Le informazioni pubblicate in questa pagina sono gestite in completa autonomia da MARIA LIGUORI il/la quale se ne assume ogni responsabilità
Nuzziello N, Ciaccia L and Liguori M.
Precision Medicine in Neurodegenerative Diseases: Some Promising Tips Coming from the microRNAs' World.
(2019) in Cells
Nicoletta Nuzziello and Maria Liguori
The MicroRNA Centrism in the Orchestration of Neuroinflammation in Neurodegenerative Diseases.
(2019) in Cells
Nuzziello, N.; Vilardo, L.; Pelucchi, P.; Consiglio, A.; Trojano, M.; Liguori, M.
MicroRNA and transcription factor co-regulatory network analysis: a combined bioinformatics and molecular strategy for uncovering genetic hub regulatory elements in multiple sclerosis pathogenesis
(2018) European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS 2018), Berlin, Germany, 10-12/10/2018
Mallardi A1, Nuzziello N2, Liguori M3, Avolio C4, Palazzo G5.
Counting of peripheral extracellular vesicles in Multiple Sclerosis patients by an improved nanoplasmonic assay and dynamic light scattering
(2018) in Colloids and surfaces. B, Biointerfaces (Print)
Nicoletta Nuzziello 1, Laura Vilardo 2, Paride Pelucchi 2, Arianna Consiglio 1, Sabino Liuni 1, Maria Trojano 3
and Maria Liguori 1
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis
Nicoletta Nuzziello 1, Laura Vilardo 2, Paride Pelucchi 2, Arianna Consiglio 1, Sabino Liuni 1, Maria Trojano 3
(2018) in International journal of molecular sciences (Online)
Maria Liguori,1,* Nicoletta Nuzziello,1,+ Alessandro Introna,2,+ Arianna Consiglio,1 Flavio Licciulli,1 Eustachio D'Errico,2 Antonio Scarafino,2 Eugenio Distaso,2 and Isabella L. Simone2
Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis
(2018) in Frontiers in molecular neuroscience
Liguori M.; Nuzziello N.; Licciulli F.; Consiglio A.; Simone M.; Viterbo R.G.; Creanza T.M.; Ancona N.; Tortorella C.; Margari L.; Grillo G.; Giordano P.; Liuni S.; Trojano M.
Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease.
(2018) in Human molecular genetics (Print)
Patrizia Spadafora 1, Giuseppe Tagarelli 2, Nelide Romeo 1, Maria Liguori 3
Tay Sachs in South Italy
(2017) in ISI atlas of science
Nuzziello, Nicoletta; Blonda, Maria; Licciulli, Flavio; Liuni, Sabino; Amoruso, Antonella; Valletti, Alessio; Consiglio, Arianna; Avolio, Carlo; Liguori, Maria
Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study.
(2017) in Medical sciences
Liguori, M.; Nuzziello, N.; Simone, M.; Licciulli, V. F.; Viterbo, R. G.; Ancona, N.; Consiglio, A.; Creanza, T.; De Caro, G.; Liuni, S.; Margari, L.; Trojano, M.
Molecular signatures associated with cognitive dysfunctions in pediatric multiple sclerosis
(2016) Congresso annuale dello European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS), Londra, 14-17/09/2016
Creanza, Teresa Maria; Liguori, Maria; Liuni, Sabino; Nuzziello, Nicoletta; Ancona, Nicola
Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis
(2016) in International journal of molecular sciences (Online)
Liguori M., Tagarelli G., Romeo N., Bagalà A., Spadafora P.
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy.
(2016) in Neurological sciences (Testo stamp.)
Lohmann, Katja; Schmidt, Alexander; Schillert, Arne; Winkler, Susen; Albanese, Alberto; Baas, Frank; Bentivoglio, Anna Rita; Borngraeber, Friederike; Brueggemann, Norbert; Defazio, Giovanni; Del Sorbo, Francesca; Deuschl, Guenther; Edwards, Mark J.; Gasser, Thomas; Gomez-Garre, Pilar; Graf, Julia; Groen, Justus L.; Gruenewald, Anne; Hagenah, Johann; Hemmelmann, Claudia; Jabusch, Hans-Christian; Kaji, Ryuji; Kasten, Meike; Kawakami, Hideshi; Kostic, Vladimir S.; Liguori, Maria; Mir, Pablo; Muenchau, Alexander; Ricchiuti, Felicia; Schreiber, Stefan; Siegesmund, Katharina; Svetel, Marina; Tijssen, Marina A. J.; Valente, Enza Maria; Westenberger, Ana; Zeuner, Kirsten E.; Zittel, Simone; Altenmueller, Eckart; Ziegler, Andreas; Klein, Christine
Genome-Wide Association Study in Musician's Dystonia: A Risk Variant at the Arylsulfatase G Locus?
(2014) in Movement disorders
Liguori M.; Qualtieri A.; Tortorella C.; Direnzo V.; Bagala A.; Mastrapasqua M.; Spadafora P.; Trojano M.
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration
(2014) in PloS one
ROMEO NELIDE, TAGARELLI GIUSEPPE, SPADAFORA PATRIZIA, *LIGUORI MARIA
COGNITIVE DYSFUNCTION AND QUALITY OF LIFE IN MULTIPLE SCLEROSIS DISEASE
(2014) C.I.A.N.S CONFERENCE COLLEGIUM INTERNATIONALE ACTIVITATIS NERVOSAE SUPERIORIS, VENEZIA, 28-30 MARZO 2014
M. Liguori, A.Qualtieri, C. tortorella, A.Bagalà, V. DiRenzo, P. Spadafora, M. Mastrapasqua, M.Trojano
Proteomic profiling of cerebrospinal fluid in clinically isolated syndrome
(2013) ECTRIMS 2013, Copenaghen, 2-5 Ottobre 2013
Fera F; Passamonti L; Cerasa A; Gioia MC; Liguori M; Manna I; Valentino P; Quattrone A.
The BDNF Val66Met Polymorphism Has Opposite Effects on Memory Circuits of Multiple Sclerosis Patients and Controls
(2013) in PloS one
Giuseppe Tagarelli ; Antonio Tagarelli ; Maria Liguori ; Anna Piro
Treating epilepsy in Italy between XIX and XX century
(2013) in Journal of ethnopharmacology
Magariello A, Tortorella C, Patitucci A, Tortelli R, Liguori M, Mazzei R, Conforti FL, Citrigno L, Ungaro C, Simone IL, Muglia M.
