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A Horínek

Showing results (1-10 of 23) with videos related to

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Physiological Research|September 12, 2001
Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosisM Vrablík, R Ceska, A Horínek
Physiological Research|September 13, 2000
Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patientsR Ceska, M Vrablík, A Horínek
Physiological Research|November 10, 2000
Bone mineral density in patients with apolipoprotein E type 2/2 and 4/4 genotypeT Stulc, R Ceska, A Horínek, et al.
Vnitrni Lekarstvi|October 1, 1993
[Familial hypercholesterolemia from the aspect of DNA analysis]A Horínek, J Sobra, R Ceska, et al.
Casopis Lekaru Ceskych|November 8, 1993
[Restriction fragment length polymorphisms in the families of patients with Down's syndrome (trisomy 21)]I Mazura, A Horínek, Y Franková, et al.
Casopis Lekaru Ceskych|August 23, 2000
[Hyperlipoproteinemia, the Apo-E genotype and bone density]T Stulc, R Ceska, A Horínek, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 10, 2001
Absence of the R3531C mutation in the apoB gene in Czech hypercholesterolaemic patientsM Vrablík, R Ceska, A Horínek, et al.
Casopis Lekaru Ceskych|April 19, 1995
[DNA analysis in heterozygotes in familial hypercholesterolemia]A Horínek, V Slézka, J Sobra, et al.
Ceska Gynekologie|August 23, 2000
[The spectrum of lipids in the intrauterine growth retarded fetus and in the parents]Z Hájek, P Drbohlav, R Ceska, et al.
Casopis Lekaru Ceskych|February 12, 1997
[Familial hypobetalipoproteinemia]J Sobra, A Horínek, R Ceska, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Physiological Research|September 12, 2001
Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosisM Vrablík, R Ceska, A Horínek
Physiological Research|September 13, 2000
Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patientsR Ceska, M Vrablík, A Horínek
Physiological Research|November 10, 2000
Bone mineral density in patients with apolipoprotein E type 2/2 and 4/4 genotypeT Stulc, R Ceska, A Horínek, et al.
Vnitrni Lekarstvi|October 1, 1993
[Familial hypercholesterolemia from the aspect of DNA analysis]A Horínek, J Sobra, R Ceska, et al.
Casopis Lekaru Ceskych|November 8, 1993
[Restriction fragment length polymorphisms in the families of patients with Down's syndrome (trisomy 21)]I Mazura, A Horínek, Y Franková, et al.
Casopis Lekaru Ceskych|August 23, 2000
[Hyperlipoproteinemia, the Apo-E genotype and bone density]T Stulc, R Ceska, A Horínek, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 10, 2001
Absence of the R3531C mutation in the apoB gene in Czech hypercholesterolaemic patientsM Vrablík, R Ceska, A Horínek, et al.
Casopis Lekaru Ceskych|April 19, 1995
[DNA analysis in heterozygotes in familial hypercholesterolemia]A Horínek, V Slézka, J Sobra, et al.
Ceska Gynekologie|August 23, 2000
[The spectrum of lipids in the intrauterine growth retarded fetus and in the parents]Z Hájek, P Drbohlav, R Ceska, et al.
Casopis Lekaru Ceskych|February 12, 1997
[Familial hypobetalipoproteinemia]J Sobra, A Horínek, R Ceska, et al.
Pageof 3