UNGARO, CARMINE
UNGARO, CARMINE
Istituto sull'Inquinamento Atmosferico - IIA - Sede Secondaria Rende
Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis
2020 Ungaro Carmine; Sprovieri Teresa; Morello Giovanna; Perrone Benedetta; Spampinato Antonio Gianmaria; Simone Isabella Laura; Trojsi Francesca; Monsurrò Maria Rosaria; Spataro Rossella; La Bella Vincenzo; Andò Sebastiano; Cavallaro Sebastiano; Conforti Francesca Luisa;
A novel S379A TARDBP mutation associated to late-onset sporadic ALS
2019 Sprovieri, Teresa; Ungaro, Carmine; Perrone, Benedetta; Naimo, Giuseppina Daniela; Spataro, Rossella; Cavallaro, Sebastiano; La Bella, Vincenzo; Conforti, Francesca Luisa
A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy
2019 Daniela Naimo, Giuseppina; Guarnaccia, Maria; Sprovieri, Teresa; Ungaro, Carmine; Luisa Conforti, Francesca; Andò, Sebastiano; Cavallaro, Sebastiano
Alternative Splicing of ALS Genes: Misregulation and Potential Therapies
2019 Perrone, Benedetta; LA COGNATA, Valentina; Sprovieri, Teresa; Ungaro, Carmine; Luisa Conforti, Francesca; Andò, Sebastiano; Cavallaro, Sebastiano
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report
2019 Sprovieri, Teresa; Ungaro, Carmine; Sivo, Serena; Quintiliani, Michela; Contaldo, Laria; Veredice, Chiara; Citrigno, Luigi; Muglia, Maria; Cavalcanti, Francesca; Cavallaro, Sebastiano; Maria Mercuri, Eugenio; Battaglia, Domenica
ALS and CHARGE syndrome: a clinical and genetic study
2018 Ungaro, Carmine; Citrigno, Luigi; Trojsi, Francesca; Sprovieri, Teresa; Gentile, Giulia; Muglia, Maria; Monsurro Maria, Rosaria; Tedeschi, Gioacchino; Cavallaro, Sebastiano; Conforti, FRANCESCA LUISA
Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations?
2018 Ungaro, Carmine; Mazzei, Rosalucia; Sprovieri, Teresa
Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case
2018 Ungaro, Carmine; Valentini, Sergio; Cerasa, Antonio; Lanza Pier, Luigi; Mazzei, Rosalucia
Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case.
2018 Ungaro, C; Valentini, S; Cerasa, A; Lanza, Pl; Mazzei, R
Notch3 protein expression in skin fibroblasts from CADASIL patients
2018 Qualtieri, Antonio; Ungaro, Carmine; Bagalà, Angelo; Bianchi, Silvia; Pantoni, Leonardo; Moccia, Marcello; Mazzei, Rosalucia
The spectrum of ROBO3 mutations in Horizontal Gaze Palsy With Progressive Scoliosis: an update
2018 Ungaro, Carmine; Mazzei, Rosalucia; Cavallaro, Sebastiano; Sprovieri, Teresa
Comparison of NOTCH3 expression in fibroblasts from CADASIL patients versus normal controls
2014 R. Mazzei; C. Ungaro; F. L. Conforti; S. Bianchi; A. Magariello; A. Patitucci; M. Muglia; M. T. Dotti; A. Federico; A. Qualtieri
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC
2014 Magariello, Angela; Citrigno, L; Vsofia, ; Patitucci, A; Conforti, Fl; Mazzei, R; Ungaro, C; Pappalardo, I; Zappia, M; Gonzalez, M; Zuchner, S; Muglia, M
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum
2014 Magariello A.; Citrigno L.; Zuchner S.; Gonzalez M.; Patitucci A.; Sofia V.; Conforti F.L.; Pappalardo I.; Mazzei R.; Ungaro C.; Zappia M.; Muglia M.
NOTCH3 PROTEIN LOCALIZATION IN (SKIN) FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY
2014 A Qualtieri; C Ungaro; F L Conforti; S Bianchi; A Magariello; M Muglia; A Patitucci; M T Dotti; A Federico; R Mazzei
NOTCH3 PROTEIN LOCALIZATION IN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY
2014 A Qualtieri; C Ungaro; MT Dotti; S Bianchi; FL Conforti; M Muglia; A Patitucci; A Magariello; A Federico; R Mazzei
NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY
2014 A. Qualtieri; C Ungaro; S Bianchi; F Conforti ; A .Magariello; A Patitucci ; M. Muglia; M Dotti; A Federico; R Mazzei
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene.
2013 Tortelli, R; Conforti, Fl; Cortese, R; D'Errico, E; Distaso, E; Mazzei, R; Ungaro, C; Magariello, A; Gambardella, A; Logroscino, G; Simone, Il
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia.
