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Results: 1-11 |
Results: 11
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene
Authors: Bretones, P Duprez, L Parma, J David, M Vassart, G Rodien, P
Citation: P. Bretones et al., A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene, THYROID, 11(10), 2001, pp. 977-980
Redistribution of the substitutional elements during sigma and chi phase formation in a duplex stainless steel
Authors: Duprez, L De Cooman, BC Akdut, N
Citation: L. Duprez et al., Redistribution of the substitutional elements during sigma and chi phase formation in a duplex stainless steel, STEEL RES, 72(8), 2001, pp. 311-316
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8
Authors: Vilain, C Rydlewski, C Duprez, L Heinrichs, C Abramowicz, M Malvaux, P Renneboog, B Parma, J Costagliola, S Vassart, G
Citation: C. Vilain et al., Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8, J CLIN END, 86(1), 2001, pp. 234-238
Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene
Authors: Heinrichs, C Parma, J Scherberg, NH Delange, F Van Vliet, G Duprez, L Bourdoux, P Bergmann, P Vassart, G Refetoff, S
Citation: C. Heinrichs et al., Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene, THYROID, 10(5), 2000, pp. 387-391
Microstructure evolution during isothermal annealing of a standard duplex stainless steel type 1.4462
Authors: Duprez, L De Cooman, B Akdut, N
Citation: L. Duprez et al., Microstructure evolution during isothermal annealing of a standard duplex stainless steel type 1.4462, STEEL RES, 71(10), 2000, pp. 417-422
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters
Authors: Pohlenz, J Duprez, L Weiss, RE Vassart, G Refetoff, S Costagliola, S
Citation: J. Pohlenz et al., Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters, J CLIN END, 85(7), 2000, pp. 2366-2369
A novel thyrotropin receptor mutation in an infant with severe thyrotoxicosis
Authors: Esapa, CT Duprez, L Ludgate, M Mustafa, MS Kendall-Taylor, P Vassart, G Harris, PE
Citation: Ct. Esapa et al., A novel thyrotropin receptor mutation in an infant with severe thyrotoxicosis, THYROID, 9(10), 1999, pp. 1005-1010
A mutation of the TSH receptor causing familial gestational hyperthyroidism
Authors: Rodien, P Bremont, C Luton, JP Raffin-Sanson, ML Parma, J Duprez, L Vassart, G
Citation: P. Rodien et al., A mutation of the TSH receptor causing familial gestational hyperthyroidism, M S-MED SCI, 15(5), 1999, pp. 713-717
Pathology of the TSH receptor
Authors: Duprez, L Parma, J Van Sande, J Rodien, P Sabine, C Abramowicz, M Dumont, JE Vassart, G
Citation: L. Duprez et al., Pathology of the TSH receptor, J PED END M, 12, 1999, pp. 295-302
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin
Authors: Rodien, P Bremont, C Parma, J Van Sande, J Costagliola, S Luton, JP Vassart, G Duprez, L
Citation: P. Rodien et al., Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin, N ENG J MED, 339(25), 1998, pp. 1823-1826
Evidences for an allelic variant of the human LC/CG receptor rather than agene duplication: Functional comparison of wild-type and variant receptors
Authors: Rodien, P Cetani, F Costagliola, S Tonacchera, M Duprez, L Minegishi, T Govaerts, C Vassart, G
Citation: P. Rodien et al., Evidences for an allelic variant of the human LC/CG receptor rather than agene duplication: Functional comparison of wild-type and variant receptors, J CLIN END, 83(12), 1998, pp. 4431-4434
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