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E Rocca

Showing results (41-50 of 56) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1985
A model for hemoglobin F synthesis in adult life: evidence for regulation at the level of erythroblastsC Peschle, A R Migliaccio, G Migliaccio, et al.
Blood|December 1, 1989
Granulocyte-macrophage colony-stimulating factor reactivates fetal hemoglobin synthesis in erythroblast clones from normal adultsM Gabbianelli, E Pelosi, E Bassano, et al.
Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson diseaseV Scornaienchi, G Nicoletti, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
Parkinsonism & Related Disorders|August 30, 2008
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonismPatrizia Tarantino, Donatella Civitelli, Ferdinanda Annesi, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseasePatrizia Tarantino, I C Cirò Candiano, F Annesi, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancyGiovanni Provenzano, E Mannarino, F Annesi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2007
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern ItalyElvira V De Marco, Grazia Annesi, Patrizia Tarantino, et al.
Clinical Genetics|May 2, 2007
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's diseaseD Civitelli, P Tarantino, G Nicoletti, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Annals of the New York Academy of Sciences|January 1, 1985
A model for hemoglobin F synthesis in adult life: evidence for regulation at the level of erythroblastsC Peschle, A R Migliaccio, G Migliaccio, et al.
Blood|December 1, 1989
Granulocyte-macrophage colony-stimulating factor reactivates fetal hemoglobin synthesis in erythroblast clones from normal adultsM Gabbianelli, E Pelosi, E Bassano, et al.
Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson diseaseV Scornaienchi, G Nicoletti, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
Parkinsonism & Related Disorders|August 30, 2008
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonismPatrizia Tarantino, Donatella Civitelli, Ferdinanda Annesi, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseasePatrizia Tarantino, I C Cirò Candiano, F Annesi, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancyGiovanni Provenzano, E Mannarino, F Annesi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2007
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern ItalyElvira V De Marco, Grazia Annesi, Patrizia Tarantino, et al.
Clinical Genetics|May 2, 2007
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's diseaseD Civitelli, P Tarantino, G Nicoletti, et al.
Pageof 6