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Results: 1-8 |
Results: 8

Authors: Antonini, SRR Elias, LLK Moreira, AC
Citation: Srr. Antonini et al., Hesxl gene in midline cerebral defects, J PEDIAT, 139(5), 2001, pp. 754-754

Authors: Clark, AJL Metherell, L Swords, FM Elias, LLK
Citation: Ajl. Clark et al., The molecular pathogenesis of ACTH insensitivity syndromes, ANN ENDOCR, 62(3), 2001, pp. 207-211

Authors: Elias, LLK Huebner, A Metherell, LA Canas, A Warne, GL Bitti, MLM Cianfarani, S Clayton, PE Savage, MO Clark, AJL
Citation: Llk. Elias et al., Tall stature in familial glucocorticoid deficiency, CLIN ENDOCR, 53(4), 2000, pp. 423-430

Authors: Marui, S Castro, M Latronico, AC Elias, LLK Arnhold, IJP Moreira, AC Mendonca, BB
Citation: S. Marui et al., Mutations in the type II 3 beta-hydroxysteroid dehydrogenase (HSD3B2) genecan cause premature pubarche in girls, CLIN ENDOCR, 52(1), 2000, pp. 67-75

Authors: Elias, LLK Clark, AJL
Citation: Llk. Elias et Ajl. Clark, The expression of the ACTH receptor, BRAZ J MED, 33(10), 2000, pp. 1245-1248

Authors: Swords, F Franklin, JL Huebner, A Elias, LLK Clark, AJL
Citation: F. Swords et al., Defects of adrenocorticotropin action on the adrenal, ENDOCR DEV, 2, 2000, pp. 24-36

Authors: Huebner, A Elias, LLK Clark, AJL
Citation: A. Huebner et al., ACTH resistance syndromes, J PED END M, 12, 1999, pp. 277-293

Authors: Elias, LLK Huebner, A Pullinger, GD Mirtella, A Clark, AJL
Citation: Llk. Elias et al., Functional characterization of naturally occurring mutations of the human adrenocorticotropin receptor: poor correlation of phenotype and gennotype, J CLIN END, 84(8), 1999, pp. 2766-2770
Risultati: 1-8 |