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Results: 1-9 |
Results: 9
Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome
Authors: Faivre, L Nivelon-Chevallier, A Kottler, ML Robinet, C Van Kien, PK Lorcerie, B Munnich, A Maroteaux, P Cormier-Daire, V LeMerrer, M
Citation: L. Faivre et al., Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome, AM J MED G, 99(2), 2001, pp. 132-136
Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients
Authors: Niccoli-Sire, P Murat, A Rohmer, V Franc, S Chabrier, G Baldet, L Maes, B Savagner, F Giraud, S Bezieau, S Kottler, ML Morange, S Conte-Devolx, B
Citation: P. Niccoli-sire et al., Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients, J CLIN END, 86(8), 2001, pp. 3746-3753
Activating mutations of the calcium-sensing receptor: Management of hypocalcemia
Authors: Lienhardt, A Bai, M Lagarde, JP Rigaud, M Zhang, ZX Jiang, YF Kottler, ML Brown, EM Garabedian, M
Citation: A. Lienhardt et al., Activating mutations of the calcium-sensing receptor: Management of hypocalcemia, J CLIN END, 86(11), 2001, pp. 5313-5323
A new compound heterozygous mutation of the gonadotropin-releasing hormonereceptor (L314X, Q106R) in a woman with complete hypogonadotropic hypogonadism: Chronic estrogen administration amplifies the gonadotropin defect
Authors: Kottler, ML Chauvin, S Lahlou, N Harris, CE Johnston, CJ Lagarde, JP Bouchard, P Farid, NR Counis, R
Citation: Ml. Kottler et al., A new compound heterozygous mutation of the gonadotropin-releasing hormonereceptor (L314X, Q106R) in a woman with complete hypogonadotropic hypogonadism: Chronic estrogen administration amplifies the gonadotropin defect, J CLIN END, 85(9), 2000, pp. 3002-3008
A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia
Authors: Lienhardt, A Garabedian, M Bai, M Sinding, C Zhang, ZX Lagarde, JP Boulesteix, J Rigaud, M Brown, EM Kottler, ML
Citation: A. Lienhardt et al., A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia, J CLIN END, 85(4), 2000, pp. 1695-1702
Tissue-specific pattern of variant transcripts of the human gonadotropin-releasing hormone receptor gene
Authors: Kottler, ML Bergametti, F Carre, MC Morice, S Decoret, E Lagarde, JP Starzec, A Counis, R
Citation: Ml. Kottler et al., Tissue-specific pattern of variant transcripts of the human gonadotropin-releasing hormone receptor gene, EUR J ENDOC, 140(6), 1999, pp. 561-569
Mutations of the GnRH receptor gene: A new cause of autosomal-recessive hypogonadotropic hypogonadism
Authors: Kottler, ML Counis, R Bouchard, P
Citation: Ml. Kottler et al., Mutations of the GnRH receptor gene: A new cause of autosomal-recessive hypogonadotropic hypogonadism, ARCH MED R, 30(6), 1999, pp. 481-485
LH down-regulates gonadotropin-releasing hormone (GnRH) receptor, but not GnRH, mRNA levels in the rat testis
Authors: Botte, MC Lerrant, Y Lozach, A Berault, A Counis, R Kottler, ML
Citation: Mc. Botte et al., LH down-regulates gonadotropin-releasing hormone (GnRH) receptor, but not GnRH, mRNA levels in the rat testis, J ENDOCR, 162(3), 1999, pp. 409-415
Resistance of hypogonadic patients with mutated GnRH receptor genes to pulsatile GnRH administration
Authors: Caron, P Chauvin, S Christin-Maitre, S Bennet, A Lahlou, N Counis, R Bouchard, P Kottler, ML
Citation: P. Caron et al., Resistance of hypogonadic patients with mutated GnRH receptor genes to pulsatile GnRH administration, J CLIN END, 84(3), 1999, pp. 990-996
Risultati: 1-9 |