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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
APPARENT CONGENITAL ATHYREOSIS CONTRASTING WITH NORMAL PLASMA THYROGLOBULIN LEVELS AND ASSOCIATED WITH INACTIVATING MUTATIONS IN THE THYROTROPIN RECEPTOR GENE - ARE ATHYREOSIS AND ECTOPIC THYROID DISTINCT ENTITIES
Authors: GAGNE N PARMA J DEAL C VASSART G VANVLIET G
Citation: N. Gagne et al., APPARENT CONGENITAL ATHYREOSIS CONTRASTING WITH NORMAL PLASMA THYROGLOBULIN LEVELS AND ASSOCIATED WITH INACTIVATING MUTATIONS IN THE THYROTROPIN RECEPTOR GENE - ARE ATHYREOSIS AND ECTOPIC THYROID DISTINCT ENTITIES, The Journal of clinical endocrinology and metabolism, 83(5), 1998, pp. 1771-1775
RELATIVE CONTRIBUTION OF KI-RAS GENE ANALYSIS AND BRUSH CYTOLOGY DURING ERCP FOR THE DIAGNOSIS OF BILIARY AND PANCREATIC DISEASES
Authors: VANLAETHEM JL BOURGEOIS V PARMA J DELHAYE M COCHAUX P VELU T DEVIERE J CREMER M
Citation: Jl. Vanlaethem et al., RELATIVE CONTRIBUTION OF KI-RAS GENE ANALYSIS AND BRUSH CYTOLOGY DURING ERCP FOR THE DIAGNOSIS OF BILIARY AND PANCREATIC DISEASES, Gastrointestinal endoscopy, 47(6), 1998, pp. 479-485
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
RESISTANCE TO THYROTROPIN (TSH) IN 3 FAMILIES IS NOT ASSOCIATED WITH MUTATIONS IN THE TSH RECEPTOR OR TSH
Authors: XIE J PANNAIN S POHLENZ J WEISS RE MOLTZ K MORLOT M ASTERIA C PERSANI L BECKPECCOZ P PARMA J VASSART G REFETOFF S
Citation: J. Xie et al., RESISTANCE TO THYROTROPIN (TSH) IN 3 FAMILIES IS NOT ASSOCIATED WITH MUTATIONS IN THE TSH RECEPTOR OR TSH, The Journal of clinical endocrinology and metabolism, 82(12), 1997, pp. 3933-3940
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
DOES KI-RAS ANALYSIS DURING ERCP EFFECTIVELY IMPROVE THE DIAGNOSIS OFBILIARY AND PANCREATIC DISEASES
Authors: BOURGEOIS V VANLAETHEM JL PARMA J DELHAYE M COCHAUX P VELU T DEVIERE J CREMER M
Citation: V. Bourgeois et al., DOES KI-RAS ANALYSIS DURING ERCP EFFECTIVELY IMPROVE THE DIAGNOSIS OFBILIARY AND PANCREATIC DISEASES, Gastrointestinal endoscopy, 45(4), 1997, pp. 395-395
KI-RAS MUTATIONS IN PATIENTS WITH CHRONIC-PANCREATITIS - HIGH PREVALENCE BUT UNDETERMINED RELEVANCE
Authors: VANLAETHEM JL BOURGEOIS V DELHAYE M PARMA J COCHAUX P VELU T DEVIERE J CREMER M
Citation: Jl. Vanlaethem et al., KI-RAS MUTATIONS IN PATIENTS WITH CHRONIC-PANCREATITIS - HIGH PREVALENCE BUT UNDETERMINED RELEVANCE, Gastroenterology, 112(4), 1997, pp. 490-490
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
THE TSH RECEPTOR AND THYROID-DISEASES
Authors: PASCHKE R VANSANDE J PARMA J VASSART G
Citation: R. Paschke et al., THE TSH RECEPTOR AND THYROID-DISEASES, Bailliere's clinical endocrinology and metabolism, 10(1), 1996, pp. 9-27
ONCOGENIC MUTATIONS IN THYROID ADENOMA - METHODOLOGICAL CRITERIA
Authors: TONACCHERA R CETANI F PARMA J VANSANDE J VASSART G DUMONT J
Citation: R. Tonacchera et al., ONCOGENIC MUTATIONS IN THYROID ADENOMA - METHODOLOGICAL CRITERIA, European journal of endocrinology, 135(4), 1996, pp. 444-446
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
SLIGHT INSTABILITY OF A FMR-1 ALLELE OVER 3 GENERATIONS IN A FAMILY FROM THE GENERAL-POPULATION
Authors: ABRAMOWICZ MJ PARMA J COCHAUX P
Citation: Mj. Abramowicz et al., SLIGHT INSTABILITY OF A FMR-1 ALLELE OVER 3 GENERATIONS IN A FAMILY FROM THE GENERAL-POPULATION, American journal of medical genetics, 64(2), 1996, pp. 268-269
CLINICAL-MOLECULAR CORRELATES IN A MOTHER AND 2 SONS WITH A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE (LH) RECEPTOR (LHR)
