LA BELLA, Vincenzo
LA BELLA, Vincenzo
Biomedicina, Neuroscienze e Diagnostica avanzata
A CERVICAL MYELOPATHY WITH A HIRAYAMA DISEASE-LIKE PHENOTYPE
2008-01-01 CERAMI,C; VALENTINO,F; PICCOLI,F; LA BELLA,V
A Deletion of the Nuclear Localization Signal Domain in the Fus Protein Induces Stable Post-stress Cytoplasmic Inclusions in SH-SY5Y Cells
2021-12-23 Notaro A.; Messina A.; La Bella V.
A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis
2023-07-18 Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavallaro
A Human-Humanoid Interaction through the use of BCI for Locked-In ALS Patients using neuro-biological feedback fusion
2018-01-01 Sorbello, R.; Tramonte, S.; Giardina, M.; La Bella, V.; Spataro, R.; Allison, B.; Guger, C.; Chella, A.
A NOVEL ANGIOGENIN GENE MUTATION IN A SPORADIC PATIENT WITH AMYOTROPHIC LATERAL SCLEROSIS FROM SOUTHERN ITALY
2008-01-01 Conforti, F.; Sprovieri, T.; Mazzei, R.; Ungaro, C.; LA BELLA, V.; Tessitore, A.; Patitucci, A.; Magariello, A.; Gabriele, A.; Tedeschi, G.; Simone, I.; Majorana, G.; Valentino, P.; Condino, F.; Bono, F.; Monsurro, M.; Muglia, M.; Quattrone, A.
A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review
2022-01-01 salvatore iacono, elda del giudice, albertya leon, vincenzo la bella, rossella spataro
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease
2004-01-01 LA BELLA V; LIGUORI M; CITTADELLA R; SETTIPANI N; PICCOLI T; MANNA I; QUATTRONE A; PICCOLI F
A novel S379A TARDBP mutation associated to late-onset sporadic ALS
2019-01-01 Sprovieri T.; Ungaro C.; Perrone B.; Naimo G.D.; Spataro R.; Cavallaro S.; La Bella V.; Conforti F.L.
A PATIENT WITH FRONTOTEMPORAL DEMENTIA (FTD) AND MOTOR NEURON DISEASE (MND) CARRYING THE INTRON10+29 SUBSTITUTION IN MAPT
2008-01-01 CUPIDI, C; MANNA, I; ROSSI, G; CITTADELLA, R; GIACCONE, G; GRIMALDI, G; BUGIANI, O; LA BELLA, V; PICCOLI, F; PICCOLI, T
A PATIENT WITH FRONTOTEMPORAL DEMENTIA (FTD) AND MOTOR NEURON DISEASE (MND) CARRYING THE INTRON10+29 SUBSTITUTION IN MAPT .
2008-01-01 CUPIDI, C; MANNA, I; ROSSI, G; CITTADELLA, R; GIACCONE, G; GRIMALDI, G; BUGIANI, O; LA BELLA, V; PICCOLI, F; PICCOLI, T
A PHASE I-II MULTICENTRE STUDY ON G-CSF IN AMYOTROPHIC LATERAL SCLEROSIS (STEMALS)
2008-01-01 CHIÒ A; MORA G; CAPONNETTO C; SICILIANO G; SABATELLI M; LA BELLA V; SILANI V; MOGLIA C; MANCARDI GL; TONALI P; CALVO A; MUTANI R; CORBO M; SCIMÉ R; DONOFRIO G; PETRINI M; MELAZZINI M; GUALANDI F; TARELLA C
A PHASE I-II MULTICENTRE STUDY ON G-CSF IN AMYOTROPHIC LATERAL SCLEROSIS
2007-01-01 CHIÒ A; MORA G; CAPONNETTO C; SICILIANO G; SABATELLI M; LA BELLA V; SILANI V; MOGLIA C; TONALI P; MANCARDI GL; CALVO A; MUTANI R; CORBO M; SCIMÉ R; LEONE G; PETRINI M; GUALANDI F; MELAZZINI M; TARELLA C
A rapidly progressive motor neuron disease associated to a natural killer cells leukaemia
2019-01-01 La Bella V.; Iannitto E.; Cuffaro L.; Spataro R.
