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Recommendations for the classification of diseases as CFTR-related disorders

Journal of cystic fibrosis, 2011-06, Vol.10, p.S86-S102

2011

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Ischemic preconditioning vs adenosine vs prostaglandin E1 for protection against liver ischemia/reperfusion injury

Brazilian journal of medical and biological research, 2017-01, Vol.50 (8), p.e6185-e6185

2017

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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

Journal of cystic fibrosis, 2008-05, Vol.7 (3), p.179-196

2008

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A novel prothrombin mutation in two families with prominent thrombophilia – the first cases of antithrombin resistance in a Caucasian population

Journal of thrombosis and haemostasis, 2013-10, Vol.11 (10), p.1936-1939

2013

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Matrix metalloproteinase-2 (MMP-2 ) and-9 (MMP-9) gene variants and microvascular complications in type 2 diabetes patients

Balkan journal of medical genetics, 2023-03, Vol.25 (1), p.35-40

2023

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Oxidized Alpha-1-Antitrypsin as a Potential Biomarker Associated with Onset and Severity of Chronic Obstructive Pulmonary Disease in Adult Population

Chronic obstructive pulmonary disease, 2018-09, Vol.15 (5), p.472-478

2018

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Clinical and biochemical characterization of the prothrombin Belgrade mutation in a large Serbian pedigree: new insights into the antithrombin resistance mechanism

Journal of thrombosis and haemostasis, 2017-04, Vol.15 (4), p.670-677

2017

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Association of the methionine sulfoxide reductase A rs10903323 gene polymorphism with functional activity and oxidative modification of alpha-1-antitrypsin in COPD patients

Pulmonology, 2024-03, Vol.30 (2), p.122-129

2024

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High expressed miR-183 as a potential biomarker of poor survival in tongue cancer patients

European journal of cancer (1990), 2016-07, Vol.61, p.S10-S10

2016

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The effect of metformin on TSH levels in euthyroid and hypothyroid newly diagnosed diabetes mellitus type 2 patients

Bratislavské lékarské listy, 2016, Vol.117 (8), p.433-435

2016

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C0219: The Presence of Prothrombotic Mutations and a Higher FVIII Activity Contribute to Thrombosis Development During the Breast Cancer Treatment

Thrombosis research, 2014-05, Vol.133, p.S103-S103

2014

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C0300: The C20068T Gene Variant in the 3’ End of the Prothrombin Gene is the Risk Factor for Recurrent Pregnancy Loss

Thrombosis research, 2014-05, Vol.133, p.S108-S108

2014

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ePS01.6 Application of next-generation sequencing for the analysis of CFTR in Serbian CF patients

Journal of cystic fibrosis, 2015-06, Vol.14, p.S43-S43

2015

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Are thrombophilia more multifactorial than we thought: report of mosaicism for FII G20210A and novel FII T20061C gene variants

Journal of thrombosis and haemostasis, 2012-02, Vol.10 (2), p.301-303

2012

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The effect of FII c.1787G>A (prothrombin Belgrade) mutation on prothrombin gene expression in vitro

Molecular biology (New York), 2017, Vol.51 (1), p.49-52

2017

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C0221: Genotype CYP2C19 Effects on Therapeutic Response During Clopidogrel Treatment in Patients with Carotid Artery Stenosis

Thrombosis research, 2014-05, Vol.133, p.S79-S79

2014

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Primary colorectal lymphoma:An overview

World journal of gastrointestinal oncology, 2011-01, Vol.3 (1), p.14-18

2011

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C0218: A High Prophylactic LMWH Dose Successfully Suppressed Haemostatic Activity in Pregnant Woman with a New Prothrombin FII G20031T (C.1787G>A) Mutation

Thrombosis research, 2014-05, Vol.133, p.S79-S79

2014

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9 CFTR rearrangements in Serbian patients with classical cystic fibrosis

Journal of cystic fibrosis, 2014-06, Vol.13, p.S47-S47

2014

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P-034 Clinical characteristics of the first thrombosis process among young women and those over 45 years

Thrombosis research, 2013, Vol.131, p.S85-S86

2013

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Clinically “silent” giant pheochromocytoma. case report

Acta endocrinologica (Bucharest, Romania : 2005), 2013, Vol.9 (1), p.121-129

Radojkovic, D

2013

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Performance of free-space optical systems in the presence of receiver imperfections

IOP conference series. Materials Science and Engineering, 2021-01, Vol.1032 (1), p.12002

2021

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ALPHA-1 antitrypsin affects U0126-induced cytotoxicity in colon cancer cell line (HCT116)

Molecular biology (New York), 2016, Vol.50 (1), p.153-156

2016

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The 3’ End Prothrombin Gene Variants in Serbian Patients with Idiopathic Thrombophilia

Balkan journal of medical genetics, 2014-12, Vol.17 (2), p.43-48

2014

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Recommendations for the classification of diseases as CFTR-related disorders

Ischemic preconditioning vs adenosine vs prostaglandin E1 for protection against liver ischemia/reperfusion injury

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

A novel prothrombin mutation in two families with prominent thrombophilia – the first cases of antithrombin resistance in a Caucasian population

Matrix metalloproteinase-2 (MMP-2 ) and-9 (MMP-9) gene variants and microvascular complications in type 2 diabetes patients

Oxidized Alpha-1-Antitrypsin as a Potential Biomarker Associated with Onset and Severity of Chronic Obstructive Pulmonary Disease in Adult Population

Clinical and biochemical characterization of the prothrombin Belgrade mutation in a large Serbian pedigree: new insights into the antithrombin resistance mechanism

Association of the methionine sulfoxide reductase A rs10903323 gene polymorphism with functional activity and oxidative modification of alpha-1-antitrypsin in COPD patients

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

High expressed miR-183 as a potential biomarker of poor survival in tongue cancer patients

The effect of metformin on TSH levels in euthyroid and hypothyroid newly diagnosed diabetes mellitus type 2 patients

C0219: The Presence of Prothrombotic Mutations and a Higher FVIII Activity Contribute to Thrombosis Development During the Breast Cancer Treatment

C0300: The C20068T Gene Variant in the 3’ End of the Prothrombin Gene is the Risk Factor for Recurrent Pregnancy Loss

ePS01.6 Application of next-generation sequencing for the analysis of CFTR in Serbian CF patients

Are thrombophilia more multifactorial than we thought: report of mosaicism for FII G20210A and novel FII T20061C gene variants

The effect of FII c.1787G>A (prothrombin Belgrade) mutation on prothrombin gene expression in vitro

C0221: Genotype CYP2C19 Effects on Therapeutic Response During Clopidogrel Treatment in Patients with Carotid Artery Stenosis

Primary colorectal lymphoma:An overview

C0218: A High Prophylactic LMWH Dose Successfully Suppressed Haemostatic Activity in Pregnant Woman with a New Prothrombin FII G20031T (C.1787G>A) Mutation

9 CFTR rearrangements in Serbian patients with classical cystic fibrosis

P-034 Clinical characteristics of the first thrombosis process among young women and those over 45 years

Clinically “silent” giant pheochromocytoma. case report

Performance of free-space optical systems in the presence of receiver imperfections

ALPHA-1 antitrypsin affects U0126-induced cytotoxicity in colon cancer cell line (HCT116)

The 3’ End Prothrombin Gene Variants in Serbian Patients with Idiopathic Thrombophilia

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