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia.
(2013) in European journal of neurology (Online)
Antonio Qualtieri, M. Liguori, C. Tortorella, V. Direnzo, A. Bagala', P. Spadafora, M. Mastrapasqua, M. Trojano
CSF MALDI-TOF mass spectrometry protein profiling in Clinically Isolated Syndrome.
(2013) in Neurological sciences (Online)
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 (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia
(2012) in European journal of human genetics (Online)
Zoccolella S, Vecchio E, Direnzo V, Luciannatelli E, Brancasi B, Bellomo R, Liguori M, Tortorella C
Concomitant myotonic dystrophy type 1, CIDP-like neuropathy and Hashimoto thyroiditis: a causal link?
(2012) in European journal of neurology (Online)
Spadafora P, Liguori M, Andreoli V, Quattrone A, Gambardella A
CAV3 T78M mutation as polymorphic variant in South Italy
(2012) in Neuromuscular disorders
Moscufo M, Wolfson LI, Meier D, Liguori M, Hildenbrand P, Wakefield D, Schmidt JA, Pearlson GD, Guttmann CRG.
Mobility decline in the elderly relates to lesion accrual in the splenium of the corpus callosum
(2012) in Age (Berlin. Online)
F. Trecroci, R. Cittadella, E.V. De Marco, M. Liguori, P. Spadafora, G. Di Palma, V. Andreoli
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer
(2012) xv congresso nazionale Società italiana Genetica Umana, Sorrento (Na), 21-24 novembre 2012
Spadafora P., Liguori M., Caracciolo M., Andreoli V., Manna I., Cittadella R., Trecroci F., Quattrone A., Gambardella A
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy
(2011) 15th Congress of the European Federation of Neurological Society, Budapest, 10-13 Settembre
Spadafora P., Liguori M., Caracciolo M., Manna I., Andreoli V., Cittadella R., Trecroci F., Quattrone A., Gambardella A
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy
(2011) in European journal of human genetics
Spadafora P., Andreoli V., Cittadella F., Trecroci F., Liguori M
Duchenne/Becker like phenotype and L276I mutation in FKRP gene
(2011) in American journal of human genetics
Andreoli V., Trecroci F., La Russa A., Liguori M., Spadafora P., Di Palma G., Gambardella A., Cittadella R
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report
(2011) in American journal of human genetics
Spadafora P., Liguori M., Andreoli V., Cittadella R., Trecroci F., Gambardella A
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype
(2011) in Neurological sciences (Testo stamp.)
Trecroci F., La Russa A., Cittadella R., Liguori M., Spadafora P., Di Palma G., Caracciolo M., Andreoli V
D678N mutation in a patient with an early-onset Alzheimer's Disease
(2011) in European journal of human genetics
A Magariello, M Muglia, M Liguori, A Patitucci, L Citrigno, R Mazzei, FL Conforti, C Ungaro, W Sproviero, D Bosco, M Plastino, A Gambardella
An intronic nucleotide change in the SPAST gene might produce an aberrant protein transcript
(2011) in Neurological sciences (Testo stamp.)
V. Andreoli , F. Trecroci, A. La Russa, R. Cittadella, M. Liguori, P. Spadafora, G. Di Palma, A. Gambardella, A. Quattrone
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification
(2011) in Neurological sciences (Testo stamp.)
A. Patitucci, C. Tortorella, M. Liguori, A. Magariello, R. Mazzei, FL. Conforti, W. Sproviero, L. Citrigno, A. Morabito, C. Ungaro, A. Gambardella and M. Muglia
A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY
(2011) in Neurological sciences (Testo stamp.)
Liguori M, Meier D, Hildenbrand P, Healy B, Chitnis T, Baruch NF, Khoury SJ, Weiner HL, Bakshi R, Barkhof F, Guttmann CRG.
One-year activity on subtraction MRI predicts subsequenr 4-year activity and progression in multiple sclerosis.
(2011) in Journal of neurology, neurosurgery and psychiatry
Manna I, Liguori M, Valentino P, Vena L, Condino F, Nistico R, Di Palma G, Quattrone A, Gambardella A
NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms.
(2011) in Journal of the neurological sciences
Mike A, Glanz BI, Hildenbrand P, Meier D, Bolden K, Liguori M, Dell'Oglio E, Healy BC, Bakshi R, Guttmann CRG
Identification and clinical impact of multiple sclerosis cortical lesions as assessed by routine 3T MRI
(2011) in American journal of neuroradiology
Liguori M, Healy BC, Glanz BI, Khoury SJ, Moscufo N, Weiner HL, De Jager PL, Guttmann CRG
HLA (A-B-C and DRB1) alleles and brain MRI changes in Multiple Sclerosis: a longitudinal study.
(2011) in Genes and immunity
Virginia Andreoli, Francesca Trecroci, Antonella La Russa, Rita Cittadella, Maria Liguori, Patrizia Spadafora, Manuela Caracciolo, Gemma Di Palma, Carmela Colica, Antonio Gambardella, Aldo Quattrone.
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease
(2011) in Alzheimer's & dementia (Online)
Autori: Healy BC and Liguori M./ Curatori: Weiner H. and Stankiewicz J
Predicting MS clinical course.
(2011) in , 2011
P. Spadafora , M. Liguori, I.C. Candiano, G. Spinelli, V. Andreoli, I. Manna, R. Cittadella, F. Trecroci, A. Gambardella, A. Quattrone,
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY
(2010) XLI Congress of the Italian Neurological Society, Catania
Spadafora P., Liguori M., Caracciolo M., Cirò Candiano IC., Manna I., Spinelli G., Andreoli V., Cittadella R., Trecroci F., Quattrone A., and Gambardella A
The frequency of limb girdle muscular dystrophy 1c in southern Italy
(2010) European Human Genetics Conference, Gothenburg
P. Spadafora, M. Liguori, M. Caracciolo, G. Tagarelli, A. Bagalà, I.C. Cirò Candiano, G. Spinelli, A. Gambardella, A. Quattrone
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY
(2010) XLI Congress of the Italian Neurological Society, Catania
P. Spadafora, M. Liguori, M. Caracciolo, G. Tagarelli, A. Bagalà, I.C. Cirò Candiano, G. Spinelli, A. Gambardella, A. Quattrone
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy
(2010) in American journal of human genetics
Moscufo N, Meier D, Liguori M, Schmidt JA, Panzer V, Wolfson L, Guttmann CRG
PROGRESSION OF MOBILITY IMPAIRMENT AND BRAIN WHITE MATTER LESION VOLUME IN THE ELDERLY: A TWO-YEAR LONGITUDINAL STUDY
(2010)
Liguori M, Meier D, Hildenbrand P, Healy B, Moraal B, Bakshi R, Chitnis T, Barkhof F, Guttmann CRG.
