Sfoglia per Autore
A Focus on the Beneficial Effects of Alpha Synuclein and a Re-Appraisal of Synucleinopathies
2018 Ryskalin, Larisa; Busceti, Carla L; Limanaqi, Fiona; Biagioni, Francesca; Gambardella, Stefano; Fornai, Francesco
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease
2018 Ferese, Rosangela; Scala, Simona; Biagioni, Francesca; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Colonnese, Claudio; Storto, Marianna; Fornai, Francesco; Novelli, Giuseppe; Ruggieri, Stefano; Gambardella, Stefano
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report
2018 Perrotta, Armando; Gambardella, Stefano; Ambrosini, Anna; Anastasio, Maria Grazia; Albano, Veronica; Fornai, Francesco; Pierelli, Francesco
Circulating miR-127-3p as a Potential Biomarker for Differential Diagnosis in Frontotemporal Dementia
2018 Piscopo, Paola; Grasso, Margherita; Puopolo, Maria; D'Acunto, Emanuela; Talarico, Giuseppina; Crestini, Alessio; Gasparini, Marina; Campopiano, Rosa; Gambardella, Stefano; Castellano, Anna Elisa; Bruno, Giuseppe; Denti, Michela A; Confaloni, Annamaria
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect
2018 Ferese, Rosangela; Bonetti, Monica; Consoli, Federica; Guida, Valentina; Sarkozy, Anna; Lepri, Francesca Romana; Versacci, Paolo; Gambardella, Stefano; Calcagni, Giulio; Margiotti, Katia; Piceci Sparascio, Francesca; Hozhabri, Hossein; Mazza, Tommaso; Digilio, Maria Cristina; Dallapiccola, Bruno; Tartaglia, Marco; Marino, Bruno; Hertog, Jeroen den; De Luca, Alessandro
Erratum to "Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease"
2018 Gambardella, Stefano; Ferese, Rosangela; Scala, Simona; Carboni, Stefania; Biagioni, Francesca; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Fabbiano, Francesco; Fornai, Francesco; Centonze, Diego; Ruggieri, Stefano
Revisiting the gamma loop in ALS
2017 Limanaqi, Fiona; Gambardella, Stefano; Lazzeri, Gloria; Ferrucci, Michela; Ruggieri, Stefano; Fornai, Francesco
Next Generation Sequencing and ALS: known genes, different phenotyphes
2017 Campopiano, Rosa; Ryskalin, Larisa; Giardina, Emiliano; Zampatti, Stefania; Busceti, Carla L; Biagioni, Francesca; Ferese, Rosangela; Storto, Marianna; Gambardella, Stefano; Fornai, Francesco
Neurons other than motor neurons in motor neuron disease
2017 Ruffoli, R; Biagioni, F; Busceti, Cl; Gaglione, A; Ryskalin, L; Gambardella, S; Frati, A; Fornai, F
Severe and rapidly-progressive Lafora disease associated with NHLRC1 mutation: a case report
2017 Casciato, S; Gambardella, S; Mascia, A; Quarato, Po; D'Aniello, A; Ackurina, Y; Albano, V; Fornai, F; Scala, S; Di Gennaro, G
Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion
2017 De Cinque, Marianna; Palumbo, Orazio; Mazzucco, Ermelinda; Simone, Antonella; Palumbo, Pietro; Ciavatta, Renata; Maria, Giuliana; Ferese, Rosangela; Gambardella, Stefano; Angiolillo, Antonella; Carella, Massimo; Garofalo, Silvio
Rapamycin promotes differentiation increasing beta III-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells
2017 Ferrucci, M; Biagioni, F; Lenzi, P; Gambardella, S; Ferese, R; Calierno, Mt; Falleni, A; Grimaldi, A; Frati, A; Esposito, V; Limatola, C; Fornai, F
PCR-based approach for qualitative molecular analysis of six neurotropic pathogens
2017 Ferese, R; Scorzolini, L; Campopiano, R; Albano, V; Griguoli, A M; Giardina, E; Scala, S; Ryskalin, L; D'Alessio, C; Zampatti, S; Fantozzi, R; Storto, M; Fornai, F; Gambardella, S