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
2009-01-01 Chiò,A; Schymick,JC; Restagno,G; Scholz,SW; Lombardo ,F; Lai ,SL; Mora ,G; Fung ,HC; Britton ,A; Arepalli ,S; Gibbs ,JR; Nalls ,M; Berger ,S; Kwee ,LC; Oddone ,EZ; Ding ,J; Crews ,C; Rafferty ,I; Washecka ,N; Hernandez ,D; Ferrucci ,L; Bandinelli ,S; GuralMnik ,J; Macciardi ,F; Torri ,F; Lupoli ,S; Chanock ,SJ; Thomas ,G; Hunter ,DJ; Gieger ,C; Wichmann ,HE; Calvo ,A; Mutani ,R; Battistini ,S; Giannini ,F; Caponnetto ,C; Mancardi ,GL; La Bella ,V; Valentino ,F; Monsurrò ,MR; Tedeschi ,G; Marinou ,K; Sabatelli ,M; Conte ,A; Mandrioli ,J; Sola ,P; Salvi ,F; Bartolomei ,I; Siciliano ,G; Carlesi ,C; Orrell ,RW; Talbot ,K; Simmons ,Z; Connor ,J; Pioro ,EP; Dunkley ,T; Stephan ,DA; Kasperaviciute ,D; Fisher ,EM; Jabonka ,S; Sendtner ,M; Beck ,M; Bruijn ,L; Rothstein ,J; Schmidt ,S; Singleton ,A; Hardy ,J; Traynor,BJ.
ACUTE REVERSIBLE PARKINSONISM IN A DIABETIC UREMIC PATIENT
2004-01-01 C CUPIDI; F PICCOLI; LA BELLA V
ACUTE REVERSIBLE PARKINSONISM IN A DIABETIC-UREMIC PATIENT
2006-01-01 CUPIDI C; PICCOLI F; LA BELLA V
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation
2022-12-01 Romano, Roberta; De Luca, Maria; Del Fiore, Victoria Stefania; Pecoraro, Martina; Lattante, Serena; Sabatelli, Mario; La Bella, Vincenzo; Bucci, Cecilia
ALS monocyte-derived microglia-like cells reveal cytoplasmic TDP-43 accumulation, DNA damage, and cell-specific impairment of phagocytosis associated with disease progression
2022-02-01 Quek H, Cuní-López C, Stewart R, Colletti T, Notaro A, Nguyen TH, Sun Y, Guo CC, Lupton MK, Roberts TL, Lim YC, Oikari LE, La Bella V, White AR
ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles
2019-01-01 An H.; Skelt L.; Notaro A.; Highley J.R.; Fox A.H.; La Bella V.; Buchman V.L.; Shelkovnikova T.A.
ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers
2017-01-01 Lo Bello M.; Di Fini F.; Notaro A.; Spataro R.; Conforti F.L.; La Bella V.
| Data di pubblicazione | Titolo | Autori | Tipologia | Autore(i) | File |
|---|---|---|---|---|---|
| 1-gen-2008 | A CERVICAL MYELOPATHY WITH A HIRAYAMA DISEASE-LIKE PHENOTYPE | CERAMI, ChiaraVALENTINO, FrancescaPICCOLI, FedericoLA BELLA, Vincenzo | 01 - Contributo in rivista::1.01 Articolo in rivista | CERAMI,C; VALENTINO,F; PICCOLI,F; LA BELLA,V | |
| 23-dic-2021 | A Deletion of the Nuclear Localization Signal Domain in the Fus Protein Induces Stable Post-stress Cytoplasmic Inclusions in SH-SY5Y Cells | Notaro A.La Bella V. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Notaro A.; Messina A.; La Bella V. | |
| 18-lug-2023 | A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis | Vincenzo La Bella + | 01 - Contributo in rivista::1.01 Articolo in rivista | Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavallaro | |
| 1-gen-2018 | A Human-Humanoid Interaction through the use of BCI for Locked-In ALS Patients using neuro-biological feedback fusion | SORBELLO, RosarioTramonte, SalvatoreGIARDINA, Marcello EmanueleLA BELLA, VincenzoSPATARO, RossellaCHELLA, Antonio + | 01 - Contributo in rivista::1.01 Articolo in rivista | Sorbello, R.; Tramonte, S.; Giardina, M.; La Bella, V.; Spataro, R.; Allison, B.; Guger, C.; Chella, A. | |
