Francesca Emanuela Rocca

Summary

Affiliation: National Research Council
Country: Italy

Publications

  1. ncbi request reprint Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
    Francesca Emanuela Rocca
    Consiglio Nazionale delle Ricerche ISN, C da Burga, 44, 87050 Piano Lago di Mangone CS, Italy
    Hum Genet 122:415. 2007
  2. 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
  3. ncbi request reprint Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study
    Maria Teresa Pellecchia
    Department of Neurological Sciences, University Federico II, Napoli, Italy
    Mov Disord 22:559-63. 2007

Detail Information

Publications3

  1. ncbi request reprint Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
    Francesca Emanuela Rocca
    Consiglio Nazionale delle Ricerche ISN, C da Burga, 44, 87050 Piano Lago di Mangone CS, Italy
    Hum Genet 122:415. 2007
  2. 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...
  3. ncbi request reprint Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study
    Maria Teresa Pellecchia
    Department of Neurological Sciences, University Federico II, Napoli, Italy
    Mov Disord 22:559-63. 2007
    ..In 3 homozygotes and 1 heterozygote, a 2-year follow-up single photon emission computed tomography suggested no progression of nigrostriatal deficit...