伴有嗅觉缺失的家族性低促性腺激素性性腺功能减退症 - Suppr

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超能文献

Familial hypogonadotropic hypogonadism with anosmia.

作者信息

Sparkes R S, Simpson R W, Paulsen C A

出版信息

Arch Intern Med. 1968 Jun;121(6):534-8.

PMID:5652405

Abstract

摘要

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Familial hypogonadotropic hypogonadism with anosmia.伴有嗅觉缺失的家族性低促性腺激素性性腺功能减退症

Arch Intern Med. 1968 Jun;121(6):534-8.

[Genetic considerations on Kallmann's syndrome (hypogonadotropic hypogenitalism with anosmia)].

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[Bilateral Duane syndrome associated with hypogonadotropic hypogonadism and anosmia (Kallmann syndrome)].[双侧杜安综合征合并低促性腺激素性性腺功能减退和嗅觉缺失（卡尔曼综合征）]

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Hypogandotropic hypogonadism with anosmia: the Kallmann syndrome.伴有嗅觉缺失的低促性腺激素性性腺功能减退症：卡尔曼综合征。

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[Hypogonadotropic hypogonadism with anosmia].[伴有嗅觉缺失的低促性腺激素性性腺功能减退症]

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[Familial hypogonadism with anosmia: Kallmann Syndrome].[伴有嗅觉缺失的家族性性腺功能减退：卡尔曼综合征]

Monatsschr Kinderheilkd. 1983 Apr;131(4):232-4.

Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadism.促性腺激素释放激素受体功能丧失突变：低促性腺激素性性腺功能减退的新病因。

J Pediatr Endocrinol Metab. 1999 Apr;12 Suppl 1:267-75.

引用本文的文献

Delayed puberty, eroticism, and sense of smell: A psychological study of hypogonadotropinism, osmatic and anosmatic (Kallmann's syndrome).青春期延迟、性欲和嗅觉：促性腺激素不足症、嗅觉和非嗅觉（卡尔曼综合征）的心理学研究。

Arch Sex Behav. 1971 Dec;1(4):329-44. doi: 10.1007/BF01638061.

Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.卡尔曼综合征的无脊椎动物模型：分子发病机制和新的疾病基因。

Curr Genomics. 2013 Mar;14(1):2-10. doi: 10.2174/138920213804999174.

Familial hypothalamic hypogonadotropic hypogonadism.家族性下丘脑性低促性腺激素性性腺功能减退症。

Can Med Assoc J. 1974 Mar 2;110(5):509-12.

Pituitary-testicular responsiveness in male hypogonadotropic hypogonadism.男性低促性腺激素性性腺功能减退症中的垂体-睾丸反应性

J Clin Invest. 1974 Feb;53(2):408-15. doi: 10.1172/JCI107574.

Familial spastic paraplegia with Kallmann's syndrome.伴有卡尔曼综合征的家族性痉挛性截瘫

J Neurol Neurosurg Psychiatry. 1983 Jul;46(7):671-4. doi: 10.1136/jnnp.46.7.671.

[Congenital anosmia].[先天性嗅觉缺失]

Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1970;196(2):384-6.

Studies of the pituitary-Leydig cell axis in young men with hypogonadotropic hypogonadism and hyposmia: comparison with normal men, prepuberal boys, and hypopituitary patients.低促性腺激素性性腺功能减退和嗅觉减退的年轻男性垂体-莱迪希细胞轴的研究：与正常男性、青春期前男孩和垂体功能减退患者的比较

J Clin Invest. 1969 Nov;48(11):2046-56. doi: 10.1172/JCI106170.

Pituitary and gonadal function in the infant son of a patient with hypogonadotropic hypogonadism.低促性腺激素性性腺功能减退患者幼子的垂体和性腺功能

J Endocrinol Invest. 1985 Feb;8(1):71-2. doi: 10.1007/BF03350646.

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.X染色体连锁型卡尔曼综合征：截短突变验证了候选基因。

Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):8190-4. doi: 10.1073/pnas.89.17.8190.

[Evaluating function and disorders of smell].[嗅觉功能与障碍评估]

Arch Otorhinolaryngol. 1975;210(1):67-164. doi: 10.1007/BF00453708.

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