Lista de obras - Maria Barcikowska - Dominio Público Uruguay

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene

artículo científico publicado en 2000

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene

artículo científico publicado en 1998

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

artículo científico publicado en 2012

A new familial congenital myopathy in children with desmin and dystrophin reacting plaques

scientific article published on 01 July 1995

A novel MAPT mutation, G55R, in a frontotemporal dementia patient leads to altered Tau function

artículo científico publicado en 2013

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

artículo científico publicado en 2013

APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians.

artículo científico publicado en 2013

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

artículo científico publicado en 2012

Alzheimer's disease therapy--theory and practice

artículo científico publicado en 2005

An open-label study to evaluate the safety, tolerability and efficacy of rivastigmine in patients with mild to moderate probable Alzheimer's disease in the community setting.

artículo científico publicado en 2002

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

artículo científico publicado en 2008

Analysis of UBQLN1 variants in a Polish Alzheimer's disease patient: control series

artículo científico publicado en 2008

ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease

artículo científico publicado en 2014

Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction

artículo científico publicado en 2016

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 between genetic and environmental factors and the risk of Alzheimer's disease.

artículo científico publicado en 2008

Association of pyridoxal kinase and Parkinson disease

artículo científico publicado en 2010

Association study of cholesterol-related genes in Alzheimer's disease

artículo científico publicado en 2007

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

Calbindin-1association and Parkinson’s disease

artículo científico publicado en 2009

Cell cycle regulation distinguishes lymphocytes from sporadic and familial Alzheimer's disease patients

artículo científico publicado en 2010

Changes in amyloid precursor protein and apolipoprotein E immunoreactivity following ischemic brain injury in rat with long-term survival: influence of idebenone treatment.

artículo científico publicado en 1997

Cognitive deficits and polymorphism of apolipoprotein E in Alzheimer's disease

artículo científico publicado en 2002

Combined use of biochemical and volumetric biomarkers to assess the risk of conversion of mild cognitive impairment to Alzheimer's disease

artículo científico publicado en 2016

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Conformational altered p53 as an early marker of oxidative stress in Alzheimer's disease

artículo científico publicado en 2012

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

artículo científico publicado en 2017

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

artículo científico publicado en 2015

Death-associated protein kinase 1 variation and Parkinson's disease.

artículo científico publicado en 2010

Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus

artículo científico publicado en 2015

Frontotemporal dementia: An attempt at clinical characteristics.

artículo científico publicado en 1999

GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16 ⬇️

artículo científico publicado el 29 de noviembre de 2013

Genetic variation of Omi/HtrA2 and Parkinson's disease

artículo científico publicado en 2008

Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease

artículo científico publicado en 2014

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

artículo científico publicado en 2012

Human leukocyte antigen variation and Parkinson's disease

artículo científico publicado en 2011

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

Hypertension in patients with Alzheimer's disease--prevalence, characteristics, and impact on clinical outcome. Experience of one neurology center in Poland

artículo científico publicado en 2015

Identification of a late onset Alzheimer's disease candidate risk variant at 9q21.33 in Polish patients.

artículo científico publicado en 2012

Immunohistochemical study of a case with progressive supranuclear palsy without ophthalmoplegia

artículo científico publicado el 1 de enero de 1992

Increased CD44 gene expression in lymphocytes derived from Alzheimer disease patients.

artículo científico publicado en 2010

Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population.

artículo científico publicado en 2009

Interleukin-6 gene (-174 C/G ) and apolipoprotein E gene polymorphisms and the risk of Alzheimer disease in a Polish population

artículo científico publicado en 2010

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

artículo científico publicado en 2010

Is descriptive writing useful in the differential diagnosis of logopenic variant of primary progressive aphasia, Alzheimer's disease and mild cognitive impairment?

artículo científico

LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD).

artículo científico publicado en 2013

Lactoferrin in the central nervous system

artículo científico publicado en 2005

MMP-9 and/or TIMP as predictors of ischaemic stroke in patients with symptomatic and asymptomatic atherosclerotic stenosis of carotid artery treated by stenting or endarterectomy - A review

artículo científico publicado en 2018

Magnetic resonance imaging-based hippocampal volumetry in patients with dementia of the Alzheimer type.

