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List of works by Patrizia Tarantino

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

scientific article published on 7 May 2015

A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.

scientific article published in March 2004

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

scientific article published on 8 October 2014

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy

article

Author’s reply to the comment of Sironi et al. on “Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism”

article

Biological effects of 6 mT static magnetic fields: a comparative study in different cell types

scientific article published on October 2006

Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene.

scientific article published in December 2004

Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism

article

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

scientific article published in November 2005

Dentatorubral-pallidoluysian atrophy: Haplotype of Asian origin in 2 Italian families

article

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

scientific article published on 08 February 2013

Dysbindin C–A–T haplotype is associated with thicker medial orbitofrontal cortex in healthy population

scientific article published on 22 December 2010

Erratum: Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the Parkin gene. Mov Disord 2004;19(12):1451-1453

article

FRAXE intermediate alleles are associated with Parkinson's disease.

scientific article published in September 2004

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

scientific article published on 25 September 2014

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

scientific article published on 26 April 2014

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

scientific article

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

scientific article published in February 2006

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.

scientific article published in February 2008

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

scientific article published on 5 November 2012

Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease

scientific article published on 7 March 2008

Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease

article

Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation

scientific article published on 24 April 2015

Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease

scientific article

Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia

scientific article

Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease

scientific article published on 01 November 2007

PCDH19 mutations in female patients from Southern Italy

scientific article published on 30 August 2014

Post-continuous whole body exposure of rabbits to 650 MHz electromagnetic fields: effects on liver, spleen, and brain

scientific article published on 6 April 2005

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

scientific article

Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study

scientific article published in April 2005

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

scientific article (publication date: September 2003)

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