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Takotsubo syndrome in a Sardinian amyotrophic lateral sclerosis cohort

Journal of neurology, 2024-09

2024

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REM sleep behavior disorder and periodic leg movements during sleep in ALS

Acta neurologica Scandinavica, 2017-02, Vol.135 (2), p.219-224

2017

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Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Neurology, 2010-08, Vol.75 (7), p.619-625

2010

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Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP‐43 subcellular distribution

Neuropathology and applied neurobiology, 2017-02, Vol.43 (2), p.133-153

2017

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Functional brain connectivity analysis in amyotrophic lateral sclerosis: an EEG source-space study

Biomedical physics & engineering express, 2018-04, Vol.4 (3), p.37004

2018

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Impairment of autonomic nervous system in amyotrophic lateral sclerosis

Sleep medicine, 2017-12, Vol.40, p.e271-e271

2017

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An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report (IN9-1.006)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.IN9-1.006-IN9-1.006

2012

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An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report (P01.100)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P01-P01.100

2012

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Reversible Pisa syndrome in Parkinson's disease during treatment with pergolide: a case report

Clinical neuropharmacology, 2005-09, Vol.28 (5), p.252

2005

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C9ORF72 in a Large Series of Italian and Sardinian Familial and Sporadic ALS Patients (IN9-1.003)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.IN9-1.003-IN9-1.003

2012

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C9ORF72 in a Large Series of Italian and Sardinian Familial and Sporadic ALS Patients (P05.161)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P05-P05.161

2012

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Epidemiological and clinical features of primary intrarachidian tumours in the island of Sardinia, during the 1977-1986 period

Acta neurologica, 1991-06, Vol.13 (3), p.220

1991

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Primary optic neuritis evolved in multiple sclerosis: an epidemiological study

Acta neurologica, 1993-12, Vol.15 (6), p.433

1993

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Thalamic hemorrhage. 30 cases studied: clinico-tomodensitometric correlations

Acta neurologica, 1992-02, Vol.14 (1), p.22

1992

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Sensitivity and specificity of the EEG versus CT in acute cortical and subcortical stroke

Functional neurology, 1994-11, Vol.9 (6), p.297

1994

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A behavioural simulator and its use for the validation of hypercube architectures

Microprocessing and microprogramming, 1988-08, Vol.24 (1), p.213-218

1988

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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Neuron (Cambridge, Mass.), 2011-10, Vol.72 (2), p.257-268

2011

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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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Genetic counselling in ALS: facts, uncertainties and clinical suggestions

Journal of Neurology, Neurosurgery and Psychiatry, 2014-05, Vol.85 (5), p.478-485

2014

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Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

Neurology, 2017-10, Vol.89 (18), p.1915-1922

2017

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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.784-793

2012

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PET/CT scan in traumatic brain injury: a new frontier for the prognosis from cerebellum activity?

European journal of physical and rehabilitation medicine, 2015-12, Vol.51 (6), p.849

2015

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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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Takotsubo syndrome in a Sardinian amyotrophic lateral sclerosis cohort

REM sleep behavior disorder and periodic leg movements during sleep in ALS

Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP‐43 subcellular distribution

Functional brain connectivity analysis in amyotrophic lateral sclerosis: an EEG source-space study

Impairment of autonomic nervous system in amyotrophic lateral sclerosis

An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report (IN9-1.006)

An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report (P01.100)

Reversible Pisa syndrome in Parkinson's disease during treatment with pergolide: a case report

C9ORF72 in a Large Series of Italian and Sardinian Familial and Sporadic ALS Patients (IN9-1.003)

C9ORF72 in a Large Series of Italian and Sardinian Familial and Sporadic ALS Patients (P05.161)

Epidemiological and clinical features of primary intrarachidian tumours in the island of Sardinia, during the 1977-1986 period

Primary optic neuritis evolved in multiple sclerosis: an epidemiological study

Thalamic hemorrhage. 30 cases studied: clinico-tomodensitometric correlations

Sensitivity and specificity of the EEG versus CT in acute cortical and subcortical stroke

A behavioural simulator and its use for the validation of hypercube architectures

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

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

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Addition of Metastasis-Directed Therapy to Intermittent Hormone Therapy for Oligometastatic Prostate Cancer: The EXTEND Phase 2 Randomized Clinical Trial

Genetic counselling in ALS: facts, uncertainties and clinical suggestions

Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

PET/CT scan in traumatic brain injury: a new frontier for the prognosis from cerebellum activity?

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

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