T Bruin - JoVE Visualize

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Gastroenterology|August 1, 1985

Antithrombin III metabolism in two colitis patients with acquired antithrombin III deficiencyE A Knot, J W ten Cate, T Bruin, et al.

Human Genetics|March 1, 1994

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.

Human Mutation|January 1, 1997

A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.

American Journal of Medical Genetics|August 26, 1998

Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo eventH E Henderson, S M Bijvoet, M A Mannens, et al.

Journal of Lipid Research|March 1, 1994

A compound heterozygote for lipoprotein lipase deficiency, Val69-->Leu and Gly188-->Glu: correlation between in vitro LPL activity and clinical expressionT Bruin, S Tuzgöl, W J Mulder, et al.

Blood|January 1, 1986

Purified radiolabeled antithrombin III metabolism in three families with hereditary AT III deficiency: application of a three-compartment modelE A Knot, E de Jong, J W ten Cate, et al.

Clinical Chemistry|December 10, 1999

Influence of repetitive finger puncturing on skin perfusion and capillary blood analysis in patients with diabetes mellitusJ C de Graaff, G J Hemmes, T Bruin, et al.

Journal of Lipid Research|December 1, 1993

Recurrent pancreatitis and chylomicronemia in an extended Dutch kindred is caused by a Gly154-->Ser substitution in lipoprotein lipaseT Bruin, S Tuzgöl, D E van Diermen, et al.

Human Mutation|January 1, 1994

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.

The Journal of Clinical Investigation|September 1, 1990

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.

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Showing results (11-20 of 28) with videos related to

Sort By:

Pageof 3

Gastroenterology|August 1, 1985

Antithrombin III metabolism in two colitis patients with acquired antithrombin III deficiencyE A Knot, J W ten Cate, T Bruin, et al.

Human Genetics|March 1, 1994

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.

Human Mutation|January 1, 1997

A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.

American Journal of Medical Genetics|August 26, 1998

Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo eventH E Henderson, S M Bijvoet, M A Mannens, et al.

Journal of Lipid Research|March 1, 1994

A compound heterozygote for lipoprotein lipase deficiency, Val69-->Leu and Gly188-->Glu: correlation between in vitro LPL activity and clinical expressionT Bruin, S Tuzgöl, W J Mulder, et al.

Blood|January 1, 1986

Purified radiolabeled antithrombin III metabolism in three families with hereditary AT III deficiency: application of a three-compartment modelE A Knot, E de Jong, J W ten Cate, et al.

Clinical Chemistry|December 10, 1999

Influence of repetitive finger puncturing on skin perfusion and capillary blood analysis in patients with diabetes mellitusJ C de Graaff, G J Hemmes, T Bruin, et al.

Journal of Lipid Research|December 1, 1993

Recurrent pancreatitis and chylomicronemia in an extended Dutch kindred is caused by a Gly154-->Ser substitution in lipoprotein lipaseT Bruin, S Tuzgöl, D E van Diermen, et al.

Human Mutation|January 1, 1994

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.

The Journal of Clinical Investigation|September 1, 1990

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.

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