MAZZEI, ROSALUCIA
MAZZEI, ROSALUCIA
Istituto per i Sistemi Agricoli e Forestali del Mediterraneo - ISAFOM
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
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease
2021 A Cerantonio; S De Benedittis; PL Lanza; M Muglia; F Cavalcanti; P Spadafora; N Romeo; O Gallo; G Di Palma; R Mazzei; A Qualtieri; L Citrigno;
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
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, C; Valentini, S; Cerasa, A; Lanza, Pl; Mazzei, R
Italian folk plant-based remedies to heal headache (XIX-XX century)
2018 Mazzei, R; De Marco, E V; Gallo, O; Tagarelli, G
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
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
Copy number variations and stroke
2016 Colaianni, V; Mazzei, R; Cavallaro, S
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients
2015 Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Monsurro M.R.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Nilo R.; Battistini S.; Mandrioli J.; Tanel R.; Murru M.R.; Mandich P.; Zollino M.; Conforti F.L.; Brunetti M.; Barberis M.; Restagno G.; Penco S.; Lunetta C.; Giannini F.; Ricci C.; Mancardi G.; Bartolomei I.; Corbo M.; Conte A.; Luigetti M.; Lattante S.; Marangi G.; Ossola I.; Logroscino G.; Tedeschi G.; Pugliatti M.; Pinter G.L.; Glynn S.; Gibbs J.R.; Cammarosano S.; Canosa A.; Manera U.; Bertuzzo D.; Ilardi A.; Marinou K.; Sideri R.; Pisano F.; Spataro R.; Colletti T.; Floris G.; Cannas A.; Piras V.; Marrosu F.; Marrosu M.G.; Parish L.D.; Ticca A.; Pirisi A.; Ortu E.; Cau T.B.; Loi D.; Traccis S.; Fini N.; Georgoulopoulou E.; Casale F.; Marrali G.; Fuda G.; Solamone P.; Maestri E.; Mazzei R.; Cristillo V.; Puddu R.; Costantino E.; Pani C.; Caredda C.; Origone P.; Mosca L.; Capasso M.; Turri M.; Petrucci A.; Tremolizzo L.; Santarelli M.
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.
Brown-Vialetto-Van Laere Syndrome: a case report of a family from Italy
2014 Conforti, Fl; Rspataro, ; Mazzei, R; Apatitutcci, ; Qualtieri, A; Magariello, A; Mmuglia, ; La Bella, V
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 Rosalucia Mazzei; Sergio Valentini; Francesca Luisa Conforti; Maria Muglia; Olivier Gallo; Antonio Cerasa; Alessandra Patitucci; Angela Magariello; Paolo Perrotta; Pier Luigi Lanza
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
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
| 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 | |
| Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease | 1-gen-2021 | A Cerantonio; S De Benedittis; PL Lanza; M Muglia; F Cavalcanti; P Spadafora; N Romeo; O Gallo; G Di Palma; R Mazzei; A Qualtieri; L Citrigno; | |
| 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 | |
| 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, C; Valentini, S; Cerasa, A; Lanza, Pl; Mazzei, R | |
| Italian folk plant-based remedies to heal headache (XIX-XX century) | 1-gen-2018 | Mazzei, R; De Marco, E V; Gallo, O; Tagarelli, G | |
| 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 | |
| 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 | |
| Copy number variations and stroke | 1-gen-2016 | Colaianni, V; Mazzei, R; Cavallaro, S | |
| CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients | 1-gen-2015 | Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Monsurro M.R.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Nilo R.; Battistini S.; Mandrioli J.; Tanel R.; Murru M.R.; Mandich P.; Zollino M.; Conforti F.L.; Brunetti M.; Barberis M.; Restagno G.; Penco S.; Lunetta C.; Giannini F.; Ricci C.; Mancardi G.; Bartolomei I.; Corbo M.; Conte A.; Luigetti M.; Lattante S.; Marangi G.; Ossola I.; Logroscino G.; Tedeschi G.; Pugliatti M.; Pinter G.L.; Glynn S.; Gibbs J.R.; Cammarosano S.; Canosa A.; Manera U.; Bertuzzo D.; Ilardi A.; Marinou K.; Sideri R.; Pisano F.; Spataro R.; Colletti T.; Floris G.; Cannas A.; Piras V.; Marrosu F.; Marrosu M.G.; Parish L.D.; Ticca A.; Pirisi A.; Ortu E.; Cau T.B.; Loi D.; Traccis S.; Fini N.; Georgoulopoulou E.; Casale F.; Marrali G.; Fuda G.; Solamone P.; Maestri E.; Mazzei R.; Cristillo V.; Puddu R.; Costantino E.; Pani C.; Caredda C.; Origone P.; Mosca L.; Capasso M.; Turri M.; Petrucci A.; Tremolizzo L.; Santarelli M. | |
| 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. | |
| Brown-Vialetto-Van Laere Syndrome: a case report of a family from Italy | 1-gen-2014 | Conforti, Fl; Rspataro, ; Mazzei, R; Apatitutcci, ; Qualtieri, A; Magariello, A; Mmuglia, ; La Bella, V | |
| 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 | Rosalucia Mazzei; Sergio Valentini; Francesca Luisa Conforti; Maria Muglia; Olivier Gallo; Antonio Cerasa; Alessandra Patitucci; Angela Magariello; Paolo Perrotta; Pier Luigi Lanza | |
| 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 | |
| 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 |