Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Patrizia Tarantino
Observed names:
P. TARANTINO,
P. Tarantino,
TARANTINO P,
Tarantino P,
Tarantino P.,
Tarantino, Patrizia
show all 6
Institutions:
Institute of Molecular Bioimaging and Physiology,
National Research Council
Observed institutions:
University of Messina,
National Academies of Sciences, Engineering, and Medicine,
Magna Graecia University,
University of Catania,
Institute of Molecular Bioimaging and Physiology,
Institute of Neurological Sciences,
National Research Council
show all 7
OpenAlex ID:
A5110015692
Sex Differences in Clinical and Genetic Determinants of Levodopa Peak-Dose Dyskinesias in Parkinson Disease
2005
·
Mario Zappia
, Grazia Annesi
, et al.
·
Archives of Neurology
·
201
DJ‐1 mutations and parkinsonism‐dementia‐amyotrophic lateral sclerosis complex
2005
·
Grazia Annesi
, Giovanni Savettieri
, et al.
·
Annals of Neurology
·
173
Large-scale replication and heterogeneity in Parkinson disease genetic loci
2012
·
Manu Sharma
, John P.A. Ioannidis
, et al.
·
Neurology
·
131
PDF
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences
2012
·
Angelo Labate
, Patrizia Tarantino
, et al.
·
Epilepsia
·
95
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy
2007
·
Elvira V. De Marco
, Grazia Annesi
, et al.
·
Movement Disorders
·
83
Divergent effects of the T 1174S SCN1A mutation associated with seizures and hemiplegic migraine
2013
·
Sandrine Cestèle
, Angelo Labate
, et al.
·
Epilepsia
·
66
PDF
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease
2007
·
Aldo Quattrone
, Antonio Bagnato
, et al.
·
Movement Disorders
·
66
Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus
2003
·
Grazia Annesi
, Antonio Gambardella
, et al.
·
Epilepsia
·
58
PDF
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP
2013
·
Angelo Labate
, Patrizia Tarantino
, et al.
·
Epilepsy Research
·
35
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy
2007
·
Elvira V. De Marco
, Antonio Gambardella
, et al.
·
Epilepsy Research
·
35
Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the Parkin gene
2004
·
Marianna Capecci
, Luca Passamonti
, et al.
·
Movement Disorders
·
31
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease
2015
·
Lisa Wang
, Jan O. Aasly
, et al.
·
Neurology
·
30
PDF
A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit
2004
·
Grazia Annesi
, Vito Sofia
, et al.
·
Epilepsia
·
25
PDF
Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye‐of‐the‐tiger pattern
2005
·
Paola Valentino
, Grazia Annesi
, et al.
·
Movement Disorders
·
24
An exome study of Parkinson’s disease in Sardinia, a Mediterranean genetic isolate
2014
·
Marialuisa Quadri
, Xu Yang
, et al.
·
Neurogenetics
·
20
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism
2008
·
Patrizia Tarantino
, Donatella Civitelli
, et al.
·
Parkinsonism & Related Disorders
·
19
Newly characterised 5′ and 3′ regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia
2008
·
Liana Veneziano
, Serena Guida
, et al.
·
Journal of the Neurological Sciences
·
18
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification
2015
·
Monica Gagliardi
, Maurizio Morelli
, et al.
·
Gene
·
17
Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy
2014
·
Monica Gagliardi
, Grazia Annesi
, et al.
·
Neurobiology of Aging
·
16
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia
2014
·
Laura Brighina
, Enrico Saracchi
, et al.
·
Neurodegenerative Diseases
·
16
FRAXE intermediate alleles are associated with Parkinson’s disease
2004
·
Grazia Annesi
, Giuseppe Nicoletti
, et al.
·
Neuroscience Letters
·
16
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy
2011
·
Valentina Greco
, Elvira Valeria De Marco
, et al.
·
Neurological Sciences
·
15
Dysbindin C–A–T haplotype is associated with thicker medial orbitofrontal cortex in healthy population
2010
·
Antonio Cerasa
, Aldo Quattrone
, et al.
·
NeuroImage
·
12
Lack of association between G‐protein coupled receptor kinase 5 gene and Parkinson's disease
2010
·
Patrizia Tarantino
, Elvira Valeria De Marco
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
11
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism
2011
·
Vittorio Scornaienchi
, Donatella Civitelli
, et al.
·
Parkinsonism & Related Disorders
·
9
Show more works
View as search
Works count:
49
Citation count:
1,302
H-index:
18
I10-index:
25
Year
Topic
Type
