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Human Molecular Genetics|May 1, 1996
Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifidaK Morrison, C Papapetrou, J Attwood, et al.Journal of Parkinson'S Disease|October 8, 2015
Anticholinergic Load: Is there a Cognitive Cost in Early Parkinson's Disease?Alison J Yarnall, Rachael A Lawson, Gordon W Duncan, et al.Journal of Parkinson'S Disease|June 13, 2014
Quality of life and mild cognitive impairment in early Parkinson's disease: does subtype matter?Rachael A Lawson, Alison J Yarnall, Gordon W Duncan, et al.Hospital Medicine (London, England : 1998)|September 4, 2001
Updated guidelines for the management of Parkinson's diseaseK Bhatia, D J Brooks, D J Burn, et al.Neurology|October 11, 1992
Parkinson's disease in twins studied with 18F-dopa and positron emission tomographyD J Burn, M H Mark, E D Playford, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2016
Hypothalamic volume loss is associated with reduced melatonin output in Parkinson's diseaseDavid P Breen, Cristina Nombela, Romina Vuono, et al.Annals of Neurology|February 1, 1997
Dopaminergic function in familial Parkinson's disease: a clinical and 18F-dopa positron emission tomography studyP Piccini, P K Morrish, N Turjanski, et al.Brain Sciences|February 7, 2020
Progression of Neuropsychiatric Symptoms over Time in an Incident Parkinson's Disease Cohort (ICICLE-PD)J K Dlay, G W Duncan, T K Khoo, et al.British Heart Journal|October 1, 1991
DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal originD I Wilson, I E Cross, J A Goodship, et al.Annals of Human Genetics|July 1, 1995
Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome)G E Davies, C M Howard, M J Farrer, et al.Pageof 51