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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1437-1446

2017

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CXCR4 involvement in neurodegenerative diseases

Translational psychiatry, 2018-04, Vol.8 (1), p.73-10, Article 73

2018

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C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Neurology, 2020-12, Vol.95 (24), p.e3288

2020

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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Scientific reports, 2017-08, Vol.7 (1), p.8899-16, Article 8899

2017

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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

Scientific reports, 2019-07, Vol.9 (1), p.10854-10, Article 10854

2019

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Acta neuropathologica, 2020-05, Vol.139 (5), p.959-962

2020

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Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Scientific reports, 2018-05, Vol.8 (1), p.7789-5, Article 7789

2018

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The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies design

Neurological sciences, 2017, Vol.38 (1), p.83-91

2017

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Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Neurology. Genetics, 2018-10, Vol.4 (5), p.e266-e266

2018

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Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy

Neurological sciences, 2015-05, Vol.36 (5), p.751-757

2015

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Neuropathological and Clinical Phenotype of an Italian Alzheimer Family with M239V Mutation of Presenilin 2 Gene

Journal of neuropathology and experimental neurology, 2004-03, Vol.63 (3), p.199-209

2004

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Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report

Journal of neuropathology and experimental neurology, 2019-07, Vol.78 (7), p.665-670

2019

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Brain‐derived neurotrophic factor modulates cholesterol homeostasis and Apolipoprotein E synthesis in human cell models of astrocytes and neurons

Journal of cellular physiology, 2018-09, Vol.233 (9), p.6925-6943

2018

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NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease

Aging cell, 2016-08, Vol.15 (4), p.661-672

2016

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Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

Biological psychiatry (1969), 2013-09, Vol.74 (5), p.384-391

2013

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Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

Neurology, 2015-06, Vol.84 (22), p.2266

2015

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Pathogenic Mechanisms of the Prion Protein Gene Mutations: A Review and Speculative Hypotheses for Pathogenic Potential of the Pro39Leu Mutation in the Associated FTD-Like Phenotype

Journal of neurology and neuroscience, 2017, Vol.8 (4)

2017

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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Scientific reports, 2020-07, Vol.10 (1), p.12184-12184, Article 12184

2020

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Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutation

Neurology. Genetics, 2020-06, Vol.6 (3), p.e417-e417

2020

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Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

Neurobiology of aging, 2014-11, Vol.35 (11), p.2657.e7-2657.e11

2014

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Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia

Journal of Alzheimer's disease, 2018-01, Vol.61 (3), p.1179

2018

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Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy

Neurobiology of aging, 2012-12, Vol.33 (12), p.2948.e1-2948.e10

2012

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Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia

Journal of Alzheimer's disease, 2017-01, Vol.56 (4), p.1271

2017

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Epidemiology and genetics of FTD: a door-to-door survey in Southern Italy

Neurobiology of aging, 2012-07, Vol.33 (12), p.2948.e1-2948.e10

2012

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Apolipoprotein profile in type II diabetic patients with and without coronary heart disease

Acta Diabetologica Latina, 1990-10, Vol.27 (4), p.371-377

1990

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

CXCR4 involvement in neurodegenerative diseases

C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies design

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy

Neuropathological and Clinical Phenotype of an Italian Alzheimer Family with M239V Mutation of Presenilin 2 Gene

Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report

Brain‐derived neurotrophic factor modulates cholesterol homeostasis and Apolipoprotein E synthesis in human cell models of astrocytes and neurons

NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

Pathogenic Mechanisms of the Prion Protein Gene Mutations: A Review and Speculative Hypotheses for Pathogenic Potential of the Pro39Leu Mutation in the Associated FTD-Like Phenotype

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutation

Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia

Epidemiology and genetics of FTD: a door-to-door survey in Southern Italy

Apolipoprotein profile in type II diabetic patients with and without coronary heart disease

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