A. Różycka

发表

Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.

W. Trzeciak, A. Różycka, 2003, Journal of applied genetics.

Evidence for S284L Mutation of the CHRNA4 in a White Family with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

W. Trzeciak, E. Skorupska, A. Różycka, 2003, Epilepsia.

The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy

W. Trzeciak, B. Steinborn, A. Różycka, 2009, Seizure.

Oxidative DNA damage and level of thiols as related to polymorphisms of MTHFR, MTR, MTHFD1 in Alzheimer's and Parkinson's diseases.

B. Kempisty, J. Dorszewska, W. Kozubski, 2007, Acta neurobiologiae experimentalis.

PEMT rs12325817 and PCYT1A rs7639752 polymorphisms are associated with betaine but not choline concentrations in pregnant women.

P. Jagodziński, A. Szwengiel, A. Chmurzyńska, 2018, Nutrition research.

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

P. Jagodziński, J. Dorszewska, M. Lianeri, 2013, DNA and cell biology.

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

P. Jagodziński, J. Dorszewska, W. Kozubski, 2011, Seizure.

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

P. Jagodziński, J. Dorszewska, W. Kozubski, 2014, Folia neuropathologica.

Mutations of TP53 Gene and Oxidative Stress in Alzheimer’s Disease Patients

P. Jagodziński, J. Dorszewska, W. Kozubski, 2014 .

Mutations of TP 53 Gene and Oxidative Stress in Alzheimer ’ s Disease Patients

P. Jagodziński, W. Kozubski, A. Różycka, 2014 .

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

J. Dorszewska, W. Kozubski, M. Lianeri, 2013, Current genomics.

[Ion channel dysfunction in pathogenesis of idiopathic epilepsies].

P. Jagodziński, J. Dorszewska, A. Różycka, 2011, Neurologia i neurochirurgia polska.

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

P. Jagodziński, J. Dorszewska, T. Grzelak, 2016, Maturitas.

The c.1460C>T Polymorphism of MAO-A Is Associated with the Risk of Depression in Postmenopausal Women

P. Jagodziński, A. Słopień, M. Lianeri, 2012, TheScientificWorldJournal.

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.

P. Jagodziński, B. Kempisty, J. Dorszewska, 2009, DNA and cell biology.

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.

J. Dorszewska, W. Kozubski, W. Trzeciak, 2005, DNA and cell biology.

Polymorphic variants of genes involved in choline pathway and the risk of intrauterine fetal death.

A. Seremak-Mrozikiewicz, K. Drews, A. Kamiński, 2017, Ginekologia polska.

Associations between folate and choline intake, homocysteine metabolism, and genetic polymorphism of MTHFR, BHMT and PEMT in healthy pregnant Polish women.

A. Chmurzyńska, A. Malinowska, A. Seremak-Mrozikiewicz, 2020, Nutrition & dietetics: the journal of the Dietitians Association of Australia.

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

P. Jagodziński, J. Dorszewska, W. Kozubski, 2013, Current genomics.

Relationship of Postoperative Pain and PONV after Minimally Invasive Surgery with the Serotonin Concentrations and Receptors’ Gene Polymorphisms

P. Jagodziński, A. Duleba, L. Pawelczyk, 2021, Journal of personalized medicine.

Coexistence of ACE (I/D) and PAI-1 (4G/5G) gene variants in recurrent miscarriage in Polish population.

A. Seremak-Mrozikiewicz, K. Drews, A. Różycka, 2016, Ginekologia polska.

Original article Expression of 8-oxoguanine DNA glycosylase 1 (OGG1) and the level of p53 and TNF-αlpha proteins in peripheral lymphocytes of patients with Alzheimer’s disease

P. Jagodziński, B. Kempisty, J. Dorszewska, 2011 .

A transcript coding for a partially duplicated form of α7 nicotinic acetylcholine receptor is absent from the CD4+ T-lymphocytes of patients with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).

P. Jagodziński, B. Kempisty, J. Dorszewska, 2013, Folia neuropathologica.

Importance of polymorphic variants of phosphatidylethanolamine N-methyltransferase (PEMT) gene in the etiology of intrauterine fetal death in the Polish population.

A. Seremak-Mrozikiewicz, K. Drews, A. Różycka, 2018, European Journal of Obstetrics, Gynecology, and Reproductive Biology.