Early MS Activity on Subtraction MRI strongly predicts lesion accrual and atrophy over 5 years.
(2010)
Mike A, Glanz B, Hildenbrand P, Meier D, Bolden K, DellOglio E, Healy BC, Liguori M, Bakshi R, Guttmann CRG.
3T MRI Frequency of MS Cortical Lesions and Their Relationship with Cognitive Performance
(2010)
Liguori M, Healy BC, Tran D, Glanz BI, Wolfish C, Khoury S, Weiner HL, De Jager PL, Guttmann CRG.
HLA Allele Interactions associated with Multiple Sclerosis Activity, Severity, and Progression
(2010)
CERASA A, TONGIORGI E, FERA F, GIOIA MC, VALENTINO P, LIGUORI M, MANNA I, ZITO G, PASSAMONTI L, NISTICO R, QUATTRONE A
The effects of BDNF Val66Met polymorphism on brain function in controls and patients with multiple sclerosis: an imaging genetic study
(2010) in Behavioural brain research
Healy BC, Liguori M, Tran D, Chitnis T, Glanz B, Wolfish C, Gauthier S, Buckle G, Houtchens M, Stazzone L, Khoury S, Hartzmann R, Fernandez-Vina M, Hafler DA, Weiner HL, Guttmann CR, De Jager PL
HLA B*44: protective effects in MS susceptibility and MRI outcome measures
(2010) in Neurology
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 Putative Alzheimer's Disease Risk Allele in PCK1 Influences Brain Atrophy in Multiple Sclerosis
(2010) in PloS one
Sampat MP, Healy BC, Meier DS, Dell'Oglio E, Liguori M, Guttmann CR
Disease modeling in multiple sclerosis: assessment and quantification of sources of variability in brain parenchymal fraction measurements
(2010) in NeuroImage (Orlando Fla., Print)
Magariello A; Muglia M; Patitucci A; Ungaro C; Mazzei R; Gabriele AL; Sprovieri T; Citrigno L; Conforti FL; Liguori M; Gambardella A; Bono F; Piccoli T; Patti F; Zappia M; Mancuso M; Iemolo F; Quattrone A.
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia
(2010) in Journal of the neurological sciences
Spadafora P., Liguori M., Caracciolo M., Cirò Candiano IC., Manna I., Spinelli G., Andreoli V., Cittadella R., Trecroci F.,Quattrone A.,and Gambardella A.
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy
(2010)
Moscufo N, Meier D, Liguori M, Schmidt JA, Panzer V, Wolfson L, Guttmann CRG.
Progression of Mobility Impairment and Brain White Matter Lesion Volume in the Elderly: a two-years longitudinal study
(2010)
C Ungaro, FL Conforti, M Liguori, M Trojano, F Condino, I Manna, V Andreoli, A Magariello, A Patitucci, AL Gabriele, L Citrigno, W Sproviero, M Muglia, A Gambardella, R Mazzei.
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis
(2010) International Annual Meeting of the European Society of Human Genetics, Gothenburg, Sweden
V. Andreoli, F. Trecroci, A. La Russa, R. Cittadella, P. Spadafora, I.C. Cirò Candiano, M. Liguori, A. Gambardella and A. Quattrone.
Molecular characterization of the Presenilin-2 gene in Italian patients with familial Alzheimer Disease.
(2010) XLI Congress of the Italian Neurological Society, Catania
V. Andreoli, R. Cittadella, F. Trecroci, A. La Russa, M. Liguori, G. Nicoletti, M. Caracciolo, G. Di Palma and A. Quattrone.
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2.
(2009) Alzheimers and Parkinsons Diseases: Advances, Concepts and New Challenges, 9th International Conference AD/PD, Prague, Czech Republic.
Valentino P, Labate A, Nisticò R, Pirritano D, Cerasa A, Liguori M, Bastone L, Crescibene L, Quattrone A.
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.
(2009) in Multiple sclerosis
Gioia MC, Cerasa A, Valentino P, Fera F, Nisticò R, Liguori M, Lanza P, Quattrone A.
Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study.
(2009) in Brain and cognition
Passamonti L; Cerasa A; Liguori M; Gioia MC; Nisticò R; Valentino P; Quattrone A; Fera F
Neurobiological mechanisms underlying emotional processing in Relapsing-Remitting Multiple Sclerosis
(2009) in Brain (Print)
Liguori M, Mazzei R, Ungaro C, Simone IL, Gambardella A, Plasmati I, Fera F, Aguglia U, Lanza P, Bono F, Chiumarulo L, Conforti FL, Consoli D, Quattrone A.
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL.
(2009) in Neurology
Cerasa A, Tongiorgi E, Fera F, Gioia MC, Valentino P, Liguori M, Manna I, Zito G, Passamonti L, Nisticò R, Quattrone A.
The effects of BDNF Val(66)Met polymorphism on brain function in controls and patients with multiple sclerosis: An imaging genetic study.
(2009) in Behavioural brain research
Liguori M, Fera F, Patitucci A, Manna I, Condino F, Valentino P, Telarico P, Cerasa A, Gioia MC, di Palma G, Quattrone A.
A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis.
(2009) in Brain research
Martino D, Muglia M, Abbruzzese G, Berardelli A, Girlanda P, Liguori M, Livrea P, Quattrone A, Roselli F, Sprovieri T, Valente EM, Defazio G.
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia
(2009) in European journal of neurology (Print)
Ungaro C; Mazzei R; Conforti FL; Sprovieri T; Servillo P; Liguori M; Citrigno L; Gabriele AL; Magariello A; Patitucci A; Muglia M and A. Quattrone
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene.
