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L Duprez

Showing results (11-20 of 26) with videos related to

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Nature|October 14, 1993
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomasJ Parma, L Duprez, J Van Sande, et al.
Annales D'Endocrinologie|January 1, 1993
[Thyrotropin receptor. Control of the gene expression and structure function relationships]G Vassart, J Parma, L Duprez, et al.
Clinical Endocrinology|June 1, 1996
TSH receptor and diseaseM Tonacchera, J Van Sande, J Parma, et al.
Thyroid : Official Journal of the American Thyroid Association|November 24, 1999
A novel thyrotropin receptor mutation in an infant with severe thyrotoxicosisC T Esapa, L Duprez, M Ludgate, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2000
Pathology of the TSH receptorL Duprez, J Parma, J Van Sande, et al.
Annals of the New York Academy of Sciences|September 7, 1995
The G protein-coupled receptor family and one of its members, the TSH receptorG Vassart, F Desarnaud, L Duprez, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2001
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8C Vilain, C Rydlewski, L Duprez, et al.
The Journal of Clinical Investigation|July 1, 1994
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitusM J Abramowicz, M Andrien, E Dupont, et al.
The New England Journal of Medicine|December 17, 1998
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropinP Rodien, C Brémont, M L Sanson, et al.
The New England Journal of Medicine|January 19, 1995
Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor geneP Kopp, J van Sande, J Parma, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Nature|October 14, 1993
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomasJ Parma, L Duprez, J Van Sande, et al.
Annales D'Endocrinologie|January 1, 1993
[Thyrotropin receptor. Control of the gene expression and structure function relationships]G Vassart, J Parma, L Duprez, et al.
Clinical Endocrinology|June 1, 1996
TSH receptor and diseaseM Tonacchera, J Van Sande, J Parma, et al.
Thyroid : Official Journal of the American Thyroid Association|November 24, 1999
A novel thyrotropin receptor mutation in an infant with severe thyrotoxicosisC T Esapa, L Duprez, M Ludgate, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2000
Pathology of the TSH receptorL Duprez, J Parma, J Van Sande, et al.
Annals of the New York Academy of Sciences|September 7, 1995
The G protein-coupled receptor family and one of its members, the TSH receptorG Vassart, F Desarnaud, L Duprez, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2001
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8C Vilain, C Rydlewski, L Duprez, et al.
The Journal of Clinical Investigation|July 1, 1994
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitusM J Abramowicz, M Andrien, E Dupont, et al.
The New England Journal of Medicine|December 17, 1998
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropinP Rodien, C Brémont, M L Sanson, et al.
The New England Journal of Medicine|January 19, 1995
Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor geneP Kopp, J van Sande, J Parma, et al.
Pageof 3