囊性纤维化中的输精管。 - Suppr

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The vas deferens in cystic fibrosis.

作者信息

Valman H B, France N E

出版信息

Lancet. 1969 Sep 13;2(7620):566-7. doi: 10.1016/s0140-6736(69)90263-3.

DOI:10.1016/s0140-6736(69)90263-3

PMID:4185534

Abstract

摘要

相似文献

The vas deferens in cystic fibrosis.囊性纤维化中的输精管。

Lancet. 1969 Sep 13;2(7620):566-7. doi: 10.1016/s0140-6736(69)90263-3.

Abnormality of the epididymis and vas deferens in cystic fibrosis.囊性纤维化患者附睾和输精管的异常

Arch Pathol. 1969 Dec;88(6):569-80.

Male infertility as the only presenting sign of cystic fibrosis when homozygous for the mild mutation R117H.当纯合携带轻度突变R117H时，男性不育作为囊性纤维化的唯一表现症状。

J Med Genet. 1993 Sep;30(9):797. doi: 10.1136/jmg.30.9.797.

Genital abnormalities in male patients with cystic fibrosis.

J Urol. 1971 Oct;106(4):568-74. doi: 10.1016/s0022-5347(17)61343-0.

Significance of absent vas deferens at hernia repair in infants and children.婴幼儿疝修补术中输精管缺如的意义。

J Pediatr Surg. 1975 Oct;10(5):765-9. doi: 10.1016/0022-3468(75)90382-6.

Letter: Cystic fibrosis and absence of vas deferens.信函：囊性纤维化与输精管缺如

Urology. 1975 Jan;5(1):158. doi: 10.1016/0090-4295(75)90330-1.

Ductal epithelial cells cultured from human foetal epididymis and vas deferens: relevance to sterility in cystic fibrosis.从人胎儿附睾和输精管培养的导管上皮细胞：与囊性纤维化不育症的相关性。

J Cell Sci. 1989 Apr;92 ( Pt 4):687-90. doi: 10.1242/jcs.92.4.687.

[Is male infertility caused by congenital bilateral atrophy of the vas deferens a clinical form of mucoviscidosis?].先天性双侧输精管萎缩所致男性不育是胰腺囊性纤维化的一种临床类型吗？

Rev Med Interne. 1993;14(10):981. doi: 10.1016/s0248-8663(05)80099-2.

[Cystic fibrosis of the pancreas and lung].[胰腺和肺部的囊性纤维化]

Wien Med Wochenschr. 1985 Jun 30;135(12):307-9.

Congenital absence of vas deferens and cystic fibrosis.先天性输精管缺如与囊性纤维化。

Minerva Pediatr. 2003 Feb;55(1):43-7, 47-50.

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The Aging Patient with Cystic Fibrosis.患有囊性纤维化的老年患者

Drugs Aging. 2025 Apr 24. doi: 10.1007/s40266-025-01207-3.

Genetics of the congenital absence of the vas deferens.先天性输精管缺失的遗传学研究。

Hum Genet. 2021 Jan;140(1):59-76. doi: 10.1007/s00439-020-02122-w. Epub 2020 Feb 5.

Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.囊性纤维化跨膜调节基因的突变与体内跨上皮电位

Am J Respir Crit Care Med. 2006 Oct 1;174(7):787-94. doi: 10.1164/rccm.200509-1377OC. Epub 2006 Jul 13.

Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.先天性双侧输精管缺如与囊性纤维化。一种遗传共性。

World J Urol. 1993;11(2):82-8. doi: 10.1007/BF00182034.

Bronchial mucous glands in the newborn with cystic fibrosis.患有囊性纤维化的新生儿的支气管黏液腺。

Eur J Pediatr. 1982 Dec;139(4):240-3. doi: 10.1007/BF00442171.

Localization of cystic fibrosis transmembrane conductance regulator mRNA in human fetal lung tissue by in situ hybridization.通过原位杂交对人胎儿肺组织中囊性纤维化跨膜传导调节因子mRNA进行定位。

J Clin Invest. 1992 Aug;90(2):619-25. doi: 10.1172/JCI115901.

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