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Results:
1-8
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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
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