ESPOSITO, TERESA

ESPOSITO, TERESA  

Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli  

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Titolo Data di pubblicazione Autore(i) File
Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies 1-gen-2024 Carrillo, Federica; Palomba, Nicole Piera; Ghirimoldi, Marco; Didò, Camilla; Fortunato, Giorgio; Khoso, Shahzaib; Giloni, Tiziana; Santilli, Marco; Bocci, Tommaso; Priori, Alberto; Pietracupa, Sara; Modugno, Nicola; Barberis, Elettra; Manfredi, Marcello; Signorelli, Paola; Esposito, Teresa
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients 1-gen-2023 Piera Palomba, Nicole; Fortunato, Giorgio; Pepe, Giuseppe; Modugno, Nicola; Pietracupa, Sara; Damiano, Immacolata; Mascio, Giada; Carrillo, Federica; DI GIOVANNANTONIO, LUCA GIOVANNI; Ianiro, Laura; Martinello, Katiuscia; Volpato, Viola; Desiato, Vincenzo; Acri, Riccardo; Storto, Marianna; Nicoletti, Ferdinando; Webber, Caleb; Simeone, Antonio; Fucile, Sergio; Maglione, Vittorio; Esposito, Teresa
Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population. 1-gen-2022 Stanzione, Rosita; Cotugno, Maria; Forte, Maurizio; Bianchi, Franca; Marchitti, Simona; Piera Palomba, Nicole; Esposito, Teresa; Zanda, Bastianina; Sanna, Alessandra; Rubattu, Speranza
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease 1-gen-2021 Tirozzi, A; Modugno, N; Palomba, Np; Ferese, R; Lombardi, A; Olivola, E; Gialluisi, A; Esposito, T
Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease 1-gen-2021 Konig, E; Nicoletti, A; Pattaro, C; Annesi, G; Melotti, R; Gialluisi, A; Schwienbacher, C; Picard, A; Blankenburg, H; Pichler, I; Modugno, N; Ciullo, M; Esposito, T; Domingues, Fs; Hicks, Aa; Zappia, M; Pramstaller, Pp
Identification of sixteen novel candidate genes for late onset Parkinson's disease 1-gen-2021 Gialluisi, A; Reccia, Mg; Modugno, N; Nutile, T; Lombardi, A; DI GIOVANNANTONIO, LUCA GIOVANNI; Pietracupa, S; Ruggiero, D; Scala, S; Gambardella, S; Iacoviello, L; Gianfrancesco, F; Acampora, D; D'Esposito, M; Simeone, A; Ciullo, M; Esposito, T
Novel autophagic vacuolar myopathies: Phenotype and genotype features 1-gen-2021 Napolitano, F; Terracciano, C; Bruno, G; De Blasiis, P; Lombardi, L; Gialluisi, A; Gianfrancesco, F; De Giovanni, D; Tummolo, A; Di Iorio, G; Limongelli, G; Esposito, T; Anna Beatrice Melone, M; Sampaolo, S
Rare variants in autophagy and non-autophagy genes in late-onset pompe disease: Suggestions of their disease-modifying role in two Italian families 1-gen-2021 Napolitano, F; Bruno, G; Terracciano, C; Franzese, G; Palomba, Np; Scotto Di Carlo, F; Signoriello, E; De Blasiis, P; Navarro, S; Gialluisi, A; Melone, Mab; Sampaolo, S; Esposito, T
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone 1-gen-2020 Scotto di Carlo, F; Pazzaglia, L; Esposito, T; Gianfrancesco, F
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population 1-gen-2020 Gialluisi, A; Reccia, Mg; Tirozzi, A; Nutile, T; Lombardi, A; De Sanctis, C; Varanese, S; Pietracupa, S; Modugno, N; Simeone, A; Ciullo, M; Esposito, T
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology 1-gen-2020 Scotto di Carlo, F; Pazzaglia, L; Mumm, S; Benassi, Ms; De Chiara, A; Franchi, A; Parafioriti, A; Righi, A; Esposito, T; Whyte, Mp; Gianfrancesco, F
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 1-gen-2019 Napolitano, Filomena; Di Iorio, Valentina; Di Iorio, Giuseppe; Melone Mariarosa Anna, Beatrice; Gianfrancesco, Fernando; Simonelli, Francesca; Esposito, Teresa; Testa, Francesco; Sampaolo, Simone
Intrafamilial "DOA-plus" phenotype variability related to different OMI/HTRA2 expression. 1-gen-2019 Napolitano, F; Terracciano, C; Bruno, G; Nesti, C; Barillari, Mr; Barillari, U; Santorelli, Fm; Melone, Mab; Esposito, T; Sampaolo, S
Procedimenti di analisi genetica della malattia di Parkinson 1-gen-2019 Teresa Esposito ; Marina Ciullo e Antonio Simeone per CNRIGB e i dott.ri Mafalda Giovanna Reccia e Alessandro Gialluisi per NeuromedTitolarità CNR; Istituto Neurologico Mediterraneo NEUROMED SpA
Autosomal dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. 1-gen-2018 Napolitano, F; Di Iorio, V; Testa, F; Tirozzi, A; Reccia, M G; Lombardi, L; Farina, O; Simonelli, F; Gianfrancesco, F; Di Iorio, G; Melone, M A B; Esposito, T; Sampaolo, S
Successful long-term therapy with flecainide in a family with paramyotonia congenita 1-gen-2018 Terracciano, C; Farina, O; Esposito, T; Lombardi, L; Napolitano, F; Blasiis, Pd; Ciccone, G; Todisco, V; Tuccillo, F; Bernardini, S; Di Iorio, G; Melone, Mab; Sampaolo, S
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location 1-gen-2018 Scotto di Carlo, F; Divisato, G; Iacoangeli, M; Esposito, T; Gianfrancesco, F
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy 1-gen-2018 Pascarella, A; Terracciano, C; Farina, O; Lombardi, L; Esposito, T; Napolitano, F; Franzese, G; Panella, G; Tuccillo, F; la Marca, G; Bernardini, S; Boffo, S; Giordano, A; Di Iorio, G; Melone, Mab; Sampaolo, S
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone. 1-gen-2018 Divisato, G; di Carlo, Fs; Petrillo, N; Esposito, T; Gianfrancesco, F
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation. 1-gen-2017 Esposito, Teresa; De Stefano, Giovanni; Reccia Mafalda, Giovanna; Di Lorenzo, Ilaria; Napolitano, Filomena; Scalabri, Francesco; Lombardi, Alessia; Saleem Moin, A; Griffiths Lyn, R; Gianfrancesco, Fernando