(2009) in Journal of neuroscience research
C Ungaro, FL Conforti, M Muglia, A Patitucci, AL Gabriele, A Magariello, L Citrigno, W Sproviero, M Liguori, M Trojano, A Gambardella, R Mazzei
Multiple sclerosis: polymorphism ILE587VAL in the eIF2B5 gene as susceptibility factor
(2009)
Passamonti L, Cerasa A, Liguori M, Gioia MC, Valentino P, Nisticò R, Quattrone A, Fera F
Neurobiological mechanisms underlying emotional processing in relapsing-remitting multiple sclerosis
(2009) SIN, Padova
C Ungaro, FL Conforti, T Sprovieri, P Servillo, M Liguori, L Citrigno, AL Gabriele, A Magariello, A Patitucci, M Muglia and R Mazzei
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy
(2008) 18th Meeting of the European Neurological Society, Nizza, France, JUN 07-11, 2008
Cittadella Rita
Andreoli Virginia
Trecroci Francesca
Spadafora Patrizia
Ida Manna
Liguori maria
Mutation analysis if the CAPN3 gene in Italian patients with suspected LGMD type 2." 31 Maggio
Cittadella Rita
Andreoli Virginia
Trecroci Francesca
Spadafora Patrizia
Ida Manna
(2008) European Human Genetics Conference, Barcellona, Spain, 31 Maggio - 3 Giugno
C Ungaro, FL Conforti, T Sprovieri, P Servillo, M Liguori, L Citrigno, AL Gabriele, A Magariello, A Patitucci, M Muglia and R Mazzei
Extended polymorphic and mutational analysis of the NOTCH3 gene in patients affected by leukoencephalopathy
(2008) The 12th Congress of the European Federation of Neurological Societies (EFNS), Madrid
A. La Russa, P. Valentino, V. Andreoli, F. Trecroci, I. Manna, M. Liguori, P. Spadafora, R. Cittadella.
Mutation analysis of the CAPN3 gene in Italian patients with suspected LGMD type 2.
(2008) in European journal of human genetics
R. Cittadella, A. La Russa, P. Valentino, V. Andreoli, F. Trecroci, I. Manna, M. Liguori, P. Spadafora, A. Quattrone.
A novel mutation in FKRP gene in Italian patient with LGMD.
(2008) in European journal of human genetics
P. Spadafora, M. Liguori, P. Valentino, R. Cittadella, A. La Russa, I. Manna, I. Candiano, V. Andreoli, and A. Quattrone.
Mutational screening of the CAPN3 in LGMD patients from Southern Italy.
(2008) in Neurological sciences (Testo stamp.)
T. Maci, F. Le Pira, L. Marturano, M. Liguori, R. Cittadella, A. Quattrone, M. Zappia
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease
(2008) in Neurological sciences (Testo stamp.)
Valentino P, Labate A, Nisticò R, Pirritano D, Cerasa A, Liguori M, Bastone L, Crescibene L, Quattrone A.
Anti-GM1antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.
(2008) in Multiple sclerosis
Cerasa A, Gioia MC, Labate A, Liguori M, Lanza P, Quattrone A.
Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume.
(2008) in NeuroReport (Oxf.)
Liguori M. 1; La Russa A. 1; Manna I. 1; Andreoli V. 1; Caracciolo M. 1; Spadafora P. 1; Cittadella R. 1; and Quattrone A. 1-2
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
(2008) in Journal of neurology (Print)
Manna I, Liguori M, Valentino P, Condino F, La Russa A, Clodomiro A, Nisticò R, Di Palma G, Quattrone A.
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis.
(2008) in Journal of the neurological sciences
Cerasa A, Fera F, Gioia MC, Passamonti L, Liguori M, Lanza P, Muglia M, Magariello A, Quattrone A.
Ventro-Lateral Prefrontal activity during working memory processing is modulated by MAO A genetic variation.
(2008) in Brain research
Ungaro C, Sprovieri T, Conforti FL, Consoli D, Citrigno L, Liguori M, Quattrone A, Mazzei R.
Gene symbol: NOTCH3. Disease CADASIL.
(2008) in Human genetics
Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La Morgia C, Montagna P, Liguori M, Zanna C et al.
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
(2008) in Brain (Print)
Valentino P, Pirritano D, Bono F, Quattrone A, Muglia M, Nisticò R, Liguori M, Citrigno L, Quattrone A, Aguglia U, Aguglia U, Branca D.
Genetic screening for familial amyloid polyneuropathy in patients with idiopathic carpal tunnel syndrome.
(2008) in Journal of the peripheral nervous system
Ungaro, Carmine; Sprovieri, Teresa; Conforti, Francesca Luisa; Consoli, Domenico; Citrigno, Luigi; Liguori, Maria; Quattrone, A.; Mazzei, Rosalucia
Gene symbol: NOTCH3. Disease: CADASIL.
(2008)
Ungaro, Carmine; Sprovieri, Teresa; Conforti, Francesca Luisa; Consoli, Domenico; Citrigno, Luigi; Liguori, Maria; Quattrone, A.; Mazzei, Rosalucia
Gene symbol: NOTCH3. Disease: CADASIL.
(2008)
V. Andreoli, F. Trecroci, R. Cittadella, A. La Russa, M. Caracciolo, G. Di Palma, M. Liguori, I. Manna, P. Spadafora and A. Quattrone
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimers Disease
(2008) XXXIX Congress of the Italian Neurological Society,, Napoli, Italia
A. La Russa, V. Andreoli, F. Trecroci, I.Manna, I.C.Cirò Candiano, P.Spadafora, M. Liguori, R. Cittadella.
Neuropatia ottica ereditaria di Lebers e Sclerosi Multipla: Hardings syndrome.
(2008) XI Congresso Nazionale S.I.G.U., Genova, Italia
C Ungaro, FL Conforti, T Sprovieri, P Servillo, M Liguori, L Citrigno, AL Gabriele, A Magariello, A Patitucci, M Muglia, R Mazzei.
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy.
(2008) The American Society of Human Genetics, Philadelphia
C Ungaro, FL Conforti, T Sprovieri, P Servillo, M Liguori, L Citrigno, AL Gabriele, A Magariello, A Patitucci, M Muglia and R Mazzei.
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy.
(2008) XI Congresso nazionale della Società Italiana di Genetica Umana (SIGU), Genova
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 evaluation of cadasil progression by diffusion magnetic resonance imaging.
(2008) Società Italiana di Neurologia (SIN), Napoli
1I. Manna, 1M. Liguori, 2P. Valentino, 1F. Condino, 2R. Nisticò, 1P. Spadafora, 1G. Di Palma, 1,2 A. Quattrone.
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs.
