Lista de obras -

A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation.

artículo científico publicado en 2017

APOE genetic variants and apoE, miR-107 and miR-650 levels in Alzheimer's disease

artículo científico publicado en 2019

Abstracts and short papers from the 5th Congress of the Polish Thyroid Association, Poznan, 3-5 September, 2015: Poznan, Poland. 3-5 September 2015.

artículo científico publicado en 2016

Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson's Disease

artículo científico publicado en 2015

Apoptotic proteins in the course of aging of central nervous system in the rat.

artículo científico publicado en 2004

Assessment of serum selenium concentration in patients with autoimmune thyroiditis in Poznan district

artículo científico publicado en 2018

Association of atherosclerotic risk factors with carotid adventitial thickness assessed by ultrasonography.

scientific article published on July 2009

Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.

scientific article published on 11 September 2013

Biothiols and oxidative stress markers and polymorphisms of and genes in Alzheimer's disease patients

article

Cell biology of normal brain aging: synaptic plasticity-cell death.

artículo científico publicado en 2013

Expression and polymorphisms of gene 8-oxoguanine glycosylase 1 and the level of oxidative DNA damage in peripheral blood lymphocytes of patients with Alzheimer's disease.

artículo científico publicado en 2009

Free sterols in the rat white matter following experimental global ischemia

artículo científico publicado en 1997

Genetic factors in Parkinson's disease.

artículo científico publicado en 2013

Genetic variants in diseases of the extrapyramidal system.

artículo científico publicado en 2014

Genetics of Parkinson's disease and other diseases of the extrapyramidal system.

artículo científico

Homocysteine Level and Mechanisms of Injury in Parkinson's Disease as Related to MTHFR, MTR, and MTHFD1 Genes Polymorphisms and L-Dopa Treatment.

artículo científico publicado en 2013

Hyperhomocysteinemia in bipolar depression: clinical and biochemical correlates.

artículo científico publicado en 2013

Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.

artículo científico publicado en 2017

MTHFR, MTR, and MTHFD1 gene polymorphisms compared to homocysteine and asymmetric dimethylarginine concentrations and their metabolites in epileptic patients treated with antiepileptic drugs

artículo científico publicado en 2011

Memantine - neuroprotective drug in aging brain

artículo científico publicado en 2013

Molecular Effects of L-dopa Therapy in Parkinson's Disease

artículo científico

Molecular factors in migraine

artículo científico publicado en 2016

Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease

artículo científico publicado en 2013

Mutations in the exon 7 of Trp53 gene and the level of p53 protein in double transgenic mouse model of Alzheimer's disease

artículo científico publicado en 2014

Neuroplasticity in the Pathology of Neurodegenerative Diseases

scientific article published on 27 May 2020

Oxidative damage to DNA, p53 gene expression and p53 protein level in the process of aging in rat brain.

artículo científico publicado en 2004

Polymorphism of the COMT, MAO, DAT, NET and 5-HTT Genes, and Biogenic Amines in Parkinson's Disease ⬇️

artículo científico publicado en 2013

Polymorphisms of COMT (c.649G>A), MAO-A (c.1460C>T), NET (c.1287G>A) Genes and the Level of Catecholamines, Serotonin in Patients with Parkinson's Disease.

artículo científico publicado en 2017

Polymorphisms of the CHRNA4 gene encoding the alpha4 subunit of nicotinic acetylcholine receptor as related to the oxidative DNA damage and the level of apoptotic proteins in lymphocytes of the patients with Alzheimer's disease

artículo científico publicado en 2005

Primary progressive multiple sclerosis and neurofibromatosis type 1

artículo científico publicado en 2019

Pulsatility index in carotid arteries is increased in levothyroxine-treated Hashimoto disease

artículo científico publicado en 2015

Serum homocysteine levels are decreased in levothyroxine-treated women with autoimmune thyroiditis.

scientific article published on March 2014

The MAOA, COMT, MTHFR and ESR1 gene polymorphisms are associated with the risk of depression in menopausal women.

