Lista de obras - Maria Liguori - Dominio Público Uruguay

A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis.

artículo científico publicado en 2008

A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease.

artículo científico publicado en 2004

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.

artículo científico publicado en 2008

A putative Alzheimer's disease risk allele in PCK1 influences brain atrophy in multiple sclerosis

artículo científico publicado en 2010

A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population

article

Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis

artículo científico publicado en 2005

Age at onset in multiple sclerosis

artículo científico publicado en 2000

Age-related disability in multiple sclerosis

artículo científico publicado en 2002

Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.

artículo científico publicado en 2008

Apolipoprotein E genotype does not influence the progression of multiple sclerosis

artículo científico publicado en 2003

Association between Synapsin III gene promoter polymorphisms and multiple sclerosis

artículo científico publicado en 2004

Association between miRNAs expression and cognitive performances of Pediatric Multiple Sclerosis patients: A pilot study

artículo científico publicado en 2019

Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study.

artículo científico publicado en 2001

Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia.

artículo científico publicado en 2009

CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene.

artículo científico publicado en 2009

CAV3 T78M mutation as polymorphic variant in South Italy

artículo científico publicado en 2012

CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers

artículo científico publicado en 2003

CONVENTIONAL MRI AND NOTCH3 GENE SCREENING IN SPORADIC CADASIL

article

Changes of serum sICAM-1 and MMP-9 induced by rIFN -1b treatment in relapsing-remitting MS

artículo científico publicado en 1999

Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease

artículo científico publicado en 2017

Comparison of clinical and demographic features between affected pairs of Italian multiple sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms.

artículo científico publicado en 1999

Concomitant myotonic dystrophy type 1, CIDP-like neuropathy and Hashimoto thyroiditis: a causal link?

artículo científico publicado en 2012

Course and prognosis in early-onset MS: comparison with adult-onset forms

artículo científico publicado en 2002

Disease modeling in multiple sclerosis: assessment and quantification of sources of variability in brain parenchymal fraction measurements.

artículo científico publicado en 2010

Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis

article

Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene

artículo científico publicado en 2007

First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia.

artículo científico publicado en 2013

Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis.

artículo científico publicado en 2004

Gene dosage influences the age at onset of SCA2 in a family from southern Italy

artículo científico publicado en 2007

Gene symbol: NOTCH3

artículo científico publicado en 2007

Gene symbol: NOTCH3

artículo científico publicado en 2007

Gene symbol: NOTCH3. Disease: CADASIL

artículo científico publicado en 2008

Genetic screening for familial amyloid polyneuropathy in patients with idiopathic carpal tunnel syndrome

artículo científico publicado en 2008

Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosis

artículo científico publicado en 2006

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

artículo científico publicado en 2013

HLA (A-B-C and -DRB1) alleles and brain MRI changes in multiple sclerosis: a longitudinal study

article

HLA B*44: protective effects in MS susceptibility and MRI outcome measures

artículo científico publicado en 2010

HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe.

artículo científico publicado en 2004

High resolution proton MR spectroscopy of cerebrospinal fluid in MS patients. Comparison with biochemical changes in demyelinating plaques

artículo científico publicado en 1996

Identification and clinical impact of multiple sclerosis cortical lesions as assessed by routine 3T MR imaging.

artículo científico publicado en 2011

Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis

artículo científico publicado en 2002

Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume

artículo científico publicado en 2008

Impact of individual cognitive profile on visuo-motor reorganization in relapsing–remitting multiple sclerosis

artículo científico publicado en 2007

Integrated Analysis of microRNA and mRNA Expression Profiles: An Attempt to Disentangle the Complex Interaction Network in Attention Deficit Hyperactivity Disorder

scientific article published on 22 October 2019

Interferon beta in relapsing-remitting multiple sclerosis: an independent postmarketing study in southern Italy

artículo científico publicado en 2003

Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis ⬇️

artículo científico publicado en 2018

Investigating the role of brain-derived neurotrophic factor in relapsing-remitting multiple sclerosis

artículo científico publicado en 2007

Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families

article

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

artículo científico publicado en 2006

Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis.

scientific article published on 15 June 2016

Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study.

artículo científico publicado en 2017

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

artículo científico publicado en 2005

Multiple sclerosis in childhood: clinical features of 149 cases

artículo científico publicado en 1997

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

artículo científico publicado en 2009

Neurobiological mechanisms underlying emotional processing in relapsing-remitting multiple sclerosis

artículo científico publicado en 2009

Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study

artículo científico publicado en 2009

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

artículo científico publicado en 2008

One year activity on subtraction MRI predicts subsequent 4 year activity and progression in multiple sclerosis

artículo científico publicado en 2011

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

scientific article published on 25 April 2005

Precision Medicine in Neurodegenerative Diseases: Some Promising Tips Coming from the microRNAs' World

scientific article published on 27 December 2019

Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis.

artículo científico publicado en 2007

Presenilin enhancer-2 gene: identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease

artículo científico publicado en 2011

Prognostic significance of metabolic changes detected by proton magnetic resonance spectroscopy in ischaemic stroke

artículo científico publicado en 1996

Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus.

