FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2089525801> ?p ?o ?g. }

• W2089525801 endingPage "817" @default.
• W2089525801 startingPage "797" @default.
• W2089525801 abstract "Absence, dysfunction or low levels of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) protein result in a broad range of clinical manifestations with CF with pancreatic insufficiency at the severe end of the phenotypic spectrum and, at the other end relatively mild clinical conditions, including several forms of male infertility. The condition of congenital bilateral absence of the vas deferens (CBAVD) is in 75-80% of the patients associated with defects in the CFTR gene. In the remaining patients, CBAVD is also associated with urinary tract malformations, and this form of CBAVD is not related to CF. Congenital unilateral absence of the vas deferens also seems to be associated with CF except when associated with renal abnormalities at the ipsilateral side of the absent vas. A possible role of the CFTR protein in the aetiology of infertility due to defects in sperm production and maturation has also been suggested recently. In contrast, Young's syndrome is probably not related to CF. The relation between some conditions of male infertility and CF implies appropriate clinical examination of the patients, CFTR mutation analysis and genetic counselling. Because infertility can now in many cases be treated by artificial reproductive technology couples have an increased risk of having children with CF or infertility if the female partner is also a carrier of a CFTR mutation. Couples should be well informed about these risks and risk prevention including pre-implantation diagnosis. Follow-up studies of children born to these couples are mandatory, whether male infertility is linked to CF or not." @default.
• W2089525801 created "2016-06-24" @default.
• W2089525801 creator A5064129202 @default.
• W2089525801 creator A5091520627 @default.
• W2089525801 date "1997-12-01" @default.
• W2089525801 modified "2023-09-27" @default.
• W2089525801 title "8b The genetics of male infertility in relation to cystic fibrosis" @default.
• W2089525801 cites W136842601 @default.
• W2089525801 cites W151468225 @default.
• W2089525801 cites W1547921699 @default.
• W2089525801 cites W1557739264 @default.
• W2089525801 cites W1785425168 @default.
• W2089525801 cites W185124257 @default.
• W2089525801 cites W1870473073 @default.
• W2089525801 cites W18726059 @default.
• W2089525801 cites W1936565108 @default.
• W2089525801 cites W1957129715 @default.
• W2089525801 cites W1967063520 @default.
• W2089525801 cites W1969697265 @default.
• W2089525801 cites W1970775609 @default.
• W2089525801 cites W1971359074 @default.
• W2089525801 cites W1973058630 @default.
• W2089525801 cites W1978105937 @default.
• W2089525801 cites W1978151850 @default.
• W2089525801 cites W1980180966 @default.
• W2089525801 cites W1985524501 @default.
• W2089525801 cites W1985771789 @default.
• W2089525801 cites W1986585175 @default.
• W2089525801 cites W1993032589 @default.
• W2089525801 cites W1994434210 @default.
• W2089525801 cites W2001940881 @default.
• W2089525801 cites W2006031676 @default.
• W2089525801 cites W2010623159 @default.
• W2089525801 cites W2011670409 @default.
• W2089525801 cites W2016073646 @default.
• W2089525801 cites W2017588023 @default.
• W2089525801 cites W2017865016 @default.
• W2089525801 cites W2020396998 @default.
• W2089525801 cites W2021002510 @default.
• W2089525801 cites W2021739826 @default.
• W2089525801 cites W2023243075 @default.
• W2089525801 cites W2023249258 @default.
• W2089525801 cites W2028369954 @default.
• W2089525801 cites W2033909465 @default.
• W2089525801 cites W2033926035 @default.
• W2089525801 cites W2035733328 @default.
• W2089525801 cites W2039529907 @default.
• W2089525801 cites W2039599894 @default.
• W2089525801 cites W2048858469 @default.
• W2089525801 cites W2049678897 @default.
• W2089525801 cites W2050717506 @default.
• W2089525801 cites W2051365970 @default.
• W2089525801 cites W2052588826 @default.
• W2089525801 cites W2060388916 @default.
• W2089525801 cites W2065331071 @default.
• W2089525801 cites W2066672702 @default.
• W2089525801 cites W2066875617 @default.
• W2089525801 cites W2068233575 @default.
• W2089525801 cites W2068880491 @default.
• W2089525801 cites W2072098956 @default.
• W2089525801 cites W2077610722 @default.
• W2089525801 cites W2081804379 @default.
• W2089525801 cites W2091146409 @default.
• W2089525801 cites W2094020724 @default.
• W2089525801 cites W2102715410 @default.
• W2089525801 cites W2114109104 @default.
• W2089525801 cites W2116365881 @default.
• W2089525801 cites W2116830768 @default.
• W2089525801 cites W2120428327 @default.
• W2089525801 cites W2122484880 @default.
• W2089525801 cites W2124025846 @default.
• W2089525801 cites W2125391335 @default.
• W2089525801 cites W2126609769 @default.
• W2089525801 cites W2134698048 @default.
• W2089525801 cites W2139574634 @default.
• W2089525801 cites W2145274467 @default.
• W2089525801 cites W2151705053 @default.
• W2089525801 cites W2256625486 @default.
• W2089525801 cites W2295931084 @default.
• W2089525801 cites W2327703579 @default.
• W2089525801 cites W2332588487 @default.
• W2089525801 cites W2336764462 @default.
• W2089525801 cites W2337925307 @default.
• W2089525801 cites W2399234860 @default.
• W2089525801 cites W2410048061 @default.
• W2089525801 cites W2417081063 @default.
• W2089525801 cites W3021613968 @default.
• W2089525801 cites W4301019251 @default.
• W2089525801 cites W4319308443 @default.
• W2089525801 cites W91911604 @default.
• W2089525801 doi "https://doi.org/10.1016/s0950-3552(97)80014-4" @default.
• W2089525801 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9692018" @default.
• W2089525801 hasPublicationYear "1997" @default.
• W2089525801 type Work @default.
• W2089525801 sameAs 2089525801 @default.
• W2089525801 citedByCount "21" @default.
• W2089525801 countsByYear W20895258012013 @default.
• W2089525801 countsByYear W20895258012015 @default.

• next