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Visual impairment in FOXG1 -mutated individuals and mice

Neuroscience, 2016-06, Vol.324, p.496-508

2016

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Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings

Neurological sciences, 2021-07, Vol.42 (7), p.3039-3042

2021

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AARS2‐related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

Acta neurologica Scandinavica, 2018-10, Vol.138 (4), p.278-283

2018

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Pendular nystagmus, palatal tremor and progressive ataxia in GM2-gangliosidosis

European journal of neurology, 2015-06, Vol.22 (6), p.e67-e69

2015

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New insights in Neanderthal palaeoecology using stable oxygen isotopes preserved in small mammals as palaeoclimatic tracers in Teixoneres Cave (Moià, northeastern Iberia)

Archaeological and anthropological sciences, 2022-06, Vol.14 (6), Article 106

2022

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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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Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families

Journal of the neurological sciences, 2017-11, Vol.382, p.29-35

2017

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Eye movement abnormalities in a patient with Zellweger spectrum disorder

Neurological sciences, 2016-06, Vol.37 (6), p.1013-1015

2016

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Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex

Journal of chemical theory and computation, 2023-08, Vol.19 (15), p.4863-4882

2023

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Who provides physical therapy in the United States? An analysis using data from the 2011 Medical Expenditure Panel Survey

Physiotherapy, 2015-05, Vol.101, p.e179-e179

2015

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Correction to Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex

Journal of chemical theory and computation, 2024-01, Vol.20 (2), p.990-991

2024

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Nonlinear analysis of saccade speed fluctuations during combined action and perception tasks

Journal of neuroscience methods, 2014-07, Vol.232, p.102-109

2014

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Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene

Neurological sciences, 2016-01, Vol.37 (1), p.143-145

2016

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Homozygosity for P.Cys183ser mutation in Notch3 gene may influence the severity of clinical presentation? Report of an Italian family

Journal of the neurological sciences, 2013-10, Vol.333, p.e658-e658

2013

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Oculomotor changes in multiple system atrophy: Clinical, MRI and laboratory features in eight patients

Journal of the neurological sciences, 2013-10, Vol.333, p.e666-e666

2013

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P10.14 Quantitative analysis of horizontal slow saccades in spinocerebellar ataxia type 2

Clinical neurophysiology, 2011, Vol.122, p.S108-S108

2011

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Four novel CYP27A1 mutations in seven Italian patients with CTX

European journal of neurology, 2010-10, Vol.17 (10), p.1259-1262

2010

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SARS-CoV-2 infects the human kidney and drives fibrosis in kidney organoids

Cell stem cell, 2022-02, Vol.29 (2), p.217-231.e8

2022

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Evaluating the Influence of Motor Control on Selective Attention through a Stochastic Model : The Paradigm of Motor Control Dysfunction in Cerebellar Patient

BioMed research international, 2014-01, Vol.2014 (2014), p.1-13

2014

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Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids

Journal of the neurological sciences, 2013-10, Vol.333, p.e691-e691

2013

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Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke’s encephalopathy

Neurological sciences, 2013-10, Vol.34 (10), p.1867-1869

2013

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CT and MRI of Wernicke’s encephalopathy

Radiologia medica, 2011-03, Vol.116 (2), p.319-333

2011

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Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL

Journal of the neurological sciences, 2013-10, Vol.333, p.e660-e660

2013

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High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy

Clinical genetics, 2012-09, Vol.82 (3), p.277-282

2012

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Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay

International journal of neuroscience, 2011-04, Vol.121 (4), p.201-208

2011

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Visual impairment in FOXG1 -mutated individuals and mice

Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings

AARS2‐related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

Pendular nystagmus, palatal tremor and progressive ataxia in GM2-gangliosidosis

New insights in Neanderthal palaeoecology using stable oxygen isotopes preserved in small mammals as palaeoclimatic tracers in Teixoneres Cave (Moià, northeastern Iberia)

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

Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families

Eye movement abnormalities in a patient with Zellweger spectrum disorder

Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex

Who provides physical therapy in the United States? An analysis using data from the 2011 Medical Expenditure Panel Survey

Correction to Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex

Nonlinear analysis of saccade speed fluctuations during combined action and perception tasks

Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene

Homozygosity for P.Cys183ser mutation in Notch3 gene may influence the severity of clinical presentation? Report of an Italian family

Oculomotor changes in multiple system atrophy: Clinical, MRI and laboratory features in eight patients

P10.14 Quantitative analysis of horizontal slow saccades in spinocerebellar ataxia type 2

Four novel CYP27A1 mutations in seven Italian patients with CTX

SARS-CoV-2 infects the human kidney and drives fibrosis in kidney organoids

Evaluating the Influence of Motor Control on Selective Attention through a Stochastic Model : The Paradigm of Motor Control Dysfunction in Cerebellar Patient

Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids

Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke’s encephalopathy

CT and MRI of Wernicke’s encephalopathy

Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL

High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy

Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay

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