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Whether Prolyl Hydroxylase Blocker-Roxadustat-In the Treatment of Anemia in Patients with Chronic Kidney Disease Is the Future?

International journal of environmental research and public health, 2021-02, Vol.18 (4), p.1612

2021

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Tirzepatide — a dual GIP/GLP-1 receptor agonist — a new antidiabetic drug with potential metabolic activity in the treatment of type 2 diabetes

Endokrynologia polska, 2022-01

2022

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Mesenchymal Stem Cells-Potential Applications in Kidney Diseases

International journal of molecular sciences, 2019-05, Vol.20 (10), p.2462

2019

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Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke

Journal of stroke and cerebrovascular diseases, 2018-07, Vol.27 (7), p.1885-1889

2018

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Fabry disease – a genetically conditioned extremely rare disease with a very unusual course

Intractable & Rare Diseases Research, 2022/02/28, Vol.11(1), pp.34-36

2022

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Association between Selected Polymorphisms rs12086634, rs846910, rs4844880, rs3753519 of 11β-Hydroxysteroid Dehydrogenase Type 1 ( HSD11B1 ) and the Presence of Insulin Resistance in the Polish Population of People Living in Upper Silesia

International journal of environmental research and public health, 2021-09, Vol.18 (19), p.10168

2021

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Why PRP works only on certain patients with tennis elbow? Is PDGFB gene a key for PRP therapy effectiveness? A prospective cohort study

BMC musculoskeletal disorders, 2021-08, Vol.22 (1), p.710-710, Article 710

2021

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Association of chemotactic cytokine receptor 5 (CCR5) gene polymorphism (59029 A/G, rs1799987) with diabetic kidney disease in patients with type 2 diabetes from Poland

Endokrynologia Polska, 2022-01, Vol.73 (1), p.103-109

2022

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Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population

Journal of autism and developmental disorders, 2022-10, Vol.52 (10), p.4213-4218

2022

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Pentoxifylline and Methylprednisolone Additively Alleviate Kidney Failure and Prolong Survival of Rats after Renal Warm Ischemia-Reperfusion

International journal of molecular sciences, 2018-01, Vol.19 (1), p.221

2018

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DIAPH2, PTPRD and HIC1 Gene Polymorphisms and Laryngeal Cancer Risk

International journal of environmental research and public health, 2021-07, Vol.18 (14), p.7486

2021

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Calcium intake and osteoporosis: the influence of calcium intake from dairy products on hip bone mineral density and fracture incidence – a population-based study in women over 55 years of age

Public health nutrition, 2014-02, Vol.17 (2), p.383-389

2014

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Influence of education, marital status, occupation, and the place of living on skeletal status, fracture prevalence, and the course and effectiveness of osteoporotic therapy in women in the RAC-OST-POL Study

Journal of bone and mineral metabolism, 2014, Vol.32 (1), p.89-95

2014

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Association of CX3CR1 Gene Polymorphisms with Fractalkine, Fractalkine Receptor, and C-Reactive Protein Levels in Patients with Kidney Failure

International journal of environmental research and public health, 2021-02, Vol.18 (4), p.2202

2021

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Relationship between CETP gene polymorphisms with coronary artery disease in Polish population

Molecular biology reports, 2018-12, Vol.45 (6), p.1929-1935

2018

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Treatment of classic phenylketonuria in Poland in the years 2009–2015 based on the database of the Polish National Health Fund

Pediatric endocrinology, diabetes, and metabolism, 2020, Vol.26 (3), p.118-124

2020

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Analysis of the association between rs12917707 and rs11864909 single nucleotide polymorphisms in the region of the uromoduline gene and chronic kidney disease - a family-based study

Annals of Agricultural and Environmental Medicine, 2017-09, Vol.24 (3), p.464-466

2017

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The relationship between CYP7A1 polymorphisms, coronary artery disease & serum lipid markers

Biomarkers in medicine, 2019-10, Vol.13 (14), p.1199-1208

2019

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Correlation between serum low-density lipoprotein cholesterol concentration and arterial wall stiffness

Kardiologia polska (1957), 2018-01, Vol.76 (12), p.1712-1716

2018

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Protein tyrosine phosphatase‐22 (PTPN‐22) polymorphism in the pathogenesis of chronic urticaria

