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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1989 2
1990 3
1991 3
1992 6
1993 5
1994 2
1995 4
1996 8
1997 6
1998 9
1999 9
2000 9
2001 9
2002 6
2003 4
2004 10
2005 9
2006 9
2007 8
2008 10
2009 9
2010 12
2011 7
2012 6
2013 7
2014 6
2015 3
2016 3
2017 6
2018 5
2019 10
2020 2
2021 0
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191 results
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Page 1
Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting.
Gravholt CH, Andersen NH, Conway GS, Dekkers OM, Geffner ME, Klein KO, Lin AE, Mauras N, Quigley CA, Rubin K, Sandberg DE, Sas TCJ, Silberbach M, Söderström-Anttila V, Stochholm K, van Alfen-van derVelden JA, Woelfle J, Backeljauw PF; International Turner Syndrome Consensus Group. Gravholt CH, et al. Among authors: conway gs. Eur J Endocrinol. 2017 Sep;177(3):G1-G70. doi: 10.1530/EJE-17-0430. Eur J Endocrinol. 2017. PMID: 28705803 Review.
Swyer syndrome.
King TF, Conway GS. King TF, et al. Among authors: conway gs. Curr Opin Endocrinol Diabetes Obes. 2014 Dec;21(6):504-10. doi: 10.1097/MED.0000000000000113. Curr Opin Endocrinol Diabetes Obes. 2014. PMID: 25314337 Review.
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD.
Buonocore F, Clifford-Mobley O, King TFJ, Striglioni N, Man E, Suntharalingham JP, Del Valle I, Lin L, Lagos CF, Rumsby G, Conway GS, Achermann JC. Buonocore F, et al. Among authors: conway gs. J Endocr Soc. 2019 Oct 10;3(12):2341-2360. doi: 10.1210/js.2019-00306. eCollection 2019 Dec 1. J Endocr Soc. 2019. PMID: 31745530 Free PMC article.
Perrault Syndrome.
Newman WG, Friedman TB, Conway GS, Demain LAM. Newman WG, et al. Among authors: conway gs. 2014 Sep 25 [updated 2018 Sep 6]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 25254289 Free Books & Documents. Review.
Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome.
McElreavey K, Jorgensen A, Eozenou C, Merel T, Bignon-Topalovic J, Tan DS, Houzelstein D, Buonocore F, Warr N, Kay RGG, Peycelon M, Siffroi JP, Mazen I, Achermann JC, Shcherbak Y, Leger J, Sallai A, Carel JC, Martinerie L, Le Ru R, Conway GS, Mignot B, Van Maldergem L, Bertalan R, Globa E, Brauner R, Jauch R, Nef S, Greenfield A, Bashamboo A. McElreavey K, et al. Among authors: conway gs. Genet Med. 2020 Jan;22(1):150-159. doi: 10.1038/s41436-019-0606-y. Epub 2019 Jul 24. Genet Med. 2020. PMID: 31337883 Free PMC article.
Conway GS, Jacobs HS. Conway GS, et al. BMJ. 1990 Sep 29;301(6753):619-20. doi: 10.1136/bmj.301.6753.619. BMJ. 1990. PMID: 2224213 Free PMC article. No abstract available.
Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients.
Arlt W, Willis DS, Wild SH, Krone N, Doherty EJ, Hahner S, Han TS, Carroll PV, Conway GS, Rees DA, Stimson RH, Walker BR, Connell JM, Ross RJ; United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE). Arlt W, et al. Among authors: conway gs. J Clin Endocrinol Metab. 2010 Nov;95(11):5110-21. doi: 10.1210/jc.2010-0917. Epub 2010 Aug 18. J Clin Endocrinol Metab. 2010. PMID: 20719839 Free PMC article.
Management of hirsutism.
Koulouri O, Conway GS. Koulouri O, et al. Among authors: conway gs. BMJ. 2009 Mar 27;338:b847. doi: 10.1136/bmj.b847. BMJ. 2009. PMID: 19329515 Review. No abstract available.
191 results
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