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Journal of Clinical Lipidology
|
December 7, 2016
Familial combined hyperlipidemia and hyperlipoprotein(a) as phenotypic mimics of familial hypercholesterolemia: Frequencies, associations and predictions
Katrina L Ellis, Jing Pang, Dick C Chan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2018
A Comparative Analysis of Phenotypic Predictors of Mutations in Familial Hypercholesterolemia
Dick C Chan, Jing Pang, Amanda J Hooper, et al.
Atherosclerosis
|
October 2, 2018
Homozygous familial hypercholesterolaemia in Vietnam: Case series, genetics and cascade testing of families
Thanh Huong Truong, Ngoc Thanh Kim, Mai Ngoc Thi Nguyen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 10, 2013
Impact of interpretative commenting on lipid profiles in people at high risk of familial hypercholesterolaemia
Damon A Bell, Robert Bender, Amanda J Hooper, et al.
Atherosclerosis
|
May 13, 2014
Detecting familial hypercholesterolaemia in the community: impact of a telephone call from a chemical pathologist to the requesting general practitioner
Damon A Bell, Amanda J Hooper, Glenn Edwards, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 23, 2013
Non-alcoholic steatohepatitis-related cirrhosis in a patient with APOB L343V familial hypobetalipoproteinaemia
Liesl V Heeks, Amanda J Hooper, Leon A Adams, et al.
Annals of Clinical Biochemistry
|
September 25, 2012
Opportunistic screening for familial hypercholesterolaemia via a community laboratory
Damon A Bell, Amanda J Hooper, Robert Bender, et al.
Journal of Paediatrics and Child Health
|
April 8, 2018
Parent-child genetic testing for familial hypercholesterolaemia in an Australian context
Jing Pang, Andrew C Martin, Timothy R Bates, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 19, 2020
Coronary artery disease and the risk-associated LPA variants, rs3798220 and rs10455872, in patients with suspected familial hypercholesterolaemia
Michael M Page, Katrina L Ellis, Jing Pang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 3, 2009
A novel ABCA1 nonsense mutation, R1270X, in Tangier disease associated with an unrecognised bleeding tendency
Amanda J Hooper, Ken Robertson, Lydia Ng, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 125) with videos related to
Sort By:
Page
of 13
Journal of Clinical Lipidology
|
December 7, 2016
Familial combined hyperlipidemia and hyperlipoprotein(a) as phenotypic mimics of familial hypercholesterolemia: Frequencies, associations and predictions
Katrina L Ellis, Jing Pang, Dick C Chan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2018
A Comparative Analysis of Phenotypic Predictors of Mutations in Familial Hypercholesterolemia
Dick C Chan, Jing Pang, Amanda J Hooper, et al.
Atherosclerosis
|
October 2, 2018
Homozygous familial hypercholesterolaemia in Vietnam: Case series, genetics and cascade testing of families
Thanh Huong Truong, Ngoc Thanh Kim, Mai Ngoc Thi Nguyen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 10, 2013
Impact of interpretative commenting on lipid profiles in people at high risk of familial hypercholesterolaemia
Damon A Bell, Robert Bender, Amanda J Hooper, et al.
Atherosclerosis
|
May 13, 2014
Detecting familial hypercholesterolaemia in the community: impact of a telephone call from a chemical pathologist to the requesting general practitioner
Damon A Bell, Amanda J Hooper, Glenn Edwards, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 23, 2013
Non-alcoholic steatohepatitis-related cirrhosis in a patient with APOB L343V familial hypobetalipoproteinaemia
Liesl V Heeks, Amanda J Hooper, Leon A Adams, et al.
Annals of Clinical Biochemistry
|
September 25, 2012
Opportunistic screening for familial hypercholesterolaemia via a community laboratory
Damon A Bell, Amanda J Hooper, Robert Bender, et al.
Journal of Paediatrics and Child Health
|
April 8, 2018
Parent-child genetic testing for familial hypercholesterolaemia in an Australian context
Jing Pang, Andrew C Martin, Timothy R Bates, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 19, 2020
Coronary artery disease and the risk-associated LPA variants, rs3798220 and rs10455872, in patients with suspected familial hypercholesterolaemia
Michael M Page, Katrina L Ellis, Jing Pang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 3, 2009
A novel ABCA1 nonsense mutation, R1270X, in Tangier disease associated with an unrecognised bleeding tendency
Amanda J Hooper, Ken Robertson, Lydia Ng, et al.
Page
of 13