Mitochondrial dysfunctions in neurodegeneration

Francesca Maltecca

Maltecca Francesca

Email: maltecca.francesca@hsr.it
Location: DIBIT1 3A2, 44A (lab) and 46 (office)

Group leader, Mitochondrial dysfunctions in neurodegeneration Unit

Francesca Maltecca has a background in human genetics, with specific training and competence in inherited cerebellar ataxias, and also a solid experience in cerebellar physiology and pathology. Indeed, her past and present research work includes the dissection of molecular mechanisms of inherited cerebellar ataxias with primary or secondary mitochondrial origin, but also of other neurodegenerative diseases (dominant optic atrophy, multiple sclerosis). In particular, she has published some seminal works on the pathogenesis of SCA28, SPAX5 and ARSACS. She is member of the Ataxia Global Initiative, where she co-coordinates the working group dedicated to preclinical trials in mouse models of ataxia. She is also part of an international research consortium studying drug development in recessive ataxias (Treat-ARCA), funded by the European Joint Program for Rare Diseases. She has been awarded twice with the Young Investigator Award for the Spinocerebellar Ataxia Research, from National Ataxia Foundation, US. Her expertise involves human genetics, cell biology, neurobiology and mouse model phenotyping.

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