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1. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Issue 11 (2nd November 2012)

2. A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease. Issue 7 (22nd February 2021)

3. Circulating Brain‐Enriched MicroRNAs for Detection and Discrimination of Idiopathic and Genetic Parkinson's Disease. Issue 3 (4th December 2019)

4. Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. (13th October 2015)

5. Peripheral alpha-synuclein levels in patients with genetic and non-genetic forms of Parkinson's disease. (April 2020)

6. Population‐specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO‐PD) consortium. Issue 12 (2nd August 2013)

7. Serum uric acid level as a putative biomarker in Parkinson's disease patients carrying GBA1 mutations: 2-Year data from the PPMI study. (March 2021)

8. The relationship between environmental factors and different Parkinson's disease subtypes in Greece: Data analysis of the Hellenic Biobank of Parkinson's disease. (October 2019)