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Showing results (421-430 of 561) with videos related to

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Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Human mismatch repair genes and their association with hereditary non-polyposis colon cancerR D Kolodner, N R Hall, J Lipford, et al.
Genomics|December 1, 1994
Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutationsR D Kolodner, N R Hall, J Lipford, et al.
International Journal of Geriatric Psychiatry|August 29, 2012
Frequency, prevalence, incidence and risk factors associated with visual hallucinations in a sample of patients with Parkinson's disease: a longitudinal 4-year studyG Gibson, P G Mottram, D J Burn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 3, 2017
Stability of mild cognitive impairment in newly diagnosed Parkinson's diseaseRachael A Lawson, Alison J Yarnall, Gordon W Duncan, et al.
Animal : an International Journal of Animal Bioscience|September 28, 2025
Application of milk mid-infrared spectroscopy for prediction of energy balance and associated traits in Fleckvieh and Holstein Friesian dairy cowsS Gruber, G Terler, A Steinwidder, et al.
Movement Disorders Clinical Practice|May 7, 2020
Impact of the COVID-19 Pandemic on Parkinson's Disease and Movement DisordersStella M Papa, Patrik Brundin, Victor S C Fung, et al.
Archives of Neurology|April 25, 2012
Frontotemporal dementia in elderly individualsAtik Baborie, Tim D Griffiths, Evelyn Jaros, et al.
Archives of Neurology|April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2020
Impact of the COVID-19 Pandemic on Parkinson's Disease and Movement DisordersStella M Papa, Patrik Brundin, Victor S C Fung, et al.
Journal of Medical Genetics|June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndromeS Lindsay, M Ireland, O O'Brien, et al.
Pageof 57

Showing results (421-430 of 561) with videos related to

Sort By:
Pageof 57
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Human mismatch repair genes and their association with hereditary non-polyposis colon cancerR D Kolodner, N R Hall, J Lipford, et al.
Genomics|December 1, 1994
Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutationsR D Kolodner, N R Hall, J Lipford, et al.
International Journal of Geriatric Psychiatry|August 29, 2012
Frequency, prevalence, incidence and risk factors associated with visual hallucinations in a sample of patients with Parkinson's disease: a longitudinal 4-year studyG Gibson, P G Mottram, D J Burn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 3, 2017
Stability of mild cognitive impairment in newly diagnosed Parkinson's diseaseRachael A Lawson, Alison J Yarnall, Gordon W Duncan, et al.
Animal : an International Journal of Animal Bioscience|September 28, 2025
Application of milk mid-infrared spectroscopy for prediction of energy balance and associated traits in Fleckvieh and Holstein Friesian dairy cowsS Gruber, G Terler, A Steinwidder, et al.
Movement Disorders Clinical Practice|May 7, 2020
Impact of the COVID-19 Pandemic on Parkinson's Disease and Movement DisordersStella M Papa, Patrik Brundin, Victor S C Fung, et al.
Archives of Neurology|April 25, 2012
Frontotemporal dementia in elderly individualsAtik Baborie, Tim D Griffiths, Evelyn Jaros, et al.
Archives of Neurology|April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2020
Impact of the COVID-19 Pandemic on Parkinson's Disease and Movement DisordersStella M Papa, Patrik Brundin, Victor S C Fung, et al.
Journal of Medical Genetics|June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndromeS Lindsay, M Ireland, O O'Brien, et al.
Pageof 57