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Clinical Genetics
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April 1, 1997
A novel V415A mutation in exon 9 of the low density lipoprotein receptor gene causing familial hypercholesterolemia
P Lombardi, J C Defesche, S W Kamerling, et al.
Frontiers in Immunology
|
June 29, 2026
Type I interferon pathway activation in connective tissue disease associated interstitial lung disease
Tobias M Defesche, Thomas Koudstaal, Marjan A Versnel, et al.
Genetic Testing
|
June 25, 2003
Identification of a new mutation, S305C, in exon 7 of the low-density lipoprotein receptor gene in a Brazilian family with homozygous familial hypercholesterolemia
Laura van de Kerkhof, Silvia J Van Eijk, Joep C Defesche, et al.
Annals of Neurology
|
May 1, 1990
An unusual variant of Becker muscular dystrophy
M de Visser, E Bakker, J C Defesche, et al.
Clinical Genetics
|
December 1, 1996
Identification of a double mutation in the low-density lipoprotein receptor gene causing familial hypercholesterolemia
P Lombardi, S W Kamerling, J C Defesche, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
March 1, 1994
Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100
A F Stalenhoef, J C Defesche, H A Kleinveld, et al.
Journal of Clinical Lipidology
|
September 29, 2016
Ten years of lipoprotein apheresis for familial hypercholesterolemia in Malaysia: A creative approach by a cardiologist in a developing country
Kah Lin Khoo, Michael M Page, Yin Mei Liew, et al.
JAMA
|
March 11, 2015
Association between familial hypercholesterolemia and prevalence of type 2 diabetes mellitus
Joost Besseling, John J P Kastelein, Joep C Defesche, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 18, 1999
[Tracing of patients with familial hypercholesterolemia in the Netherlands]
M A Umans-Eckenhausen, J C Defesche, R L Scheerder, et al.
The Netherlands Journal of Medicine
|
February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemia
J C Defesche, P J Lansberg, P W Reymer, et al.
Page
of 18
Search research articles
Search
Showing results (41-50 of 178) with videos related to
Sort By:
Page
of 18
Clinical Genetics
|
April 1, 1997
A novel V415A mutation in exon 9 of the low density lipoprotein receptor gene causing familial hypercholesterolemia
P Lombardi, J C Defesche, S W Kamerling, et al.
Frontiers in Immunology
|
June 29, 2026
Type I interferon pathway activation in connective tissue disease associated interstitial lung disease
Tobias M Defesche, Thomas Koudstaal, Marjan A Versnel, et al.
Genetic Testing
|
June 25, 2003
Identification of a new mutation, S305C, in exon 7 of the low-density lipoprotein receptor gene in a Brazilian family with homozygous familial hypercholesterolemia
Laura van de Kerkhof, Silvia J Van Eijk, Joep C Defesche, et al.
Annals of Neurology
|
May 1, 1990
An unusual variant of Becker muscular dystrophy
M de Visser, E Bakker, J C Defesche, et al.
Clinical Genetics
|
December 1, 1996
Identification of a double mutation in the low-density lipoprotein receptor gene causing familial hypercholesterolemia
P Lombardi, S W Kamerling, J C Defesche, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
March 1, 1994
Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100
A F Stalenhoef, J C Defesche, H A Kleinveld, et al.
Journal of Clinical Lipidology
|
September 29, 2016
Ten years of lipoprotein apheresis for familial hypercholesterolemia in Malaysia: A creative approach by a cardiologist in a developing country
Kah Lin Khoo, Michael M Page, Yin Mei Liew, et al.
JAMA
|
March 11, 2015
Association between familial hypercholesterolemia and prevalence of type 2 diabetes mellitus
Joost Besseling, John J P Kastelein, Joep C Defesche, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 18, 1999
[Tracing of patients with familial hypercholesterolemia in the Netherlands]
M A Umans-Eckenhausen, J C Defesche, R L Scheerder, et al.
The Netherlands Journal of Medicine
|
February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemia
J C Defesche, P J Lansberg, P W Reymer, et al.
Page
of 18