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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-thyroxin
J Wortsman, D C Papadimitriou, M Borges, et al.
Human Mutation
|
October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The Netherlands
Sigrid 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 variants
Roeland 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 polymorphisms
P 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 mutations
Melchior 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 Mutations
Xavier-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 report
P 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 hypercholesterolaemia
Sigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Page
of 18
Search research articles
Search
Showing results (21-30 of 178) with videos related to
Sort By:
Page
of 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-thyroxin
J Wortsman, D C Papadimitriou, M Borges, et al.
Human Mutation
|
October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The Netherlands
Sigrid 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 variants
Roeland 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 polymorphisms
P 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 mutations
Melchior 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 Mutations
Xavier-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 report
P 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 hypercholesterolaemia
Sigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Page
of 18