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The Adiponectin Paradox for All-Cause and Cardiovascular Mortality

Diabetes (New York, N.Y.), 2018-01, Vol.67 (1), p.12-22

2018

Volltextzugriff (PDF)

On the emerging role of GALNT2 on intermediate metabolism and adipogenesis

Acta diabetologica, 2022-09, Vol.59 (9), p.1255-1256

2022

Volltextzugriff (PDF)

GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Acta diabetologica, 2024, Vol.61 (8), p.1007-1013

2024

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Correction: GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Acta diabetologica, 2024, Vol.61 (8), p.1015-1015

2024

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GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling

International Journal of Obesity, 2019-12, Vol.43 (12), p.2448-2457

2019

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Morphological and molecular characterization of GALNT2-mediated adipogenesis

International Journal of Obesity, 2021-06, Vol.45 (6), p.1362-1366

2021

Volltextzugriff (PDF)

MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Acta diabetologica, 2023-01, Vol.60 (1), p.131-135

2023

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Correction to: MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Acta diabetologica, 2023-03, Vol.60 (3), p.459-459

2023

Volltextzugriff (PDF)

Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients

Acta diabetologica, 2022-08, Vol.59 (8), p.1113-1116

2022

Volltextzugriff (PDF)

All-cause mortality prediction models in type 2 diabetes: applicability in the early stage of disease

Acta diabetologica, 2021-10, Vol.58 (10), p.1425-1428

2021

Volltextzugriff (PDF)

A Haplotype at the Adiponectin Locus Is Associated With Obesity and Other Features of the Insulin Resistance Syndrome

Diabetes (New York, N.Y.), 2002-07, Vol.51 (7), p.2306-2312

2002

Volltextzugriff (PDF)

The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy

Acta diabetologica, 2020-05, Vol.57 (5), p.589-596

2020

Volltextzugriff (PDF)

Pathogenic variants of MODY-genes in adult patients with early-onset type 2 diabetes

Acta diabetologica, 2022-05, Vol.59 (5), p.747-750

2022

Volltextzugriff (PDF)

Moving Toward the Implementation of Precision Medicine Needs Highly Discriminatory, Validated, Inexpensive, and Easy-to-Use Prediction Models

Diabetes care, 2020-04, Vol.43 (4), p.701-703

2020

Volltextzugriff (PDF)

Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

Acta diabetologica, 2019-05, Vol.56 (5), p.515-523

2019

Volltextzugriff (PDF)

Type 2 Deiodinase Polymorphism (Threonine 92 Alanine) Predicts l-Thyroxine Dose to Achieve Target Thyrotropin Levels in Thyroidectomized Patients

The journal of clinical endocrinology and metabolism, 2008-03, Vol.93 (3), p.910-913

2008

Volltextzugriff (PDF)

Erratum. The Adiponectin Paradox for All-Cause and Cardiovascular Mortality. Diabetes 2018;67:12-22

Diabetes (New York, N.Y.), 2018-12, Vol.67 (12), p.2710-2710

2018

Volltextzugriff (PDF)

Unveiling Novel Markers and Modeling Clinical Prediction of Treatment Effects Are Equally Important for Implementing Precision Therapeutics

Diabetes (New York, N.Y.), 2023-08, Vol.72 (8), p.1057-1059

2023

Volltextzugriff (PDF)

Complications following endoscopic intracranial procedures in children

Child's nervous system, 2007-06, Vol.23 (6), p.633-644

2007

Volltextzugriff (PDF)

The +276 G/T Single Nucleotide Polymorphism of the Adiponectin Gene Is Associated With Coronary Artery Disease in Type 2 Diabetic Patients

Diabetes care, 2004-08, Vol.27 (8), p.2015-2020

2004

Volltextzugriff (PDF)

Some Doubts About the Mantra on the Deleterious Cardiovascular Effects of Sulfonylureas

Diabetes (New York, N.Y.), 2017-08, Vol.66 (8), p.2069-2071

2017

Volltextzugriff (PDF)

Endoscopic third ventriculostomy in the treatment of hydrocephalus in posterior fossa tumors in children

Child's nervous system, 2004-11, Vol.20 (11-12), p.828-833

2004

Volltextzugriff (PDF)

Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do

Current opinion in pharmacology, 2020-12, Vol.55, p.157-164

2020

Volltextzugriff (PDF)

Intracranial pressure monitoring and lumbar puncture after endoscopic third ventriculostomy in children

Neurosurgery, 2006-01, Vol.58 (1), p.126-136

2006

Volltextzugriff (PDF)

The Need to Increase Clinical Skills and Change the Genetic Testing Strategy for Monogenic Diabetes

Diabetes (New York, N.Y.), 2022-03, Vol.71 (3), p.379-380

2022

Volltextzugriff (PDF)

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The Adiponectin Paradox for All-Cause and Cardiovascular Mortality

On the emerging role of GALNT2 on intermediate metabolism and adipogenesis

GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Correction: GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling

Morphological and molecular characterization of GALNT2-mediated adipogenesis

MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Correction to: MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients

All-cause mortality prediction models in type 2 diabetes: applicability in the early stage of disease

A Haplotype at the Adiponectin Locus Is Associated With Obesity and Other Features of the Insulin Resistance Syndrome

The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy

Pathogenic variants of MODY-genes in adult patients with early-onset type 2 diabetes

Moving Toward the Implementation of Precision Medicine Needs Highly Discriminatory, Validated, Inexpensive, and Easy-to-Use Prediction Models

Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

Type 2 Deiodinase Polymorphism (Threonine 92 Alanine) Predicts l-Thyroxine Dose to Achieve Target Thyrotropin Levels in Thyroidectomized Patients

Erratum. The Adiponectin Paradox for All-Cause and Cardiovascular Mortality. Diabetes 2018;67:12-22

Unveiling Novel Markers and Modeling Clinical Prediction of Treatment Effects Are Equally Important for Implementing Precision Therapeutics

Complications following endoscopic intracranial procedures in children

The +276 G/T Single Nucleotide Polymorphism of the Adiponectin Gene Is Associated With Coronary Artery Disease in Type 2 Diabetic Patients

Some Doubts About the Mantra on the Deleterious Cardiovascular Effects of Sulfonylureas

Endoscopic third ventriculostomy in the treatment of hydrocephalus in posterior fossa tumors in children

Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do

Intracranial pressure monitoring and lumbar puncture after endoscopic third ventriculostomy in children

The Need to Increase Clinical Skills and Change the Genetic Testing Strategy for Monogenic Diabetes

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