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PATITUCCI, ALESSANDRA

PATITUCCI, ALESSANDRA  

Istituto per i Sistemi Agricoli e Forestali del Mediterraneo - ISAFOM  

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Risultati 1 - 20 di 89 (tempo di esecuzione: 0.047 secondi).
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 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
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