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Results:
1-8
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Results: 8
Authors:
Macchia, PE
Bagattini, M
Lupoli, G
Vitale, M
Vitale, G
Fenzi, G
Citation: Pe. Macchia et al., High dose intravenous corticosteroid therapy for Graves' ophthalmopathy, J ENDOC INV, 24(3), 2001, pp. 152-158
Authors:
Macchia, PE
Takeuchi, Y
Kawai, T
Cua, K
Gauthier, K
Chassande, O
Seo, H
Hayashi, Y
Samarut, J
Murata, Y
Weiss, RE
Refetoff, S
Citation: Pe. Macchia et al., Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha, P NAS US, 98(1), 2001, pp. 349-354
Authors:
Macchia, PE
Citation: Pe. Macchia, Recent advances in understanding the molecular basis of primary congenitalhypothyroidism, MOL MED TOD, 6(1), 2000, pp. 36-42
Authors:
Reutrakul, S
Sadow, PM
Pannain, S
Pohlenz, J
Carvalho, GA
Macchia, PE
Weiss, RE
Refetoff, S
Citation: S. Reutrakul et al., Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations inthyroid hormone receptor beta or alpha genes, J CLIN END, 85(10), 2000, pp. 3609-3617
Authors:
Macchia, PE
De Felice, M
Di Lauro, R
Citation: Pe. Macchia et al., Molecular genetics of congenital hypothyroidism, CUR OP GEN, 9(3), 1999, pp. 289-294
Authors:
Macchia, PE
Mattei, MG
Lapi, P
Fenzi, G
Di Lauro, R
Citation: Pe. Macchia et al., Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2), BIOCHIMIE, 81(5), 1999, pp. 433-440
Authors:
Tell, G
Pellizzari, L
Esposito, G
Pucillo, C
Macchia, PE
Di Lauro, R
Damante, G
Citation: G. Tell et al., Structural defects of a Pax8 mutant that give rise to congenital hypothyroidism, BIOCHEM J, 341, 1999, pp. 89-93
Authors:
Pohlenz, J
Weiss, RE
Macchia, PE
Pannain, S
Lau, IT
Ho, H
Refetoff, S
Citation: J. Pohlenz et al., Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene, J CLIN END, 84(11), 1999, pp. 3919-3928
Risultati:
1-8
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