| 1-gen-2008 | A NOVEL ANGIOGENIN GENE MUTATION IN A SPORADIC PATIENT WITH AMYOTROPHIC LATERAL SCLEROSIS FROM SOUTHERN ITALY | LA BELLA, Vincenzo + | 01 - Contributo in rivista::1.01 Articolo in rivista | Conforti, F.; Sprovieri, T.; Mazzei, R.; Ungaro, C.; LA BELLA, V.; Tessitore, A.; Patitucci, A.; Magariello, A.; Gabriele, A.; Tedeschi, G.; Simone, I.; Majorana, G.; Valentino, P.; Condino, F.; Bono, F.; Monsurro, M.; Muglia, M.; Quattrone, A. | |
| 1-gen-2022 | A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review | salvatore iaconovincenzo la bellarossella spataro + | 01 - Contributo in rivista::1.01 Articolo in rivista | salvatore iacono, elda del giudice, albertya leon, vincenzo la bella, rossella spataro | |
| 1-gen-2004 | A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease | LA BELLA, VincenzoPICCOLI, TommasoPICCOLI, Federico + | 01 - Contributo in rivista::1.01 Articolo in rivista | LA BELLA V; LIGUORI M; CITTADELLA R; SETTIPANI N; PICCOLI T; MANNA I; QUATTRONE A; PICCOLI F | |
| 1-gen-2019 | A novel S379A TARDBP mutation associated to late-onset sporadic ALS | La Bella V. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Sprovieri T.; Ungaro C.; Perrone B.; Naimo G.D.; Spataro R.; Cavallaro S.; La Bella V.; Conforti F.L. | |
| 1-gen-2008 | A PATIENT WITH FRONTOTEMPORAL DEMENTIA (FTD) AND MOTOR NEURON DISEASE (MND) CARRYING THE INTRON10+29 SUBSTITUTION IN MAPT | CUPIDI, ChiaraROSSI, Giacomo GiuseppeGRIMALDI, GiulianaLA BELLA, VincenzoPICCOLI, FedericoPICCOLI, Tommaso + | 10 - Proceedings::Proceedings | CUPIDI, C; MANNA, I; ROSSI, G; CITTADELLA, R; GIACCONE, G; GRIMALDI, G; BUGIANI, O; LA BELLA, V; PICCOLI, F; PICCOLI, T | |
| 1-gen-2008 | A PATIENT WITH FRONTOTEMPORAL DEMENTIA (FTD) AND MOTOR NEURON DISEASE (MND) CARRYING THE INTRON10+29 SUBSTITUTION IN MAPT . | CUPIDI, ChiaraROSSI, Giacomo GiuseppeGRIMALDI, GiulianaLA BELLA, VincenzoPICCOLI, FedericoPICCOLI, Tommaso + | 10 - Proceedings::Proceedings | CUPIDI, C; MANNA, I; ROSSI, G; CITTADELLA, R; GIACCONE, G; GRIMALDI, G; BUGIANI, O; LA BELLA, V; PICCOLI, F; PICCOLI, T | |
| 1-gen-2008 | A PHASE I-II MULTICENTRE STUDY ON G-CSF IN AMYOTROPHIC LATERAL SCLEROSIS (STEMALS) | CAPONNETTO, ChiaraLA BELLA, Vincenzo + | 10 - Proceedings::Proceedings | CHIÒ A; MORA G; CAPONNETTO C; SICILIANO G; SABATELLI M; LA BELLA V; SILANI V; MOGLIA C; MANCARDI GL; TONALI P; CALVO A; MUTANI R; CORBO M; SCIMÉ R; DONOFRIO G; PETRINI M; MELAZZINI M; GUALANDI F; TARELLA C | |
| 1-gen-2007 | A PHASE I-II MULTICENTRE STUDY ON G-CSF IN AMYOTROPHIC LATERAL SCLEROSIS | CAPONNETTO, ChiaraLA BELLA, Vincenzo + | 10 - Proceedings::Proceedings | CHIÒ A; MORA G; CAPONNETTO C; SICILIANO G; SABATELLI M; LA BELLA V; SILANI V; MOGLIA C; TONALI P; MANCARDI GL; CALVO A; MUTANI R; CORBO M; SCIMÉ R; LEONE G; PETRINI M; GUALANDI F; MELAZZINI M; TARELLA C | |
