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Hyperthecosis: an inheritable form of polycystic ovarian disease.

作者信息

Wilroy R S, Givens J R, Wiser W L, Coleman S A, Andersen R N, Summitt R L

出版信息

Birth Defects Orig Artic Ser. 1975;11(4):81-5.

PMID:1156689
Abstract
摘要

相似文献

1
Hyperthecosis: an inheritable form of polycystic ovarian disease.卵泡膜细胞增殖症:一种多囊卵巢疾病的遗传形式。
Birth Defects Orig Artic Ser. 1975;11(4):81-5.
2
Familial hyperthecosis: comparison of endocrinologic and histologic findings with polycystic ovarian disease.
Am J Obstet Gynecol. 1973 Dec 1;117(7):976-82. doi: 10.1016/0002-9378(73)90071-9.
3
[Relations between polycystic ovary and idiopathic hirsutism].[多囊卵巢与特发性多毛症之间的关系]
G Clin Med. 1988 Mar;69(3):183-5.
4
Dynamics of suppression and recovery of plasma FSH, LH, androstenedione and testosterone in polycystic ovarian disease using an oral contraceptive.
J Clin Endocrinol Metab. 1974 May;38(5):727-35. doi: 10.1210/jcem-38-5-727.
5
Primary polycystic ovary syndrome in a premenarchal girl. A case report.
J Reprod Med. 1985 Apr;30(4):361-5.
6
[Interrelationship of abnormal family history in the first degree relatives and clinical phenotype of patients with polycystic ovary syndrome].[多囊卵巢综合征患者一级亲属异常家族史与临床表型的相互关系]
Zhonghua Fu Chan Ke Za Zhi. 2007 Nov;42(11):756-60.
7
The androgenic profile of women with non-insulin-dependent diabetes mellitus.非胰岛素依赖型糖尿病女性的雄激素水平
J Reprod Med. 2004 Sep;49(9):746-52.
8
Effect of spironolactone on testosterone and LHRH responsiveness in women with polycystic ovarian disease.螺内酯对多囊卵巢疾病女性睾酮及促黄体生成素释放激素反应性的影响。
Isr J Med Sci. 1984 Jul;20(7):630-3.
9
Shorter CAG repeats in the androgen receptor gene may enhance hyperandrogenicity in polycystic ovary syndrome.雄激素受体基因中较短的CAG重复序列可能会增强多囊卵巢综合征中的高雄激素血症。
Gynecol Endocrinol. 2008 Dec;24(12):669-73. doi: 10.1080/09513590802342841.
10
Serum anti-Müllerian hormone levels remain high until late reproductive age and decrease during metformin therapy in women with polycystic ovary syndrome.血清抗苗勒管激素水平在育龄后期之前一直保持较高水平,而在多囊卵巢综合征女性接受二甲双胍治疗期间会下降。
Hum Reprod. 2005 Jul;20(7):1820-6. doi: 10.1093/humrep/deh850. Epub 2005 Mar 31.

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Whole Exome Sequencing Reveals Rare Variants in Genes Associated with Metabolic Disorders in Women with PCOS.全外显子组测序揭示了多囊卵巢综合征女性中与代谢紊乱相关基因的罕见变异。
J Hum Reprod Sci. 2023 Oct-Dec;16(4):307-316. doi: 10.4103/jhrs.jhrs_13_23. Epub 2023 Dec 29.
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An Investigation of Steroid Biosynthesis Pathway Genes in Women with Polycystic Ovary Syndrome.多囊卵巢综合征女性甾体生物合成途径基因的研究
J Hum Reprod Sci. 2022 Jul-Sep;15(3):240-249. doi: 10.4103/jhrs.jhrs_86_22. Epub 2022 Sep 30.
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Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.
通过全外显子组测序进一步描绘家族性多囊卵巢综合征(PCOS):鉴定出与PCOS相关的罕见FBN3和FN1基因变异。
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Polycystic ovary syndrome: definition, aetiology, diagnosis and treatment.多囊卵巢综合征:定义、病因、诊断与治疗。
Nat Rev Endocrinol. 2018 May;14(5):270-284. doi: 10.1038/nrendo.2018.24. Epub 2018 Mar 23.
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Fetal programming of polycystic ovary syndrome.多囊卵巢综合征的胎儿编程。
World J Diabetes. 2015 Jul 10;6(7):936-42. doi: 10.4239/wjd.v6.i7.936.
6
Prevalence of metabolic syndrome in the family members of women with polycystic ovary syndrome from North India.印度北部多囊卵巢综合征女性家庭成员中代谢综合征的患病率。
Indian J Endocrinol Metab. 2014 May;18(3):364-9. doi: 10.4103/2230-8210.131186.
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Polycystic ovary syndrome: etiology, pathogenesis and diagnosis.多囊卵巢综合征:病因、发病机制与诊断。
Nat Rev Endocrinol. 2011 Apr;7(4):219-31. doi: 10.1038/nrendo.2010.217. Epub 2011 Jan 25.
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Genetics of polycystic ovary syndrome.多囊卵巢综合征的遗传学
Hippokratia. 2009 Oct;13(4):216-23.
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The Genetic Basis of the Polycystic Ovary Syndrome: A Literature Review Including Discussion of PPAR-gamma.多囊卵巢综合征的遗传学基础:文献综述,包括对 PPAR-γ的讨论。
PPAR Res. 2007;2007:49109. doi: 10.1155/2007/49109.
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The role of genes and environment in the etiology of PCOS.基因与环境在多囊卵巢综合征病因学中的作用。
Endocrine. 2006 Aug;30(1):19-26. doi: 10.1385/ENDO:30:1:19.