Goldenhar-Gorlin syndrome. A case with congenital trigeminal neuropathy

What is in our seas? Assessing anthropogenic litter on the seafloor of the central Mediterranean Sea.

Environmental pollution (Barking, Essex : 1987)·2020

Anodal tDCS of the swallowing motor cortex for treatment of dysphagia in multiple sclerosis: a pilot open-label study.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology·2018

The importance of the reproducibility of oropharyngeal swallowing in amyotrophic lateral sclerosis. An electrophysiological study.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology·2017

Long-Term Nicergoline Treatment of Mild to Moderate Senile Dementia : Results of a Multicentre, Double-Blind, Placebo-Controlled Study.

Clinical drug investigation·2016

Specific patterns of laryngeal electromyography during wakefulness are associated to sleep disordered breathing and nocturnal stridor in multiple system atrophy.

Parkinsonism & related disorders·2016

Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients.

European journal of clinical pharmacology·2016

False positive of ADA determination in cerebrospinal fluid.

Acta neurologica·1994

Post-radiation cerebral lesions in adults.

Acta neurologica·1994

A case of type I Arnold-Chiari malformation of anomalous onset.

Acta neurologica·1994

BAEP and E.M.G. changes from whiplash injuries.

Acta neurologica·1994

S.P.E.C.T., E.E.G. and M.R.I. investigations in complex partial epilepsy.

Acta neurologica·1994

Early cognitive impairment in multiple sclerosis detected by a screening with a vocabulary-test.

Acta neurologica·1994

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

[Analysis of clinical phenotypes and pathogenicity of a c.4476+5G>T variant of SCN1A gene in a Chinese pedigree affected with Genetic epilepsy with febrile seizures plus].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

APOL1 kidney disease: a critical narrative review of molecular mechanisms, clinical heterogeneity, and the emerging therapeutic landscape.

International urology and nephrology·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

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Goldenhar-Gorlin syndrome. A case with congenital trigeminal neuropathy

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What is in our seas? Assessing anthropogenic litter on the seafloor of the central Mediterranean Sea.

Anodal tDCS of the swallowing motor cortex for treatment of dysphagia in multiple sclerosis: a pilot open-label study.

The importance of the reproducibility of oropharyngeal swallowing in amyotrophic lateral sclerosis. An electrophysiological study.

Long-Term Nicergoline Treatment of Mild to Moderate Senile Dementia : Results of a Multicentre, Double-Blind, Placebo-Controlled Study.

Specific patterns of laryngeal electromyography during wakefulness are associated to sleep disordered breathing and nocturnal stridor in multiple system atrophy.

Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients.

False positive of ADA determination in cerebrospinal fluid.

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A case of type I Arnold-Chiari malformation of anomalous onset.

BAEP and E.M.G. changes from whiplash injuries.

S.P.E.C.T., E.E.G. and M.R.I. investigations in complex partial epilepsy.

Early cognitive impairment in multiple sclerosis detected by a screening with a vocabulary-test.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Familial short stature: genetic architecture, risk stratification, and precision management.

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

[Analysis of clinical phenotypes and pathogenicity of a c.4476+5G>T variant of SCN1A gene in a Chinese pedigree affected with Genetic epilepsy with febrile seizures plus].

APOL1 kidney disease: a critical narrative review of molecular mechanisms, clinical heterogeneity, and the emerging therapeutic landscape.

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Goldenhar-Gorlin syndrome. A case with congenital trigeminal neuropathy

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