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Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects

BMC medicine, 2017-02, Vol.15 (1), p.41-41, Article 41

2017

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HTRA1 expression profile and activity on TGF‐β signaling in HTRA1 mutation carriers

Journal of cellular physiology, 2020-10, Vol.235 (10), p.7120-7127

2020

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Application of the DSM-5 Criteria for Major Neurocognitive Disorder to Vascular MCI Patients

Dementia and geriatric cognitive disorders extra, 2018-01, Vol.8 (1), p.104-116

2018

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News on the journal Neurological Sciences in 2017

Neurological sciences, 2018, Vol.39 (1), p.15-21

2018

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CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients

Journal of neurology, 2015-01, Vol.262 (1), p.134-141

2015

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POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients

Neurological sciences, 2022-02, Vol.43 (2), p.1071-1077

2022

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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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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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Longitudinal changes in MoCA performances in patients with mild cognitive impairment and small vessel disease. Results from the VMCI-Tuscany Study

Cerebral circulation - cognition and behavior, 2021-01, Vol.2, p.100008, Article 100008

2021

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Arterial stiffness in patients with deep and lobar intracerebral hemorrhage

대한뇌졸중학회지, 2014, 16(3), 13, pp.184-188

2014

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Advances in clinical neurology through the journal “Neurological Sciences” (2015–2016)

Neurological sciences, 2017, Vol.38 (1), p.9-18

2017

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Hereditary cerebral small vessel diseases: A review

Journal of the neurological sciences, 2012-11, Vol.322 (1), p.25-30

2012

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Ad-hoc modifications of cyclic mimetics of SOCS1 protein: Structural and functional insights

European journal of medicinal chemistry, 2022-12, Vol.243, p.114781-114781, Article 114781

2022

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Hippocampal atrophy and white matter lesions characteristics can predict evolution to dementia in patients with vascular mild cognitive impairment

Journal of the neurological sciences, 2024-09, Vol.464, p.123163, Article 123163

2024

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Development and psychometric properties of a neuropsychological battery for mild cognitive impairment with small vessel disease: the VMCI-Tuscany Study

Journal of Alzheimer's disease, 2015-01, Vol.43 (4), p.1313-1323

2015

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Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

CNS neuroscience & therapeutics, 2017-09, Vol.23 (9), p.759-765

2017

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Validation of Empoli Embolic Stroke of Undetermined Source Atrial Fibrillation (E 2 AF) Score for Detecting Atrial Fibrillation in Patients With Embolic Stroke of Undetermined Source

The Neurologist (Baltimore, Md.), 2023-11, Vol.28 (6), p.426-428

2023

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Update on several/certain adult-onset genetic leukoencephalopathies: clinical signs and molecular confirmation

Journal of Alzheimer's disease, 2014-01, Vol.42 Suppl 3 (s3), p.S27-S35

2014

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Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene

Journal of Alzheimer's disease, 2016-01, Vol.49 (1), p.27-30

2016

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Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene

Journal of neurology, 2014-04, Vol.261 (4), p.768-772

2014

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A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids

Journal of Alzheimer's disease, 2015-01, Vol.47 (2), p.319-322

2015

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Use of Agro Waste Biomass for α-Amylase Production by Anoxybacillus amylolyticus: Purification and Properties

Journal of microbial & biochemical technology, 2014, Vol.6 (6)

Paola Di Donato, Ilaria Finore

2014

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Huntington's disease gene expansion associates with early onset nonprogressive chorea

Movement disorders, 2013-05, Vol.28 (5), p.684-684

2013

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The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL

Neurobiology of aging, 2013-09, Vol.34 (9), p.2234.e9-2234.e12

2013

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Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Neurological sciences, 2017-07, Vol.38 (7), p.1333-1336

2017

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Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects

HTRA1 expression profile and activity on TGF‐β signaling in HTRA1 mutation carriers

Application of the DSM-5 Criteria for Major Neurocognitive Disorder to Vascular MCI Patients

News on the journal Neurological Sciences in 2017

CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients

POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients

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

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

Longitudinal changes in MoCA performances in patients with mild cognitive impairment and small vessel disease. Results from the VMCI-Tuscany Study

Arterial stiffness in patients with deep and lobar intracerebral hemorrhage

Advances in clinical neurology through the journal “Neurological Sciences” (2015–2016)

Hereditary cerebral small vessel diseases: A review

Ad-hoc modifications of cyclic mimetics of SOCS1 protein: Structural and functional insights

Hippocampal atrophy and white matter lesions characteristics can predict evolution to dementia in patients with vascular mild cognitive impairment

Development and psychometric properties of a neuropsychological battery for mild cognitive impairment with small vessel disease: the VMCI-Tuscany Study

Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

Validation of Empoli Embolic Stroke of Undetermined Source Atrial Fibrillation (E 2 AF) Score for Detecting Atrial Fibrillation in Patients With Embolic Stroke of Undetermined Source

Update on several/certain adult-onset genetic leukoencephalopathies: clinical signs and molecular confirmation

Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene

Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene

A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids

Use of Agro Waste Biomass for α-Amylase Production by Anoxybacillus amylolyticus: Purification and Properties

Huntington's disease gene expansion associates with early onset nonprogressive chorea

The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL

Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

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