Lista de obras - Beata Pepłońska - Dominio Público Uruguay

A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene.

artículo científico publicado en 2013

Analysis of APBB2 gene polymorphisms in sporadic Alzheimer's disease.

artículo científico publicado en 2008

Association between Cerebrospinal Fluid Biomarkers for Alzheimer's Disease, APOE Genotypes and Auditory Verbal Learning Task in Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease.

artículo científico publicado en 2016

Association of apolipoprotein E and myeloperoxidase genotypes to clinical course of familial and sporadic multiple sclerosis

artículo científico publicado en 2004

Association of serotoninergic pathway gene variants with elite athletic status in the Polish population

artículo científico publicado en 2019

Behavioural pathology in Alzheimer's disease with special reference to apolipoprotein E genotype

artículo científico publicado en 2002

CYP46: a risk factor for Alzheimer's disease or a coincidence?

artículo científico publicado en 2005

Changes in the Hormonal Profile of Athletes following a Combat Sports Performance

artículo científico publicado en 2020

DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups.

artículo científico publicado en 2017

Earlier onset of Alzheimer's disease: risk polymorphisms within PRNP, PRND, CYP46, and APOE genes.

artículo científico publicado en 2009

Genetic variants associated with physical and mental characteristics of the elite athletes in the Polish population.

artículo científico publicado en 2016

Homocysteine, apolipoproteine E and methylenetetrahydrofolate reductase in Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2003

Hyperhomocysteinemia and methylenetetrahydrofolate reductase polymorphism in patients with Parkinson's disease

scientific article published on 19 June 2006

Hypermethylation of TRIM59 and KLF14 Influences Cell Death Signaling in Familial Alzheimer's Disease.

artículo científico publicado en 2018

Modified aging of elite athletes revealed by analysis of epigenetic age markers

artículo científico publicado en 2018

Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed frontotemporal dementia

artículo científico publicado en 2003

Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland

artículo científico publicado en 2003

Neurocognition of centenarians: neuropsychological study of élite centenarians

artículo científico publicado en 2007

Overactive BRCA1 Affects Presenilin 1 in Induced Pluripotent Stem Cell-Derived Neurons in Alzheimer's Disease.

artículo científico publicado en 2018

Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD

artículo científico publicado en 2004

Prion protein gene M129 allele is a risk factor for Alzheimer's disease.

artículo científico publicado en 2006

Regulatory region single nucleotide polymorphisms of the apolipoprotein E gene as risk factors for Alzheimer's disease

artículo científico publicado en 2018

Sigma Receptor Type 1 Gene Variation in a Group of Polish Patients with Alzheimer’s Disease and Mild Cognitive Impairment

artículo científico publicado en 2007

Simultaneous analysis of five genetic risk factors in Polish patients with Alzheimer's disease

artículo científico publicado en 2003

Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population

artículo científico publicado en 2003

TOMM40 and APOE common genetic variants are not Parkinson's disease risk factors.

artículo científico publicado en 2013

TOMM40 rs10524523 polymorphism's role in late-onset Alzheimer's disease and in longevity

artículo científico publicado en 2012

TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.

artículo científico publicado en 2018

The -22c/t polymorphism in presenilin 1 gene is not connected with late-onset and early-onset familial Alzheimer's disease in Poland.

artículo científico publicado en 2004

The E318G substitution in PSEN1 gene is not connected with Alzheimer's disease in a large Polish cohort

artículo científico publicado en 2004

The rate of conversion of mild cognitive impairment to dementia: predictive role of depression.

artículo científico publicado en 2007

Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: Genetic and bioinformatic assessment

artículo científico publicado en 2006

Two polymorphisms of presenilin-2 gene (PSEN2) 5' regulatory region are not associated with Alzheimer's disease (AD) in the Polish population.

artículo científico publicado en 2007

Lista de obras de Beata Pepłońska

A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene.

Analysis of APBB2 gene polymorphisms in sporadic Alzheimer's disease.

Association between Cerebrospinal Fluid Biomarkers for Alzheimer's Disease, APOE Genotypes and Auditory Verbal Learning Task in Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease.

Association of apolipoprotein E and myeloperoxidase genotypes to clinical course of familial and sporadic multiple sclerosis

Association of serotoninergic pathway gene variants with elite athletic status in the Polish population

Behavioural pathology in Alzheimer's disease with special reference to apolipoprotein E genotype

CYP46: a risk factor for Alzheimer's disease or a coincidence?

Changes in the Hormonal Profile of Athletes following a Combat Sports Performance

DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups.

Earlier onset of Alzheimer's disease: risk polymorphisms within PRNP, PRND, CYP46, and APOE genes.

Genetic variants associated with physical and mental characteristics of the elite athletes in the Polish population.

Homocysteine, apolipoproteine E and methylenetetrahydrofolate reductase in Alzheimer's disease and mild cognitive impairment

Hyperhomocysteinemia and methylenetetrahydrofolate reductase polymorphism in patients with Parkinson's disease

Hypermethylation of TRIM59 and KLF14 Influences Cell Death Signaling in Familial Alzheimer's Disease.

Modified aging of elite athletes revealed by analysis of epigenetic age markers

Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed frontotemporal dementia

Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland

Neurocognition of centenarians: neuropsychological study of élite centenarians

Overactive BRCA1 Affects Presenilin 1 in Induced Pluripotent Stem Cell-Derived Neurons in Alzheimer's Disease.

Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD

Prion protein gene M129 allele is a risk factor for Alzheimer's disease.

Regulatory region single nucleotide polymorphisms of the apolipoprotein E gene as risk factors for Alzheimer's disease

Sigma Receptor Type 1 Gene Variation in a Group of Polish Patients with Alzheimer’s Disease and Mild Cognitive Impairment

Simultaneous analysis of five genetic risk factors in Polish patients with Alzheimer's disease

Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population

TOMM40 and APOE common genetic variants are not Parkinson's disease risk factors.

TOMM40 rs10524523 polymorphism's role in late-onset Alzheimer's disease and in longevity

TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.

The -22c/t polymorphism in presenilin 1 gene is not connected with late-onset and early-onset familial Alzheimer's disease in Poland.

The E318G substitution in PSEN1 gene is not connected with Alzheimer's disease in a large Polish cohort

The rate of conversion of mild cognitive impairment to dementia: predictive role of depression.

Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: Genetic and bioinformatic assessment

Two polymorphisms of presenilin-2 gene (PSEN2) 5' regulatory region are not associated with Alzheimer's disease (AD) in the Polish population.