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Gary Adamson

Showing results (61-70 of 73) with videos related to

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BMC Nephrology|February 15, 2018
Establishing a clinical phenotype for cachexia in end stage kidney disease - study protocolJoanne Reid, Helen R Noble, Gary Adamson, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|November 18, 2019
Estimating the Prevalence of Muscle Wasting, Weakness, and Sarcopenia in Hemodialysis PatientsAdrian Slee, Clare McKeaveney, Gary Adamson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 5, 2020
Using a generic definition of cachexia in patients with kidney disease receiving haemodialysis: a longitudinal (pilot) studyClare McKeaveney, Adrian Slee, Gary Adamson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 6, 2021
ErratumClare McKeaveney, Adrian Slee, Gary Adamson, et al.
The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Brain : a Journal of Neurology|September 13, 2015
CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementiaSamir Abdelkarim, Sarah Morgan, Vincent Plagnol, et al.
American Journal of Human Genetics|February 26, 2013
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK populationJon Beck, Mark Poulter, Davina Hensman, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
BMC Nephrology|February 15, 2018
Establishing a clinical phenotype for cachexia in end stage kidney disease - study protocolJoanne Reid, Helen R Noble, Gary Adamson, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|November 18, 2019
Estimating the Prevalence of Muscle Wasting, Weakness, and Sarcopenia in Hemodialysis PatientsAdrian Slee, Clare McKeaveney, Gary Adamson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 5, 2020
Using a generic definition of cachexia in patients with kidney disease receiving haemodialysis: a longitudinal (pilot) studyClare McKeaveney, Adrian Slee, Gary Adamson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 6, 2021
ErratumClare McKeaveney, Adrian Slee, Gary Adamson, et al.
The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Brain : a Journal of Neurology|September 13, 2015
CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementiaSamir Abdelkarim, Sarah Morgan, Vincent Plagnol, et al.
American Journal of Human Genetics|February 26, 2013
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK populationJon Beck, Mark Poulter, Davina Hensman, et al.
Pageof 8