Works matching IS 00778923 AND DT 1985 AND VI 458 AND IP 1
Results: 30
The Association Between Congenital Adrenal Hyperplasia and HLA in Southern Italy.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 46, doi. 10.1111/j.1749-6632.1985.tb14589.x
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Biochemical Properties of Cytochrome P-450 in Relation to Steroid Oxygenation<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 216, doi. 10.1111/j.1749-6632.1985.tb14606.x
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Structure Organization and Expression of the Major Histocompatibility Class III Genes.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 269, doi. 10.1111/j.1749-6632.1985.tb14612.x
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Deoxycorticosterone Biosynthesis in Kidney Tissue of Experimental Animals: Characterization of Steroid 21-Hydroxylase Activity in Guinea Pig Kidney<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 232, doi. 10.1111/j.1749-6632.1985.tb14608.x
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Different Gene Defects in the Salt-Wasting (SW), Simple Virilizing (SV), and Nonclassical (NC) Types of Congenital Adrenal Hyperplasia (CAH).
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 71, doi. 10.1111/j.1749-6632.1985.tb14592.x
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Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 111, doi. 10.1111/j.1749-6632.1985.tb14597.x
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Evidence that Variation among Untreated Rabbits in Hepatic Progesterone 21-Hydroxylase Activity Is Indicative of Enzyme Heterogeneity Rather than a Transient Inductive Effect<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 225, doi. 10.1111/j.1749-6632.1985.tb14607.x
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Cytochrome P-450: Physiology of Steroidogenesis<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 203, doi. 10.1111/j.1749-6632.1985.tb14605.x
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Modern Medical Therapy of Congenital Adrenal Hyperplasia A Decade of Experience<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 165, doi. 10.1111/j.1749-6632.1985.tb14601.x
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Introduction.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. ix, doi. 10.1111/j.1749-6632.1985.tb14584.x
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Clinical and Endocrinological Aspects of 21-Hydroxylase Deficiency<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 1, doi. 10.1111/j.1749-6632.1985.tb14585.x
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Regulation of Cytochrome P-450<sub>17</sub>α Activity and Synthesis in Bovine Adrenocortical Cells<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 252, doi. 10.1111/j.1749-6632.1985.tb14610.x
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Extended MHC Haplotypes in Salt-Losing 21-Hydroxylase Deficiency<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 28, doi. 10.1111/j.1749-6632.1985.tb14586.x
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The Use of Gamma Interferon to Increase HLA Antigen Expression on Cultured Amniotic Cells Used for the Prenatal Diagnosis of 21-Hydroxylase Deficiency<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 148, doi. 10.1111/j.1749-6632.1985.tb14599.x
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HLA Associations in 21-Hydroxylase Deficiency (Congenital and Late-Onset Adrenal Hyperplasia) in France.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 41, doi. 10.1111/j.1749-6632.1985.tb14588.x
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HLA Associations in Late-Onset 21-Hydroxylase Deficiency in Israel.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 52, doi. 10.1111/j.1749-6632.1985.tb14590.x
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Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 85, doi. 10.1111/j.1749-6632.1985.tb14594.x
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Neonatal Screening for Congenital Adrenal Hyperplasia in Japan.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 103, doi. 10.1111/j.1749-6632.1985.tb14596.x
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Effect of Hydrocortisone Dose Schedule on Adrenal Steroid Secretion in Congenital Adrenal Hyperplasia.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 182, doi. 10.1111/j.1749-6632.1985.tb14603.x
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Monitoring Treatment in Congenital Adrenal Hyperplasia Use of Serial Measurements of 17-OH-Progesterone in Plasma, Capillary Blood, and Saliva<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 193, doi. 10.1111/j.1749-6632.1985.tb14604.x
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An Approach to the Molecular Biology of Congenital Adrenal Hyperplasia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 238, doi. 10.1111/j.1749-6632.1985.tb14609.x
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Newborn Screening for Congenital Adrenal Hyperplasia with Special Reference to Screening in Alaska<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 90, doi. 10.1111/j.1749-6632.1985.tb14595.x
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Prenatal Therapy in Congenital Adrenal Hyperplasia Attempted Prevention of Abnormal External Genital Masculinization by Pharmacologic Suppression of the Fetal Adrenal Gland in Utero.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 156, doi. 10.1111/j.1749-6632.1985.tb14600.x
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The Human Major Histocompatibility Complex Genes and Proteins<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 262, doi. 10.1111/j.1749-6632.1985.tb14611.x
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Molecular Cloning of Steroid 21-Hydroxylase<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 277, doi. 10.1111/j.1749-6632.1985.tb14613.x
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The HLA Associations in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in a Yugoslav Population.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 36, doi. 10.1111/j.1749-6632.1985.tb14587.x
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Pitfalls in Prenatal Diagnosis of 21-Hydroxylase Deficiency by Amniotic Fluid Steroid Analysis? A Six Years Experience in 102 Pregnancies at Risk<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 130, doi. 10.1111/j.1749-6632.1985.tb14598.x
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HLA-B14 and Nonclassical 21-Hydroxylase Deficiency in a Heterogeneous New York Population<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 65, doi. 10.1111/j.1749-6632.1985.tb14591.x
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The Coexistence of IgA Deficiency and 21-Hydroxylase Deficiency Marked by Specific MHC Supratypes.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 76, doi. 10.1111/j.1749-6632.1985.tb14593.x
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LHRH Analog Treatment of Central Precocious Puberty Complicating Congenital Adrenal Hyperplasia.
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- Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 174, doi. 10.1111/j.1749-6632.1985.tb14602.x
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