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BMC Medical Genetics
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April 9, 2016
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
Rubika Balendra, James Uphill, Claire Collinson, et al.
International Journal of Clinical Pharmacy
|
October 21, 2025
Addressing potentially inappropriate prescribing in care homes: regional evaluation of a pharmacist-led model in Northern Ireland
Ann Sinéad Doherty, Gary Adamson, John Mallett, et al.
BMJ Open
|
October 16, 2024
Post-rehabilitation programme to support upper limb recovery in community-dwelling stroke survivors: a mixed methods cluster-feasibility controlled trial
Katy Pedlow, Niamh C Kennedy, Natalie Klempel, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experience
Jane Owen, Jon Beck, Tracy Campbell, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 3, 2017
A novel prion protein variant in a patient with semantic dementia
Joanna Kenny, Ione Woollacott, Carolin Koriath, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2017
Methods for Molecular Diagnosis of Human Prion Disease
Jonathan D F Wadsworth, Gary Adamson, Susan Joiner, et al.
JMIR Research Protocols
|
May 6, 2026
Co-Design of a Physical Activity Maintenance Intervention for People With Stroke: Protocol for a Mixed Methods Study
Katy Pedlow, Suzanne McDonough, Natalie Duff, et al.
Human Mutation
|
June 29, 2010
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit
Jon A Beck, Mark Poulter, Tracy A Campbell, et al.
Human Molecular Genetics
|
April 30, 2004
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease
Jonathan A Beck, Mark Poulter, Tracy A Campbell, et al.
Neurobiology of Aging
|
March 2, 2015
Rare structural genetic variation in human prion diseases
Ana Lukic, James Uphill, Craig A Brown, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
BMC Medical Genetics
|
April 9, 2016
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
Rubika Balendra, James Uphill, Claire Collinson, et al.
International Journal of Clinical Pharmacy
|
October 21, 2025
Addressing potentially inappropriate prescribing in care homes: regional evaluation of a pharmacist-led model in Northern Ireland
Ann Sinéad Doherty, Gary Adamson, John Mallett, et al.
BMJ Open
|
October 16, 2024
Post-rehabilitation programme to support upper limb recovery in community-dwelling stroke survivors: a mixed methods cluster-feasibility controlled trial
Katy Pedlow, Niamh C Kennedy, Natalie Klempel, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experience
Jane Owen, Jon Beck, Tracy Campbell, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 3, 2017
A novel prion protein variant in a patient with semantic dementia
Joanna Kenny, Ione Woollacott, Carolin Koriath, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2017
Methods for Molecular Diagnosis of Human Prion Disease
Jonathan D F Wadsworth, Gary Adamson, Susan Joiner, et al.
JMIR Research Protocols
|
May 6, 2026
Co-Design of a Physical Activity Maintenance Intervention for People With Stroke: Protocol for a Mixed Methods Study
Katy Pedlow, Suzanne McDonough, Natalie Duff, et al.
Human Mutation
|
June 29, 2010
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit
Jon A Beck, Mark Poulter, Tracy A Campbell, et al.
Human Molecular Genetics
|
April 30, 2004
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease
Jonathan A Beck, Mark Poulter, Tracy A Campbell, et al.
Neurobiology of Aging
|
March 2, 2015
Rare structural genetic variation in human prion diseases
Ana Lukic, James Uphill, Craig A Brown, et al.
Page
of 8