All papers authored by Flavia Palombo
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2023
Claudio Fiorini 
,
Andrea Degiorgi,
Maria Lucia Cascavilla,
Concetta Valentina Tropeano,
Chiara La Morgia,
Marco Battista,
Danara Ormanbekova,
Flavia Palombo ,
Michele Carbonelli,
Francesco Bandello,
Valerio Carelli,
Alessandra Maresca ,
Piero Barboni,
Enrico Baruffini ,
Leonardo Caporali
,
Andrea Degiorgi,
Maria Lucia Cascavilla,
Concetta Valentina Tropeano,
Chiara La Morgia,
Marco Battista,
Danara Ormanbekova,
Flavia Palombo ,
Michele Carbonelli,
Francesco Bandello,
Valerio Carelli,
Alessandra Maresca ,
Piero Barboni,
Enrico Baruffini ,
Leonardo Caporali
RecessiveMECRpathogenic variants cause an LHON-like optic neuropathy
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2021
Flavia Palombo ,
Camille Peron,
Leonardo Caporali,
Angelo Iannielli,
Alessandra Maresca ,
Ivano Di Meo,
Claudio Fiorini,
Alice Segnali,
Francesca L. Sciacca,
Ambra Rizzo,
Sonia Levi,
Anu Suomalainen,
Alessandro Prigione,
Vania Broccoli,
Valerio Carelli
and 1 other authors
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,
Camille Peron,
Leonardo Caporali,
Angelo Iannielli,
Alessandra Maresca ,
Ivano Di Meo,
Claudio Fiorini,
Alice Segnali,
Francesca L. Sciacca,
Ambra Rizzo,
Sonia Levi,
Anu Suomalainen,
Alessandro Prigione,
Vania Broccoli,
Valerio Carelli
and 1 other authors
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Sarah L. Stenton ,
Natalia L. Sheremet ,
Claudia B. Catarino ,
Natalia A. Andreeva,
Zahra Assouline,
Piero Barboni,
Ortal Barel,
Riccardo Berutti ,
Igor O. Bychkov ,
Leonardo Caporali ,
Mariantonietta Capristo,
P. Charbel Issa,
Michele Carbonelli,
Maria Lucia Cascavilla,
Peter Charbel Issa
and 40 other authors
,
Natalia L. Sheremet ,
Claudia B. Catarino ,
Natalia A. Andreeva,
Zahra Assouline,
Piero Barboni,
Ortal Barel,
Riccardo Berutti ,
Igor O. Bychkov ,
Leonardo Caporali ,
Mariantonietta Capristo,
P. Charbel Issa,
Michele Carbonelli,
Maria Lucia Cascavilla,
Peter Charbel Issa
and 40 other authors
Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy
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2019
Valentina Del Dotto,
Farid Ullah ,
Ivano Di Meo ,
Pamela Magini,
Mirjana Gusic,
Alessandra Maresca ,
Leonardo Caporali ,
Flavia Palombo ,
Francesca Tagliavini,
Evan Harris Baugh,
Bertil Macao,
Zsolt Szilagyi,
Camille Peron,
Margaret A. Gustafson,
Kamal Khan
and 32 other authors
,
Ivano Di Meo ,
Pamela Magini,
Mirjana Gusic,
Alessandra Maresca ,
Leonardo Caporali ,
Flavia Palombo ,
Francesca Tagliavini,
Evan Harris Baugh,
Bertil Macao,
Zsolt Szilagyi,
Camille Peron,
Margaret A. Gustafson,
Kamal Khan
and 32 other authors
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
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