睾丸女性化综合征中靶器官缺陷的进一步证据。 - Suppr

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超能文献

Further evidence of a target organ defect in the syndrome of testicular feminization.

作者信息

French F S, Van Wyk J J, Baggett B, Easterling W E, Talbert L M, Johnston F R, Forchielli E, Dey A C

出版信息

J Clin Endocrinol Metab. 1966 May;26(5):493-503. doi: 10.1210/jcem-26-5-493.

DOI:10.1210/jcem-26-5-493

PMID:5949337

Abstract

摘要

相似文献

Further evidence of a target organ defect in the syndrome of testicular feminization.睾丸女性化综合征中靶器官缺陷的进一步证据。

J Clin Endocrinol Metab. 1966 May;26(5):493-503. doi: 10.1210/jcem-26-5-493.

Absence of response to dihydrotestosterone in the syndrome of testicular feminization.睾丸女性化综合征中对双氢睾酮无反应

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Br Med J. 1968 Jan 27;1(5586):208-10. doi: 10.1136/bmj.1.5586.208.

In vivo studies on testosterone metabolism by skin of normal males and patients with the syndrome of testicular feminization.正常男性和睾丸女性化综合征患者皮肤对睾酮代谢的体内研究。

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An explanation for the target organ unresponsiveness to testosterone in the testicular feminization syndrome.睾丸女性化综合征中靶器官对睾酮无反应的一种解释。

J Clin Endocrinol Metab. 1969 Mar;29(3):422-5. doi: 10.1210/jcem-29-3-422.

Blood production rate of dihydrotestosterone in the syndrome of male pseudohermaphroditism with testicular feminization.睾丸女性化型男性假两性畸形中双氢睾酮的血生成率

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Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo.

J Clin Endocrinol Metab. 1971 May;32(5):604-10. doi: 10.1210/jcem-32-5-604.

Steroid hormone formation by testes of a male pseudohermaphrodite.

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Clinical and endocrinologic characterization of a patients with the syndrome of incomplete testicular feminization.一名不完全性睾丸女性化综合征患者的临床及内分泌特征

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Further in vivo studies in male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect (compared to a case of testicular feminization).对因睾丸17-酮类固醇还原酶缺陷导致男性假两性畸形伴男性乳腺增生的进一步体内研究（与睾丸女性化病例相比）。

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引用本文的文献

An uncommon large deletion in the androgen-receptor gene in a XY female with complete androgen insensitivity syndrome.一名患有完全性雄激素不敏感综合征的XY女性雄激素受体基因存在罕见的大片段缺失。

J Endocrinol Invest. 2006 May;29(5):457-61. doi: 10.1007/BF03344130.

Intersex problems in the neonate.新生儿的两性畸形问题。

Indian J Pediatr. 1982 Jul-Aug;49(399):555-75. doi: 10.1007/BF02834565.

High dose androgen therapy in male pseudohermaphroditism due to 5 alpha-reductase deficiency and disorders of the androgen receptor.高剂量雄激素疗法治疗因5α-还原酶缺乏和雄激素受体异常所致的男性假两性畸形。

J Clin Invest. 1984 Oct;74(4):1496-508. doi: 10.1172/JCI111563.

Testicular feminization: a study of two cases, one with a seminoma.睾丸女性化：两例病例研究，其中一例伴有精原细胞瘤。

Can Med Assoc J. 1968 Mar 2;98(9):438-45.

Studies on testosterone metabolism in subjects with testicular feminization syndrome.睾丸女性化综合征患者的睾酮代谢研究。

J Clin Invest. 1970 Jan;49(1):31-40. doi: 10.1172/JCI106219.

[Leydig cell function test. Assessment of plasma testosterone levels by competitive protein binding before and after HCG stimulation].[睾丸间质细胞功能测试。通过人绒毛膜促性腺激素刺激前后的竞争性蛋白结合法评估血浆睾酮水平]

Klin Wochenschr. 1971 Jan 15;49(2):91-100. doi: 10.1007/BF01497306.

Hormones and the immunological capacity. 3. The immunodeficiency disease of the hypopituitary Snell-Bagg dwarf mouse.激素与免疫能力。3. 垂体功能减退的斯内尔-巴格侏儒小鼠的免疫缺陷疾病。

Clin Exp Immunol. 1971 Aug;9(2):209-25.

["Transsexualism" in testicular feminization].睾丸女性化中的“易性癖”

Klin Wochenschr. 1972 Jul 15;50(14):696-701. doi: 10.1007/BF01495528.

[Hard-to-classify forms of intersexuality. 3. Biosynthesis of steroids in testis of a case of male pseudohermaphroditism].[难以分类的两性畸形形式。3. 一例男性假两性畸形患者睾丸中类固醇的生物合成]

Klin Wochenschr. 1970 Aug 15;48(16):996-1001. doi: 10.1007/BF01484404.

Familial occurrence of persistent Mullerian structures in otherwise normal males.在其他方面正常的男性中持续性苗勒管结构的家族性发生。

Br Med J. 1973 Mar 31;1(5856):771-3. doi: 10.1136/bmj.1.5856.771.

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