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L Duprez

Showing results (1-10 of 26) with videos related to

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The Journal of Clinical Investigation|June 15, 1997
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid glandM J Abramowicz, L Duprez, J Parma, et al.
Thyroid : Official Journal of the American Thyroid Association|November 22, 2001
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor geneP Bretones, L Duprez, J Parma, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2000
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symportersJ Pohlenz, L Duprez, R E Weiss, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1997
Two autonomous nodules of a patient with multinodular goiter harbor different activating mutations of the thyrotropin receptor geneL Duprez, J Hermans, J Van Sande, et al.
Molecular and Cellular Endocrinology|April 1, 1994
Constitutively active receptors as a disease-causing mechanismJ Parma, L Duprez, J Van Sande, et al.
Annales D'Endocrinologie|January 1, 1996
Activating mutations of the TSH receptor gene cause thyroid diseasesG Vassart, J Van Sande, J Parma, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptorsP Rodien, F Cetani, S Costagliola, et al.
Trends in Endocrinology and Metabolism: TEM|April 15, 2008
TSH Receptor Mutations and Thyroid DiseaseL Duprez, J Parma, J Van Sande, et al.
Prenatal Diagnosis|July 21, 2005
Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?M Staebler, C Donner, N Van Regemorter, et al.
FEBS Letters|June 16, 1997
Constitutive activation of the TSH receptor by spontaneous mutations affecting the N-terminal extracellular domainL Duprez, J Parma, S Costagliola, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|June 15, 1997
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid glandM J Abramowicz, L Duprez, J Parma, et al.
Thyroid : Official Journal of the American Thyroid Association|November 22, 2001
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor geneP Bretones, L Duprez, J Parma, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2000
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symportersJ Pohlenz, L Duprez, R E Weiss, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1997
Two autonomous nodules of a patient with multinodular goiter harbor different activating mutations of the thyrotropin receptor geneL Duprez, J Hermans, J Van Sande, et al.
Molecular and Cellular Endocrinology|April 1, 1994
Constitutively active receptors as a disease-causing mechanismJ Parma, L Duprez, J Van Sande, et al.
Annales D'Endocrinologie|January 1, 1996
Activating mutations of the TSH receptor gene cause thyroid diseasesG Vassart, J Van Sande, J Parma, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptorsP Rodien, F Cetani, S Costagliola, et al.
Trends in Endocrinology and Metabolism: TEM|April 15, 2008
TSH Receptor Mutations and Thyroid DiseaseL Duprez, J Parma, J Van Sande, et al.
Prenatal Diagnosis|July 21, 2005
Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?M Staebler, C Donner, N Van Regemorter, et al.
FEBS Letters|June 16, 1997
Constitutive activation of the TSH receptor by spontaneous mutations affecting the N-terminal extracellular domainL Duprez, J Parma, S Costagliola, et al.
Pageof 3