artículo científico publicado en 1999

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

artículo científico publicado en 1993

Mitochondrial DNA haplogroups and subhaplogroups are associated with Parkinson’s disease risk in a Polish PD cohort

artículo científico publicado en 2008

Mitochondrial haplogroup H and Alzheimer's disease--is there a connection?

artículo científico publicado en 2008

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

artículo científico publicado en 2015

Mitochondrial transcription factor A variants and the risk of Parkinson's disease

artículo científico publicado en 2010

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

N-acetylaspartate, choline, myoinositol, glutamine and glutamate (glx) concentration changes in proton MR spectroscopy (1H MRS) in patients with mild cognitive impairment (MCI).

artículo científico publicado en 2011

Neurocognition of centenarians: neuropsychological study of élite centenarians

artículo científico publicado en 2007

New therapeutic approaches in Alzheimer's disease

artículo científico publicado en 2004

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

artículo científico publicado en 2018

PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroups

artículo científico publicado en 2012

PIN1 gene variants in Alzheimer's disease

artículo científico publicado en 2009

Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population

artículo científico publicado en 2011

Phagocytosis of ?/A4 amyloid fibrils of the neuritic neocortical plaques ⬇️

artículo científico publicado el 1 de enero de 1991

Plasma adiponectin array in women with Alzheimer's disease

scientific article published on 17 August 2018

Plasma beta amyloid and cytokine profile in women with Alzheimer's disease.

artículo científico publicado en 2008

Plasma leptin levels and free leptin index in women with Alzheimer's disease

artículo científico publicado en 2015

Polish Centenarians Programme. Multidisciplinary studies of successful ageing: aims, methods, and preliminary results

artículo científico publicado en 2007

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

artículo científico publicado en 2004

PrP amyloid plaques in Creutzfeldt-Jakob disease of short duration: immunohistochemical studies of 5 cases from Poland.

artículo científico publicado en 1991

Predicting the conversion of mild cognitive impairment to Alzheimer's disease based on the volumetric measurements of the selected brain structures in magnetic resonance imaging

artículo científico publicado en 2015

Prediction of deterioration of mild cognitive impairment with CT and SPECT.

artículo científico publicado en 2007

Prevalence of major and minor depression in elderly persons with mild cognitive impairment--MADRS factor analysis.

artículo científico publicado en 2004

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

artículo científico publicado en 2006

Radiological Evaluation of Strategic Structures in Patients with Mild Cognitive Impairment and Early Alzheimer's Disease

artículo científico publicado en 2016

Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions

artículo científico publicado en 2011

Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study

artículo científico publicado en 2011

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

artículo científico publicado en 2015

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

Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease.

artículo científico publicado en 2010

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 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease

artículo científico publicado en 2013

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 Erlangen Score Algorithm in the diagnosis and prediction of the progression from subjective cognitive decline and mild cognitive impairment to Alzheimer-type dementia

artículo científico publicado en 2018

The Impact of Mitochondrial and Nuclear DNA Variants on Late-Onset Alzheimer's Disease Risk

artículo científico publicado en 2011

The Role of Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in the Pathophysiology of Neurodegeneration: A Literature Study ⬇️

artículo científico publicado el 1 de enero de 2013

The diagnostic value of EEG in Alzheimer disease: correlation with the severity of mental impairment.

artículo científico publicado en 2001

The prion protein M129V polymorphism: longevity and cognitive impairment among Polish centenarians

artículo científico publicado en 2013

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

artículo científico publicado en 2007

Transport of Human β-Amyloid Peptide Through the Rat Blood-Brain Barrier After Global Cerebral Ischemia ⬇️

artículo científico publicado el 1 de enero de 1997

Tubulovesicular structures in Creutzfeldt-Jakob disease

artículo científico publicado el 1 de enero de 1992

Tubulovesicular structures in human and experimental Creutzfeldt-Jakob disease

artículo científico publicado en 1991

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

Ubiquitin expression in globose tangles in the locus coeruleus in brains of patients with Alzheimer's and Parkinson's diseases

artículo científico publicado el 17 de febrero de 1992

Ultrafiltrate of blood plasma modulates amyloid-β aggregation.

artículo científico publicado en 2011

Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish population

artículo científico publicado en 2008

Writing in Richardson variant of progressive supranuclear palsy in comparison to progressive non-fluent aphasia

artículo científico publicado en 2015

[Fronto-temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): clinical criteria].

artículo científico publicado en 2003

Lista de obras de Maria Barcikowska

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

A new familial congenital myopathy in children with desmin and dystrophin reacting plaques

A novel MAPT mutation, G55R, in a frontotemporal dementia patient leads to altered Tau function

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

APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians.

