PATITUCCI, ALESSANDRA
PATITUCCI, ALESSANDRA
Istituto per i Sistemi Agricoli e Forestali del Mediterraneo - ISAFOM - Sede Secondaria Rende
Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches
2024 Mazzei, Rosalucia; Genovese, Claudia; Magariello, Angela; Patitucci, Alessandra; Russo, Giampiero; Tagarelli, Giuseppe
A review of the antimicrobial potential of herbal drugs used in popular Italian medicine (1850s-1950s) to treat bacterial skin diseases
2020 Mazzei, R; Leonti, M; Spadafora, S; Patitucci, A; Tagarelli, G
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders
2018 La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments
2017 Magariello A.; Russo C.; Citrigno L.; Zuchner S.; Patitucci A.; Mazzei R.; Conforti F.L.; Ferlazzo E.; Aguglia U.; Muglia M
A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B
2016 Cortese, Rosa; Zoccolella, Stefano; Muglia, Maria; Patitucci, Alessandra; Scarafino, Antonio; Paolicelli, Damiano; Laura Simone, Isabella
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness
2014 Muglia M.; Citrigno L.; D'Errico E.; Magariello A.; Distaso E.; Gasparro A.A.; Scarafino A.; Patitucci A.; Conforti F.L.; Mazzei R.; Cortese R.; Tortelli R.; L. Simone I.
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
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC
2014 Magariello, Angela; Citrigno, L; Sofia, V; Patitucci, A; Conforti, F; Mazzei, R; Pappalardo, I; Mzappia, ; 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.
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case
2014 Mazzei, Rosalucia; Valentini, Sergio; Conforti, FRANCESCA LUISA; Muglia, Maria; Gallo, Olivier; Cerasa, Antonio; Patitucci, Alessandra; Magariello, Angela; Perrotta, Paolo; Lanza, PIER LUIGI
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case
2014 Rosalucia Mazzei; Sergio Valentini; Francesca Luisa Conforti; Maria Muglia; Olivier Gallo; Antonio Cerasa; Alessandra Patitucci; Angela Magariello; Paolo Perrotta; Pier Luigi Lanza
MUTATIONAL ANALISYS OF GJB1, MPZ AND PMP22 GENES IN CMT PATIENTS FROM SOUTHERN ITALY
2014 Alessandra Patitucci; A. Magariello ; F. Conforti ; R. Mazzei ; A. Mazzeo ; I. Simone ; M. Muglia
Mutational screening of GJB1, MPZ and PMP22 genes in a cohort of CMT patients from Southern Italy
2014 Patitucci, A; Magariello, A; Conforti, Fl; Mazzei, R; Mazzeo, A; Simone, Il; 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
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
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia
2012 A. Magariello; C. Tortorella; A. Patitucci; R. Tortelli; M. Liguori; R. Mazzei; F. L. Conforti; L. Citrigno; C. Ungaro; I. L. Simone; M. Muglia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches | 1-gen-2024 | Mazzei, Rosalucia; Genovese, Claudia; Magariello, Angela; Patitucci, Alessandra; Russo, Giampiero; Tagarelli, Giuseppe | |
| A review of the antimicrobial potential of herbal drugs used in popular Italian medicine (1850s-1950s) to treat bacterial skin diseases | 1-gen-2020 | Mazzei, R; Leonti, M; Spadafora, S; Patitucci, A; Tagarelli, G | |
| NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders | 1-gen-2018 | La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano | |
| Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments | 1-gen-2017 | Magariello A.; Russo C.; Citrigno L.; Zuchner S.; Patitucci A.; Mazzei R.; Conforti F.L.; Ferlazzo E.; Aguglia U.; Muglia M | |
| A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B | 1-gen-2016 | Cortese, Rosa; Zoccolella, Stefano; Muglia, Maria; Patitucci, Alessandra; Scarafino, Antonio; Paolicelli, Damiano; Laura Simone, Isabella | |
| A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness | 1-gen-2014 | Muglia M.; Citrigno L.; D'Errico E.; Magariello A.; Distaso E.; Gasparro A.A.; Scarafino A.; Patitucci A.; Conforti F.L.; Mazzei R.; Cortese R.; Tortelli R.; L. Simone I. | |
| 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 | |
| EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC | 1-gen-2014 | Magariello, Angela; Citrigno, L; Sofia, V; Patitucci, A; Conforti, F; Mazzei, R; Pappalardo, I; Mzappia, ; 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. | |
| Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case | 1-gen-2014 | Mazzei, Rosalucia; Valentini, Sergio; Conforti, FRANCESCA LUISA; Muglia, Maria; Gallo, Olivier; Cerasa, Antonio; Patitucci, Alessandra; Magariello, Angela; Perrotta, Paolo; Lanza, PIER LUIGI | |
| Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case | 1-gen-2014 | Rosalucia Mazzei; Sergio Valentini; Francesca Luisa Conforti; Maria Muglia; Olivier Gallo; Antonio Cerasa; Alessandra Patitucci; Angela Magariello; Paolo Perrotta; Pier Luigi Lanza | |
| MUTATIONAL ANALISYS OF GJB1, MPZ AND PMP22 GENES IN CMT PATIENTS FROM SOUTHERN ITALY | 1-gen-2014 | Alessandra Patitucci; A. Magariello ; F. Conforti ; R. Mazzei ; A. Mazzeo ; I. Simone ; M. Muglia | |
| Mutational screening of GJB1, MPZ and PMP22 genes in a cohort of CMT patients from Southern Italy | 1-gen-2014 | Patitucci, A; Magariello, A; Conforti, Fl; Mazzei, R; Mazzeo, A; Simone, Il; 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 | |
| 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 | |
| A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia | 1-gen-2012 | A. Magariello; C. Tortorella; A. Patitucci; R. Tortelli; M. Liguori; R. Mazzei; F. L. Conforti; L. Citrigno; C. Ungaro; I. L. Simone; M. Muglia |