Search research articles
Contact Us
Filters
Showing results (1-10 of 67) with videos related to
Page
of 7
Sort By:
Organizational Behavior and Human Decision Processes
|
July 20, 2001
Attribute Framing and Goal Framing Effects in Health Decisions
Parthasarathy Krishnamurthy, Patrick Carter, Edward Blair
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
May 30, 2007
Eliciting expert opinion for economic models: an applied example
José Leal, Sarah Wordsworth, Rosa Legood, et al.
Trends in Genetics : TIG
|
April 25, 2003
Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion
Houman Ashrafian, Charles Redwood, Edward Blair, et al.
Journal of Cardiology Cases
|
December 15, 2018
Effective cascade screening through identification of a mutation in <i>RYR2</i> in a large family with a history of sudden death
Claire Bailey, Edward Blair, Clifford Garratt, et al.
The British Journal of Cardiology
|
March 19, 2026
Sudden cardiac death associated with a pathogenic genetic variant in <i>HCN4</i>
Gokul Parameswaran, Edward Blair, Hugh C Watkins, et al.
European Journal of Human Genetics : EJHG
|
May 2, 2013
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications
Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Ulnar Mammary syndrome and TBX3: expanding the phenotype
Helen Linden, Rosy Williams, Janet King, et al.
Pediatric Radiology
|
May 12, 2017
Multiple long bone cysts revealed by MRI in trichorhinophalangeal syndrome type II predisposing to pathological fractures
Praveen Konala, Nigel Kiely, Charlotte Noakes, et al.
Ophthalmic Genetics
|
December 15, 2005
Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome)
M Anandan, Neroli J Porter, Andrea H Nemeth, et al.
American Journal of Medical Genetics. Part A
|
October 4, 2011
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Organizational Behavior and Human Decision Processes
|
July 20, 2001
Attribute Framing and Goal Framing Effects in Health Decisions
Parthasarathy Krishnamurthy, Patrick Carter, Edward Blair
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
May 30, 2007
Eliciting expert opinion for economic models: an applied example
José Leal, Sarah Wordsworth, Rosa Legood, et al.
Trends in Genetics : TIG
|
April 25, 2003
Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion
Houman Ashrafian, Charles Redwood, Edward Blair, et al.
Journal of Cardiology Cases
|
December 15, 2018
Effective cascade screening through identification of a mutation in <i>RYR2</i> in a large family with a history of sudden death
Claire Bailey, Edward Blair, Clifford Garratt, et al.
The British Journal of Cardiology
|
March 19, 2026
Sudden cardiac death associated with a pathogenic genetic variant in <i>HCN4</i>
Gokul Parameswaran, Edward Blair, Hugh C Watkins, et al.
European Journal of Human Genetics : EJHG
|
May 2, 2013
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications
Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Ulnar Mammary syndrome and TBX3: expanding the phenotype
Helen Linden, Rosy Williams, Janet King, et al.
Pediatric Radiology
|
May 12, 2017
Multiple long bone cysts revealed by MRI in trichorhinophalangeal syndrome type II predisposing to pathological fractures
Praveen Konala, Nigel Kiely, Charlotte Noakes, et al.
Ophthalmic Genetics
|
December 15, 2005
Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome)
M Anandan, Neroli J Porter, Andrea H Nemeth, et al.
American Journal of Medical Genetics. Part A
|
October 4, 2011
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, et al.
Page
of 7