Author pages are created from data sourced from our academic publisher partnerships and public sources.
Posterior cortical atrophy.
Two patients had a steadily progressive disorder of higher cortical function dominated by the early development of cortical visual deficits. In one, a right visual inattention progressed over a… Expand
Language disorders in dementia of the Alzheimer type
The language profile of a group of 18 Alzheimer patients is documented and their performance on a standard aphasia test battery compared to a group of institutionalized, nonneurologically impaired… Expand
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
- G. Sutherland, G. Halliday, +7 authors G. Mellick
- Movement disorders : official journal of the…
- 30 April 2009
Recent whole genome association studies provided little evidence that polymorphisms at the familial Parkinsonism loci influence the risk for Parkinson's disease (PD). However, these studies are not… Expand
Parkinson's disease and family history.
The study of family history in Parkinson's disease (PD) has resulted in considerable debate over the role of genetic factors in the development of PD. Despite this, family history is consistently… Expand
A 24 year old woman presented with generalised livedo reticularis and progressive intellectual decline. A CT scan of her head showed multifocal low density areas, consistent with cerebral infarction.… Expand
Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias.
- Jeremy R. B. Newman, G. Sutherland, +5 authors G. Mellick
- Parkinsonism & related disorders
- 1 May 2012
Genes involved in familial dystonia syndromes (DYT genes) are ideal candidates for investigating whether common genetic variants influence the susceptibility to sporadic primary dystonia. To date,… Expand
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy
- Alice‐Ann Sullivan, B. Teh, S. Jeavons, M. Schalling, R. Boyle
- Journal of Clinical Neuroscience
- 1 April 1997
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is a recently described genetic disease characterized by recurrent subcortical infarcts and… Expand
Lhermitte‐duclos disease and cowden disease: A third case
Carotid sinus hypersensitivity in elderly nursing home patients.
- A. L. Murphy, B. Rowbotham, R. Boyle, C. Thew, J. A. Fardoulys, K. Wilson
- Australian and New Zealand journal of medicine
- 1 February 1986
Fourteen of 100 geriatric nursing home patients were shown to have evidence of carotid sinus hypersensitivity. The incidence of syncope and falls was noted in prospective follow-up over 33 months.… Expand