artículo científico publicado en 2003

Prospective study of multiple sclerosis with early onset

artículo científico publicado en 2002

Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration

artículo científico publicado en 2014

Proton magnetic resonance spectroscopy in patients with ischemic stroke

artículo científico publicado en 1994

Seeking a standardized normalization method for the quantification of microRNA expression

scientific article published on 08 March 2019

Serum and CSF anti-GM1 antibodies in patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy

scientific article published on 01 January 1993

The BDNF Val66Met polymorphism has opposite effects on memory circuits of multiple sclerosis patients and controls.

artículo científico publicado en 2013

The MicroRNA Centrism in the Orchestration of Neuroinflammation in Neurodegenerative Diseases

artículo científico publicado en 2019

The effects of BDNF Val66Met polymorphism on brain function in controls and patients with multiple sclerosis: an imaging genetic study

artículo científico publicado en 2009

The role of VLA4 polymorphisms in multiple sclerosis: an association study.

artículo científico publicado en 2007

Treating epilepsy in Italy between XIX and XX century

artículo científico publicado en 2012

Lista de obras de Maria Liguori

A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis.

A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease.

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.

A putative Alzheimer's disease risk allele in PCK1 influences brain atrophy in multiple sclerosis

A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population

Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis

Age at onset in multiple sclerosis

Age-related disability in multiple sclerosis

Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.

Apolipoprotein E genotype does not influence the progression of multiple sclerosis

Association between Synapsin III gene promoter polymorphisms and multiple sclerosis

Association between miRNAs expression and cognitive performances of Pediatric Multiple Sclerosis patients: A pilot study

Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study.

Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia.

CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene.

CAV3 T78M mutation as polymorphic variant in South Italy

CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers

CONVENTIONAL MRI AND NOTCH3 GENE SCREENING IN SPORADIC CADASIL

Changes of serum sICAM-1 and MMP-9 induced by rIFN -1b treatment in relapsing-remitting MS

Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease

Comparison of clinical and demographic features between affected pairs of Italian multiple sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms.

Concomitant myotonic dystrophy type 1, CIDP-like neuropathy and Hashimoto thyroiditis: a causal link?

Course and prognosis in early-onset MS: comparison with adult-onset forms

Disease modeling in multiple sclerosis: assessment and quantification of sources of variability in brain parenchymal fraction measurements.

Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis

Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene

First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia.

Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis.

Gene dosage influences the age at onset of SCA2 in a family from southern Italy

Gene symbol: NOTCH3

Gene symbol: NOTCH3

Gene symbol: NOTCH3. Disease: CADASIL

Genetic screening for familial amyloid polyneuropathy in patients with idiopathic carpal tunnel syndrome

Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosis

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

HLA (A-B-C and -DRB1) alleles and brain MRI changes in multiple sclerosis: a longitudinal study

HLA B*44: protective effects in MS susceptibility and MRI outcome measures

HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe.

High resolution proton MR spectroscopy of cerebrospinal fluid in MS patients. Comparison with biochemical changes in demyelinating plaques

Identification and clinical impact of multiple sclerosis cortical lesions as assessed by routine 3T MR imaging.

Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis

Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume

Impact of individual cognitive profile on visuo-motor reorganization in relapsing–remitting multiple sclerosis

Integrated Analysis of microRNA and mRNA Expression Profiles: An Attempt to Disentangle the Complex Interaction Network in Attention Deficit Hyperactivity Disorder

Interferon beta in relapsing-remitting multiple sclerosis: an independent postmarketing study in southern Italy

Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis ⬇️

Investigating the role of brain-derived neurotrophic factor in relapsing-remitting multiple sclerosis

Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis.

Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study.

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

Multiple sclerosis in childhood: clinical features of 149 cases

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

Neurobiological mechanisms underlying emotional processing in relapsing-remitting multiple sclerosis

Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

One year activity on subtraction MRI predicts subsequent 4 year activity and progression in multiple sclerosis

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

Precision Medicine in Neurodegenerative Diseases: Some Promising Tips Coming from the microRNAs' World

Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis.

Presenilin enhancer-2 gene: identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease

Prognostic significance of metabolic changes detected by proton magnetic resonance spectroscopy in ischaemic stroke

Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus.

Prospective study of multiple sclerosis with early onset

Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration

Proton magnetic resonance spectroscopy in patients with ischemic stroke

Seeking a standardized normalization method for the quantification of microRNA expression

Serum and CSF anti-GM1 antibodies in patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy

The BDNF Val66Met polymorphism has opposite effects on memory circuits of multiple sclerosis patients and controls.

The MicroRNA Centrism in the Orchestration of Neuroinflammation in Neurodegenerative Diseases

The effects of BDNF Val66Met polymorphism on brain function in controls and patients with multiple sclerosis: an imaging genetic study

The role of VLA4 polymorphisms in multiple sclerosis: an association study.

Treating epilepsy in Italy between XIX and XX century