BARTOLETTI STELLA, ANNA
BARTOLETTI STELLA, ANNA
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
Personale tecnico amm.vo
Phospholipase Family Enzymes in Lung Cancer: Looking for Novel Therapeutic Approaches.
2023 Sara Salucci , Beatrice Aramini, Anna Bartoletti-Stella, Ilaria Versari, Giovanni Martinelli, William Blalock, Franco Stella, Irene Faenza
The Cytotoxic Effect of Curcumin in Rhabdomyosarcoma Is Associated with the Modulation of AMPK, AKT/mTOR, STAT, and p53 Signaling
2023 Salucci, Sara; Bavelloni, Alberto; Stella, Anna Bartoletti; Fabbri, Francesco; Vannini, Ivan; Piazzi, Manuela; Volkava, Karyna; Scotlandi, Katia; Martinelli, Giovanni; Faenza, Irene; Blalock, William
Combined Treatment with PI3K Inhibitors BYL-719 and CAL-101 Is a Promising Antiproliferative Strategy in Human Rhabdomyosarcoma Cells
2022 Manuela Piazzi; Alberto Bavelloni; Vittoria Cenni; Sara Salucci; Anna Bartoletti Stella; Enrica Tomassini; Katia Scotlandi; William L. Blalock; Irene Faenza
Extra Virgin Olive Oil (EVOO), a Mediterranean Diet Component, in the Management of Muscle Mass and Function Preservation.
2022 Sara Salucci, Anna Bartoletti-Stella, Alberto Bavelloni, Beatrice Aramini, William L. Blalock, Francesco Fabbri, Ivan Vannini, Vittorio Sambri , Franco Stella, Irene Faenza
Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease
2022 Tarozzi, Martina; Baiardi, Simone; Sala, Claudia; Bartoletti-Stella, Anna; Parchi, Piero; Capellari, Sabina; Castellani, Gastone
Binary transformation of sequencing data to explore functional genetic patterns.
2020 Martina Tarozzi, Anna Bartoletti-Stella, Daniele Dall'Olio, Tommaso Matteuzzi, Sabina Capellari, Gastone Castellani
CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia
2020 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.
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene
2018 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
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing
2018 Bartoletti-Stella, Anna; Baiardi, Simone; Stanzani-Maserati, Michelangelo; Piras, Silvia; Caffarra, Paolo; Raggi, Alberto; Pantieri, Roberta; Baldassari, Sara; Caporali, Leonardo; Abu-Rumeileh, Samir; Linarello, Simona; Liguori, Rocco; Parchi, Piero; Capellari, Sabina
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance
2018 Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Casalena, Alfonsina; Oppi, Federico; Ambrosetto, Giovanni; Montagna, Pasquale; Liguori, Rocco; Parchi, Piero; Capellari, Sabina
Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease
2018 Baiardi, Simone; Capellari, Sabina; Bartoletti Stella, Anna; Parchi, Piero
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature
2017 Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Pession, Annalisa; De Massis, Patrizia; Oppi, Federico; Stanzani-Maserati, Michelangelo; Pasini, Elena; Baiardi, Simone; Avoni, Patrizia; Parchi, Piero; Liguori, Rocco; Capellari, Sabina
Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation
2017 Terlizzi, Rossana; Valentino, Maria Lucia; Bartoletti-Stella, Anna; Columbaro, Marta; Piras, Silvia; Stanzani-Maserati, Michelangelo; Quadri, Marialuisa; Breedveld, Guido J.; Bonifati, Vincenzo; Martinelli, Paolo; Parchi, Piero; Capellari, Sabina
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency
2016 Donadio, V; Liguori, R.; Incensi, A.; Chiaro, G.; Bartoletti-Stella, A.; Capellari, S.; Cortelli, P.
A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia
2015 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
Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva
2011 BARTOLETTI-STELLA A.; SALFI N.; CECCARELLI C.; ATTIMONELLI M.; ROMEO G.; GASPARRE G.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 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 |
| 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 |
| 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 |
| 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.pdf; 40478_2022_1483_MOESM1_ESM.docx |
| 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 |
| 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 | - |
| 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 | - |
| 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 | - |
| 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 | - |
| 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 | - |
| 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 | - |
| 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 | - |