Allergy (Copenhagen), 2011-10, Vol.66 (10), p.1392-1393

2011

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The incidence rate of hospitalized lysosomal storage diseases in Poland in 2013-2015 based on data from the National Health Fund

Pediatric endocrinology, diabetes, and metabolism, 2021, Vol.27 (3), p.191-198

2021

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Uremic pruritus and serum brain-derived neurotrophic factor in diabetic and non-diabetic haemodialysis patients

Postȩpy dermatologii i alergologii, 2020-12, Vol.37 (6), p.932-937

2020

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Association of single nucleotide polymorphism (rs741301) of the ELMO1 gene with diabetic kidney disease in Polish patients with type 2 diabetes: a pilot study

Endokrynologia polska, 2020-01, Vol.71 (1), p.66-72

2020

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Falls in RAC-OST-POL Study: epidemiological study in postmenopausal women aged over 55 years

Endokrynologia Polska, 2016, Vol.67 (2), p.185-189

2016

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Relationship between rs4674344 CYP27A1 gene polymorphism and coronary artery disease in a Polish population

Kardiologia polska, 2020-01, Vol.78 (1), p.65-67

2020

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Whether Prolyl Hydroxylase Blocker-Roxadustat-In the Treatment of Anemia in Patients with Chronic Kidney Disease Is the Future?

Tirzepatide — a dual GIP/GLP-1 receptor agonist — a new antidiabetic drug with potential metabolic activity in the treatment of type 2 diabetes

Mesenchymal Stem Cells-Potential Applications in Kidney Diseases

Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke

Fabry disease – a genetically conditioned extremely rare disease with a very unusual course

Association between Selected Polymorphisms rs12086634, rs846910, rs4844880, rs3753519 of 11β-Hydroxysteroid Dehydrogenase Type 1 ( HSD11B1 ) and the Presence of Insulin Resistance in the Polish Population of People Living in Upper Silesia

Why PRP works only on certain patients with tennis elbow? Is PDGFB gene a key for PRP therapy effectiveness? A prospective cohort study

Association of chemotactic cytokine receptor 5 (CCR5) gene polymorphism (59029 A/G, rs1799987) with diabetic kidney disease in patients with type 2 diabetes from Poland

Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population

Pentoxifylline and Methylprednisolone Additively Alleviate Kidney Failure and Prolong Survival of Rats after Renal Warm Ischemia-Reperfusion

DIAPH2, PTPRD and HIC1 Gene Polymorphisms and Laryngeal Cancer Risk

Calcium intake and osteoporosis: the influence of calcium intake from dairy products on hip bone mineral density and fracture incidence – a population-based study in women over 55 years of age

Influence of education, marital status, occupation, and the place of living on skeletal status, fracture prevalence, and the course and effectiveness of osteoporotic therapy in women in the RAC-OST-POL Study

Association of CX3CR1 Gene Polymorphisms with Fractalkine, Fractalkine Receptor, and C-Reactive Protein Levels in Patients with Kidney Failure

Relationship between CETP gene polymorphisms with coronary artery disease in Polish population

Treatment of classic phenylketonuria in Poland in the years 2009–2015 based on the database of the Polish National Health Fund

Analysis of the association between rs12917707 and rs11864909 single nucleotide polymorphisms in the region of the uromoduline gene and chronic kidney disease - a family-based study

The relationship between CYP7A1 polymorphisms, coronary artery disease & serum lipid markers

Correlation between serum low-density lipoprotein cholesterol concentration and arterial wall stiffness

Protein tyrosine phosphatase‐22 (PTPN‐22) polymorphism in the pathogenesis of chronic urticaria

The incidence rate of hospitalized lysosomal storage diseases in Poland in 2013-2015 based on data from the National Health Fund

Uremic pruritus and serum brain-derived neurotrophic factor in diabetic and non-diabetic haemodialysis patients

Association of single nucleotide polymorphism (rs741301) of the ELMO1 gene with diabetic kidney disease in Polish patients with type 2 diabetes: a pilot study

Falls in RAC-OST-POL Study: epidemiological study in postmenopausal women aged over 55 years

Relationship between rs4674344 CYP27A1 gene polymorphism and coronary artery disease in a Polish population

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