Methamphetamine increases Prion Protein and induces dopamine-dependent expression of protease resistant PrPsc
2017 Ferrucci, M; Ryskalin, L; Biagioni, F; Gambardella, S; Busceti, Cl; Falleni, A; Lazzeri, G; Fornai, F
mTOR-Dependent Cell Proliferation in the Brain
2017 Ryskalin, L; Lazzeri, G; Flaibani, M; Biagioni, F; Gambardella, S; Frati, A; Fornai, F
Loud Noise Exposure Produces DNA, Neurotransmitter and Morphological Damage within Specific Brain Areas
2017 Frenzilli, G; Ryskalin, L; Ferrucci, M; Cantafora, E; Chelazzi, S; Giorgi, Fs; Lenzi, P; Scarcelli, V; Frati, A; Biagioni, F; Gambardella, S; Falleni, A; Fornai, F
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing
2017 Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, L T; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease)
2017 Ferese, Rosangela; Albano, Veronica; Falconi, Mattia; Iacovelli, Federico; Campopiano, Rosa; Scala, Simona; Griguoli, Anna Maria; Gaglione, Anderson; Giardina, Emiliano; Zampatti, Stefania; Storto, Marianna; Fornai, Francesco; D'Alessio, Carmelo; Novelli, Giuseppe; Gambardella, Stefano
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity
2017 Gambardella, S; Ferese, R; Biagioni, F; Busceti, Cl; Campopiano, R; Griguoli, Amp; Limanaqi, F; Novelli, G; Storto, M; Fornai, F
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS)
2016 Ferese, R; Zampatti, S; Griguoli, Amp; Fornai, F; Giardina, E; Barrano, G; Albano, V; Campopiano, R; Scala, S; Novelli, G; Gambardella, S
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A Focus on the Beneficial Effects of Alpha Synuclein and a Re-Appraisal of Synucleinopathies | 1-gen-2018 | Ryskalin, Larisa; Busceti, Carla L; Limanaqi, Fiona; Biagioni, Francesca; Gambardella, Stefano; Fornai, Francesco | |
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease | 1-gen-2018 | Ferese, Rosangela; Scala, Simona; Biagioni, Francesca; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Colonnese, Claudio; Storto, Marianna; Fornai, Francesco; Novelli, Giuseppe; Ruggieri, Stefano; Gambardella, Stefano | |
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report | 1-gen-2018 | Perrotta, Armando; Gambardella, Stefano; Ambrosini, Anna; Anastasio, Maria Grazia; Albano, Veronica; Fornai, Francesco; Pierelli, Francesco | |
Circulating miR-127-3p as a Potential Biomarker for Differential Diagnosis in Frontotemporal Dementia | 1-gen-2018 | Piscopo, Paola; Grasso, Margherita; Puopolo, Maria; D'Acunto, Emanuela; Talarico, Giuseppina; Crestini, Alessio; Gasparini, Marina; Campopiano, Rosa; Gambardella, Stefano; Castellano, Anna Elisa; Bruno, Giuseppe; Denti, Michela A; Confaloni, Annamaria | |
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect | 1-gen-2018 | Ferese, Rosangela; Bonetti, Monica; Consoli, Federica; Guida, Valentina; Sarkozy, Anna; Lepri, Francesca Romana; Versacci, Paolo; Gambardella, Stefano; Calcagni, Giulio; Margiotti, Katia; Piceci Sparascio, Francesca; Hozhabri, Hossein; Mazza, Tommaso; Digilio, Maria Cristina; Dallapiccola, Bruno; Tartaglia, Marco; Marino, Bruno; Hertog, Jeroen den; De Luca, Alessandro | |
Erratum to "Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease" | 1-gen-2018 | Gambardella, Stefano; Ferese, Rosangela; Scala, Simona; Carboni, Stefania; Biagioni, Francesca; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Fabbiano, Francesco; Fornai, Francesco; Centonze, Diego; Ruggieri, Stefano | |
