SINGLE SUBCUTANEOUS DOSES OF A LUTEINIZING-HORMONE-RELEASING HORMONE ANTAGONIST SUPPRESS SERUM GONADOTROPIN AND TESTOSTERONE LEVELS IN NORMAL MEN

被引：42

作者：

PAVLOU, SN ^{[1
]}

DEBOLD, CR ^{[1
]}

ISLAND, DP ^{[1
]}

WAKEFIELD, G ^{[1
]}

RIVIER, J ^{[1
]}

VALE, W ^{[1
]}

RABIN, D ^{[1
]}

机构：

[1] SALK INST BIOL STUDIES, LA JOLLA, CA 92037 USA

来源：

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 1986年 / 63卷 / 02期

关键词：

D O I：

10.1210/jcem-63-2-303

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：303 / 308

页数：6

共 29 条

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[5] THE CHANGING RATIO OF BIOACTIVE TO IMMUNOREACTIVE LUTEINIZING-HORMONE (LH) THROUGH PUBERTY PRINCIPALLY REFLECTS CHANGING LH RADIOIMMUNOASSAY DOSE-RESPONSE CHARACTERISTICS [J].

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[6] THE DYNAMICS OF GONADOTROPIN INHIBITION IN WOMEN INDUCED BY AN ANTAGONISTIC ANALOG OF GONADOTROPIN-RELEASING HORMONE [J].

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[7] HYPOTHALAMIC REGULATION OF PITUITARY GONADOTROPIN-RELEASING HORMONE RECEPTORS - EFFECTS OF HYPOTHALAMIC-LESIONS AND A GONADOTROPIN-RELEASING HORMONE ANTAGONIST [J].

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