artículo científico publicado en 2015

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

artículo científico publicado en 2018

The Role of Vitamin D Receptor Gene Polymorphisms in Thyroid-Associated Orbitopathy

artículo científico publicado en 2019

The effect of UGT1A9, CYP2B6 and CYP2C9 genes polymorphism on individual differences in propofol pharmacokinetics among Polish patients undergoing general anaesthesia

artículo científico publicado en 2016

The immunological, biochemical and molecular bases of canine senescence and carcinogenesis: a review

artículo científico publicado en 2012

Vitamin B12 level may be related to the efficacy of single ketamine infusion in bipolar depression

artículo científico publicado en 2013

[Homocysteine and cognitive functions in bipolar depression]

scientific article published on 01 November 2014

Lista de obras de

A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation.

APOE genetic variants and apoE, miR-107 and miR-650 levels in Alzheimer's disease

Abstracts and short papers from the 5th Congress of the Polish Thyroid Association, Poznan, 3-5 September, 2015: Poznan, Poland. 3-5 September 2015.

Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson's Disease

Apoptotic proteins in the course of aging of central nervous system in the rat.

Assessment of serum selenium concentration in patients with autoimmune thyroiditis in Poznan district

Association of atherosclerotic risk factors with carotid adventitial thickness assessed by ultrasonography.

Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.

Biothiols and oxidative stress markers and polymorphisms of and genes in Alzheimer's disease patients

Cell biology of normal brain aging: synaptic plasticity-cell death.

Expression and polymorphisms of gene 8-oxoguanine glycosylase 1 and the level of oxidative DNA damage in peripheral blood lymphocytes of patients with Alzheimer's disease.

Free sterols in the rat white matter following experimental global ischemia

Genetic factors in Parkinson's disease.

Genetic variants in diseases of the extrapyramidal system.

Genetics of Parkinson's disease and other diseases of the extrapyramidal system.

Homocysteine Level and Mechanisms of Injury in Parkinson's Disease as Related to MTHFR, MTR, and MTHFD1 Genes Polymorphisms and L-Dopa Treatment.

Hyperhomocysteinemia in bipolar depression: clinical and biochemical correlates.

Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.

MTHFR, MTR, and MTHFD1 gene polymorphisms compared to homocysteine and asymmetric dimethylarginine concentrations and their metabolites in epileptic patients treated with antiepileptic drugs

Memantine - neuroprotective drug in aging brain

Molecular Effects of L-dopa Therapy in Parkinson's Disease

Molecular factors in migraine

Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease

Mutations in the exon 7 of Trp53 gene and the level of p53 protein in double transgenic mouse model of Alzheimer's disease

Neuroplasticity in the Pathology of Neurodegenerative Diseases

Oxidative damage to DNA, p53 gene expression and p53 protein level in the process of aging in rat brain.

Polymorphism of the COMT, MAO, DAT, NET and 5-HTT Genes, and Biogenic Amines in Parkinson's Disease ⬇️

Polymorphisms of COMT (c.649G>A), MAO-A (c.1460C>T), NET (c.1287G>A) Genes and the Level of Catecholamines, Serotonin in Patients with Parkinson's Disease.

Polymorphisms of the CHRNA4 gene encoding the alpha4 subunit of nicotinic acetylcholine receptor as related to the oxidative DNA damage and the level of apoptotic proteins in lymphocytes of the patients with Alzheimer's disease

Primary progressive multiple sclerosis and neurofibromatosis type 1

Pulsatility index in carotid arteries is increased in levothyroxine-treated Hashimoto disease

Serum homocysteine levels are decreased in levothyroxine-treated women with autoimmune thyroiditis.

The MAOA, COMT, MTHFR and ESR1 gene polymorphisms are associated with the risk of depression in menopausal women.

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

The Role of Vitamin D Receptor Gene Polymorphisms in Thyroid-Associated Orbitopathy

The effect of UGT1A9, CYP2B6 and CYP2C9 genes polymorphism on individual differences in propofol pharmacokinetics among Polish patients undergoing general anaesthesia

The immunological, biochemical and molecular bases of canine senescence and carcinogenesis: a review

Vitamin B12 level may be related to the efficacy of single ketamine infusion in bipolar depression

[Homocysteine and cognitive functions in bipolar depression]