Lista de obras - Gianluca Floris - Dominio Público Uruguay

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

artículo científico publicado en 2011

ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations

artículo científico publicado en 2012

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

artículo científico publicado en 2015

Aberrant sexual behaviours in Parkinson’s disease during dopaminergic treatment

artículo científico publicado en 2007

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

artículo científico publicado en 2021

Bipolar affective disorder and Parkinson's disease: a rare, insidious and often unrecognized association.

artículo científico publicado en 2002

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

artículo científico publicado en 2013

C9ORF72repeat expansion and bipolar disorder - is there a link? No mutation detected in a Sardinian cohort of patients with bipolar disorder

artículo científico publicado en 2014

Capgras syndrome in Parkinson's disease: two new cases and literature review.

artículo científico publicado en 2016

Chronic delusional hallucinatory psychosis in early-onset Parkinson's disease: drug-induced complication or sign of an idiopathic psychiatric illness?

artículo científico publicado en 2001

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Description (reporting the actual words used in written letters) of the neuropsychological and psychopathological modifications produced by dopaminergic treatment in a young patient with Parkinson's disease.

artículo científico publicado en 2005

Effect of dose and frequency of interferon beta-1a administration on clinical and magnetic resonance imaging parameters in relapsing-remitting multiple sclerosis

artículo científico publicado en 2006

Fluctuating off-period hemidystonia with Pisa syndrome in advanced Parkinson's disease.

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.

artículo científico publicado en 2008

Genetic architecture of ALS in Sardinia

artículo científico publicado en 2014

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

artículo científico publicado en 2021

Hypersexual behaviour, frotteurism and delusional jealousy in a young parkinsonian patient during dopaminergic therapy with pergolide: A rare case of iatrogenic paraphilia

artículo científico publicado en 2006

Isolated bipallidal lesions caused by extrapontine myelinolysis.

artículo científico publicado en 2013

Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene

artículo científico publicado en 2011

Medulloblastoma induces unusual headache with clinical picture of basilar-type migraine complicated by ischaemic infarcts.

artículo científico publicado en 2006

Mitoxantrone treatment in patients with early relapsing-remitting multiple sclerosis.

artículo científico publicado en 2007

Othello syndrome in Parkinson disease patients without dementia.

artículo científico publicado en 2009

Pathological gambling, delusional parasitosis and adipsia as a post-haemorrhagic syndrome: a case report

artículo científico publicado en 2008

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

artículo científico publicado en 2015

Pisa-Like Syndrome Under Baclofen in a Patient With Spastic Hemiparesis due to Ischemic Stroke

scientific article published on 01 September 2015

Reversible Pisa syndrome in patients with Parkinson's disease on dopaminergic therapy

artículo científico publicado en 2009

TBK1 is associated with ALS and ALS-FTD in Sardinian patients

artículo científico publicado en 2016

Transient unilateral spatial neglect during aura in a woman with sporadic hemiplegic migraine

artículo científico publicado en 2013

Ultrarapid mood cycling in a Parkinsonian patient: is not always simply an "on-off" fluctuation--a case report.

artículo científico publicado en 2007

[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.

artículo científico publicado en 2005

Lista de obras de Gianluca Floris

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

ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

Aberrant sexual behaviours in Parkinson’s disease during dopaminergic treatment

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Bipolar affective disorder and Parkinson's disease: a rare, insidious and often unrecognized association.

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

C9ORF72repeat expansion and bipolar disorder - is there a link? No mutation detected in a Sardinian cohort of patients with bipolar disorder

Capgras syndrome in Parkinson's disease: two new cases and literature review.

Chronic delusional hallucinatory psychosis in early-onset Parkinson's disease: drug-induced complication or sign of an idiopathic psychiatric illness?

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

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

Description (reporting the actual words used in written letters) of the neuropsychological and psychopathological modifications produced by dopaminergic treatment in a young patient with Parkinson's disease.

Effect of dose and frequency of interferon beta-1a administration on clinical and magnetic resonance imaging parameters in relapsing-remitting multiple sclerosis

Fluctuating off-period hemidystonia with Pisa syndrome in advanced Parkinson's disease.

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

Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.

Genetic architecture of ALS in Sardinia

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Hypersexual behaviour, frotteurism and delusional jealousy in a young parkinsonian patient during dopaminergic therapy with pergolide: A rare case of iatrogenic paraphilia

Isolated bipallidal lesions caused by extrapontine myelinolysis.

Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene

Medulloblastoma induces unusual headache with clinical picture of basilar-type migraine complicated by ischaemic infarcts.

Mitoxantrone treatment in patients with early relapsing-remitting multiple sclerosis.

Othello syndrome in Parkinson disease patients without dementia.

Pathological gambling, delusional parasitosis and adipsia as a post-haemorrhagic syndrome: a case report

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

Pisa-Like Syndrome Under Baclofen in a Patient With Spastic Hemiparesis due to Ischemic Stroke

Reversible Pisa syndrome in patients with Parkinson's disease on dopaminergic therapy

TBK1 is associated with ALS and ALS-FTD in Sardinian patients

Transient unilateral spatial neglect during aura in a woman with sporadic hemiplegic migraine

Ultrarapid mood cycling in a Parkinsonian patient: is not always simply an "on-off" fluctuation--a case report.

[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.