Patrizia Tarantino

Catanzaro, Italy

Last Updated: 09/26/2026

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Found 13 publications

Role of G-protein coupled receptor kinase 5 gene in cognitive impairment in Parkinson's disease.

Role of G-protein coupled receptor kinase 5 gene in cognitive impairment in Parkinson's disease.

Journal: Psychiatry research

Published: May 05, 2015

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.

Journal: Gene

Published: March 24, 2015

Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation.

Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation.

Journal: Journal of the neurological sciences

Published: February 07, 2015

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.

Journal: Epilepsia

Published: January 20, 2015

An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate.

An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate.

Journal: Neurogenetics

Published: July 21, 2014

PCDH19 mutations in female patients from Southern Italy.

PCDH19 mutations in female patients from Southern Italy.

Journal: Seizure

Published: May 29, 2014

Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia.

Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia.

Journal: Neuro-degenerative diseases

Published: April 28, 2014

Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy.

Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy.

Journal: Neurobiology of aging

Published: April 02, 2014

Sacsin-related spastic ataxia caused by a novel missense mutation p.Arg272His in a patient from Sicily, southern Italy.

Sacsin-related spastic ataxia caused by a novel missense mutation p.Arg272His in a patient from Sicily, southern Italy.

Journal: Cerebellum (London, England)

Published: January 23, 2013

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.

Journal: Epilepsia

Published: January 15, 2013

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.

Journal: Epilepsia

Published: November 07, 2012

Spinocerebellar ataxia type 7: report of a new Italian family.

Spinocerebellar ataxia type 7: report of a new Italian family.

Journal: Internal medicine (Tokyo, Japan)

Published: October 16, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026