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Defesche

Showing results (21-30 of 178) with videos related to

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Journal of the American College of Cardiology|May 17, 2005
What promise does PCSK9 hold?John J P Kastelein, Sigrid W Fouchier, Joep C Defesche
Clinical Chemistry|January 1, 1989
Thermal inactivation of L-thyroxinJ Wortsman, D C Papadimitriou, M Borges, et al.
Human Mutation|October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The NetherlandsSigrid W Fouchier, John J P Kastelein, Joep C Defesche
European Heart Journal|March 7, 2012
Cardiovascular risk in relation to functionality of sequence variants in the gene coding for the low-density lipoprotein receptor: a study among 29,365 individuals tested for 64 specific low-density lipoprotein-receptor sequence variantsRoeland Huijgen, Iris Kindt, Joep C Defesche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Differential diagnosis of genetic disease by DNA restriction fragment length polymorphismsP A Bolhuis, J C Defesche, H J van der Helm
Journal of Inherited Metabolic Disease|September 15, 2006
Lipoprotein lipase gene analyses in one Turkish family and three different Chinese families with severe hypertriglyceridaemia: one novel and several established mutationsMelchior C Nierman, Jorge Peter, Kah-Lin Khoo, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Is detection and treatment of familial hypercholesterolemia indicated in children?]H D Bakker, A Wiegman, J C Defesche, et al.
Annals of Internal Medicine|November 7, 2018
Abetalipoproteinemia From Previously Unreported Gene MutationsXavier-Philippe Aers, Bart P Leroy, Joep C Defesche, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 12, 1999
The role of chemotherapy in intracranial germinoma: a case reportP S Hupperets, H F Defesche, L M de Bruijckere, et al.
European Journal of Human Genetics : EJHG|September 29, 2005
Management of hereditary dyslipidaemia; the paradigm of autosomal dominant hypercholesterolaemiaSigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Pageof 18

Showing results (21-30 of 178) with videos related to

Sort By:
Pageof 18
Journal of the American College of Cardiology|May 17, 2005
What promise does PCSK9 hold?John J P Kastelein, Sigrid W Fouchier, Joep C Defesche
Clinical Chemistry|January 1, 1989
Thermal inactivation of L-thyroxinJ Wortsman, D C Papadimitriou, M Borges, et al.
Human Mutation|October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The NetherlandsSigrid W Fouchier, John J P Kastelein, Joep C Defesche
European Heart Journal|March 7, 2012
Cardiovascular risk in relation to functionality of sequence variants in the gene coding for the low-density lipoprotein receptor: a study among 29,365 individuals tested for 64 specific low-density lipoprotein-receptor sequence variantsRoeland Huijgen, Iris Kindt, Joep C Defesche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Differential diagnosis of genetic disease by DNA restriction fragment length polymorphismsP A Bolhuis, J C Defesche, H J van der Helm
Journal of Inherited Metabolic Disease|September 15, 2006
Lipoprotein lipase gene analyses in one Turkish family and three different Chinese families with severe hypertriglyceridaemia: one novel and several established mutationsMelchior C Nierman, Jorge Peter, Kah-Lin Khoo, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Is detection and treatment of familial hypercholesterolemia indicated in children?]H D Bakker, A Wiegman, J C Defesche, et al.
Annals of Internal Medicine|November 7, 2018
Abetalipoproteinemia From Previously Unreported Gene MutationsXavier-Philippe Aers, Bart P Leroy, Joep C Defesche, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 12, 1999
The role of chemotherapy in intracranial germinoma: a case reportP S Hupperets, H F Defesche, L M de Bruijckere, et al.
European Journal of Human Genetics : EJHG|September 29, 2005
Management of hereditary dyslipidaemia; the paradigm of autosomal dominant hypercholesterolaemiaSigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Pageof 18