AAAAAA

   
Results: 1-15 |
Results: 15
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
Mutation analysis of the Epac-Rap1 signaling pathway in cold thyroid follicular adenomas
Authors: Vanvooren, V Allgeier, A Nguyen, M Massart, C Parma, J Dumont, JE Van Sande, J
Citation: V. Vanvooren et al., Mutation analysis of the Epac-Rap1 signaling pathway in cold thyroid follicular adenomas, EUR J ENDOC, 144(6), 2001, pp. 605-610
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
Hb Ube-2 [alpha 68(E17)Asn -> Asp] and Hb Hafnia [beta 116(G18)His+Gln] observed during neonatal screening in Brussels
Authors: Cotton, F Hansen, V Lin, C Parma, J Cochaux, P Damis, E Vertongen, F Gulbis, B
Citation: F. Cotton et al., Hb Ube-2 [alpha 68(E17)Asn -> Asp] and Hb Hafnia [beta 116(G18)His+Gln] observed during neonatal screening in Brussels, HEMOGLOBIN, 24(1), 2000, pp. 65-69
Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies
Authors: Mircescu, H Parma, J Huot, C Deal, C Oligny, LL Vassart, G Van Vliet, G
Citation: H. Mircescu et al., Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies, J PEDIAT, 137(4), 2000, pp. 585-587
A quantitative study of peripheral blood stem cell contamination in diffuse large-cell non-Hodgkin's lymphoma: one-half of patients significantly mobilize malignant cells
Authors: Jacquy, C Soree, A Lambert, F Bosly, A Ferrant, A Andre, M Parma, J Kentos, A Martiat, P
Citation: C. Jacquy et al., A quantitative study of peripheral blood stem cell contamination in diffuse large-cell non-Hodgkin's lymphoma: one-half of patients significantly mobilize malignant cells, BR J HAEM, 110(3), 2000, pp. 631-637
Gene rearrangement and Chernobyl related thyroid cancers
Authors: Santoro, M Thomas, GA Vecchio, G Williams, GH Fusco, A Chiappetta, G Pozcharskaya, V Bogdanova, TI Demidchik, EP Cherstvoy, ED Voscoboinik, L Tronko, ND Carss, A Bunnell, H Tonnachera, M Parma, J Dumont, JE Keller, G Hofler, H Williams, ED
Citation: M. Santoro et al., Gene rearrangement and Chernobyl related thyroid cancers, BR J CANC, 82(2), 2000, pp. 315-322
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor
Authors: Tiosano, D Pannain, S Vassart, G Parma, J Gershoni-Baruch, R Mandel, H Lotan, R Zaharan, Y Pery, M Weiss, RE Refetoff, S Hochberg, Z
Citation: D. Tiosano et al., The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor, THYROID, 9(9), 1999, pp. 887-894
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
Long-term follow-up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr)
Authors: Lavard, L Sehested, A Jacobsen, BB Muller, J Perrild, H Feldt-Rasmussen, U Parma, J Vassart, G
Citation: L. Lavard et al., Long-term follow-up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr), HORMONE RES, 51(1), 1999, pp. 43-46
Peripheral blood stem cell contamination in mantle cell non-Hodgkin lymphoma: the case for purging?
Authors: Jacquy, C Lambert, F Soree, A Van Daele, S Heusterspreute, M Bosly, A Ferrant, A Parma, J Bron, D Martiat, P
Citation: C. Jacquy et al., Peripheral blood stem cell contamination in mantle cell non-Hodgkin lymphoma: the case for purging?, BONE MAR TR, 23(7), 1999, pp. 681-686
A germline mutation of the thyrotropin receptor gene associated with thyrotoxicosis and mitral valve prolapse in a Chinese family
Authors: Khoo, DHC Parma, J Rajasoorya, C Ho, SC Vassart, G
Citation: Dhc. Khoo et al., A germline mutation of the thyrotropin receptor gene associated with thyrotoxicosis and mitral valve prolapse in a Chinese family, J CLIN END, 84(4), 1999, pp. 1459-1462
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
Risultati: 1-15 |