LIGUORI, MARIA
LIGUORI, MARIA
Istituto di Tecnologie Biomediche - ITB
3T MRI Frequency of MS Cortical Lesions and Their Relationship with Cognitive Performance
2010 Mike A; Glanz B; Hildenbrand P; Meier D; Bolden K; DellOglio E; Healy BC; Liguori M; Bakshi R; Guttmann CRG.
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation.
2007 A.La Russa; M. Liguori; I. Manna; V. Andreoli; M. Caracciolo; P. Spadafora; R. Cittadella; A. Quattrone.
A longitudinal evaluation of cadasil progression by diffusion magnetic resonance imaging.
2008 Liguori M; Lanza P; Mazzei R; Consoli D; Garreffa G; Carnevale S; Bosco D; Cerasa A; Caracciolo M; Gallo O; Gioia MC; Quattrone A
A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis.
2009 Liguori M; Fera F; Patitucci A; Manna I; Condino F; Valentino P; Telarico P; Cerasa A; Gioia MC; di Palma G; Quattrone A.
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
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
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
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy
2011 Spadafora, P; Liguori, M; Caracciolo, M; Andreoli, V; Manna, I; Cittadella, R; Trecroci, F; Quattrone, A; Gambardella, A
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease.
2004 La Bella V;Liguori M;Cittadella R;Settipani N;Piccoli T;Manna I;Quattrone A;Piccoli F.
A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY
2011 A. Patitucci; C. Tortorella; M. Liguori; A. Magariello; R. Mazzei; FL. Conforti; W. Sproviero; L. Citrigno; A. Morabito; C. Ungaro; A. Gambardella;M. Muglia
A novel mutation in FKRP gene in Italian patient with LGMD.
2008 R. Cittadella; A. La Russa; P. Valentino; V. Andreoli; F. Trecroci; I. Manna; M. Liguori; P. Spadafora; A. Quattrone.
A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy
2006 Ungaro, C; Liguori, M; Conforti, Fl; Sprovieri, T; Di Palma, G; Patitucci, A; Magariello, A; Gabriele, Al; Muglia, M; Mazzei, R
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy
2007 Mazzei, R; Ungaro, C; Conforti, Fl; Liguori, M; Sprovieri, T; DI PALMA, Gemma; Patitucci, A; Magariello, A; Gabriele, Al; Citrigno, L; Muglia, M; Quattrone, A
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
2008 Liguori, M; La Russa, A; Manna, I; Andreoli, V; Caracciolo, M; Spadafora, P; Cittadella, R; Quattrone, A
A Pilot Longitudinal Evaluation of MicroRNAs for Monitoring the Cognitive Impairment in Pediatric Multiple Sclerosis
2020 Nicoletta Nuzziello; Arianna Consiglio; Rosa Gemma Viterbo; Flavio Licciulli; Sabino Liuni; Maria Trojano;Maria Liguori.
A Predictive Model for MicroRNA Expressions in Pediatric Multiple Sclerosis Detection
2019 Casalino G.; Castellano G.; Consiglio A.; Liguori M.; Nuzziello N.; Primiceri D.
A Putative Alzheimer's Disease Risk Allele in PCK1 Influences Brain Atrophy in Multiple Sclerosis
2010 Xia, Z; Chibnik, Lb; Glanz, Bi; Liguori, M; Shulman, Jm; Tran, D; Khoury, Sj; Chitnis, T; Holyoak, T; Weiner, Hl; Guttmann, Cr; De Jager, Pl
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population.
