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Immunology and Allergy Clinics of North America
|
April 26, 2022
Pharmacogenomics of Drug Hypersensitivity: Technology and Translation
Rebecca Kuruvilla, Kathryn Scott, Sir Munir Pirmohamed
Urology
|
December 13, 2021
Robotic Assisted Caval Replacement for Recurrent Renal Cell Carcinoma Invading the Wall of the Inferior Vena Cava
Kathryn Scott, Jared Manwaring, Kwame Amankwah, et al.
Clinical and Translational Science
|
May 7, 2010
Association of a polymorphic variant of the adiponectin gene with insulin resistance in african americans
Claudia Specchia, Kathryn Scott, Paolo Fortina, et al.
Law and Human Behavior
|
September 15, 2022
Evaluator empathy in risk assessment interviews
Kathryn Scott, Marcus T Boccaccini, Gabriele Trupp, et al.
Haematologica
|
July 22, 2008
Genetic variation in genes expressed in the germinal center and risk of B cell lymphoma among Caucasians
Kathryn Scott, Peter J Adamson, Eleanor V Willett, et al.
Thorax
|
April 23, 2022
COVID-19 associated phrenic nerve mononeuritis: a case series
Sheonagh MacPhail Law, Kathryn Scott, Ahmed Alkarn, et al.
Blood
|
June 8, 2007
RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphoma
Kathryn Scott, Peter J Adamson, Sharon L Barrans, et al.
Clinical and Translational Science
|
December 21, 2010
Variants in genes involved in functional pathways associated with hypertension in African Americans
Maria P Martinez Cantarin, Adam Ertel, Stephanie Deloach, et al.
BMJ Open
|
January 15, 2018
A study protocol for a non-randomised comparison trial evaluating the feasibility and effectiveness of a mobile cognitive-behavioural programme with integrated coaching for anxious adults in primary care
Eva Szigethy, Francis Solano, Meredith Wallace, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 30, 2013
Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family
George J Feldman, Javad Parvizi, Mark Levenstien, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Immunology and Allergy Clinics of North America
|
April 26, 2022
Pharmacogenomics of Drug Hypersensitivity: Technology and Translation
Rebecca Kuruvilla, Kathryn Scott, Sir Munir Pirmohamed
Urology
|
December 13, 2021
Robotic Assisted Caval Replacement for Recurrent Renal Cell Carcinoma Invading the Wall of the Inferior Vena Cava
Kathryn Scott, Jared Manwaring, Kwame Amankwah, et al.
Clinical and Translational Science
|
May 7, 2010
Association of a polymorphic variant of the adiponectin gene with insulin resistance in african americans
Claudia Specchia, Kathryn Scott, Paolo Fortina, et al.
Law and Human Behavior
|
September 15, 2022
Evaluator empathy in risk assessment interviews
Kathryn Scott, Marcus T Boccaccini, Gabriele Trupp, et al.
Haematologica
|
July 22, 2008
Genetic variation in genes expressed in the germinal center and risk of B cell lymphoma among Caucasians
Kathryn Scott, Peter J Adamson, Eleanor V Willett, et al.
Thorax
|
April 23, 2022
COVID-19 associated phrenic nerve mononeuritis: a case series
Sheonagh MacPhail Law, Kathryn Scott, Ahmed Alkarn, et al.
Blood
|
June 8, 2007
RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphoma
Kathryn Scott, Peter J Adamson, Sharon L Barrans, et al.
Clinical and Translational Science
|
December 21, 2010
Variants in genes involved in functional pathways associated with hypertension in African Americans
Maria P Martinez Cantarin, Adam Ertel, Stephanie Deloach, et al.
BMJ Open
|
January 15, 2018
A study protocol for a non-randomised comparison trial evaluating the feasibility and effectiveness of a mobile cognitive-behavioural programme with integrated coaching for anxious adults in primary care
Eva Szigethy, Francis Solano, Meredith Wallace, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 30, 2013
Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family
George J Feldman, Javad Parvizi, Mark Levenstien, et al.
Page
of 3