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T P Leren

Showing results (1-10 of 73) with videos related to

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Acta Pharmacologica Et Toxicologica|March 1, 1985
Doxazosin increases low density lipoprotein receptor activityT P Leren
Clinical Genetics|November 4, 2004
Cascade genetic screening for familial hypercholesterolemiaT P Leren
Clinical Genetics|April 22, 2004
Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemiaT P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 10, 1986
[Total cholesterol. Reference values and criteria for treatment]T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1993
[Molecular genetic causes of familial hypercholesterolemia]T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1983
[Hyperosmolar nonketotic diabetic coma]O Bruserud, T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 20, 1987
[Biochemical defects in familial hypercholesterolemia]T P Leren, H Tolleshaug
Scandinavian Journal of Clinical and Laboratory Investigation|June 1, 1988
Studies of serum lipids in hypercholesterolaemic rabbits treated with doxazosinT P Leren, K Berg
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1997
[Is there a need for genetic/molecular diagnosis of familial hypercholesterolemia?]T P Leren, L Ose
European Journal of Clinical Investigation|December 1, 1995
Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?T P Leren, I Hjermann
Pageof 8

Showing results (1-10 of 73) with videos related to

Sort By:
Pageof 8
Acta Pharmacologica Et Toxicologica|March 1, 1985
Doxazosin increases low density lipoprotein receptor activityT P Leren
Clinical Genetics|November 4, 2004
Cascade genetic screening for familial hypercholesterolemiaT P Leren
Clinical Genetics|April 22, 2004
Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemiaT P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 10, 1986
[Total cholesterol. Reference values and criteria for treatment]T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1993
[Molecular genetic causes of familial hypercholesterolemia]T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1983
[Hyperosmolar nonketotic diabetic coma]O Bruserud, T P Leren
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 20, 1987
[Biochemical defects in familial hypercholesterolemia]T P Leren, H Tolleshaug
Scandinavian Journal of Clinical and Laboratory Investigation|June 1, 1988
Studies of serum lipids in hypercholesterolaemic rabbits treated with doxazosinT P Leren, K Berg
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1997
[Is there a need for genetic/molecular diagnosis of familial hypercholesterolemia?]T P Leren, L Ose
European Journal of Clinical Investigation|December 1, 1995
Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?T P Leren, I Hjermann
Pageof 8