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Alzheimer's disease therapy--theory and practice

An open-label study to evaluate the safety, tolerability and efficacy of rivastigmine in patients with mild to moderate probable Alzheimer's disease in the community setting.

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

Analysis of UBQLN1 variants in a Polish Alzheimer's disease patient: control series

ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease

Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction

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 between genetic and environmental factors and the risk of Alzheimer's disease.

Association of pyridoxal kinase and Parkinson disease

Association study of cholesterol-related genes in Alzheimer's disease

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

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

Calbindin-1association and Parkinson’s disease

Cell cycle regulation distinguishes lymphocytes from sporadic and familial Alzheimer's disease patients

Changes in amyloid precursor protein and apolipoprotein E immunoreactivity following ischemic brain injury in rat with long-term survival: influence of idebenone treatment.

Cognitive deficits and polymorphism of apolipoprotein E in Alzheimer's disease

Combined use of biochemical and volumetric biomarkers to assess the risk of conversion of mild cognitive impairment to Alzheimer's disease

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Conformational altered p53 as an early marker of oxidative stress in Alzheimer's disease

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

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

Death-associated protein kinase 1 variation and Parkinson's disease.

Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease

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

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus

Frontotemporal dementia: An attempt at clinical characteristics.

GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16 ⬇️

Genetic variation of Omi/HtrA2 and Parkinson's disease

Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

Human leukocyte antigen variation and Parkinson's disease

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.

Hypertension in patients with Alzheimer's disease--prevalence, characteristics, and impact on clinical outcome. Experience of one neurology center in Poland

Identification of a late onset Alzheimer's disease candidate risk variant at 9q21.33 in Polish patients.

Immunohistochemical study of a case with progressive supranuclear palsy without ophthalmoplegia

Increased CD44 gene expression in lymphocytes derived from Alzheimer disease patients.

Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population.

Interleukin-6 gene (-174 C/G ) and apolipoprotein E gene polymorphisms and the risk of Alzheimer disease in a Polish population

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

Is descriptive writing useful in the differential diagnosis of logopenic variant of primary progressive aphasia, Alzheimer's disease and mild cognitive impairment?

LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD).

Lactoferrin in the central nervous system

MMP-9 and/or TIMP as predictors of ischaemic stroke in patients with symptomatic and asymptomatic atherosclerotic stenosis of carotid artery treated by stenting or endarterectomy - A review

Magnetic resonance imaging-based hippocampal volumetry in patients with dementia of the Alzheimer type.

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

Mitochondrial DNA haplogroups and subhaplogroups are associated with Parkinson’s disease risk in a Polish PD cohort

Mitochondrial haplogroup H and Alzheimer's disease--is there a connection?

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

Mitochondrial transcription factor A variants and the risk of Parkinson's disease

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

N-acetylaspartate, choline, myoinositol, glutamine and glutamate (glx) concentration changes in proton MR spectroscopy (1H MRS) in patients with mild cognitive impairment (MCI).

Neurocognition of centenarians: neuropsychological study of élite centenarians

New therapeutic approaches in Alzheimer's disease

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

PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroups

PIN1 gene variants in Alzheimer's disease

Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population

Phagocytosis of ?/A4 amyloid fibrils of the neuritic neocortical plaques ⬇️

Plasma adiponectin array in women with Alzheimer's disease

Plasma beta amyloid and cytokine profile in women with Alzheimer's disease.

Plasma leptin levels and free leptin index in women with Alzheimer's disease

Polish Centenarians Programme. Multidisciplinary studies of successful ageing: aims, methods, and preliminary results

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

PrP amyloid plaques in Creutzfeldt-Jakob disease of short duration: immunohistochemical studies of 5 cases from Poland.

Predicting the conversion of mild cognitive impairment to Alzheimer's disease based on the volumetric measurements of the selected brain structures in magnetic resonance imaging

Prediction of deterioration of mild cognitive impairment with CT and SPECT.

Prevalence of major and minor depression in elderly persons with mild cognitive impairment--MADRS factor analysis.

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

Radiological Evaluation of Strategic Structures in Patients with Mild Cognitive Impairment and Early Alzheimer's Disease