(2008) Società Italiana di Neurologia (SIN), Napoli (Italy)
I. Manna 1, M. Liguori 1, F. Fera 3, A. Patitucci 1, F. Condino 1, P. Valentino 2, A. Cerasa 1, MC. Gioia 1, P. Spadafora 1, P. Telarico 4 , L. Vena 1, G. Di Palma1, and Quattrone A1,2.
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS).
(2008) Società Italiana di Genetica Umana (SIGU), Genova (Italy)
Gioia MC, Cerasa A, Valentino P, Lanza P, Liguori M, Nisticò R, Pirritano D, Canino M, Quattrone A.
Personality predicts functional activation during working memory demand in patients with multiple sclerosis
(2008) Società Italiana di Neurologia (SIN), Napoli
V. Andreoli, F. Trecroci, A. Nucera, A. La Russa, M. Liguori, I. Manna, P. Spadafora, M. Caracciolo, G. Di Palma, R. Cittadella.
Screening for MELAS mutations in Italian patients having stroke-like episodes.
(2008) European Human Genetic Conference 2008, Barcelona, Spain.
R Mazzei, C Ungaro, FL Conforti, T Sprovieri, P Servillo, M Liguori, L Citrigno, AL Gabriele, A Magariello, A Patitucci, M Muglia, A Quattrone.
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy
(2008) XXXIX Congresso della Società Italiana di Neurologia, SIN, Napoli
Ungaro C., Conforti F.L., Liguori M., Muglia M., Sprovieri T., Patitucci A., Magariello A., Gabriele A.L., Quattrone A., Mazzei R.
Familial multiple sclerosis is not associated with eIF2B5 gene mutation in Southern Italy.
(2007) in Journal of the neurological sciences
Mazzei R, Conforti FL, Ungaro C, Liguori M, Magariello A, Gabriele AL, Patitucci A, Sprovieri T, Muglia M, Quattrone A
Gene symbol: NOTCH3.
(2007) in Human genetics
Gioia MC, Cerasa A, Liguori M, Passamonti L, Condino F, Vercillo L, Valentino P, Clodomiro A, Quattrone A, Fera F.
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis
(2007) in Brain research
Liguori M,Fera F,Gioia MC,Valentino P,Manna I,Condino F,Cerasa F,La Russa A,Clodomiro A,Paolillo A,Nisticò R,Vercillo L,Cittadella R,Quattrone A.
Investigating the role of brain-derived neurotrophic factor in relapsing-remitting multiple sclerosis.
(2007) in Genes, brain and behavior (Print)
Virginia Andreoli, Giuseppe Nicoletti, Nelide Romeo, Francesca Condino, Antonella La Russa, Maria Liguori, Ida Manna, Patrizia Spadafora, Aldo Quattrone, Rita Cittadella.
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene.
(2007) in Neurochemical research
V. Andreoli, R. Cittadella, P. Valentino, F. Condino, A. La Russa, M. Liguori, I. Manna, P. Spadafora, R. Nisticò, D. Pirritano, A. Clodomiro, and A. Quattrone.
The role of VLA4 polymorphisms in Multiple Sclerosis: an association study.
(2007) in Journal of neuroimmunology (Print)
Spadafora P, Annesi G, Liguori M, Tarantino P, Cutuli N, Carrideo S, Ciro Candiano IC, De Marco EV, Civitelli D, Annesi F, Giuffrida S, Quattrone A
Gene dosage influences the age at onset of SCA2 in a family from southern Italy
(2007) in Clinical genetics
Liguori M., F. Fera, A. Patitucci, P. Valentino, I. Manna, F. Condino, A. Cerasa, M.C. Gioia, R. Nisticò, A. Clodomiro, A. La Russa, P. Spadafora, R. Cittadella, A. Quattrone.
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS).
(2007) in Neurological sciences (Testo stamp.)
R Mazzei, C Ungaro, FL Conforti, M Liguori, T Sprovieri, G Di Palma, A Patitucci, A Magariello, AL Gabriele, L Citrigno, M Muglia, A Quattrone.
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy
(2007) V Incontro dell'Istituto di Neuroscienze, Cagliari
Liguori M., F. Fera, A. Patitucci, I. Manna, P. Valentino, F. Condino, A. Cerasa, M. Gioia, R. Cittadella, A. Quattrone
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis
(2007) 23 Congresso ECTRIMS, Praga 11-14 Ottobre, 2007, Praga 11-14 Ottobre, 2007
M Liguori, R Mazzei, C Ungaro, FL Conforti, T Sprovieri, A Magariello, A Patitucci, AL Gabriele, M Muglia, A Quattrone
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL
(2007) V Incontro dellIstituto di Neuroscienze, Cagliari
Manna I, Liguori M., P. Valentino, F. Condino, A. Clodomiro, A. La Russa, R. Nisticò, G. Di Palma, A. Quattrone
Preliminary evidence of NOS2A protective effect in patients with Relapsing-Remitting Multiple Sclerosis
(2007) XXXVIII Congresso della Società Italiana di Neurologia,, Firenze 13-17 Ottobre 2007
A. Cerasa, MC. Gioia, F. Fera, M. Liguori, L. Passamonti, A. Magariello, M. Muglia, P. Lanza, A. Quattrone.
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation
(2007) National Congress of Italian Society of Neuroscience, Verona
MC. Gioia, A. Cerasa, F. Fera, M. Liguori, L. Passamonti, P. Valentino, A. Clodomiro, A. Quattrone
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis
(2007) V incontro dellIstituo di Neuroscienze del CNR, cagliari
F.Fera, M. Liguori, MC Gioia, A. Cerasa, P. Valentino, A. Clodomiro, A. Quattrone
The BOLD response to episodic encoding and retrieval in RR-MS
(2007) V incontro dellIstituo di Neuroscienze del CNR, cagliari
I Manna, Liguori M, P Valentino, A La Russa, F Condino, A Clodomiro, R Nisticò, G Di Palma and A Quattrone
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis
(2007) V Incontro dellIstituto di Neuroscienze, Cagliari 3-5 giugno 2007
L. Bastone, T. Ferraro, A. Bagalà, M. Casaletto, M.G. Perri, F. Condino, Liguori M., R.L. Mazzei, L. Crescibene.
Glutamate and multiple sclerosis.
