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Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease

Frontiers in neurology, 2020-11, Vol.11, p.577362-577362

2020

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Visual System Involvement in CADASIL

Journal of stroke and cerebrovascular diseases, 2013-11, Vol.22 (8), p.1377-1384

2013

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The role of dentate nuclei in human oculomotor control: insights from cerebrotendinous xanthomatosis

The Journal of physiology, 2017-06, Vol.595 (11), p.3607-3620

2017

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APOE 2 is associated with white matter hyperintensity volume in CADASIL

Journal of cerebral blood flow and metabolism, 2016-01, Vol.36 (1), p.199-203

2016

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Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias

Brain (London, England : 1878), 2011-03, Vol.134 (Pt 3), p.879-891

2011

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Postpartum psychiatric disturbances as an unrecognized onset of CADASIL

Acta psychiatrica Scandinavica, 2005-09, Vol.112 (3), p.241-241

2005

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Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

Journal of the neurological sciences, 2015-03, Vol.350 (1), p.107-109

2015

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Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies

Journal of the peripheral nervous system, 2012-12, Vol.17 (4), p.391-398

2012

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Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Stroke (1970), 2010-02, Vol.41 (2), p.218-223

2010

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APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

Journal of cerebral blood flow and metabolism, 2016-01, Vol.36 (1), p.199-203

2016

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Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4

Neurological sciences, 2014-08, Vol.35 (8), p.1287-1291

2014

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Right-to-Left Shunt in CADASIL Patients : Prevalence and Correlation With Clinical and MRI Findings

Stroke (1970), 2008-07, Vol.39 (7), p.2155-2157

2008

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Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis

Brain (London, England : 1878), 2001-01, Vol.124 (1), p.121-131

2001

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Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Stroke (1970), 2007-02, Vol.38 (2), p.276-280

2007

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Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities

Journal of neurology, 2006-11, Vol.253 (11), p.1471-1477

2006

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Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study

Journal of neurology, 2001-05, Vol.248 (5), p.403-409

2001

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Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.2847-2858

2015

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Quantification of Brain Damage in Cerebrotendinous Xanthomatosis with Magnetization Transfer MR Imaging

American journal of neuroradiology : AJNR, 2003-03, Vol.24 (3), p.495-500

2003

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MR evidence of structural and metabolic changes in brains of patients with Werner's syndrome

Journal of neurology, 2003-10, Vol.250 (10), p.1169-1173

2003

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Age and sex prevalence estimate of Joubert syndrome in Italy

Neurology, 2020-02, Vol.94 (8)

2020

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Congenital myopathies: clinical phenotypes and new diagnostic tools

Italian journal of pediatrics, 2017-11, Vol.43 (1), p.101-101, Article 101

2017

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A recessive ataxia diagnosis algorithm for the next generation sequencing era

Annals of neurology, 2017-12, Vol.82 (6), p.892-899

2017

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Operationalizing mild cognitive impairment criteria in small vessel disease: the VMCI-Tuscany Study

Alzheimer's & dementia, 2016-04, Vol.12 (4), p.407-418

2016

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APOE ɛ 2 is associated with white matter hyperintensity volume in CADASIL

Journal of cerebral blood flow and metabolism, 2015-04, Vol.36 (1), p.199-203

2015

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Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease

Visual System Involvement in CADASIL

The role of dentate nuclei in human oculomotor control: insights from cerebrotendinous xanthomatosis

APOE 2 is associated with white matter hyperintensity volume in CADASIL

Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias

Postpartum psychiatric disturbances as an unrecognized onset of CADASIL

Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies

Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4

Right-to-Left Shunt in CADASIL Patients : Prevalence and Correlation With Clinical and MRI Findings

Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis

Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities

Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study

Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Quantification of Brain Damage in Cerebrotendinous Xanthomatosis with Magnetization Transfer MR Imaging

MR evidence of structural and metabolic changes in brains of patients with Werner's syndrome

Age and sex prevalence estimate of Joubert syndrome in Italy

Congenital myopathies: clinical phenotypes and new diagnostic tools

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

A recessive ataxia diagnosis algorithm for the next generation sequencing era

Operationalizing mild cognitive impairment criteria in small vessel disease: the VMCI-Tuscany Study

APOE ɛ 2 is associated with white matter hyperintensity volume in CADASIL

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