Authors: ROSENFIELD RL ROSENTHAL IM REFETOFF S RICH BH BARNES RB SUNTHORNTHEPVARAKUL T PARMA J
Citation: Rl. Rosenfield et al., CLINICAL-MOLECULAR CORRELATES IN A MOTHER AND 2 SONS WITH A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE (LH) RECEPTOR (LHR), Pediatric research, 39(4), 1996, pp. 569-569
FUNCTIONAL-CHARACTERISTICS OF 3 NEW GERMLINE MUTATIONS OF THE THYROTROPIN RECEPTOR GENE CAUSING AUTOSOMAL-DOMINANT TOXIC THYROID HYPERPLASIA
Authors: TONACCHERA M VANSANDE J CETANI F SWILLENS S SCHVARTZ C WINISZEWSKI P PORTMANN L DUMONT JE VASSART G PARMA J
Citation: M. Tonacchera et al., FUNCTIONAL-CHARACTERISTICS OF 3 NEW GERMLINE MUTATIONS OF THE THYROTROPIN RECEPTOR GENE CAUSING AUTOSOMAL-DOMINANT TOXIC THYROID HYPERPLASIA, The Journal of clinical endocrinology and metabolism, 81(2), 1996, pp. 547-554
RESPONSE TO CHALLENGE WITH GONADOTROPIN-RELEASING-HORMONE AGONIST IN A MOTHER AND HER 2 SONS WITH A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR - A CLINICAL RESEARCH-CENTER STUDY
Authors: ROSENTHAL IM REFETOFF S RICH B BARNES RB SUNTHORNTHEPVARAKUL T PARMA J ROSENFIELD RL
Citation: Im. Rosenthal et al., RESPONSE TO CHALLENGE WITH GONADOTROPIN-RELEASING-HORMONE AGONIST IN A MOTHER AND HER 2 SONS WITH A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR - A CLINICAL RESEARCH-CENTER STUDY, The Journal of clinical endocrinology and metabolism, 81(10), 1996, pp. 3802-3806
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
SOMATIC MUTATIONS CAUSING CONSTITUTIVE ACTIVITY OF THE THYROTROPIN RECEPTOR ARE THE MAJOR CAUSE OF HYPERFUNCTIONING THYROID ADENOMAS - IDENTIFICATION OF ADDITIONAL MUTATIONS ACTIVATING BOTH THE CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE AND INOSITOL PHOSPHATE-CA2+ CASCADES
Authors: PARMA J VANSANDE J SWILLENS S TONACCHERA M DUMONT J VASSART G
Citation: J. Parma et al., SOMATIC MUTATIONS CAUSING CONSTITUTIVE ACTIVITY OF THE THYROTROPIN RECEPTOR ARE THE MAJOR CAUSE OF HYPERFUNCTIONING THYROID ADENOMAS - IDENTIFICATION OF ADDITIONAL MUTATIONS ACTIVATING BOTH THE CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE AND INOSITOL PHOSPHATE-CA2+ CASCADES, Molecular endocrinology, 9(6), 1995, pp. 725-733
MOLECULAR-GENETICS OF THYROID-DISORDERS
Authors: LEDENT C PARMA J VANSANDE J VASSART G
Citation: C. Ledent et al., MOLECULAR-GENETICS OF THYROID-DISORDERS, MS. Medecine sciences, 11(2), 1995, pp. 215-221
POSITIVE CONTROL OF PROLIFERATION BY THE CYCLIC-AMP CASCADE - AN ONCOGENIC MECHANISM OF HYPER-FUNCTIONAL ADENOMA
Authors: LEDENT C PARMA J PIRSON I TATON M ROGER P MAENHAUT C VANSAUDE J POHL V LAMY F PARMENTIER M VASSART G DUMONT JE
Citation: C. Ledent et al., POSITIVE CONTROL OF PROLIFERATION BY THE CYCLIC-AMP CASCADE - AN ONCOGENIC MECHANISM OF HYPER-FUNCTIONAL ADENOMA, Journal of endocrinological investigation, 18(2), 1995, pp. 120-122
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
SOMATIC AND GERMLINE MUTATIONS OF THE TSH RECEPTOR GENE IN THYROID-DISEASES
Authors: VANSANDE J PARMA J TONACCHERA M SWILLENS S DUMONT J VASSART G
Citation: J. Vansande et al., SOMATIC AND GERMLINE MUTATIONS OF THE TSH RECEPTOR GENE IN THYROID-DISEASES, The Journal of clinical endocrinology and metabolism, 80(9), 1995, pp. 2577-2585
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
MOLECULAR-GENETICS OF THYROID-DISEASES
Authors: LEDENT C PARMA J DUMONT J VASSART G TARGOVNIK H
Citation: C. Ledent et al., MOLECULAR-GENETICS OF THYROID-DISEASES, European journal of endocrinology, 130(1), 1994, pp. 8-14
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