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Общее количество найденных документов : 5
Показаны документы с 1 по 5
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1.
| Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne // Clin. Endocrinol., 1998. Vol. 48, N 2.-С.209-215
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2.
| Prenatal dexamethasone treatment does not prevent alterations of the hypothalamic pituitary adrenal axis in steroid 21-hydroxylase deficient mice // Endocrinology, 1999. Vol. 140, N 7.-С.3354-3362
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3.
| Prenatal dexamethasone treatment does not prevent alterations of the hypothalamic pituitary adrenal axis in steroid 21-hydroxylase deficient mice // Endocrinology, 1999. Vol. 140, N 7.-С.3354-3362
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4.
| Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency // Clin. Endocrinol., 2004. Vol. 61, N 1.-С.94-101
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5.
| CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency // J. Clin. Endocrinol. and Metab., 2003. Vol. 88, N 12.-С.5680-5688
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