Lista de obras -

APOE epsilon 2/epsilon 4 genotype a risk factor for primary progressive aphasia in women

artículo científico publicado en 2009

An atypical case of acute disseminated encephalomyelitis associated with cytomegalovirus infection

artículo científico publicado en 2015

An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.

artículo científico publicado en 2010

Apoe epsilon2-epsilon4 genotype is a possible risk factor for primary progressive aphasia

artículo científico publicado en 2006

Apolipoprotein E epsilon4 allele differently affects the patterns of neuropsychological presentation in early- and late-onset Alzheimer's disease patients

artículo científico publicado en 2004

Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease

artículo científico publicado en 2008

BuChE K variant is decreased in Alzheimer's disease not in fronto-temporal dementia

artículo científico publicado en 2010

Cerebellar degeneration associated with mGluR1 autoantibodies as a paraneoplastic manifestation of prostate adenocarcinoma.

artículo científico publicado en 2013

Cognitive and behavioral determinants of psychotic symptoms in Alzheimer's disease.

artículo científico publicado en 2015

EPA and DHA Differentially Affect In Vitro Inflammatory Cytokine Release by Peripheral Blood Mononuclear Cells from Alzheimer’s Patients ⬇️

artículo científico publicado el 1 de octubre de 2012

Effectiveness of a high-throughput genetic analysis in the identification of responders/non-responders to CYP2D6-metabolized drugs.

artículo científico publicado en 2011

Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

article

Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients

artículo científico publicado en 2003

Neural substrates of the 'low-level' system for speech articulation: Evidence from primary opercular syndrome.

artículo científico publicado en 2016

Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

artículo científico publicado en 2016

Polymorphism C in the serotonin transporter gene in depression-free elderly patients with vascular dementia

artículo científico publicado en 2010

Possible relationship between Al/ferritin complex and Alzheimer's disease.

artículo científico publicado en 2012

Psychotic symptoms in Alzheimer's disease and 5-HTTLPR polymorphism of the serotonin transporter gene: evidence for an association

artículo científico publicado en 2009

R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

artículo científico publicado en 2013

Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre study

artículo científico publicado en 2012

Role of CLU, PICALM, and TNK1 Genotypes in Aging With and Without Alzheimer's Disease

artículo científico publicado en 2017

Role of cytochrome P4502D6 functional polymorphisms in the efficacy of donepezil in patients with Alzheimer's disease.

artículo científico publicado en 2011

Sleep palsy involving different nerves: Role of ultrasound.

artículo científico publicado en 2015

Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele

scientific article published on 07 March 2008

TOMM40, APOE, and APOC1 in Primary Progressive Aphasia and Frontotemporal Dementia

article

The APOE Gene Locus in Frontotemporal Dementia and Primary Progressive Aphasia

article

The RELN Locus in Alzheimer's Disease

scholarly article by Davide Seripa et al published 11 June 2008 in Journal of Alzheimer's Disease

The RELN locus in Alzheimer's disease

artículo científico publicado en 2008

The Serotonin Transporter Gene Locus in Late-Life Major Depressive Disorder

article

The complex interaction between APOE promoter and AD: an Italian case-control study

artículo científico publicado en 2009

The serotonin transporter gene locus in late-life major depressive disorder

artículo científico publicado en 2013

Lista de obras de

APOE epsilon 2/epsilon 4 genotype a risk factor for primary progressive aphasia in women

An atypical case of acute disseminated encephalomyelitis associated with cytomegalovirus infection

An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.

Apoe epsilon2-epsilon4 genotype is a possible risk factor for primary progressive aphasia

Apolipoprotein E epsilon4 allele differently affects the patterns of neuropsychological presentation in early- and late-onset Alzheimer's disease patients

Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease

BuChE K variant is decreased in Alzheimer's disease not in fronto-temporal dementia

Cerebellar degeneration associated with mGluR1 autoantibodies as a paraneoplastic manifestation of prostate adenocarcinoma.

Cognitive and behavioral determinants of psychotic symptoms in Alzheimer's disease.

EPA and DHA Differentially Affect In Vitro Inflammatory Cytokine Release by Peripheral Blood Mononuclear Cells from Alzheimer’s Patients ⬇️

Effectiveness of a high-throughput genetic analysis in the identification of responders/non-responders to CYP2D6-metabolized drugs.

Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients

Neural substrates of the 'low-level' system for speech articulation: Evidence from primary opercular syndrome.

Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

Polymorphism C in the serotonin transporter gene in depression-free elderly patients with vascular dementia

Possible relationship between Al/ferritin complex and Alzheimer's disease.

Psychotic symptoms in Alzheimer's disease and 5-HTTLPR polymorphism of the serotonin transporter gene: evidence for an association

R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre study

Role of CLU, PICALM, and TNK1 Genotypes in Aging With and Without Alzheimer's Disease

Role of cytochrome P4502D6 functional polymorphisms in the efficacy of donepezil in patients with Alzheimer's disease.

Sleep palsy involving different nerves: Role of ultrasound.

Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele

TOMM40, APOE, and APOC1 in Primary Progressive Aphasia and Frontotemporal Dementia

The APOE Gene Locus in Frontotemporal Dementia and Primary Progressive Aphasia

The RELN Locus in Alzheimer's Disease

The RELN locus in Alzheimer's disease

The Serotonin Transporter Gene Locus in Late-Life Major Depressive Disorder

The complex interaction between APOE promoter and AD: an Italian case-control study

The serotonin transporter gene locus in late-life major depressive disorder