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Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations

Journal of neurology, 2015-02, Vol.262 (2), p.375-384

2015

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Vitamin D responsive elements within the HLA-DRB1 promoter region in Sardinian multiple sclerosis associated alleles

PloS one, 2012-07, Vol.7 (7), p.e41678-e41678

2012

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One Platform, a Thousand Worlds: On Twitter Irony in the Early Response to the COVID-19 Pandemic in Italy

Social media + society, 2020-07, Vol.6 (3), p.2056305120948254-2056305120948254

2020

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Pediatric schwannoma of the hypoglossal nerve: a case report and narrative literature overview

Frontiers in oncology, 2024-05, Vol.14, p.1400335

2024

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Bipolar affective disorder preceding frontotemporal dementia in a patient with C9ORF72 mutation: is there a genetic link between these two disorders?

Journal of neurology, 2013-04, Vol.260 (4), p.1155-1157

2013

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Geographic differences in the incidence of Huntington’s disease in Sardinia, Italy

Neurological sciences, 2021-12, Vol.42 (12), p.5177-5181

2021

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Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?

Journal of neurology, 2012-08, Vol.259 (8), p.1749-1751

2012

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Dealing With Brain MRI Findings in Pediatric Patients With Endocrinological Conditions: Less Is More?

Frontiers in endocrinology (Lausanne), 2022-01, Vol.12, p.780763-780763

2022

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Minimizing unnecessary brain magnetic resonance imaging in pediatric endocrinology: a retrospective cohort analysis

Frontiers in endocrinology (Lausanne), 2024-09, Vol.15, p.1456541

2024

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Memetising the pandemic: memes, covid-19 mundanity and political cultures

Information, communication & society, 2021-12, Vol.24 (16), p.2422-2441

2021

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A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD

Neurobiology of aging, 2011-12, Vol.32 (12), p.2327.e1-2327.e5

2011

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Adolescent girl with a huge pelvic collection

Surgery, 2022-05, Vol.171 (5), p.e21-e22

2022

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Myositis ossificans mimicking sarcoma: a not so rare bioptic diagnostic pitfall

Italian journal of pediatrics, 2020-07, Vol.46 (1), p.1-110, Article 110

2020

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Neck stiffness and bone osteolytic lesion in a 3-years old child: a case report

Italian journal of pediatrics, 2023-09, Vol.49 (1), p.132-5, Article 132

2023

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Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-05, Vol.17 (3-4), p.245-248

2016

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“I Can Share Politics But I Don’t Discuss It”: Everyday Practices of Political Talk on Facebook

Social media + society, 2017-10, Vol.3 (4)

2017

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TARDBP Ala382Thr Mutation in Multiple Sclerosis: A Possible Role in Brain Atrophy

Current medical imaging reviews, 2018-02, Vol.14 (1), p.95-98

2018

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CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

Neurobiology of aging, 2015-04, Vol.36 (4), p.1767.e3-1767.e6

2015

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HFE p.H63D polymorphism does not influence ALS phenotype and survival

Neurobiology of aging, 2015-10, Vol.36 (10), p.2906.e7-2906.e11

2015

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Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-03, Vol.16 (1-2), p.8-15

2015

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Progressive apraxia of speech in a patient with a C9orf72 mutation

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-10, Vol.17 (7-8), p.608-609

2016

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School in Italy: a safe place for children and adolescents

Italian journal of pediatrics, 2021-02, Vol.47 (1), p.23-23, Article 23

2021

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Severe onset of inflammatory myositis in a child: think to paraneoplastic myositis

Italian journal of pediatrics, 2021-07, Vol.47 (1), p.1-146, Article 146

2021

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Intranasal dexmedetomidine and intravenous ketamine for procedural sedation in a child with alpha-mannosidosis: a magic bullet?

Italian journal of pediatrics, 2019-09, Vol.45 (1), p.119-119, Article 119

2019

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Charcot–Marie–Tooth disease: genetic subtypes in the Sardinian population

Neurological sciences, 2017-06, Vol.38 (6), p.1019-1025

2017

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Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations

Vitamin D responsive elements within the HLA-DRB1 promoter region in Sardinian multiple sclerosis associated alleles

One Platform, a Thousand Worlds: On Twitter Irony in the Early Response to the COVID-19 Pandemic in Italy

Pediatric schwannoma of the hypoglossal nerve: a case report and narrative literature overview

Bipolar affective disorder preceding frontotemporal dementia in a patient with C9ORF72 mutation: is there a genetic link between these two disorders?

Geographic differences in the incidence of Huntington’s disease in Sardinia, Italy

Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?

Dealing With Brain MRI Findings in Pediatric Patients With Endocrinological Conditions: Less Is More?

Minimizing unnecessary brain magnetic resonance imaging in pediatric endocrinology: a retrospective cohort analysis

Memetising the pandemic: memes, covid-19 mundanity and political cultures

A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD

Adolescent girl with a huge pelvic collection

Myositis ossificans mimicking sarcoma: a not so rare bioptic diagnostic pitfall

Neck stiffness and bone osteolytic lesion in a 3-years old child: a case report

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

“I Can Share Politics But I Don’t Discuss It”: Everyday Practices of Political Talk on Facebook

TARDBP Ala382Thr Mutation in Multiple Sclerosis: A Possible Role in Brain Atrophy

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

HFE p.H63D polymorphism does not influence ALS phenotype and survival

Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype

Progressive apraxia of speech in a patient with a C9orf72 mutation

School in Italy: a safe place for children and adolescents

Severe onset of inflammatory myositis in a child: think to paraneoplastic myositis

Intranasal dexmedetomidine and intravenous ketamine for procedural sedation in a child with alpha-mannosidosis: a magic bullet?

Charcot–Marie–Tooth disease: genetic subtypes in the Sardinian population

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