J L de Gennes|G Turpin|J Truffert|B Labrousse - JoVE Visualize

Showing results (61-70 of 245) with videos related to

Pageof 25

Sort By:

Acta Endocrinologica|August 1, 1988

The immunocytochemical heterogeneity of silent pituitary adenomasH M Heshmati, G Turpin, M Kujas, et al.

Annales D'Endocrinologie|July 1, 1979

[Determination of 6 pituitary hormones in the cerebrospinal fluid. Control subjects, prolactin adenomas, empty sella syndrome and hypothalamic disorders (author's transl)]G Turpin, H M Heshmati, M Roger, et al.

Arteriosclerosis (Dallas, Tex.)|September 1, 1985

Direct fetal blood examination for prenatal diagnosis of homozygous familial hypercholesterolemiaJ L de Gennes, F Daffos, F Dairou, et al.

Annales De Medecine Interne|January 1, 1985

[Results of bromocriptine treatment of giant or invasive prolactin adenomas. Apropos of 20 cases]H Scherrer, G Turpin, J L De Gennes, et al.

Presse Medicale (Paris, France : 1983)|May 19, 1984

[Mucigenous cysts of the pituitary gland. 3 cases]G Turpin, M Kujas, R Van Effenterre, et al.

The Journal of Biological Chemistry|December 15, 1989

An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-IIS S Fojo, J L de Gennes, J Chapman, et al.

Haemostasis|January 1, 1989

Plasma factor VII, triglyceride concentration and fibrin degradation products in primary hyperlipidemia: a clinical and laboratory studyJ Carvalho de Sousa, E Bruckert, P Giral, et al.

Haemostasis|January 1, 1989

Coagulation factor VII and plasma triglycerides. Decreased catabolism as a possible mechanism of factor VII hyperactivityJ Carvalho de Sousa, E Bruckert, P Giral, et al.

Human Mutation|January 1, 1992

Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.

Annales De Genetique|January 1, 1990

A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequencyP Benlian, S Amselem, N Loux, et al.

Pageof 25

Showing results (61-70 of 245) with videos related to

Sort By:

Pageof 25

Acta Endocrinologica|August 1, 1988

The immunocytochemical heterogeneity of silent pituitary adenomasH M Heshmati, G Turpin, M Kujas, et al.

Annales D'Endocrinologie|July 1, 1979

[Determination of 6 pituitary hormones in the cerebrospinal fluid. Control subjects, prolactin adenomas, empty sella syndrome and hypothalamic disorders (author's transl)]G Turpin, H M Heshmati, M Roger, et al.

Arteriosclerosis (Dallas, Tex.)|September 1, 1985

Direct fetal blood examination for prenatal diagnosis of homozygous familial hypercholesterolemiaJ L de Gennes, F Daffos, F Dairou, et al.

Annales De Medecine Interne|January 1, 1985

[Results of bromocriptine treatment of giant or invasive prolactin adenomas. Apropos of 20 cases]H Scherrer, G Turpin, J L De Gennes, et al.

Presse Medicale (Paris, France : 1983)|May 19, 1984

[Mucigenous cysts of the pituitary gland. 3 cases]G Turpin, M Kujas, R Van Effenterre, et al.

The Journal of Biological Chemistry|December 15, 1989

An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-IIS S Fojo, J L de Gennes, J Chapman, et al.

Haemostasis|January 1, 1989

Plasma factor VII, triglyceride concentration and fibrin degradation products in primary hyperlipidemia: a clinical and laboratory studyJ Carvalho de Sousa, E Bruckert, P Giral, et al.

Haemostasis|January 1, 1989

Coagulation factor VII and plasma triglycerides. Decreased catabolism as a possible mechanism of factor VII hyperactivityJ Carvalho de Sousa, E Bruckert, P Giral, et al.

Human Mutation|January 1, 1992

Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.

Annales De Genetique|January 1, 1990

A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequencyP Benlian, S Amselem, N Loux, et al.

Pageof 25