http://www.cnr.it/ontology/cnr/individuo/unitaDiPersonaleInterno/MATRICOLA10890
PATRIZIA TARANTINO
- Type
- Label
- PATRIZIA TARANTINO (literal)
- PATRIZIA TARANTINO (literal)
- Http://www.w3.org/2002/07/owl#sameAs
- Persona in rapporto
- Autore CNR di
- Spinocerebellar ataxia type 7: report of a new Italian family. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- 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)
- Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- PCDH19 mutations in female patients from Southern Italy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association study between HFE, TF, TFR1 genes and Parkinson disease. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. (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)
- MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- 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)
- GENETIC STUDY OF SCN1A-RELATED EPILEPSIES IN SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- ANALISI CLINICO-GENETICA IN UNA FAMIGLIA ITALIANA CON ATASSIA SPINOCEREBELLARE AUTOSOMICO-DOMINANTE (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)
- Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- 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)
- Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. (Articolo in rivista) (Prodotto della ricerca)
- Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association study between the LINGO1 gene and Parkinsons disease in the Italian population (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- 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)
- Fraxe intermediate alleles are associated with Parkinson's disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
- 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)
- Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population (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)
- 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)
- Clinical and genetic analysis of a four-generation family with autosomal dominant cerebellar ataxia (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- 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)
- ROUTINE MRI MEASUREMENT OF THE BRAINSTEM STRUCTURES IN PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE 1 AND 2 ON: CORRELATION WITH CLINICAL AND GENETIC DATA (Comunicazione a convegno) (Prodotto della ricerca)
- Screening of genes causing Huntington disease like phenotype. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Molecular studies of the PANK2 gene in patients with PKAN (Abstract/Poster in atti di convegno) (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)
- 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)
- Dentatorubral pallidoluysian atrophy: clinical and genetic analysis of a Sicilian pedigree (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS (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 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)
- Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). (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)
- Coautore
- Nome
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- Afferisce a
- Ha pubblicazioni con
Incoming links:
- Coautore
- Ha pubblicazioni con
- Ha afferente
- Rapporto con persona
- Autore CNR
- Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (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)
- Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association study between the LINGO1 gene and Parkinsons disease in the Italian population (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- 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)
- Fragile X premutation alleles in movement disorders. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Clinical and genetic analysis of a four-generation family with autosomal dominant cerebellar ataxia (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)
- Fraxe intermediate alleles are associated with Parkinson's disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
- Dentatorubral pallidoluysian atrophy: clinical and genetic analysis of a Sicilian pedigree (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)
- Screening of genes causing Huntington disease like phenotype. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- ROUTINE MRI MEASUREMENT OF THE BRAINSTEM STRUCTURES IN PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE 1 AND 2 ON: CORRELATION WITH CLINICAL AND GENETIC DATA (Comunicazione a convegno) (Prodotto della ricerca)
- DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS (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)
- G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSONS DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). (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)
- 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)
- GENETIC STUDY OF SCN1A-RELATED EPILEPSIES IN SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- 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)
- MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY (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)
- Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. (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)
- Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- ANALISI CLINICO-GENETICA IN UNA FAMIGLIA ITALIANA CON ATASSIA SPINOCEREBELLARE AUTOSOMICO-DOMINANTE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
- 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)
- 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)
- Spinocerebellar ataxia type 7: report of a new Italian family. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. (Articolo in rivista) (Prodotto della ricerca)
- An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. (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)
- PCDH19 mutations in female patients from Southern Italy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)