(2007) 23 Congresso ECTRIMS,, Praga 11-14 Ottobre, 2007
A. Cerasa, VS Mattay, MC. Gioia, M. Liguori, P. Lanza, I. Manna,
Brain-derived neurotrophic factor val66met polymorphysm and the cortical response to spatial working memory
(2007) V incontro dellIstituo di Neuroscienze del CNR, Cagliari
Manna I, P. Valentino, F. Condino, Liguori M., A. La Russa, A. Clodomiro, R. Nisticò, G. Di Palma, V. Andreoli, R. Cittadella, A. Quattrone
No association between estrogen receptor 1 gene polymorphisms and susceptibility to multiple sclerosis
(2007) 23 Congresso ECTRIMS, Praga 11-14 Ottobre, 2007, Praga 11-14 Ottobre, 2007
Manna I, Liguori M., P. Valentino, F. Condino, A. Carpino, A. La Russa, A. Clodomiro, R. Nisticò, G. Di Palma, A. Quattrone
Relapsing-remitting multiple sclerosis and protective effect of a NOS2A gene variant
(2007) 23 Congresso ECTRIMS,, Praga 11-14 Ottobre, 2007
A.La Russa, M. Liguori, I. Manna, V. Andreoli, M. Caracciolo, P. Spadafora, R. Cittadella, A. Quattrone.
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation.
(2007) V° Incontro dellIstituto di Neuroscienze-Consiglio Nazionale delle Ricerche., Cagliari
A. Cerasa, F. Fera, MC. Gioia, M. Liguori, L. Passamonti, P. Valentino, A. Clodomiro, A. Quattrone
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis
(2007) V incontro dellIstituo di Neuroscienze del CNR, Cagliari
M. Casaletto, A. Bagalà, L. Bastone, T. Ferraro, M.G. Perri, Liguori M., L. Crescibene
Serum prolactin concentrations in patients with multiple sclerosis
(2007) Atti del 23 Congresso ECTRIMS, Praga 11-14 Ottobre, 2007, Praga 11-14 Ottobre, 2007
R Mazzei, M Liguori, FL Conforti, C Ungaro, M Muglia, T Sprovieri, A Patitucci, A Magariello, AL Gabriele, L Citrigno, L Crescibene, A Quattrone.
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis.
(2007) del 23 Congresso ECTRIMS,, Praga 11-14 Ottobre, 2007
F. Fera, A. Cerasa, MC. Gioia, M. Liguori, A. Quattrone, K. Pardatscher.
Visualizing genetic influences on Human brain function: Interactive effects of BNDF and COMT allelic variations on a spatial working memory network
(2007) Associazione Italiana di Neuroradiologia, Bergamo
A. Cerasa, MC Gioia, F Fera, M Liguori, L. Passamonti, F. Condino, P. Valentino, A. Clodomiro,M. Canino, A. Quattrone
Impact of brain atrophy and cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis
(2007) Società Italiana di Neurologia, Firenze
V. Andreoli , P. Valentino, F. Condino, F. Trecroci, A. La Russa, M. Liguori, R. Cittadella.
An examination of the Apo-1/Fas polymorphisms in Italian patients with multiple sclerosis.
(2006) Congresso dell'Associazione Italiana di Neuroimmunologia, AINI, Bari, Italia
V. Andreoli, M. Liguori, F. Trecroci, A. La Russa, R.Cittadella.
Mutational analysis of the presenilin 2 gene in a group of Italian patients with familial Alzheimer's disease.
(2006) in American journal of human genetics
*M Liguori , *MC Gioia, °P Valentino, *I Manna, *F Condino, *A Cerasa, °A Clodomiro, *A La Russa, , °R. Nisticò, *R Cittadella, ^*F Fera and °*A Quattrone
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION
(2006) in Neurological sciences (Testo stamp.)
I. Manna, P. Valentino, A. La Russa, F. Condino, M. Liguori, R. Nisticò, A. Clodomiro, M. Canino, R. Cittadella, A. Quattrone.
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis.
(2006) in Neurological sciences (Testo stamp.)
A Cerasa, VS Mattay, MC Gioia, M Liguori, I manna, A La Russa, R Cittadella, DR Weinberger, A Quattrone, F Fera
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory.
(2006) in Human brain mapping (Print)
V. Andreoli, P. Valentino, F. Condino, L. Nicoletti, I. Manna, A. La Russa, M. Liguori, R. Cittadella.
The Fas gene polymorhisms in Italian patients with Sporadic Alzheimers Disease.
(2006) in American journal of human genetics
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
(2006) in Brain research bulletin
Ban M, Booth D, Heard R, Stewart G, Goris A, Vandenbroeck K, Dubois B, Laaksonen M, Ilonen J, Alizadeh M, Edan G, Babron MC, Brassat D, Clanet M, Cournu-Rebeix I, Fontaine B, Semana G, Goedde R, Epplen J, Weber A, Infante-Duarte C, Zipp F, Rajda C, Bencsi
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans.
(2006) in Journal of neuroimmunology (Print)
MANNA I, VALENTINO P, LA RUSSA A, CONDINO F, NISTICO R, LIGUORI M, CLODOMIRO A, ANDREOLI V, PIRRITANO D, CITTADELLA R, QUATTRONE A
Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosis
(2006) in Journal of negative results in biomedicine
R Mazzei,1 C Ungaro,1 M Liguori,1 FL Conforti,1 A Gambardella,1,2 T Sprovieri,1 A Magariello,1 A Patitucci,1 A Qualtieri,1 M. Muglia,1 A. Quattrone.1,2
Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL
(2006) in Neurological sciences (Testo stamp.)
C. Ungaro, T. Sprovieri, M. Muglia, F.L. Conforti, A. Patitucci, M. Liguori, A. Magariello, A.L. Gabriele, R. Mazzei
Ricerca di mutazioni nel gene jag1 e loro possibile implicazione nella modulazione di fenotipi simili al Cadasil
(2006) IX Congresso Nazionale della Società Italiana di Genetica Umana, Lido di Venezia, Venezia
La Russa, M. Liguori, I. Manna, V. Andreoli, M. Caracciolo, P. Spadafora, R. Cittadella, A. Quattrone.
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità.
(2006) 9° Congresso Nazionale S.I.G.U., Venezia, Italia.
