Patrizia Tarantino

Summary

Affiliation: National Research Council
Country: Italy

Publications

  1. ncbi request reprint Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
    Patrizia Tarantino
    Consiglio Nazionale delle Ricerche ISN, C da Burga, 44, 87050 Piano Lago di Mangone CS, Italy
    Hum Genet 122:415. 2007
  2. doi request reprint Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population
    Antonio Cerasa
    Neuroimaging Research Unit, Institute of Neurological Sciences, National Research Council, Catanzaro, Italy
    Neuroimage 55:508-13. 2011
  3. ncbi request reprint Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease
    Aldo Quattrone
    Institute of Neurology, University Magna Graecia, Catanzaro, Italy
    Mov Disord 23:21-7. 2008
  4. doi request reprint Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease
    Giovanni Savettieri
    Department of Clinical Neurosciences, University of Palermo, Italy
    Parkinsonism Relat Disord 14:509-12. 2008
  5. ncbi request reprint Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy
    Elvira V De Marco
    Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy
    Mov Disord 23:460-3. 2008
  6. ncbi request reprint DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex
    Grazia Annesi
    Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy
    Ann Neurol 58:803-7. 2005
  7. ncbi request reprint Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study
    Mario Zappia
    Institute of Neurology, University Magna Graecia, Catanzaro, Italy
    Arch Neurol 62:601-5. 2005
  8. ncbi request reprint Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene
    Marianna Capecci
    Dipartimento di Scienze Neurologiche, Universita Politecnica delle Marche, Ospedale Regionale Torrette, Ancona, Italy
    Mov Disord 19:1450-2. 2004
  9. ncbi request reprint Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern
    Paola Valentino
    Institute of Neurology, University Magna Graecia Catanzaro, Catanzaro, Italy
    Mov Disord 21:252-4. 2006
  10. ncbi request reprint FRAXE intermediate alleles are associated with Parkinson's disease
    Grazia Annesi
    Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy
    Neurosci Lett 368:21-4. 2004

Collaborators

  • Francesca Emanuela Rocca
  • A Cerasa
  • Aldo Quattrone
  • G Spalletta
  • Grazia Annesi
  • Ferdinanda Annesi
  • Donatella Civitelli
  • Sara Carrideo
  • Mario Zappia
  • Elvira V De Marco
  • Patrizia Spadafora
  • Innocenza C Cirò Candiano
  • Antonio Gambardella
  • Giovanni Savettieri
  • Giuseppe Nicoletti
  • Innocenza Claudia Cirò Candiano
  • Gennarina Arabia
  • Pierfrancesco Pugliese
  • Elvira Valeria De Marco
  • Demetrio Messina
  • Paolo Ragonese
  • Marco D'Amelio
  • Francesca Condino
  • Paola Valentino
  • Manuela Caracciolo
  • Nunzio Cutuli
  • Marianna Capecci
  • Nelide Romeo
  • Giuseppe Salemi
  • Valeria Terruso
  • Fabiana Novellino
  • Giovanni Provenzano
  • Maurizio Morelli
  • Francesco Naso
  • Domenico Consoli
  • Innocenza C Cirò-Candiano
  • Tommaso Piccoli
  • Vincenzo La Bella
  • Brigida Fierro
  • Federico Piccoli
  • Massimo Scerrati
  • Michele Bellesi
  • Rita Barone
  • Luca Passamonti
  • Vito Sofia
  • Maria Gabriella Ceravolo
  • Innocenza Cirò Candiano
  • Maurizio Iacoangeli
  • Riccardo Ricciuti
  • Leandro Provinciali
  • Letterio Morgante
  • Emilio Lepiane
  • Angela Aurora Pasqua
  • Umberto Aguglia
  • Gemma Incorpora
  • Agata Polizzi
  • Lorenzo Pavone
  • Patrizia Ventura
  • Angelo Labate

Detail Information

Publications12

  1. ncbi request reprint Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
    Patrizia Tarantino
    Consiglio Nazionale delle Ricerche ISN, C da Burga, 44, 87050 Piano Lago di Mangone CS, Italy
    Hum Genet 122:415. 2007
  2. doi request reprint Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population
    Antonio Cerasa
    Neuroimaging Research Unit, Institute of Neurological Sciences, National Research Council, Catanzaro, Italy
    Neuroimage 55:508-13. 2011
    ....
  3. ncbi request reprint Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease
    Aldo Quattrone
    Institute of Neurology, University Magna Graecia, Catanzaro, Italy
    Mov Disord 23:21-7. 2008
    ..Our findings also demonstrate that MIGB uptake has a heterogeneous pattern in genetic PD, because it was differently impaired in patients with different mutations in the same gene or with the same gene mutation...
  4. doi request reprint Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease
    Giovanni Savettieri
    Department of Clinical Neurosciences, University of Palermo, Italy
    Parkinsonism Relat Disord 14:509-12. 2008
    ..The present study supports the view that PINK1 is a pathogenic gene in some Italian families with EOPD and contributes to define the PINK1-associated phenotype...
  5. ncbi request reprint Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy
    Elvira V De Marco
    Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy
    Mov Disord 23:460-3. 2008
    ..2%) had a heterozygous substitution (P = 0.0018). These results strongly suggest that Italian carriers of a GBA mutation have an increased risk of developing PD...
  6. ncbi request reprint DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex
    Grazia Annesi
    Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy
    Ann Neurol 58:803-7. 2005
    ..Both mutations cosegregated with the disease and were detected in a heterozygous state in the patients' mother and their healthy siblings. Our findings expand the spectrum of clinical presentations associated with mutations in DJ-1 gene...
  7. ncbi request reprint Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study
    Mario Zappia
    Institute of Neurology, University Magna Graecia, Catanzaro, Italy
    Arch Neurol 62:601-5. 2005
    ....
  8. ncbi request reprint Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene
    Marianna Capecci
    Dipartimento di Scienze Neurologiche, Universita Politecnica delle Marche, Ospedale Regionale Torrette, Ancona, Italy
    Mov Disord 19:1450-2. 2004
    ....
  9. ncbi request reprint Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern
    Paola Valentino
    Institute of Neurology, University Magna Graecia Catanzaro, Catanzaro, Italy
    Mov Disord 21:252-4. 2006
    ..Therefore, the present observation reinforces the notion of the phenotypic and genetic heterogeneity in PKAN...
  10. ncbi request reprint FRAXE intermediate alleles are associated with Parkinson's disease
    Grazia Annesi
    Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy
    Neurosci Lett 368:21-4. 2004
    ..4%) subjects with PD and in only one of the 370 (0.27%) healthy controls (P < 0.001), thus indicating that these relatively large alleles may be associated with PD...
  11. ncbi request reprint A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit
    Grazia Annesi
    Epilepsia 45:294-5. 2004
  12. ncbi request reprint Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus
    Grazia Annesi
    Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy
    Epilepsia 44:1257-8. 2003