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Amanda J Hooper

Showing results (61-70 of 125) with videos related to

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Annals of Clinical Biochemistry|June 3, 2009
Hypobetalipoproteinaemia secondary to chronic hepatitis C virus infection in a patient with familial hypercholesterolaemiaAbdulhadi I Bima, Amanda J Hooper, Frank M van Bockxmeer, et al.
Pathology|May 21, 2025
Dual-reporting aldosterone by mass spectrometry and immunoassay in the seated saline suppression test may enhance subtype classification of patients with primary aldosteronismNicola Sawyer, Paul Glendenning, Markus P Schlaich, et al.
Annals of Clinical Biochemistry|September 16, 2020
Homozygous autosomal recessive hypercholesterolaemia in a South Asian child presenting with multiple cutaneous xanthomataV Thadchanamoorthy, Kavinda Dayasiri, S I Majitha, et al.
Endocrinology, Diabetes & Metabolism Case Reports|January 10, 2022
Monogenic diabetes due to an INSR mutation in a child with severe insulin resistanceElaine E Sanderson, Mark Shah, Amanda J Hooper, et al.
Pathology|June 26, 2026
Impact of the 2025 Endocrine Society clinical practice guideline on the diagnosis and management of primary aldosteronism for the clinical laboratoryNicola K Sawyer, Paul Glendenning, Markus P Schlaich, et al.
The New Zealand Medical Journal|April 3, 2010
Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB geneChris Florkowski, John Hedley, Vivienne Bickley, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|May 21, 2014
Lipoprotein apheresis and new therapies for severe familial hypercholesterolemia in adults and childrenMichael M Page, Damon A Bell, Amanda J Hooper, et al.
Journal of Paediatrics and Child Health|October 1, 2025
Incidental Finding of Severe Hypertriglyceridaemia and Diagnosis of Familial Chylomicronaemia Syndrome in a FamilyV Thadchanamoorthy, Kavinda Dayasiri, Hemika Yoganathan, et al.
Pathology|January 2, 2019
Update on the diagnosis, treatment and management of rare genetic lipid disordersDavid M Ng, John R Burnett, Damon A Bell, et al.
Global Pediatric Health|July 12, 2017
Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia RetinalisDinesha Maduri Vidanapathirana, Thushara Rodrigo, Samantha Waidyanatha, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
Annals of Clinical Biochemistry|June 3, 2009
Hypobetalipoproteinaemia secondary to chronic hepatitis C virus infection in a patient with familial hypercholesterolaemiaAbdulhadi I Bima, Amanda J Hooper, Frank M van Bockxmeer, et al.
Pathology|May 21, 2025
Dual-reporting aldosterone by mass spectrometry and immunoassay in the seated saline suppression test may enhance subtype classification of patients with primary aldosteronismNicola Sawyer, Paul Glendenning, Markus P Schlaich, et al.
Annals of Clinical Biochemistry|September 16, 2020
Homozygous autosomal recessive hypercholesterolaemia in a South Asian child presenting with multiple cutaneous xanthomataV Thadchanamoorthy, Kavinda Dayasiri, S I Majitha, et al.
Endocrinology, Diabetes & Metabolism Case Reports|January 10, 2022
Monogenic diabetes due to an INSR mutation in a child with severe insulin resistanceElaine E Sanderson, Mark Shah, Amanda J Hooper, et al.
Pathology|June 26, 2026
Impact of the 2025 Endocrine Society clinical practice guideline on the diagnosis and management of primary aldosteronism for the clinical laboratoryNicola K Sawyer, Paul Glendenning, Markus P Schlaich, et al.
The New Zealand Medical Journal|April 3, 2010
Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB geneChris Florkowski, John Hedley, Vivienne Bickley, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|May 21, 2014
Lipoprotein apheresis and new therapies for severe familial hypercholesterolemia in adults and childrenMichael M Page, Damon A Bell, Amanda J Hooper, et al.
Journal of Paediatrics and Child Health|October 1, 2025
Incidental Finding of Severe Hypertriglyceridaemia and Diagnosis of Familial Chylomicronaemia Syndrome in a FamilyV Thadchanamoorthy, Kavinda Dayasiri, Hemika Yoganathan, et al.
Pathology|January 2, 2019
Update on the diagnosis, treatment and management of rare genetic lipid disordersDavid M Ng, John R Burnett, Damon A Bell, et al.
Global Pediatric Health|July 12, 2017
Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia RetinalisDinesha Maduri Vidanapathirana, Thushara Rodrigo, Samantha Waidyanatha, et al.
Pageof 13