CITTADELLA, RITA
CITTADELLA, RITA
Istituto per la Ricerca e l'Innovazione Biomedica -IRIB
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
Copy Number Variants in Alzheimer's Disease
2017 Cuccaro, Denis; DE MARCO, ELVIRA VALERIA; Cittadella, Rita; Cavallaro, Sebastiano
Huntington's disease-like syndrome: a case report
2016 Avantaggiato, F; Minafra, B; Zangaglia, R; De Marco, Ev; Cittadella, R; Pacchetti, C
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease
2014 Andreoli, Virginia; DE MARCO, ELVIRA VALERIA; Trecroci, Francesca; Cittadella, Rita; DI PALMA, Gemma; Gambardella, Antonio
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy
2011 Spadafora P.; Liguori M.; Caracciolo M.; Manna I.; Andreoli V.; Cittadella R.; Trecroci F.; Quattrone A.; Gambardella A
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification
2011 V. Andreoli ; F. Trecroci; A. La Russa; R. Cittadella; M. Liguori; P. Spadafora; G. Di Palma; A. Gambardella; A. Quattrone
D678N mutation in a patient with an early-onset Alzheimer's Disease
2011 Trecroci F.; La Russa A.; Cittadella R.; Liguori M.; Spadafora P.; Di Palma G.; Caracciolo M.; Andreoli V
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report
2011 Andreoli, V; Trecroci, F; La Russa, A; Liguori, M; Spadafora, P; Di Palma, G; Gambardella, A; Cittadella, R
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype
2011 Spadafora P.; Liguori M.; Andreoli V.; Cittadella R.; Trecroci F.; Gambardella A
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man
2011 La Russa, Antonella; Cittadella, Rita; Andreoli, Virginia; Valentino, Paola; Trecroci, Francesca; Caracciolo, Manuela; Gallo, Olivier; Gambardella, Antonio; Quattrone, Aldo
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
2011 La Russa, A; Cittadella, R; Andreoli, V; Valentino, P; Trecroci, F; Caracciolo, M; Gallo, O; Gambardella, A; Quattrone, A
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease.
2011 V. Andreoli; F. Trecroci; A. La Russa; R. Cittadella; P. Spadafora; G. Di Palma; M. Caracciolo; A. Gambardella; A. Quattrone
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease
2011 Andreoli, Virginia; Trecroci, Francesca; La Russa, Antonella; Cittadella, Rita; Liguori, Maria; Spadafora, Patrizia; Caracciolo, Manuela; Di Palma, Gemma; Colica, Carmela; Gambardella, Antonio; Quattrone, Aldo
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.
2010 La Russa, A; Cittadella, R; De Marco, Ev; Valentino, P; Andreoli, V; Trecroci, F; Latorre, V; Gambardella, A; Quattrone, A
CASP-9 : a susceptibility locus for multiple sclerosis in Italy.
2009 Andreoli, V; Trecroci, F; La Russa, A; Valentino, P; Condino, F; Latorre, V; Nisticò, R; Pirritano, D; Del Giudice, F; Canino, M; Cittadella, R; Quattrone, A
CASP-9: a susceptibility locus for multiple sclerosis in Italy.
2009 Andreoli, V; Trecroci, F; La Russa, A; Valentino, P; Condino, F; La Torre, V; Nisticò, R; Pirritano, D; Del Giudice, F; Canino, M; Cittadella, R; Gambardella, A; Quattrone, A
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome.
2009 La Russa, A; Valentino, P; Andreoli, V; Trecroci, F; C Cirò Candiano, I; Spadafora, P; Cittadella, R
NOTCH3 gene mutations and mtDNA variations
2009 C Ungaro; A La Russa; R Mazzei; R Cittadella; FL Conforti; V Andreoli; L Citrigno; A Gabriele; F Trecroci; A Magariello; A Patitucci; M Muglia; A Quattrone; A Gambardella
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease.
