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You searched for: Author/Creator Ross, Owen A.

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1. [P1–334]: CHARACTERIZATION OF THE CLINICAL AND NEUROIMAGING FEATURES OF PATIENTS WITH DEMENTIA WITH LEWY BODIES ASSOCIATED WITH VARIANTS IN GLUCOCEREBROSIDASE (GBA). (1st July 2017)

2. A genome-wide association study in multiple system atrophy. (11th October 2016)

3. 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)

4. A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease. Issue 11 (November 2015)

6. Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease. Issue 8 (3rd August 2018)

7. An examination of atypical primary progressive aphasia variants. (31st December 2021)

8. APOE ε4 is associated with severity of Lewy body pathology independent of Alzheimer pathology. (18th September 2018)

9. APOE2 Exacerbates TDP‐43 Related Toxicity in the Absence of Alzheimer Pathology. Issue 4 (10th January 2023)