2013 Magariello, A; Tortorella, C; Patitucci, A; Tortelli, R; Liguori, M; Mazzei, R; Conforti, Fl; Citrigno, L; Ungaro, C; Simone, Il; Muglia, M
R521C mutation in the FUS gene in a large Italian family
2013 R. Mazzei; R. Tortelli; A. Patitucci; A. Magariello; M. Muglia; R. Cortese; E. D'Errico; C. Ungaro; G. Logroscino; I. L. Simone; F.L. Conforti
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis | 1-gen-2020 | Ungaro Carmine; Sprovieri Teresa; Morello Giovanna; Perrone Benedetta; Spampinato Antonio Gianmaria; Simone Isabella Laura; Trojsi Francesca; Monsurrò Maria Rosaria; Spataro Rossella; La Bella Vincenzo; Andò Sebastiano; Cavallaro Sebastiano; Conforti Francesca Luisa; | |
| A novel S379A TARDBP mutation associated to late-onset sporadic ALS | 1-gen-2019 | Sprovieri, Teresa; Ungaro, Carmine; Perrone, Benedetta; Naimo, Giuseppina Daniela; Spataro, Rossella; Cavallaro, Sebastiano; La Bella, Vincenzo; Conforti, Francesca Luisa | |
| A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy | 1-gen-2019 | Daniela Naimo, Giuseppina; Guarnaccia, Maria; Sprovieri, Teresa; Ungaro, Carmine; Luisa Conforti, Francesca; Andò, Sebastiano; Cavallaro, Sebastiano | |
| Alternative Splicing of ALS Genes: Misregulation and Potential Therapies | 1-gen-2019 | Perrone, Benedetta; LA COGNATA, Valentina; Sprovieri, Teresa; Ungaro, Carmine; Luisa Conforti, Francesca; Andò, Sebastiano; Cavallaro, Sebastiano | |
| Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report | 1-gen-2019 | Sprovieri, Teresa; Ungaro, Carmine; Sivo, Serena; Quintiliani, Michela; Contaldo, Laria; Veredice, Chiara; Citrigno, Luigi; Muglia, Maria; Cavalcanti, Francesca; Cavallaro, Sebastiano; Maria Mercuri, Eugenio; Battaglia, Domenica | |
| ALS and CHARGE syndrome: a clinical and genetic study | 1-gen-2018 | Ungaro, Carmine; Citrigno, Luigi; Trojsi, Francesca; Sprovieri, Teresa; Gentile, Giulia; Muglia, Maria; Monsurro Maria, Rosaria; Tedeschi, Gioacchino; Cavallaro, Sebastiano; Conforti, FRANCESCA LUISA | |
| Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations? | 1-gen-2018 | Ungaro, Carmine; Mazzei, Rosalucia; Sprovieri, Teresa | |
| Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case | 1-gen-2018 | Ungaro, Carmine; Valentini, Sergio; Cerasa, Antonio; Lanza Pier, Luigi; Mazzei, Rosalucia | |
| Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case. | 1-gen-2018 | Ungaro, C; Valentini, S; Cerasa, A; Lanza, Pl; Mazzei, R | |
| Notch3 protein expression in skin fibroblasts from CADASIL patients | 1-gen-2018 | Qualtieri, Antonio; Ungaro, Carmine; Bagalà, Angelo; Bianchi, Silvia; Pantoni, Leonardo; Moccia, Marcello; Mazzei, Rosalucia | |
| The spectrum of ROBO3 mutations in Horizontal Gaze Palsy With Progressive Scoliosis: an update | 1-gen-2018 | Ungaro, Carmine; Mazzei, Rosalucia; Cavallaro, Sebastiano; Sprovieri, Teresa | |
| Comparison of NOTCH3 expression in fibroblasts from CADASIL patients versus normal controls | 1-gen-2014 | R. Mazzei; C. Ungaro; F. L. Conforti; S. Bianchi; A. Magariello; A. Patitucci; M. Muglia; M. T. Dotti; A. Federico; A. Qualtieri | |
| Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC | 1-gen-2014 | Magariello, Angela; Citrigno, L; Vsofia, ; Patitucci, A; Conforti, Fl; Mazzei, R; Ungaro, C; Pappalardo, I; Zappia, M; Gonzalez, M; Zuchner, S; Muglia, M | |
| Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum | 1-gen-2014 | Magariello A.; Citrigno L.; Zuchner S.; Gonzalez M.; Patitucci A.; Sofia V.; Conforti F.L.; Pappalardo I.; Mazzei R.; Ungaro C.; Zappia M.; Muglia M. | |
| NOTCH3 PROTEIN LOCALIZATION IN (SKIN) FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY | 1-gen-2014 | A Qualtieri; C Ungaro; F L Conforti; S Bianchi; A Magariello; M Muglia; A Patitucci; M T Dotti; A Federico; R Mazzei | |
| NOTCH3 PROTEIN LOCALIZATION IN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY | 1-gen-2014 | A Qualtieri; C Ungaro; MT Dotti; S Bianchi; FL Conforti; M Muglia; A Patitucci; A Magariello; A Federico; R Mazzei | |
| NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY | 1-gen-2014 | A. Qualtieri; C Ungaro; S Bianchi; F Conforti ; A .Magariello; A Patitucci ; M. Muglia; M Dotti; A Federico; R Mazzei | |
| Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene. | 1-gen-2013 | Tortelli, R; Conforti, Fl; Cortese, R; D'Errico, E; Distaso, E; Mazzei, R; Ungaro, C; Magariello, A; Gambardella, A; Logroscino, G; Simone, Il | |
| First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. | 1-gen-2013 | Magariello, A; Tortorella, C; Patitucci, A; Tortelli, R; Liguori, M; Mazzei, R; Conforti, Fl; Citrigno, L; Ungaro, C; Simone, Il; Muglia, M | |
| R521C mutation in the FUS gene in a large Italian family | 1-gen-2013 | R. Mazzei; R. Tortelli; A. Patitucci; A. Magariello; M. Muglia; R. Cortese; E. D'Errico; C. Ungaro; G. Logroscino; I. L. Simone; F.L. Conforti |