2009 V. Andreoli; F. Trecroci; A. La Russa; R. Cittadella; P. Spadafora; G. Di Palma; M. Caracciolo; A. Quattrone.
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease
2008 T. Maci; F. Le Pira; L. Marturano; M. Liguori; R. Cittadella; A. Quattrone; M. Zappia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Copy Number Variants in Alzheimer's Disease | 1-gen-2017 | Cuccaro, Denis; DE MARCO, ELVIRA VALERIA; Cittadella, Rita; Cavallaro, Sebastiano | |
| Huntington's disease-like syndrome: a case report | 1-gen-2016 | Avantaggiato, F; Minafra, B; Zangaglia, R; De Marco, Ev; Cittadella, R; Pacchetti, C | |
| Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease | 1-gen-2014 | Andreoli, Virginia; DE MARCO, ELVIRA VALERIA; Trecroci, Francesca; Cittadella, Rita; DI PALMA, Gemma; Gambardella, Antonio | |
| A novel CAPN3 gene mutation in a LGMD patient from Southern Italy | 1-gen-2011 | Spadafora P.; Liguori M.; Caracciolo M.; Manna I.; Andreoli V.; Cittadella R.; Trecroci F.; Quattrone A.; Gambardella A | |
| Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification | 1-gen-2011 | V. Andreoli ; F. Trecroci; A. La Russa; R. Cittadella; M. Liguori; P. Spadafora; G. Di Palma; A. Gambardella; A. Quattrone | |
| D678N mutation in a patient with an early-onset Alzheimer's Disease | 1-gen-2011 | Trecroci F.; La Russa A.; Cittadella R.; Liguori M.; Spadafora P.; Di Palma G.; Caracciolo M.; Andreoli V | |
| Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report | 1-gen-2011 | Andreoli, V; Trecroci, F; La Russa, A; Liguori, M; Spadafora, P; Di Palma, G; Gambardella, A; Cittadella, R | |
| Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype | 1-gen-2011 | Spadafora P.; Liguori M.; Andreoli V.; Cittadella R.; Trecroci F.; Gambardella A | |
| Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man | 1-gen-2011 | La Russa, Antonella; Cittadella, Rita; Andreoli, Virginia; Valentino, Paola; Trecroci, Francesca; Caracciolo, Manuela; Gallo, Olivier; Gambardella, Antonio; Quattrone, Aldo | |
| Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. | 1-gen-2011 | La Russa, A; Cittadella, R; Andreoli, V; Valentino, P; Trecroci, F; Caracciolo, M; Gallo, O; Gambardella, A; Quattrone, A | |
| Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. | 1-gen-2011 | V. Andreoli; F. Trecroci; A. La Russa; R. Cittadella; P. Spadafora; G. Di Palma; M. Caracciolo; A. Gambardella; A. Quattrone | |
| Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease | 1-gen-2011 | Andreoli, Virginia; Trecroci, Francesca; La Russa, Antonella; Cittadella, Rita; Liguori, Maria; Spadafora, Patrizia; Caracciolo, Manuela; Di Palma, Gemma; Colica, Carmela; Gambardella, Antonio; Quattrone, Aldo | |
| Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. | 1-gen-2010 | La Russa, A; Cittadella, R; De Marco, Ev; Valentino, P; Andreoli, V; Trecroci, F; Latorre, V; Gambardella, A; Quattrone, A | |
| CASP-9 : a susceptibility locus for multiple sclerosis in Italy. | 1-gen-2009 | Andreoli, V; Trecroci, F; La Russa, A; Valentino, P; Condino, F; Latorre, V; Nisticò, R; Pirritano, D; Del Giudice, F; Canino, M; Cittadella, R; Quattrone, A | |
| CASP-9: a susceptibility locus for multiple sclerosis in Italy. | 1-gen-2009 | Andreoli, V; Trecroci, F; La Russa, A; Valentino, P; Condino, F; La Torre, V; Nisticò, R; Pirritano, D; Del Giudice, F; Canino, M; Cittadella, R; Gambardella, A; Quattrone, A | |
| Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. | 1-gen-2009 | La Russa, A; Valentino, P; Andreoli, V; Trecroci, F; C Cirò Candiano, I; Spadafora, P; Cittadella, R | |
| NOTCH3 gene mutations and mtDNA variations | 1-gen-2009 | C Ungaro; A La Russa; R Mazzei; R Cittadella; FL Conforti; V Andreoli; L Citrigno; A Gabriele; F Trecroci; A Magariello; A Patitucci; M Muglia; A Quattrone; A Gambardella | |
| Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. | 1-gen-2009 | V. Andreoli; F. Trecroci; A. La Russa; R. Cittadella; P. Spadafora; G. Di Palma; M. Caracciolo; A. Quattrone. | |
| A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease | 1-gen-2008 | T. Maci; F. Le Pira; L. Marturano; M. Liguori; R. Cittadella; A. Quattrone; M. Zappia |