 698-701, 2018 06.
Article
in English
| MEDLINE | ID: mdl-28466964
9.
Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study.
Br J Haematol
; 162(1): 112-9, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23617394
10.
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
Blood
; 117(24): 6673-80, 2011 Jun 16.
Article
in English
| MEDLINE | ID: mdl-21467542
11.
Effects of a Combination of Empagliflozin Plus Metformin vs. Metformin Monotherapy on NAFLD Progression in Type 2 Diabetes: The IMAGIN Pilot Study.
Biomedicines
; 11(2)2023 Jan 23.
Article
in English
| MEDLINE | ID: mdl-36830859
12.
Impact of gliflozins on cardiac remodeling in patients with type 2 diabetes mellitus & reduced ejection fraction heart failure: A pilot prospective study. GLISCAR study.
Diabetes Res Clin Pract
; 200: 110686, 2023 Jun.
Article
in English
| MEDLINE | ID: mdl-37100231
13.
Mortality and risk factors of vaccinated and unvaccinated frail patients with COVID-19 treated with anti-SARS-CoV-2 monoclonal antibodies: A real-world study.
Int J Infect Dis
; 131: 155-161, 2023 Jun.
Article
in English
| MEDLINE | ID: mdl-36944382
14.
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation).
Haematologica
; 97(1): 82-8, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-21933849
15.
Coronary Microvascular Dysfunction in Diabetes Mellitus: Pathogenetic Mechanisms and Potential Therapeutic Options.
Biomedicines
; 10(9)2022 Sep 14.
Article
in English
| MEDLINE | ID: mdl-36140374
16.
Association between Renal Function at Admission and COVID-19 in-Hospital Mortality in Southern Italy: Findings from the Prospective Multicenter Italian COVOCA Study.
J Clin Med
; 11(20)2022 Oct 17.
Article
in English
| MEDLINE | ID: mdl-36294442
17.
Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis.
Thromb Haemost
; 91(1): 129-40, 2004 Jan.
Article
in English
| MEDLINE | ID: mdl-14691578
18.
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes.
Mol Cytogenet
; 5(1): 39, 2012 Oct 01.
Article
in English
| MEDLINE | ID: mdl-23025896
19.
Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.
PLoS One
; 7(4): e35986, 2012.
Article
in English
| MEDLINE | ID: mdl-22558294
20.
Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.
Thromb Haemost
; 103(4): 826-32, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-20174760