Chrisovalantou Huridou

4PUBLICATIONS
76CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsGene mappingMedical infection agents (incl. prions)Neurogenetics
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Publications (4)

|Feb 25, 2026
The DNA/RNA autophagy protein SIDT2 as a novel neuropathological hallmark in Huntington disease.

Sanaz Gabery, Sofia Bergh, Chrisovalantou Huridou

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Aug 01, 2024
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy.

Jonasz J Weber, Leah Czisch, Priscila Pereira Sena

|Apr 28, 2022
Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17.

Jonasz Jeremiasz Weber, Stefanie Cari Anger, Priscila Pereira Sena

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