http://www.cnr.it/ontology/cnr/individuo/unitaDiPersonaleEsterno/ID9392
VITTORIO SCORNAIENCHI
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- VITTORIO SCORNAIENCHI (literal)
- VITTORIO SCORNAIENCHI (literal)
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- ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSONS DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- PARKIN, PINK1 AND DJ-1 HETEROZYGOUS MUTATIONS IN SOUTHERN ITALIAN PATIENTS WITH EARLY-ONSET PARKINSONISM (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Association study between HFE, TF, TFR1 genes and Parkinson disease. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- PINK1 mutations and the risk of Parkinsons disease in family members of Southern Italy (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Pink1 mutations and the risk of Parkinsons disease in family members of Southern Italy (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- Mitochondrial DNA haplogroups and the risk of Parkinson disease in a cohort of patients from South Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Fragile X premutation alleles in movement disorders. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- GIGYF2 (TRNC15) mutation analysis in patients with familial Parkinsons disease with autosomal-dominant transmission. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Association study between HFE, TF, TFR genes and Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Genetic analysis of SCA2 and SCA17 in familial Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Genetic analysis of SCA2 and SCA17 in familial Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Mutational Analysis of the DCX, LIS1 and FLNA genes in patients with neuronal migration disorder from Southern Italy. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Alpha synuclein in familial parkinsons disease and lewy body dementia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- G-463A myeloperoxidase polymorphism and parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mutational analysis of the DCX and LIS1 genes in patients with Lissencephaly and Subcortical band heterotopia from Southern Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- LRRK2 mutation analysis in a cohort of Parkinsons Disease patients with a dominant pattern of inheritance from Southern Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Association study between G-protein-coupled receptor kinase 5 gene and Parkinsons disease (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Molecular studies of the PANK2 gene in patients with PKAN (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- FRAGILE X PREMUTATION ALLELES IN MOVEMENT DISORDERS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- TWO NOVEL PCDH19 MUTATIONS IN DRAVET SYNDROME (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY (Abstract/Comunicazione in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1305)
- Analisi mutazionale del gene GIGYF2 (TRNC15) in pazienti con malattia di Parkinson con trasmissione autosomica dominante. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Alpha-synuclein in familial Parkinsons disease and Lewy Body Dementia (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- FREQUENZA DELLE MUTAZIONI IN ETEROZIGOSI NEI GENI PARK2 PINK1 E DJ-1 IN PAZIENTI DEL SUD-ITALIA CON MALATTIA DI PARKINSON AD ESORDIO PRECOCE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Frequency analysis of autosomal dominant spinocerebellar ataxia (AD-SCA) in the patients from southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- A functional G-463A polymorphism in the myeloperoxidase gene promoter and Parkinsons disease (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- STUDIO DI ASSOCIAZIONE TRA I GENI HFE, TF, TFR E LA MALATTIA DI PARKINSON (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Fragile X premutation alleles in movement disorders. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- ANALISI MUTAZIONALE DEI GENI RESPONSABILI DELLA MALATTIA DI PARKINSON AD ESORDIO PRECOCE IN UNA POPOLAZIONE DEL SUD ITALIA (Abstract/Poster in convegno) (Prodotto della ricerca)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. (Articolo in rivista) (Prodotto della ricerca)
- LRRK2 exons 31, 34, 35, 38 and 48 mutation analysis in a cohort of PD patients with a dominant pattern of inheritance from South Italy. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- DJ-1 is a Parkinson's disease susceptibility gene in southern Italy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
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- Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. (Articolo in rivista) (Prodotto della ricerca)
- Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- Pink1 mutations and the risk of Parkinsons disease in family members of Southern Italy (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- Frequency analysis of autosomal dominant spinocerebellar ataxia (AD-SCA) in the patients from southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Fragile X premutation alleles in movement disorders. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- A functional G-463A polymorphism in the myeloperoxidase gene promoter and Parkinsons disease (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- STUDIO DI ASSOCIAZIONE TRA I GENI HFE, TF, TFR E LA MALATTIA DI PARKINSON (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- ANALISI MUTAZIONALE DEI GENI RESPONSABILI DELLA MALATTIA DI PARKINSON AD ESORDIO PRECOCE IN UNA POPOLAZIONE DEL SUD ITALIA (Abstract/Poster in convegno) (Prodotto della ricerca)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Association study between HFE, TF, TFR genes and Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Genetic analysis of SCA2 and SCA17 in familial Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Genetic analysis of SCA2 and SCA17 in familial Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Mutational Analysis of the DCX, LIS1 and FLNA genes in patients with neuronal migration disorder from Southern Italy. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Association study between G-protein-coupled receptor kinase 5 gene and Parkinsons disease (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Mutational analysis of the DCX and LIS1 genes in patients with Lissencephaly and Subcortical band heterotopia from Southern Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- LRRK2 mutation analysis in a cohort of Parkinsons Disease patients with a dominant pattern of inheritance from Southern Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Molecular studies of the PANK2 gene in patients with PKAN (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- TWO NOVEL PCDH19 MUTATIONS IN DRAVET SYNDROME (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY (Abstract/Comunicazione in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1305)
- G-463A myeloperoxidase polymorphism and parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- FRAGILE X PREMUTATION ALLELES IN MOVEMENT DISORDERS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Alpha-synuclein in familial Parkinsons disease and Lewy Body Dementia (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- FREQUENZA DELLE MUTAZIONI IN ETEROZIGOSI NEI GENI PARK2 PINK1 E DJ-1 IN PAZIENTI DEL SUD-ITALIA CON MALATTIA DI PARKINSON AD ESORDIO PRECOCE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Analisi mutazionale del gene GIGYF2 (TRNC15) in pazienti con malattia di Parkinson con trasmissione autosomica dominante. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Ceruloplasmin gene variations and Parkinsons disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Alpha synuclein in familial parkinsons disease and lewy body dementia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSONS DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- PARKIN, PINK1 AND DJ-1 HETEROZYGOUS MUTATIONS IN SOUTHERN ITALIAN PATIENTS WITH EARLY-ONSET PARKINSONISM (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Association study between HFE, TF, TFR1 genes and Parkinson disease. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- PINK1 mutations and the risk of Parkinsons disease in family members of Southern Italy (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Fragile X premutation alleles in movement disorders. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Mitochondrial DNA haplogroups and the risk of Parkinson disease in a cohort of patients from South Italy (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- GIGYF2 (TRNC15) mutation analysis in patients with familial Parkinsons disease with autosomal-dominant transmission. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinsons disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- LRRK2 exons 31, 34, 35, 38 and 48 mutation analysis in a cohort of PD patients with a dominant pattern of inheritance from South Italy. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- DJ-1 is a Parkinson's disease susceptibility gene in southern Italy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)