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Alessia Nasca

Scopus Author ID ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Mitochondrial Dna

Intellectual Disability

Top Venues

EMBO molecular medicine

Journal of human genetics

International journal of molecular sciences

Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta

University of Milano-Bicocca (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta Sep 1o 2010

Italy

Biologist / Researcher :: Unit of Medical Genetics and Neurogenetics

Education History

University of Milano-Bicocca

Italy

MSC

Publications

Mirko Baglivo, Alessia Nasca, Eleonora Lamantea, Stefano Vinci, Manuela Spagnolo, Silvia Marchet, Holger Prokisch, Alessia Catania, Costanza Lamperti, Daniele Ghezzi
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects. International journal of molecular sciences 24 (16) (2023)
Alessia Nasca, Andrea Legati, Megi Meneri, Melisa Emel Ermert, Chiara Frascarelli, Nadia Zanetti, Manuela Garbellini, Giacomo Pietro Comi, Alessia Catania, Costanza Lamperti, Dario Ronchi, Daniele Ghezzi
Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions. Cells 11 (6) (2022)
Alessia Nasca, Ivano Di Meo, Yakov Fellig, Ann Saada, Orly Elpeleg, Daniele Ghezzi, Shimon Edvardson
A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy. Journal of human genetics 66 (8) (2021)
Ahmad Alahmad, Alessia Nasca, Juliana Heidler, Kyle Thompson, Monika Oláhová, Andrea Legati, Eleonora Lamantea, Jana Meisterknecht, Manuela Spagnolo, Langping He, Seham Alameer, Fahad Hakami, Abeer Almehdar, Anna Ardissone, Charlotte L Alston, Robert McFarland, Ilka Wittig, Daniele Ghezzi, Robert W Taylor
Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I. EMBO molecular medicine 12 (11) (2020)