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2. Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17) due to microtubule‐associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy. (8th March 2017)

3. DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients. (September 2015)

4. Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke. Issue 2 (6th August 2012)

5. Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke risk. (29th May 2015)

6. Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke risk. (29th May 2015)