Vincenzo Trischitta


Titolo Pubblicato in Anno
All-cause mortality prediction models in type 2 diabetes: applicability in the early stage of disease ACTA DIABETOLOGICA 2021
A Serum Resistin and Multicytokine Inflammatory Pathway Is Linked with and Helps Predict All-cause Death in Diabetes THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 2021
Correction to: Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation JOURNAL OF THROMBOSIS AND THROMBOLYSIS 2021
The synergic association of hs-CRP and serum amyloid P component in predicting all-cause mortality in patients with type 2 diabetes DIABETES CARE 2020
PPARA polymorphism influences the cardiovascular benefit of fenofibrate in type 2 diabetes: Findings from accord-lipid DIABETES 2020
Moving toward the implementation of precision medicine needs highly discriminatory, validated, inexpensive, and easy-to-use prediction models DIABETES CARE 2020
Association of the 1q25 Diabetes-Specific Coronary Heart Disease Locus With Alterations of the γ-Glutamyl Cycle and Increased Methylglyoxal Levels in Endothelial Cells DIABETES 2020
Contribution of rare and common genetic variants to early-onset type 2 diabetes DIABETOLOGIA 2020
Ruolo della variabilità genetica nel diabete tipo 2 (DT2) ad insorgenza precoce. SID 2020 2020
Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do CURRENT OPINION IN PHARMACOLOGY 2020
EstimatioN oF mORtality risk in type2 diabetiC patiEnts (ENFORCE): an inexpensive and parsimonious prediction model THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2019
A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients CARDIOVASCULAR DIABETOLOGY 2019
Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation PLOS ONE 2019
Association of a homozygous GCK missense mutation with mild diabetes MOLECULAR GENETICS & GENOMIC MEDICINE 2019
GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling INTERNATIONAL JOURNAL OF OBESITY 2019
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing ACTA DIABETOLOGICA 2019
The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy ACTA DIABETOLOGICA 2019
Serum amyloid component P improves the ability of C-reactive protein to predict all-cause mortality in patients with type 2 diabetes DIABETOLOGIADIABETOLOGIA 2019
Unraveling the genetic background of early-onset type 2 diabetes: a step forward toward precision medicine SIGU 2019 2019
Insights from Molecular Characterization of Adult Patients of Families with Multigenerational Diabetes Mellitus DIABETES 2018

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