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Diffusion Tensor Imaging Shows Different Topographic Involvement of the Thalamus in Progressive Supranuclear Palsy and Corticobasal Degeneration

American journal of neuroradiology : AJNR, 2009-09, Vol.30 (8), p.1482-1487

2009

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Stereotypic behaviors in degenerative dementias

Journal of neurology, 2012-11, Vol.259 (11), p.2452-2459

2012

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Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome

Journal of the neurological sciences, 2016-09, Vol.368, p.300-303

2016

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Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy

Neurology, 1999-08, Vol.53 (3), p.502-502

1999

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Atypical presentation of Creutzfeldt–Jakob disease: The first Italian case associated with E196K mutation in the PRNP gene

Journal of the neurological sciences, 2008-12, Vol.275 (1), p.145-147

2008

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Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy

Journal of neurology, neurosurgery and psychiatry, 2000-09, Vol.69 (3), p.313-318

2000

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Cerebral Amyloid Angiopathy-Related Inflammation: An Emerging Disease

The neuroradiology journal, 2011-04, Vol.24 (2), p.253-257

2011

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Levodopa reduces risk factors for vascular disease in parkinsonian patients

Journal of neurology, 2008-08, Vol.255 (8), p.1266-1267

2008

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Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy

Neurological sciences, 2001-06, Vol.22 (3), p.247-251

2001

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Affective symptoms in multiple system atrophy and Parkinson’s disease: response to levodopa therapy

Journal of neurology, neurosurgery and psychiatry, 1999-04, Vol.66 (4), p.541-544

1999

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Reduced risk factors for vascular disorders in parkinson disease patients : A case-control study

Stroke (1970), 2006-05, Vol.37 (5), p.1184-1188

2006

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Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

Brain (London, England : 1878), 2008-09, Vol.131 (9), p.2321-2331

2008

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Cognitive and behavioral disturbances in Parkinson's disease

Neurological sciences, 2003-05, Vol.24 Suppl 1, p.S30-s31

2003

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Progressive dysarthria: definition and clinical follow-up

Neurological sciences, 2003-10, Vol.24 (3), p.211-212

2003

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Progressive myoclonic ataxia with intrathecal immune activation in six patients

Neurological sciences, 2007-08, Vol.28 (4), p.199-204

2007

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Unusual association of sporadic olivopontocerebellar atrophy and motor neuron disease

Neurological sciences, 2002-12, Vol.23 (5), p.243-245

2002

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Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients

Neurology, 1993-11, Vol.43 (11), p.2262-2262

1993

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Distal-proximal differences in limb apraxia in corticobasal degeneration but not progressive supranuclear palsy

Neurological sciences, 2003-10, Vol.24 (3), p.213-214

2003

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Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene

American journal of human genetics, 1996-08, Vol.59 (2), p.475-477

1996

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Neurophysiological features in relation to clinical signs in clinically diagnosed corticobasal degeneration

Neurological sciences, 2003-04, Vol.24 (1), p.16-23

2003

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Limb apraxia in corticobasal degeneration and progressive supranuclear palsy

Neurology, 2005-02, Vol.64 (3), p.448-453

2005

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Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy

Radiology, 1990-03, Vol.174 (3 Pt 1), p.693-696

1990

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Chorea in patients with AIDS

Acta neurologica Scandinavica, 1999-11, Vol.100 (5), p.332-336

1999

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Cognitive and psychiatric characterization of patients with Huntington's disease and their at-risk relatives

Neurological sciences, 2002-09, Vol.23 Suppl 2, p.S105-s106

2002

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Clinical and neuroradiological aspects of Sneddon's syndrome and primary antiphospholipid antibody syndrome. A follow-up study

Neurological sciences, 2000-06, Vol.21 (3), p.157-164

2000

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Diffusion Tensor Imaging Shows Different Topographic Involvement of the Thalamus in Progressive Supranuclear Palsy and Corticobasal Degeneration

Stereotypic behaviors in degenerative dementias

Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome

Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy

Atypical presentation of Creutzfeldt–Jakob disease: The first Italian case associated with E196K mutation in the PRNP gene

Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy

Cerebral Amyloid Angiopathy-Related Inflammation: An Emerging Disease

Levodopa reduces risk factors for vascular disease in parkinsonian patients

Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy

Affective symptoms in multiple system atrophy and Parkinson’s disease: response to levodopa therapy

Reduced risk factors for vascular disorders in parkinson disease patients : A case-control study

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

Cognitive and behavioral disturbances in Parkinson's disease

Progressive dysarthria: definition and clinical follow-up

Progressive myoclonic ataxia with intrathecal immune activation in six patients

Unusual association of sporadic olivopontocerebellar atrophy and motor neuron disease

Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients

Distal-proximal differences in limb apraxia in corticobasal degeneration but not progressive supranuclear palsy

Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene

Neurophysiological features in relation to clinical signs in clinically diagnosed corticobasal degeneration

Limb apraxia in corticobasal degeneration and progressive supranuclear palsy

Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy

Chorea in patients with AIDS

Cognitive and psychiatric characterization of patients with Huntington's disease and their at-risk relatives

Clinical and neuroradiological aspects of Sneddon's syndrome and primary antiphospholipid antibody syndrome. A follow-up study

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