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BMC Neurology
|
August 20, 2015
Effects of botulinum toxin A and/or bimanual task-oriented therapy on upper extremity activities in unilateral Cerebral Palsy: a clinical trial
Lucianne Speth, Yvonne Janssen-Potten, Eugene Rameckers, et al.
Archives of Internal Medicine
|
October 25, 1993
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia
J C Defesche, K L Pricker, M R Hayden, et al.
European Heart Journal
|
November 9, 2006
Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia
Olga W Souverein, Joep C Defesche, Aeilko H Zwinderman, et al.
Human Genetics
|
April 1, 1989
DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases
J C Defesche, M de Vissar, E Bakker, et al.
Seminars in Vascular Medicine
|
June 17, 2004
Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands
David Wonderling, Marina A W Umans-Eckenhausen, Dalya Marks, et al.
Circulation
|
May 20, 2025
Efficacy and Safety of Inclisiran in Adolescents With Genetically Confirmed Homozygous Familial Hypercholesterolemia: Results From the Double-Blind, Placebo-Controlled Part of the ORION-13 Randomized Trial
Albert Wiegman, Amy L Peterson, Robert A Hegele, et al.
Journal of Epidemiology and Community Health
|
June 20, 2001
Results from a family and DNA based active identification programme for familial hypercholesterolaemia
A H ten Asbroek, P J de Mheen, J C Defesche, et al.
Molecular Genetics and Metabolism
|
February 12, 2009
Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses
Øystein L Holla, Sigve Nakken, Morten Mattingsdal, et al.
Nature Reviews. Disease Primers
|
December 9, 2017
Familial hypercholesterolaemia
Joep C Defesche, Samuel S Gidding, Mariko Harada-Shiba, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 1, 1997
Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia
S N Pimstone, J C Defesche, S M Clee, et al.
Page
of 18
Search research articles
Search
Showing results (61-70 of 178) with videos related to
Sort By:
Page
of 18
BMC Neurology
|
August 20, 2015
Effects of botulinum toxin A and/or bimanual task-oriented therapy on upper extremity activities in unilateral Cerebral Palsy: a clinical trial
Lucianne Speth, Yvonne Janssen-Potten, Eugene Rameckers, et al.
Archives of Internal Medicine
|
October 25, 1993
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia
J C Defesche, K L Pricker, M R Hayden, et al.
European Heart Journal
|
November 9, 2006
Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia
Olga W Souverein, Joep C Defesche, Aeilko H Zwinderman, et al.
Human Genetics
|
April 1, 1989
DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases
J C Defesche, M de Vissar, E Bakker, et al.
Seminars in Vascular Medicine
|
June 17, 2004
Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands
David Wonderling, Marina A W Umans-Eckenhausen, Dalya Marks, et al.
Circulation
|
May 20, 2025
Efficacy and Safety of Inclisiran in Adolescents With Genetically Confirmed Homozygous Familial Hypercholesterolemia: Results From the Double-Blind, Placebo-Controlled Part of the ORION-13 Randomized Trial
Albert Wiegman, Amy L Peterson, Robert A Hegele, et al.
Journal of Epidemiology and Community Health
|
June 20, 2001
Results from a family and DNA based active identification programme for familial hypercholesterolaemia
A H ten Asbroek, P J de Mheen, J C Defesche, et al.
Molecular Genetics and Metabolism
|
February 12, 2009
Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses
Øystein L Holla, Sigve Nakken, Morten Mattingsdal, et al.
Nature Reviews. Disease Primers
|
December 9, 2017
Familial hypercholesterolaemia
Joep C Defesche, Samuel S Gidding, Mariko Harada-Shiba, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 1, 1997
Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia
S N Pimstone, J C Defesche, S M Clee, et al.
Page
of 18