C Ungaro, M Liguori, FL Conforti, P Servillo, T Sprovieri, A Patitucci, AL Gabriele, A Magariello, M Muglia, R Mazzei
Il Ruolo Della Rm Nello Screening Sul Gene Notch3: Distinguere I Soggetti Cadasil Apparentemente Sporadici Da Altre Leucoencefalopatie
(2006) IX Congresso Nazionale della Società Italiana di Genetica Umana, Lido di Venezia, Venezia
C Ungaro,1 FL Conforti,1 M Liguori,1 A Gambardella,1,2 T Sprovieri,1 A Magariello,1 AL Gabriele,1 A Patitucci,1 A Qualtieri,1 M Muglia,1 R Mazzei1
Due nuove mutazioni non coinvolgenti residui di cisteina in pazienti affetti da CADASIL
(2006) IX Congresso Nazionale della Società Italiana di Genetica Umana (S.I.G.U.), Lido di Venezia
V. Andreoli, M. Liguori, F. Trecroci, A. La Russa, R. Cittadella.
Analisi mutazionale del gene della Presenilina 2 in pazienti italiani, affetti da malattia di Alzheimer familiare.
(2006) 9° Congresso Nazionale S.I.G.U., Venezia, Italia.
1A. Clodomiro, 1P. Valentino, 1D. Pirritano, 1R. Nisticò, 1M. Canino, 2L. Crescibene, 2L. Bastone, 2F. Condino, 2M. Liguori, 1,2A. Quattrone
Investigation of the relationship between anti-GM1 antibodies and brain atrophy in multiple sclerosis
(2006) XXXVII Congress of the Italian Neurological Society, Bari
MC Gioia, F Fera, A Cerasa, M Liguori, O Gallo, L Passamonti, P Valentino, A Clodomiro, A Quattrone
Cognitive impairment drives adaptive cortical reorganization in Relapsing-Remitting Multiple Sclerosis.
(2006) Human Brain Mapping, Firenze
Mazzei R,* Ungaro C,* Liguori M,* Conforti FL,* Gambardella A,*° Sprovieri T,* Patitucci A,* Magariello A,* Gabriele AL,* Qualtieri A,* Muglia M.*
Two novel Notch3 mutations not involving cysteine residues in CADASIL patients
(2006) The American Society of Human Genetics, New Orleans, Louisiana
*M. Liguori, C. Ungaro, F.L. Conforti, A. Patitucci, A. Magariello, T. Sprovieri, A.L. Gabriele, M. Muglia and R. Mazzei
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING
(2006) 58th Annual Meeting Human Genetics, New Orleans - USA
M. Liguori*, R. Mazzei*, C. Ungano*, FL. Conforti*, T. Sprovieri*, A. Magariello*, A. Patitucci*, U. Aguglia^, M. Muglia* and A. Quattrone*°
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES: THE ROLE OF MRI IN THE NOTCH3 GENE SCREENING
(2006) XXXVII Congresso Società Italiana di Neurologia, Bari
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
(2006) European Society of Human Genetics, Amsterdam
Chiocchetti A, Comi C, Indelicato M, Castelli L, Mesturini R, Bensi T, Mazzarino MC, Giordano M, D'Alfonso S, Momigliano-Richiardi P, Liguori M, Zorzon M, Amoroso A, Trojano M, Monaco F, Leone M, Magnani C, Dianzani U.
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression.
(2005) in Journal of neuroimmunology (Print)
Roxburgh RH, Seaman SR, Masterman T, Hensiek AE, Sawcer SJ, Vukusic S, Achiti I, Confavreux C, Coustans M, le Page E, Edan G, McDonnell GV, Hawkins S, Trojano M, Liguori M, Cocco E, Marrosu MG, Tesser F, Leone MA, Weber A, Zipp F, Miterski B, et al.
Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.
(2005) in Neurology
A.Gambardella,U.Aguglia,R.Chifari,A.Labate,I.Manna,M.Liguori,N.Romeo,D.Messina,E.Lepiane,A.LaRussa,P.Ventura,R.Cittadella,V.Andreoli,F.Sasanelli,E.Colosimo,U.Leggio,A.Quattrone.
APOE-4 allele and disease duration affect verbal memory in mild temporal lobe epilepsy.
(2004) in Neurological sciences (Testo stamp.)
D.Messina,G.Savettieri,V.Andreoli,S.Bonavita,C.Caltagirone,R.Cittadella,D.Farina,M.C.Fazio,P.Girlanda,F.Le Pira,M.Liguori,A.Lugaresi,U.Nocentini,A.Reggio,G.Salemi,G.Tedeschi,M.Trojano, I.Manna,P.Valentino,A.Quattrone.
Gender-related effect of clinical and genetic variables on the cognitive impairment in MS.
(2004) in Neurological sciences (Testo stamp.)
A. La Russa, I. Manna, V. Andreoili, M. Liguori, P. Serra, P. Valentino, A. Clodomiro, R. Cittadella.
Intercellular adhesion molecole-1 gene (ICAM-1) polymorphism: study of association with Multiple Sclerosis.
(2004) in European journal of human genetics
Liguori M.,Cittadella R.,Manna I.,Valentino P.,La Russa A.,Serra P.,Trojano M.,Messina D.,Ruscica F.,Andreoli V.,Romeo N.,Livrea P.,Quattrone A.
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis
(2004)
Savettieri G,Messina D,Andreoli V,Bonavita S,Caltagirone C,Cittadella R,Farina D,Fazio MC,Girlanda P,Le Pira F,Liguori M,Lugaresi A,Nocentini U,ReggioA,Salemi G,Tedeschi G,Trojano M,Quattrone A.
Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis.
(2004) in Journal of neurology (Print)
Ballerini C, Guerini FR, Rombolà G, Rosati E, Massacesi L, Ferrante P, Caputo D, Talamanca LF, Naldi P, Liguori M, Alizadeh M, Momigliano-Richiardi P, D'Alfonso S.
HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe.
(2004) in Journal of neuroimmunology (Print)
La Bella V,Liguori M,Cittadella R,Settipani N,Piccoli T,Manna I,Quattrone A,Piccoli F.
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease.
(2004) in European journal of neurology (Print)
Liguori M, Cittadella R, Manna I, Valentino P, La Russa A, Serra P, Trojano M, Messina D, Ruscica F, Andreoli V, Romeo N, Livrea P, Quattrone A.
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis.
(2004) in Journal of neurology (Print)
V.Andreoli,R.Cittadella,I.Manna,A.La Russa,D.Messina,G.Savettieri,S.Bonavita,C.Caltagirone,D.Farina,M.Fazio,F.Le Pira,M.Liguori,A.Lugaresi,P.Girlanda,U.Nocentini,A.Reggio,G.Salemi,G.Tedeschi,M.Trojano,P.Valentino,A.Quattrone.
Declino cognitivo nella Sclerosi Multipla:Studi di associazione.
