Aleo, Serena Jasmine; Dotto, Valentina Del; Romagnoli, Martina; Fiorini, Claudio; Capirossi, Giada; Peron, Camille; Maresca, Alessandra; Caporali, Leonardo; Capristo, Mariantonietta; Tropeano, Concetta Valentina; Zanna, Claudia; Ross-Cisneros, Fred N.; Sadun, Alfredo A.; Pignataro, Maria Gemma; Giordano, Carla; Fasano, Chiara; Cavaliere, Andrea; Porcelli, Anna Maria; Tioli, Gaia; Musiani, Francesco; Catania, Alessia; Lamperti, Costanza; Marzoli, Stefania Bianchi; Negri, Annamaria De; Cascavilla, Maria Lucia; Battista, Marco; Barboni, Piero; Carbonelli, Michele; Amore, Giulia; Morgia, Chiara La; Smirnov, Dmitrii; Vasilescu, Catalina; Farzeen, Aiman; Blickhaeuser, Beryll; Prokisch, Holger; Priglinger, Claudia; Livonius, Bettina; Catarino, Claudia B.; Klopstock, Thomas; Tiranti, Valeria; Carelli, Valerio; Maria, Anna

New insights into idebenone therapy in relation to NQO1

ACTA OPHTHALMOLOGICA

IF2.8

2024-01-180

Recessive MECR pathogenic variants cause an LHON-like optic neuropathy

JOURNAL OF MEDICAL GENETICS

IF3.7

2023-09-2110

OAAI

Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts

SCIENTIFIC REPORTS

IF3.9

2023-08-260

OAAI

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys

MOLECULAR MEDICINE

IF6.4

2022-08-033

OAAI

Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy

病理性线粒体自噬破坏Leber遗传性视神经病变的线粒体稳态

CELL REPORTS

IF6.9

2022-07-0137

OAAI

Danese, Alberto; Patergnani, Simone; Maresca, Alessandra; Peron, Camille; Raimondi, Andrea; Caporali, Leonardo; Marchi, Saverio; La Morgia, Chiara; Del Dotto, Valentina; Zanna, Claudia; Iannielli, Angelo; Segnali, Alice; Di Meo, Ivano; Cavaliere, Andrea; Lebiedzinska-Arciszewska, Magdalena; Wieckowski, Mariusz R.; Martinuzzi, Andrea; Moraes-Filho, Milton N.; Salomao, Solange R.; Berezovsky, Adriana; Belfort, Rubens; Buser, Christopher; Ross-Cisneros, Fred N.; Sadun, Alfredo A.; Tacchetti, Carlo; Broccoli, Vania; Giorgi, Carlotta; Tiranti, Valeria; Carelli, Valerio; Pinton, Paolo

Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation

MOLECULAR GENETICS AND METABOLISM

IF3.5

2022-01-017

PRE

The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs

STEM CELL REPORTS

IF5.1

2021-08-018

OAAI

Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2021-05-059

Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy

BRAIN

IF11.7

2021-04-1533

OAAI

Bonora, Elena; Chakrabarty, Sanjiban; Kellaris, Georgios; Tsutsumi, Makiko; Bianco, Francesca; Bergamini, Christian; Ullah, Farid; Isidori, Federica; Liparulo, Irene; Diquigiovanni, Chiara; Masin, Luca; Rizzardi, Nicola; Cratere, Mariapia Giuditta; Boschetti, Elisa; Papa, Valentina; Maresca, Alessandra; Cenacchi, Giovanna; Casadio, Rita; Martelli, Pierluigi; Matera, Ivana; Ceccherini, Isabella; Fato, Romana; Raiola, Giuseppe; Arrigo, Serena; Signa, Sara; Sementa, Angela Rita; Severino, Mariasavina; Striano, Pasquale; Fiorillo, Chiara; Goto, Tsuyoshi; Uchino, Shumpei; Oyazato, Yoshinobu; Nakamura, Hisayoshi; Mishra, Sushil K.; Yeh, Yu-Sheng; Kato, Takema; Nozu, Kandai; Tanboon, Jantima; Morioka, Ichiro; Nishino, Ichizo; Toda, Tatsushi; Goto, Yu-ichi; Ohtake, Akira; Kosaki, Kenjiro; Yamaguchi, Yoshiki; Nonaka, Ikuya; Iijima, Kazumoto; Mimaki, Masakazu; Kurahashi, Hiroki; Raams, Anja; MacInnes, Alyson; Alders, Mariel; Engelen, Marc; Linthorst, Gabor; de Koning, Tom; den Dunnen, Wilfred; Dijkstra, Gerard; van Spaendonck, Karin; van Gent, Dik C.; Aronica, Eleonora M.; Picco, Paolo; Carelli, Valerio; Seri, Marco; Katsanis, Nicholas; Duijkers, Floor A. M.; Taniguchi-Ikeda, Mariko; De Giorgio, Roberto

Impaired complex I repair causes recessive Leber?s hereditary optic neuropathy Sarah L. Stenton, ... , Ilka Wittig, Holger Prokisch ...

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2021-03-1551

OAAI

Stenton, Sarah L.; Sheremet, Natalia L.; Catarino, Claudia B.; Andreeva, Natalia A.; Assouline, Zahra; Barboni, Piero; Barel, Ortal; Berutti, Riccardo; Bychkov, Igor; Caporali, Leonardo; Capristo, Mariantonietta; Carbonelli, Michele; Cascavilla, Maria L.; Issa, Peter Charbel; Freisinger, Peter; Gerber, Sylvie; Ghezzi, Daniele; Graf, Elisabeth; Heidler, Juliana; Hempel, Maja; Heon, Elise; Itkis, Yulya S.; Javasky, Elisheva; Kaplan, Josseline; Kopajtich, Robert; Kornblum, Cornelia; Kovacs-Nagy, Reka; Krylova, Tatiana D.; Kunz, Wolfram S.; La Morgia, Chiara; Lamperti, Costanza; Ludwig, Christina; Malacarne, Pedro F.; Maresca, Alessandra; Mayr, Johannes A.; Meisterknecht, Jana; Nevinitsyna, Tatiana A.; Palombo, Flavia; Pode-Shakked, Ben; Shmelkova, Maria S.; Strom, Tim M.; Tagliavini, Francesca; Tzadok, Michal; van der Ven, Amelie T.; Vignal-Clermont, Catherine; Wagner, Matias; Zakharova, Ekaterina Y.; Zhorzholadze, Nino, V; Rozet, Jean-Michel; Carelli, Valerio; Tsygankova, Polina G.; Klopstock, Thomas; Wittig, Ilka; Prokisch, Holger

Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations

HUMAN MOLECULAR GENETICS

IF3.2

2020-11-2413

OAAI

Alessandra Maresca

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