2003 Liguori M; Sawcer S; Setakis E; Compston A; Giordano M; D'Alfonso S; Mellai M; Malferrari G; Trojano M; Livrea P; De Robertis F; Massacesi L; Repice A; Ballerini C; Biagioli T; Bomprezzi R; Cannoni S; Ristori G; Salvetti M; Grimaldi LM; Biunno I; Comi G;
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis
2006 Cerasa, A; Fera, F; Gioia, Mc; Liguori, M; Passamonti, L; Nicoletti, G; Vercillo, L; Paolillo, A; Clodomiro, A; Valentino, P; Quattrone, A
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis
2007 Cerasa, A; Fera, F; Gioia, Mc; Liguori, M; Passamonti, L; Valentino, P; Clodomiro, A; Quattrone, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 3T MRI Frequency of MS Cortical Lesions and Their Relationship with Cognitive Performance | 1-gen-2010 | Mike A; Glanz B; Hildenbrand P; Meier D; Bolden K; DellOglio E; Healy BC; Liguori M; Bakshi R; Guttmann CRG. | |
| A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. | 1-gen-2007 | A.La Russa; M. Liguori; I. Manna; V. Andreoli; M. Caracciolo; P. Spadafora; R. Cittadella; A. Quattrone. | |
| A longitudinal evaluation of cadasil progression by diffusion magnetic resonance imaging. | 1-gen-2008 | Liguori M; Lanza P; Mazzei R; Consoli D; Garreffa G; Carnevale S; Bosco D; Cerasa A; Caracciolo M; Gallo O; Gioia MC; Quattrone A | |
| A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis. | 1-gen-2009 | Liguori M; Fera F; Patitucci A; Manna I; Condino F; Valentino P; Telarico P; Cerasa A; Gioia MC; di Palma G; Quattrone A. | |
| 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 | |
| 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 | |
| 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 | |
| A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy | 1-gen-2011 | Spadafora, P; Liguori, M; Caracciolo, M; Andreoli, V; Manna, I; Cittadella, R; Trecroci, F; Quattrone, A; Gambardella, A | |
| A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. | 1-gen-2004 | La Bella V;Liguori M;Cittadella R;Settipani N;Piccoli T;Manna I;Quattrone A;Piccoli F. | |
| A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY | 1-gen-2011 | A. Patitucci; C. Tortorella; M. Liguori; A. Magariello; R. Mazzei; FL. Conforti; W. Sproviero; L. Citrigno; A. Morabito; C. Ungaro; A. Gambardella;M. Muglia | |
| A novel mutation in FKRP gene in Italian patient with LGMD. | 1-gen-2008 | R. Cittadella; A. La Russa; P. Valentino; V. Andreoli; F. Trecroci; I. Manna; M. Liguori; P. Spadafora; A. Quattrone. | |
| A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy | 1-gen-2006 | Ungaro, C; Liguori, M; Conforti, Fl; Sprovieri, T; Di Palma, G; Patitucci, A; Magariello, A; Gabriele, Al; Muglia, M; Mazzei, R | |
| A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy | 1-gen-2007 | Mazzei, R; Ungaro, C; Conforti, Fl; Liguori, M; Sprovieri, T; DI PALMA, Gemma; Patitucci, A; Magariello, A; Gabriele, Al; Citrigno, L; Muglia, M; Quattrone, A | |
| A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. | 1-gen-2008 | Liguori, M; La Russa, A; Manna, I; Andreoli, V; Caracciolo, M; Spadafora, P; Cittadella, R; Quattrone, A | |
| A Pilot Longitudinal Evaluation of MicroRNAs for Monitoring the Cognitive Impairment in Pediatric Multiple Sclerosis | 1-gen-2020 | Nicoletta Nuzziello; Arianna Consiglio; Rosa Gemma Viterbo; Flavio Licciulli; Sabino Liuni; Maria Trojano;Maria Liguori. | |
| A Predictive Model for MicroRNA Expressions in Pediatric Multiple Sclerosis Detection | 1-gen-2019 | Casalino G.; Castellano G.; Consiglio A.; Liguori M.; Nuzziello N.; Primiceri D. | |
| A Putative Alzheimer's Disease Risk Allele in PCK1 Influences Brain Atrophy in Multiple Sclerosis | 1-gen-2010 | Xia, Z; Chibnik, Lb; Glanz, Bi; Liguori, M; Shulman, Jm; Tran, D; Khoury, Sj; Chitnis, T; Holyoak, T; Weiner, Hl; Guttmann, Cr; De Jager, Pl | |
| A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. | 1-gen-2003 | Liguori M; Sawcer S; Setakis E; Compston A; Giordano M; D'Alfonso S; Mellai M; Malferrari G; Trojano M; Livrea P; De Robertis F; Massacesi L; Repice A; Ballerini C; Biagioli T; Bomprezzi R; Cannoni S; Ristori G; Salvetti M; Grimaldi LM; Biunno I; Comi G; | |
| Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis | 1-gen-2006 | Cerasa, A; Fera, F; Gioia, Mc; Liguori, M; Passamonti, L; Nicoletti, G; Vercillo, L; Paolillo, A; Clodomiro, A; Valentino, P; Quattrone, A | |
| Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis | 1-gen-2007 | Cerasa, A; Fera, F; Gioia, Mc; Liguori, M; Passamonti, L; Valentino, P; Clodomiro, A; Quattrone, A |