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Mostrati risultati da 1 a 16 di 16
Titolo Autore(i) Anno Periodico Editore Tipo File
Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva BARTOLETTI-STELLA A.; SALFI N.; CECCARELLI C.; ATTIMONELLI M.; ROMEO G.; GASPARRE G. 2011-01-01 ARCHIVES OF OPHTHALMOLOGY - 1.01 Articolo in rivista -
A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia Bartoletti-Stella, Anna; Chiaro, Giacomo; Calandra-Buonaura, Giovanna; Contin, Manuela; Scaglione..., Cesa; Barletta, Giorgio; Cecere, Annagrazia; Garagnani, Paolo; Tieri, Paolo; Ferrarini, Alberto; Piras, Silvia; Franceschi, Claudio; Delledonne, Massimo; Cortelli, Pietro; Capellari, Sabina 2015-01-01 JOURNAL OF NEUROLOGY - 1.01 Articolo in rivista -
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency Donadio, V; Liguori, R.; Incensi, A.; Chiaro, G.; Bartoletti-Stella, A.; Capellari, S.; Cortelli, P. 2016-01-01 AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL - 1.01 Articolo in rivista -
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Pession, Annalisa; De Massis, Pat...rizia; Oppi, Federico; Stanzani-Maserati, Michelangelo; Pasini, Elena; Baiardi, Simone; Avoni, Patrizia; Parchi, Piero; Liguori, Rocco; Capellari, Sabina 2017-01-01 JOURNAL OF NEUROLOGY - 1.01 Articolo in rivista -
Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation Terlizzi, Rossana; Valentino, Maria Lucia; Bartoletti-Stella, Anna; Columbaro, Marta; Piras, Silv...ia; Stanzani-Maserati, Michelangelo; Quadri, Marialuisa; Breedveld, Guido J.; Bonifati, Vincenzo; Martinelli, Paolo; Parchi, Piero; Capellari, Sabina 2017-01-01 MOVEMENT DISORDERS - 1.01 Articolo in rivista -
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, ...Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio 2018-01-01 JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY - 1.01 Articolo in rivista -
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Casalena, Alfonsina; Oppi, Federi...co; Ambrosetto, Giovanni; Montagna, Pasquale; Liguori, Rocco; Parchi, Piero; Capellari, Sabina 2018-01-01 JOURNAL OF ALZHEIMER'S DISEASE - 1.01 Articolo in rivista -
Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease Baiardi, Simone; Capellari, Sabina; Bartoletti Stella, Anna; Parchi, Piero 2018-01-01 JOURNAL OF ALZHEIMER'S DISEASE - 1.01 Articolo in rivista -
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing Bartoletti-Stella, Anna; Baiardi, Simone; Stanzani-Maserati, Michelangelo; Piras, Silvia; Caffarr...a, Paolo; Raggi, Alberto; Pantieri, Roberta; Baldassari, Sara; Caporali, Leonardo; Abu-Rumeileh, Samir; Linarello, Simona; Liguori, Rocco; Parchi, Piero; Capellari, Sabina 2018-01-01 NEUROBIOLOGY OF AGING - 1.01 Articolo in rivista -
Binary transformation of sequencing data to explore functional genetic patterns. Martina Tarozzi, Anna Bartoletti-Stella, Daniele Dall'Olio, Tommaso Matteuzzi, Sabina Capellari, ...Gastone Castellani 2020-01-01 - - 4.03 Poster -
CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia Abu-Rumeileh S.; Steinacker P.; Polischi B.; Mammana A.; Bartoletti-Stella A.; Oeckl P.; Baiardi ...S.; Zenesini C.; Huss A.; Cortelli P.; Capellari S.; Otto M.; Parchi P. 2020-01-01 ALZHEIMER'S RESEARCH & THERAPY - 1.01 Articolo in rivista s13195-019-0562-4.pdf
Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease Tarozzi, Martina; Baiardi, Simone; Sala, Claudia; Bartoletti-Stella, Anna; Parchi, Piero; Capella...ri, Sabina; Castellani, Gastone 2022-01-01 ACTA NEUROPATHOLOGICA COMMUNICATIONS - 1.01 Articolo in rivista Genomic, transcriptomic and RNA editing MM1 and VV2 CJD.pdf40478_2022_1483_MOESM1_ESM.docx
Extra Virgin Olive Oil (EVOO), a Mediterranean Diet Component, in the Management of Muscle Mass and Function Preservation. Sara Salucci, Anna Bartoletti-Stella, Alberto Bavelloni, Beatrice Aramini, William L. Blalock, F...rancesco Fabbri, Ivan Vannini, Vittorio Sambri , Franco Stella, Irene Faenza 2022-01-01 NUTRIENTS - 1.01 Articolo in rivista nutrients-14-03567 Salucci S, ARAMINI B..pdf
Combined Treatment with PI3K Inhibitors BYL-719 and CAL-101 Is a Promising Antiproliferative Strategy in Human Rhabdomyosarcoma Cells Manuela Piazzi; Alberto Bavelloni; Vittoria Cenni; Sara Salucci; Anna Bartoletti Stella; Enrica T...omassini; Katia Scotlandi; William L. Blalock; Irene Faenza 2022-01-01 MOLECULES - 1.01 Articolo in rivista molecules-27-02742.pdf
Phospholipase Family Enzymes in Lung Cancer: Looking for Novel Therapeutic Approaches. Sara Salucci , Beatrice Aramini, Anna Bartoletti-Stella, Ilaria Versari, Giovanni Martinelli, Wil...liam Blalock, Franco Stella, Irene Faenza 2023-01-01 CANCERS - 1.01 Articolo in rivista cancers-15-03245 (1).pdf
The Cytotoxic Effect of Curcumin in Rhabdomyosarcoma Is Associated with the Modulation of AMPK, AKT/mTOR, STAT, and p53 Signaling Salucci, Sara; Bavelloni, Alberto; Stella, Anna Bartoletti; Fabbri, Francesco; Vannini, Ivan; Pia...zzi, Manuela; Volkava, Karyna; Scotlandi, Katia; Martinelli, Giovanni; Faenza, Irene; Blalock, William 2023-01-01 NUTRIENTS - 1.01 Articolo in rivista nutrients-15-00740.pdf
Mostrati risultati da 1 a 16 di 16
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