| 1-gen-2019 | A rapidly progressive motor neuron disease associated to a natural killer cells leukaemia | La Bella V.Iannitto E.Cuffaro L.Spataro R. | 01 - Contributo in rivista::1.01 Articolo in rivista | La Bella V.; Iannitto E.; Cuffaro L.; Spataro R. | |
| 1-gen-2009 | A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. | LA BELLA, VincenzoVALENTINO, Francesca + | 01 - Contributo in rivista::1.01 Articolo in rivista | Chiò,A; Schymick,JC; Restagno,G; Scholz,SW; Lombardo ,F; Lai ,SL; Mora ,G; Fung ,HC; Britton ,A; Arepalli ,S; Gibbs ,JR; Nalls ,M; Berger ,S; Kwee ,LC; Oddone ,EZ; Ding ,J; Crews ,C; Rafferty ,I; Washecka ,N; Hernandez ,D; Ferrucci ,L; Bandinelli ,S; GuralMnik ,J; Macciardi ,F; Torri ,F; Lupoli ,S; Chanock ,SJ; Thomas ,G; Hunter ,DJ; Gieger ,C; Wichmann ,HE; Calvo ,A; Mutani ,R; Battistini ,S; Giannini ,F; Caponnetto ,C; Mancardi ,GL; La Bella ,V; Valentino ,F; Monsurrò ,MR; Tedeschi ,G; Marinou ,K; Sabatelli ,M; Conte ,A; Mandrioli ,J; Sola ,P; Salvi ,F; Bartolomei ,I; Siciliano ,G; Carlesi ,C; Orrell ,RW; Talbot ,K; Simmons ,Z; Connor ,J; Pioro ,EP; Dunkley ,T; Stephan ,DA; Kasperaviciute ,D; Fisher ,EM; Jabonka ,S; Sendtner ,M; Beck ,M; Bruijn ,L; Rothstein ,J; Schmidt ,S; Singleton ,A; Hardy ,J; Traynor,BJ. | |
| 1-gen-2004 | ACUTE REVERSIBLE PARKINSONISM IN A DIABETIC UREMIC PATIENT | CUPIDI, ChiaraPICCOLI, FedericoLA BELLA, Vincenzo | 10 - Proceedings::Proceedings | C CUPIDI; F PICCOLI; LA BELLA V | |
| 1-gen-2006 | ACUTE REVERSIBLE PARKINSONISM IN A DIABETIC-UREMIC PATIENT | CUPIDI, ChiaraPICCOLI, FedericoLA BELLA, Vincenzo | 01 - Contributo in rivista::1.01 Articolo in rivista | CUPIDI C; PICCOLI F; LA BELLA V | |
| 1-dic-2022 | Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation | Romano, RobertaPecoraro, MartinaLa Bella, VincenzoBucci, Cecilia + | 01 - Contributo in rivista::1.01 Articolo in rivista | Romano, Roberta; De Luca, Maria; Del Fiore, Victoria Stefania; Pecoraro, Martina; Lattante, Serena; Sabatelli, Mario; La Bella, Vincenzo; Bucci, Cecilia | |
| 1-feb-2022 | ALS monocyte-derived microglia-like cells reveal cytoplasmic TDP-43 accumulation, DNA damage, and cell-specific impairment of phagocytosis associated with disease progression | Colletti TNotaro ALa Bella V + | 01 - Contributo in rivista::1.01 Articolo in rivista | Quek H, Cuní-López C, Stewart R, Colletti T, Notaro A, Nguyen TH, Sun Y, Guo CC, Lupton MK, Roberts TL, Lim YC, Oikari LE, La Bella V, White AR | |
| 1-gen-2019 | ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles | Notaro A.La Bella V. + | 01 - Contributo in rivista::1.01 Articolo in rivista | An H.; Skelt L.; Notaro A.; Highley J.R.; Fox A.H.; La Bella V.; Buchman V.L.; Shelkovnikova T.A. | |
| 1-gen-2017 | ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers | Lo Bello M.Di Fini F.Notaro A.Spataro R.La Bella V. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Lo Bello M.; Di Fini F.; Notaro A.; Spataro R.; Conforti F.L.; La Bella V. |