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vincenzo.trischitta@uniroma1.it
Vincenzo Trischitta
Professore Ordinario
Struttura:
DIPARTIMENTO DI MEDICINA SPERIMENTALE
E-mail:
vincenzo.trischitta@uniroma1.it
Pagina istituzionale corsi di laurea
Curriculum Sapienza
Pubblicazioni
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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Progetti di Ricerca
Towards precision medicine: insights into the molecular pathogenesis of early-onset type 2 diabetes.
Gruppi di ricerca
Slowly progressive autoimmune diabetes: a clinical model for novel pathways of ß-cell protection
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