Revisiting the gamma loop in ALS | 1-gen-2017 | Limanaqi, Fiona; Gambardella, Stefano; Lazzeri, Gloria; Ferrucci, Michela; Ruggieri, Stefano; Fornai, Francesco | |
Next Generation Sequencing and ALS: known genes, different phenotyphes | 1-gen-2017 | Campopiano, Rosa; Ryskalin, Larisa; Giardina, Emiliano; Zampatti, Stefania; Busceti, Carla L; Biagioni, Francesca; Ferese, Rosangela; Storto, Marianna; Gambardella, Stefano; Fornai, Francesco | |
Neurons other than motor neurons in motor neuron disease | 1-gen-2017 | Ruffoli, R; Biagioni, F; Busceti, Cl; Gaglione, A; Ryskalin, L; Gambardella, S; Frati, A; Fornai, F | |
Severe and rapidly-progressive Lafora disease associated with NHLRC1 mutation: a case report | 1-gen-2017 | Casciato, S; Gambardella, S; Mascia, A; Quarato, Po; D'Aniello, A; Ackurina, Y; Albano, V; Fornai, F; Scala, S; Di Gennaro, G | |
Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion | 1-gen-2017 | De Cinque, Marianna; Palumbo, Orazio; Mazzucco, Ermelinda; Simone, Antonella; Palumbo, Pietro; Ciavatta, Renata; Maria, Giuliana; Ferese, Rosangela; Gambardella, Stefano; Angiolillo, Antonella; Carella, Massimo; Garofalo, Silvio | |
Rapamycin promotes differentiation increasing beta III-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells | 1-gen-2017 | Ferrucci, M; Biagioni, F; Lenzi, P; Gambardella, S; Ferese, R; Calierno, Mt; Falleni, A; Grimaldi, A; Frati, A; Esposito, V; Limatola, C; Fornai, F | |
PCR-based approach for qualitative molecular analysis of six neurotropic pathogens | 1-gen-2017 | Ferese, R; Scorzolini, L; Campopiano, R; Albano, V; Griguoli, A M; Giardina, E; Scala, S; Ryskalin, L; D'Alessio, C; Zampatti, S; Fantozzi, R; Storto, M; Fornai, F; Gambardella, S | |
Methamphetamine increases Prion Protein and induces dopamine-dependent expression of protease resistant PrPsc | 1-gen-2017 | Ferrucci, M; Ryskalin, L; Biagioni, F; Gambardella, S; Busceti, Cl; Falleni, A; Lazzeri, G; Fornai, F | |
mTOR-Dependent Cell Proliferation in the Brain | 1-gen-2017 | Ryskalin, L; Lazzeri, G; Flaibani, M; Biagioni, F; Gambardella, S; Frati, A; Fornai, F | |
Loud Noise Exposure Produces DNA, Neurotransmitter and Morphological Damage within Specific Brain Areas | 1-gen-2017 | Frenzilli, G; Ryskalin, L; Ferrucci, M; Cantafora, E; Chelazzi, S; Giorgi, Fs; Lenzi, P; Scarcelli, V; Frati, A; Biagioni, F; Gambardella, S; Falleni, A; Fornai, F | |
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing | 1-gen-2017 | Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, L T; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E | |
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease) | 1-gen-2017 | Ferese, Rosangela; Albano, Veronica; Falconi, Mattia; Iacovelli, Federico; Campopiano, Rosa; Scala, Simona; Griguoli, Anna Maria; Gaglione, Anderson; Giardina, Emiliano; Zampatti, Stefania; Storto, Marianna; Fornai, Francesco; D'Alessio, Carmelo; Novelli, Giuseppe; Gambardella, Stefano | |
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity | 1-gen-2017 | Gambardella, S; Ferese, R; Biagioni, F; Busceti, Cl; Campopiano, R; Griguoli, Amp; Limanaqi, F; Novelli, G; Storto, M; Fornai, F | |
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) | 1-gen-2016 | Ferese, R; Zampatti, S; Griguoli, Amp; Fornai, F; Giardina, E; Barrano, G; Albano, V; Campopiano, R; Scala, S; Novelli, G; Gambardella, S |
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