Polyglutamine/poly (Q) diseases are a group nine hereditary neurodegenerative disorders
caused due to abnormally expanded stretches of CAG trinucleotide in functionally distinct …

In this article we have reviewed the potential role of coenzyme Q10 (CoQ10) in the
pathogenesis and treatment of a number of less common age-related disorders, for many of …

Radiation has been applied in cancer treatment to eradicate tumors and displayed great
therapeutic benefits for humans. However, it is associated with negative impacts on normal …

Background Spinocerebellar ataxia type 3 (SCA3) is an inherited, autosomal, and rare
neurodegenerative disease. Serum/plasma biomarkers or functional magnetic resonance …

Cerebellar ataxias are a wide heterogeneous group of movement disorders. Within this
broad umbrella of diseases, there are both genetics and sporadic forms. The clinical …

Ataksja (niezborność ruchowa, bezład) jest zespołem objawów charakteryzującym się
zaburzeniami równowagi i koordynacji chodu, postawy, ruchów kończyn oraz …

Background Spinocerebellar ataxia type 3 (SCA3) is an inherited, autosomal, and rare
neurodegenerative disease. Serum/plasma biomarkers or functional magnetic resonance …

Machado Joseph disease (MJD) or Spinocerebellar Ataxia Type 3 (SCA3) is a
neurodegenerative disorder characterised by an expansion of a CAG repeat in the coding …