(2004) S.I.G.U., Pisa
Romeo N.,Di Palma G.,Cavalcanti F.,Liguori M.,De Marco V.,Messina D.,Civitelli D.,Caracciolo M.
Depression and Parkinson's disease:a neuropsychological view
(2004) First Congress of the Neuropsychological Societies, Modena
Trojano M, Liguori M, Paolicelli D, Zimatore GB, De Robertis F, Avolio C, Giuliani F, Fuiani A, Livrea P; Southern Italy MS Group.
Interferon beta in relapsing-remitting multiple sclerosis: an independent postmarketing study in southern Italy.
(2003) in Multiple sclerosis
Savettieri G1,Andreoli V2, Bonavita S3, Cittadella R2, Caltagirone C4, Fazio MC5, Girlanda P5, Le Pira F6, Liguori M7, Logroscino G8, Lugaresi A9,Nocentini U4, Reggio A6,Salemi G1, Serra P2,Tedeschi G3,Toma L9,Trojano M7,Valentino P10,Quattrone A.2-10
Apolipoprotein E genotype does not influence the progression of multiple sclerosis.
(2003) in Journal of neurology (Print)
Gomez-Lira M,1; Liguori M,2; Magnani C,3; Bonamini D,1; Salviati A,4; Leone M,5; Andreoli V,2; Trojano M,6; Valentino P,7; Savettieri G,8 Quattrone A,2-7; Pignatti PF,1; Momigliano-Richiardi P,9; Giordano M.9
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers.
(2003) in Journal of neuroimmunology (Print)
Mellai M, Giordano M, D'Alfonso S, Marchini M, Scorza R, Giovanna Danieli M, Leone M, Ferro I, Liguori M, Trojano M, Ballerini C, Massacesi L, Cannoni S, Bomprezzi R, Momigliano-Richiardi P.
Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus.
(2003) in Human immunology
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,
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population.
(2003) in Journal of neuroimmunology (Print)
Simone IL, Carrara D, Tortorella C, Liguori M, Lepore V, Pellegrini F, Bellacosa A, Ceccarelli A, Pavone I, Livrea P
Course and prognosis in early-onset MS: comparison with adult-onset forms.
(2002) in Neurology
D'Alfonso S, Mellai M, Giordano M, Pastore A, Malferrari G, Naldi P, Repice A, Liguori M, Cannoni S, Milanese C, Caputo D, Savettieri G, Momigliano-Richiardi P; Italian Group for the Study of Multiple Sclerosis Genetics.
Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis.
(2002) in Journal of neuroimmunology (Print)
Ghezzi A, Pozzilli C, Liguori M, Marrosu MG, Milani N, Milanese C, Simone I, Zaffaroni M.
Prospective study of multiple sclerosis with early onset.
(2002) in Multiple sclerosis
Trojano M, Liguori M, Bosco Zimatore G, Bugarini R, Avolio C, Paolicelli D, Giuliani F, De Robertis F, Marrosu MG, Livrea P.
Age-related disability in multiple sclerosis.
(2002) in Annals of neurology
SIMONE IL, TORTORELLA C, FEDERICO F, LIGUORI M, LUCIVERO V, GIANNINI P, CARRARA D, BELLACOSA A, LIVREA P
Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study
(2001) in Neurology
LIGUORI M, MARROSU MG, PUGLIATTI M, GIULIANI F, DE ROBERTIS F, COCCO E, ZIMATORE GB, LIVREA P, TROJANO M
Age at onset in multiple sclerosis
(2000) in Neurological sciences (Testo stamp.)
D'Alfonso, Sandra; Nisticò, Lorenza; Bocchio, Daniela; Bomprezzi, Roberto; Marrosu -, Maria Giovanna; Murru, Maria Rita; Lai, Marina; Massacesi, Luca; Ballerini, Clara; Repice, Anna Maria; Salvetti, Marco; Montesperelli, Chiara; Ristori, Giovanni P.; Trojano, Maria; Liguori, Maria; Gambi, Domenico; Quattrone, A.; Tosi, Roberto M.; Momigliano-Richiardi, Patricia
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population
(2000) in Journal of neurovirology
D'Alfonso, Sandra; Nisticò, Lorenza; Zavattari, Patrizia; Marrosu -, Maria Giovanna; Murru, Raffaele; Lai, Marina; Massacesi, Luca; Ballerini, Clara; Gestri, Donella; Salvetti, Marco; Ristori, Giovanni P.; Bomprezzi, Roberto; Trojano, María; Liguori, Maria; Gambi, Domenico; Quattrone, A.; Fruci, Doriana; Cucca, Francesco; Richiardi, Patricia Momigliano; Tosi, Roberto M.
Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families
(1999) in European journal of human genetics
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PAOLICELLI D, GIULIANI F, RICCIO P, LIVREA P
Changes of serum sICAM-1 and MMP-9 induced by rIFNbeta-1b treatment in relapsing-remitting MS
TROJANO M, AVOLIO C, LIUZZI GM, RUGGIERI M, DEFAZIO G, LIGUORI M, SANTACROCE MP,
(1999) in Neurology (Online)
Trojano, M; Liguori, M; De Robertis, F; Stella, A; Guanti, G; Avolio, C; Livrea, P
Comparison of clinical and demographic features between affected pairs of Italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms
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Ghezzi, A; Deplano, V; Faroni, J; Grasso, MG; Liguori, M; Marrosu, G; Pozzilli, C; Simone, IL; Zaffaroni, M
Multiple sclerosis in childhood: Clinical features of 149 cases
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High resolution proton MR spectroscopy of cerebrospinal fluid in MS patients. Comparison with biochemical changes in demyelinating plaques
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Federico, F; Simone, IL; Conte, C; Lucivero, V; Giannini, P; Liguori, M; Picciola, E; Tortorella, C
Prognostic significance of metabolic changes detected by proton magnetic resonance spectroscopy in ischaemic stroke
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FEDERICO, F; CONTE, C; SIMONE, IL; GIANNINI, P; LIGUORI, M; PICCIOLA, E; TORTORELLA, C; FERRARI, E
PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN PATIENTS WITH ISCHEMIC STROKE
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SIMONE, IL; ANNUNZIATA, P; MAIMONE, D; LIGUORI, M; LEANTE, R; LIVREA, P
SERUM AND CSF ANTI-GM1 ANTIBODIES IN PATIENTS WITH GUILLAIN-BARRE-SYNDROME AND CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY
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