Lista de obras - Francesca Di Stefano - Dominio Público Uruguay

Abnormalities of insulin-like growth factor-I signaling and impaired cell proliferation in osteoblasts from subjects with osteoporosis

artículo científico publicado en 2007

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

C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population

artículo científico publicado en 2015

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

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

EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis

scientific article published on 07 December 2016

Exendin-4 prevents c-Jun N-terminal protein kinase activation by tumor necrosis factor-alpha (TNFalpha) and inhibits TNFalpha-induced apoptosis in insulin-secreting cells

artículo científico publicado en 2010

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

Insulin signaling in human visceral and subcutaneous adipose tissue in vivo

artículo científico publicado en 2006

Involvement of the p66Shc protein in glucose transport regulation in skeletal muscle myoblasts

artículo científico publicado en 2008

Isolated bipallidal lesions caused by extrapontine myelinolysis.

artículo científico publicado en 2013

Multiple Spontaneous Cerebral Microbleeds and Leukoencephalopathy in PSEN1-Associated Familial Alzheimer's Disease: Mirror of Cerebral Amyloid Angiopathy?

artículo científico publicado en 2015

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

artículo científico publicado en 2015

The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms

artículo científico publicado en 2013

The p66Shc protein controls redox signaling and oxidation-dependent DNA damage in human liver cells

artículo científico publicado en 2015

The phenotypical core of Alzheimer's disease-related and nonrelated variants of the corticobasal syndrome: A systematic clinical, neuropsychological, imaging, and biomarker study

artículo científico

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

artículo científico publicado en 2013

Lista de obras de Francesca Di Stefano

Abnormalities of insulin-like growth factor-I signaling and impaired cell proliferation in osteoblasts from subjects with osteoporosis

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

C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population

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.

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

EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis

Exendin-4 prevents c-Jun N-terminal protein kinase activation by tumor necrosis factor-alpha (TNFalpha) and inhibits TNFalpha-induced apoptosis in insulin-secreting cells

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?

Insulin signaling in human visceral and subcutaneous adipose tissue in vivo

Involvement of the p66Shc protein in glucose transport regulation in skeletal muscle myoblasts

Isolated bipallidal lesions caused by extrapontine myelinolysis.

Multiple Spontaneous Cerebral Microbleeds and Leukoencephalopathy in PSEN1-Associated Familial Alzheimer's Disease: Mirror of Cerebral Amyloid Angiopathy?

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms

The p66Shc protein controls redox signaling and oxidation-dependent DNA damage in human liver cells

The phenotypical core of Alzheimer's disease-related and nonrelated variants of the corticobasal syndrome: A systematic clinical, neuropsychological, imaging, and biomarker study

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