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Showing results (431-440 of 561) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 24, 2019
Pro-Saccades Predict Cognitive Decline in Parkinson's Disease: ICICLE-PDSamuel Stuart, Rachael A Lawson, Alison J Yarnall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 31, 2003
Extrapyramidal features in Parkinson's disease with and without dementia and dementia with Lewy bodies: A cross-sectional comparative studyDavid J Burn, Elise N Rowan, Thais Minett, et al.
American Journal of Medical Genetics|January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)R J Gibbons, L Brueton, V J Buckle, et al.
American Journal of Human Genetics|November 1, 1992
A prospective cytogenetic study of 36 cases of DiGeorge syndromeD I Wilson, I E Cross, J A Goodship, et al.
Parkinsonism & Related Disorders|July 31, 2014
Severity of mild cognitive impairment in early Parkinson's disease contributes to poorer quality of lifeRachael A Lawson, Alison J Yarnall, Gordon W Duncan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 2, 2003
Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for Parkinsonian disordersIrene Litvan, Kailash P Bhatia, David J Burn, et al.
American Journal of Human Genetics|December 1, 1996
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC geneD M Eccles, R van der Luijt, C Breukel, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approachP Fidalgo, M R Almeida, S West, et al.
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.
Pageof 57

Showing results (431-440 of 561) with videos related to

Sort By:
Pageof 57
Movement Disorders : Official Journal of the Movement Disorder Society|August 24, 2019
Pro-Saccades Predict Cognitive Decline in Parkinson's Disease: ICICLE-PDSamuel Stuart, Rachael A Lawson, Alison J Yarnall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 31, 2003
Extrapyramidal features in Parkinson's disease with and without dementia and dementia with Lewy bodies: A cross-sectional comparative studyDavid J Burn, Elise N Rowan, Thais Minett, et al.
American Journal of Medical Genetics|January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)R J Gibbons, L Brueton, V J Buckle, et al.
American Journal of Human Genetics|November 1, 1992
A prospective cytogenetic study of 36 cases of DiGeorge syndromeD I Wilson, I E Cross, J A Goodship, et al.
Parkinsonism & Related Disorders|July 31, 2014
Severity of mild cognitive impairment in early Parkinson's disease contributes to poorer quality of lifeRachael A Lawson, Alison J Yarnall, Gordon W Duncan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 2, 2003
Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for Parkinsonian disordersIrene Litvan, Kailash P Bhatia, David J Burn, et al.
American Journal of Human Genetics|December 1, 1996
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC geneD M Eccles, R van der Luijt, C Breukel, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approachP Fidalgo, M R Almeida, S West, et al.
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.
Pageof 57