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Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.Journal of Medical Genetics|October 1, 1993
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11J Burn, A Takao, D Wilson, et al.International Journal of Geriatric Psychiatry|November 11, 2006
Subjectively reported sleep quality and excessive daytime somnolence in Parkinson's disease with and without dementia, dementia with Lewy bodies and Alzheimer's diseaseFrauke Boddy, Elise N Rowan, Debbie Lett, et al.Gut|May 1, 1993
Colonic fermentation of complex carbohydrates in patients with familial adenomatous polyposisD M Bradburn, J C Mathers, A Gunn, et al.Journal of Medical Genetics|March 1, 1990
Cranial hemihypertrophy and neurodevelopmental prognosisJ C Dean, G F Cole, R E Appleton, et al.Neurology|August 1, 1993
Comparison of striatal 18F-dopa uptake in adult-onset dystonia-parkinsonism, Parkinson's disease, and dopa-responsive dystoniaN Turjanski, K Bhatia, D J Burn, et al.Journal of Medical Genetics|June 1, 1989
Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy geneS S Papiha, D F Roberts, A Clarke, et al.Neurology|March 9, 2005
Temporal lobe atrophy on MRI in Parkinson disease with dementia: a comparison with Alzheimer disease and dementia with Lewy bodiesC W C Tam, E J Burton, I G McKeith, et al.Journal of Medical Genetics|July 1, 1992
A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisationJ Goodship, A Curtis, I Cross, et al.Neurology|September 1, 2006
POLG1 in idiopathic Parkinson diseaseW Tiangyou, G Hudson, D Ghezzi, et al.Pageof 51