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Results: 1-13 |
Results: 13
TSH RECEPTOR MUTATIONS AND THYROID-DISEASE
Authors: DUPREZ L PARMA J VANSANDE J RODIEN P DUMONT JE VASSART G ABRAMOWICZ M
Citation: L. Duprez et al., TSH RECEPTOR MUTATIONS AND THYROID-DISEASE, Trends in endocrinology and metabolism, 9(4), 1998, pp. 133-140
FAMILIAL CONGENITAL HYPOTHYROIDISM DUE TO INACTIVATING MUTATION OF THE THYROTROPIN RECEPTOR CAUSING PROFOUND HYPOPLASIA OF THE THYROID-GLAND
Authors: ABRAMOWICZ MJ DUPREZ L PARMA J VASSART G HEINRICHS C
Citation: Mj. Abramowicz et al., FAMILIAL CONGENITAL HYPOTHYROIDISM DUE TO INACTIVATING MUTATION OF THE THYROTROPIN RECEPTOR CAUSING PROFOUND HYPOPLASIA OF THE THYROID-GLAND, The Journal of clinical investigation, 99(12), 1997, pp. 3018-3024
DIVERSITY AND PREVALENCE OF SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR AND G(S)ALPHA GENES AS A CAUSE OF TOXIC THYROID ADENOMAS
Authors: PARMA J DUPREZ L VANSANDE J HERMANS J ROCMANS P VANVLIET G COSTAGLIOLA S RODIEN P DUMONT JE VASSART G
Citation: J. Parma et al., DIVERSITY AND PREVALENCE OF SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR AND G(S)ALPHA GENES AS A CAUSE OF TOXIC THYROID ADENOMAS, The Journal of clinical endocrinology and metabolism, 82(8), 1997, pp. 2695-2701
2 AUTONOMOUS NODULES OF A PATIENT WITH MULTINODULAR GOITER HARBOR DIFFERENT ACTIVATING MUTATIONS OF THE THYROTROPIN RECEPTOR GENE
Authors: DUPREZ L HERMANS J VANSANDE J DUMONT JE VASSART G PARMA J
Citation: L. Duprez et al., 2 AUTONOMOUS NODULES OF A PATIENT WITH MULTINODULAR GOITER HARBOR DIFFERENT ACTIVATING MUTATIONS OF THE THYROTROPIN RECEPTOR GENE, The Journal of clinical endocrinology and metabolism, 82(1), 1997, pp. 306-308
CONSTITUTIVE ACTIVATION OF THE TSH RECEPTOR BY SPONTANEOUS MUTATIONS AFFECTING THE N-TERMINAL EXTRACELLULAR DOMAIN
Authors: DUPREZ L PARMA J COSTAGLIOLA S HERMANS J VANSANDE J DUMONT JE VASSART G
Citation: L. Duprez et al., CONSTITUTIVE ACTIVATION OF THE TSH RECEPTOR BY SPONTANEOUS MUTATIONS AFFECTING THE N-TERMINAL EXTRACELLULAR DOMAIN, FEBS letters, 409(3), 1997, pp. 469-474
TSH RECEPTOR AND DISEASE
Authors: TONACCHERA M VANSANDE J PARMA J DUPREZ L CETANI F COSTAGLIOLA S DUMONT JE VASSART G
Citation: M. Tonacchera et al., TSH RECEPTOR AND DISEASE, Clinical endocrinology, 44(6), 1996, pp. 621-633
ACTIVATING MUTATIONS OF THE TSH RECEPTOR GENE CAUSE THYROID-DISEASES
Authors: VASSART G VANSANDE J PARMA J TONACCHERA M DUPREZ L SWILLENS S DUMONT J
Citation: G. Vassart et al., ACTIVATING MUTATIONS OF THE TSH RECEPTOR GENE CAUSE THYROID-DISEASES, Annales d'Endocrinologie, 57(1), 1996, pp. 50-54
BRIEF REPORT - CONGENITAL HYPERTHYROIDISM CAUSED BY A MUTATION IN THETHYROTROPIN-RECEPTOR GENE
Authors: KOPP P VANSANDE J PARMA J DUPREZ L GERBER H JOSS E JAMESON JL DUMONT JE VASSART G
Citation: P. Kopp et al., BRIEF REPORT - CONGENITAL HYPERTHYROIDISM CAUSED BY A MUTATION IN THETHYROTROPIN-RECEPTOR GENE, The New England journal of medicine, 332(3), 1995, pp. 150-154
GERMLINE MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE NON-AUTOIMMUNE AUTOSOMAL-DOMINANT HYPERTHYROIDISM
Authors: DUPREZ L PARMA J VANSANDE J ALLGEIER A LECLERE J SCHVARTZ C DELISLE MJ DECOULX M ORGIAZZI J DUMONT J VASSART G
Citation: L. Duprez et al., GERMLINE MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE NON-AUTOIMMUNE AUTOSOMAL-DOMINANT HYPERTHYROIDISM, Nature genetics, 7(3), 1994, pp. 396-401
CONSTITUTIVELY ACTIVE RECEPTORS AS A DISEASE-CAUSING MECHANISM
Authors: PARMA J DUPREZ L VANSANDE J PASCHKE R TONACCHERA M DUMONT J VASSART G
Citation: J. Parma et al., CONSTITUTIVELY ACTIVE RECEPTORS AS A DISEASE-CAUSING MECHANISM, Molecular and cellular endocrinology, 100(1-2), 1994, pp. 159-162
ISODISOMY OF CHROMOSOME-6 IN A NEWBORN WITH METHYLMALONIC ACIDEMIA AND AGENESIS OF PANCREATIC BETA-CELLS CAUSING DIABETES-MELLITUS
Authors: ABRAMOWICZ MJ ANDRIEN M DUPONT E DORCHY H PARMA J DUPREZ L LEDLEY FD COURTENS W VAMOS E
Citation: Mj. Abramowicz et al., ISODISOMY OF CHROMOSOME-6 IN A NEWBORN WITH METHYLMALONIC ACIDEMIA AND AGENESIS OF PANCREATIC BETA-CELLS CAUSING DIABETES-MELLITUS, The Journal of clinical investigation, 94(1), 1994, pp. 418-421
SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE HYPERFUNCTIONING THYROID ADENOMAS
Authors: PARMA J DUPREZ L VANSANDE J COCHAUX P GERVY C MOCKEL J DUMONT J VASSART G
Citation: J. Parma et al., SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE HYPERFUNCTIONING THYROID ADENOMAS, Nature, 365(6447), 1993, pp. 649-651
THYROTROPIN RECEPTOR REGULATION OF GENE - EXPRESSION AND STRUCTURE-FUNCTION-RELATIONSHIPS
Authors: VASSART G PARMA J DUPREZ L MAENHAUT C LEDENT C VANSANDE J BRABANT G DUMONT J
Citation: G. Vassart et al., THYROTROPIN RECEPTOR REGULATION OF GENE - EXPRESSION AND STRUCTURE-FUNCTION-RELATIONSHIPS, Annales d'Endocrinologie, 54(6), 1993, pp. 367-368
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