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Amanda J Hooper

Showing results (51-60 of 125) with videos related to

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Expert Opinion on Pharmacotherapy|April 24, 2025
Sepiapterin for the treatment of phenylketonuriaRobin A Williams, Damon A Bell, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
Clinical utility gene card for: AbetalipoproteinaemiaJohn R Burnett, Damon A Bell, Amanda J Hooper, et al.
Nature Reviews. Endocrinology|May 21, 2016
Progress in the care of common inherited atherogenic disorders of apolipoprotein B metabolismKatrina L Ellis, Amanda J Hooper, John R Burnett, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 25, 2010
Pancreatitis in a child with lipemia due to novel lipoprotein lipase mutationsNitin Gupta, David Moore, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Clinical utility gene card for: Familial Hypobetalipoproteinaemia (APOB)John R Burnett, Damon A Bell, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|October 23, 2014
Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB)--Update 2014John R Burnett, Damon A Bell, Amanda J Hooper, et al.
Obesity Facts|June 25, 2025
Diverse Obesity Trajectories in a Family Including Identical Twins with a Pathogenic MC4R VariantJane Jia Xin Lim, Amanda J Hooper, Joan Khoo, et al.
Critical Reviews in Clinical Laboratory Sciences|June 11, 2011
Familial hypercholesterolemia: epidemiology, Neolithic origins and modern geographic distributionKhemanganee E Liyanage, John R Burnett, Amanda J Hooper, et al.
The Medical Journal of Australia|October 22, 2008
Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelaeHelen Mountain, Joanna M Brisbane, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|May 25, 2017
Clinical utility gene card for: Tangier diseaseAmanda J Hooper, Sally P A McCormick, Robert A Hegele, et al.
Pageof 13

Showing results (51-60 of 125) with videos related to

Sort By:
Pageof 13
Expert Opinion on Pharmacotherapy|April 24, 2025
Sepiapterin for the treatment of phenylketonuriaRobin A Williams, Damon A Bell, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
Clinical utility gene card for: AbetalipoproteinaemiaJohn R Burnett, Damon A Bell, Amanda J Hooper, et al.
Nature Reviews. Endocrinology|May 21, 2016
Progress in the care of common inherited atherogenic disorders of apolipoprotein B metabolismKatrina L Ellis, Amanda J Hooper, John R Burnett, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 25, 2010
Pancreatitis in a child with lipemia due to novel lipoprotein lipase mutationsNitin Gupta, David Moore, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Clinical utility gene card for: Familial Hypobetalipoproteinaemia (APOB)John R Burnett, Damon A Bell, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|October 23, 2014
Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB)--Update 2014John R Burnett, Damon A Bell, Amanda J Hooper, et al.
Obesity Facts|June 25, 2025
Diverse Obesity Trajectories in a Family Including Identical Twins with a Pathogenic MC4R VariantJane Jia Xin Lim, Amanda J Hooper, Joan Khoo, et al.
Critical Reviews in Clinical Laboratory Sciences|June 11, 2011
Familial hypercholesterolemia: epidemiology, Neolithic origins and modern geographic distributionKhemanganee E Liyanage, John R Burnett, Amanda J Hooper, et al.
The Medical Journal of Australia|October 22, 2008
Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelaeHelen Mountain, Joanna M Brisbane, Amanda J Hooper, et al.
European Journal of Human Genetics : EJHG|May 25, 2017
Clinical utility gene card for: Tangier diseaseAmanda J Hooper, Sally P A McCormick, Robert A Hegele, et al.
Pageof 13