Floriano Girotti

Via Celoria 11
Milan, 20133, Italy

Last Updated: 09/26/2026

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Found 16 publications

Unawareness of motor deficit in Huntington's disease.

Unawareness of motor deficit in Huntington's disease.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 02, 2026

Further insights into anti-IgLON5 disease: a case with complex clinical presentation.

Further insights into anti-IgLON5 disease: a case with complex clinical presentation.

Journal: BMC neurology
Published: July 21, 2024

Parkinsonian Syndromes in Motor Neuron Disease: A Clinical Study.

Parkinsonian Syndromes in Motor Neuron Disease: A Clinical Study.

Journal: Frontiers in aging neuroscience
Published: April 11, 2022

Correction to: Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Correction to: Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 03, 2021

Negative symptoms in Huntington's disease.

Negative symptoms in Huntington's disease.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: June 27, 2021

Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron Disorders.

Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron Disorders.

Journal: Neurology
Published: March 10, 2021

Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 23, 2021

A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease.

A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease.

Journal: Frontiers in neurology
Published: June 18, 2019

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study.

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: December 20, 2018

Stereotypic behaviours in frontotemporal dementia and progressive supranuclear palsy.

Stereotypic behaviours in frontotemporal dementia and progressive supranuclear palsy.

Journal: Cortex; a journal devoted to the study of the nervous system and behavior
Published: December 09, 2017

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.

Journal: Parkinsonism & related disorders
Published: June 22, 2017

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

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

Journal: Journal of the neurological sciences
Published: May 12, 2016
Showing 1-12 of 16

Last Updated: 09/26/2026