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AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approach

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.137

2023

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Aldo-keto reductase 1C2 (AKR1C2) as the second gene associated to non-syndromic primary lipedema: investigating activating mutation or overexpression as causative factors

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.127

2023

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Italian SARS-CoV-2 patients in intensive care: towards an identikit for subjects at risk?

European review for medical and pharmacological sciences, 2020-09, Vol.24 (18), p.9698

2020

Volltextzugriff (PDF)

Autoantibodies in patients with post-COVID syndrome: a possible link with severity?

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.48

2023

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Linking pathogenic and likely pathogenic gene variants to long-COVID symptoms

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.20

2023

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Serum proteomic profiling reveals potential inflammatory biomarkers in long-COVID patients: a comparative analysis with healthy controls

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.1

2023

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Autoantibodies detection in patients affected by autoimmune retinopathies

European review for medical and pharmacological sciences, 2023-12, Vol.27 (6 Suppl), p.57

2023

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Omics sciences and precision medicine in thyroid cancer

Clinica terapeutica, 2023-11, Vol.174, p.11-20

2023

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Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity

Genetics and molecular research, 2016-08, Vol.15 (3)

2016

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The Role of Olive Tree Polyphenols In The Prevention of COVID-19: A Scoping Review Part 2

Clinica terapeutica, 2023-11, Vol.174, p.149-153

2023

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Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach

Lymphology, 2016-06, Vol.49 (2), p.57-72

2016

Volltextzugriff (PDF)

Omics sciences and precision medicine in melanoma

Clinica terapeutica, 2023-11, Vol.174, p.29-36

2023

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Omics sciences and precision medicine in testicular cancer

Clinica terapeutica, 2023-11, Vol.174, p.21-28

2023

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Putative role of Brugada syndrome genes in familial atrial fibrillation

European review for medical and pharmacological sciences, 2019-09, Vol.23 (17), p.7582

2019

Volltextzugriff (PDF)

Omics sciences and precision medicine in kidney cancer

Clinica terapeutica, 2023-11, Vol.174, p.46-54

2023

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Omics sciences and precision medicine in pancreas cancer

Clinica terapeutica, 2023-11, Vol.174 (Suppl 2(6)), p.85-94

2023

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Omics sciences and precision medicine in Urothelial Carcinoma

Clinica terapeutica, 2023-11, Vol.174, p.1-10

2023

Volltextzugriff (PDF)

Reply to the Letter - "The development of Brugada syndrome phenotype is multifactorial, combining genetic and environmental factors"

European review for medical and pharmacological sciences, 2020-04, Vol.24 (7), p.3446

2020

Volltextzugriff (PDF)

Genetic tests for low- and middle-income countries: a literature review

Genetics and molecular research, 2017-02, Vol.16 (1)

2017

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TNFR1 -383 A˃C polymorphism and ankylosing spondylitis in a Russian Caucasian population: a preliminary study

Genetics and molecular research, 2017-03, Vol.16 (1)

2017

Volltextzugriff (PDF)

A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene

Lymphology, 2016-03, Vol.49 (1), p.15-20

2016

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Glu298Asp polymorphism in the NOS3 gene is not associated with susceptibility to chronic heart failure in a Russian population

Genetics and molecular research, 2019 (1)

2019

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Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome

Genetics and molecular research, 2016-07, Vol.15 (3)

2016

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Clinical and molecular findings in an Albanian family with familial adenomatous polyposis

Genetics and molecular research, 2017-10 (4), p.1

2017

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Genetic polymorphisms and retinal vein occlusion in an Italian population

Genetics and molecular research, 2015-01, Vol.14 (4), p.13337-13341

2015

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AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approach

Aldo-keto reductase 1C2 (AKR1C2) as the second gene associated to non-syndromic primary lipedema: investigating activating mutation or overexpression as causative factors

Italian SARS-CoV-2 patients in intensive care: towards an identikit for subjects at risk?

Autoantibodies in patients with post-COVID syndrome: a possible link with severity?

Linking pathogenic and likely pathogenic gene variants to long-COVID symptoms

Serum proteomic profiling reveals potential inflammatory biomarkers in long-COVID patients: a comparative analysis with healthy controls

Autoantibodies detection in patients affected by autoimmune retinopathies

Omics sciences and precision medicine in thyroid cancer

Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity

The Role of Olive Tree Polyphenols In The Prevention of COVID-19: A Scoping Review Part 2

Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach

Omics sciences and precision medicine in melanoma

Omics sciences and precision medicine in testicular cancer

Putative role of Brugada syndrome genes in familial atrial fibrillation

Omics sciences and precision medicine in kidney cancer

Omics sciences and precision medicine in pancreas cancer

Omics sciences and precision medicine in Urothelial Carcinoma

Reply to the Letter - "The development of Brugada syndrome phenotype is multifactorial, combining genetic and environmental factors"

Genetic tests for low- and middle-income countries: a literature review

TNFR1 -383 A˃C polymorphism and ankylosing spondylitis in a Russian Caucasian population: a preliminary study

A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene

Glu298Asp polymorphism in the NOS3 gene is not associated with susceptibility to chronic heart failure in a Russian population

Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome

Clinical and molecular findings in an Albanian family with familial adenomatous polyposis

Genetic polymorphisms and retinal vein occlusion in an Italian population

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