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

Year Number of Results
1975 1
1977 2
1979 1
1981 2
1987 1
1988 1
1989 2
1990 2
1991 1
1992 2
1993 1
1995 1
1996 5
1997 1
1998 2
1999 4
2000 1
2001 1
2002 5
2003 5
2004 2
2005 4
2006 8
2007 3
2008 5
2009 6
2010 6
2011 3
2012 6
2013 4
2014 2
2015 7
2016 5
2017 5
2018 1
2019 8
2020 5
2021 11
2022 4
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Article type
Publication date

Similar articles for PMID: 28668903

130 results
Results by year
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Page 1
Frasier syndrome: four new cases with unusual presentations.
Guaragna MS, Lutaif AC, Bittencourt VB, Piveta CS, Soardi FC, Castro LC, Belangero VM, Maciel-Guerra AT, Guerra-Junior G, Mello MP. Guaragna MS, et al. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):525-32. doi: 10.1590/s0004-27302012000800011. Arq Bras Endocrinol Metabol. 2012. PMID: 23295293
Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
Kitsiou-Tzeli S, Deligiorgi M, Malaktari-Skarantavou S, Vlachopoulos C, Megremis S, Fylaktou I, Traeger-Synodinos J, Kanaka-Gantenbein C, Stefanadis C, Kanavakis E. Kitsiou-Tzeli S, et al. Hormones (Athens). 2012 Jul-Sep;11(3):361-7. doi: 10.14310/horm.2002.1366. Hormones (Athens). 2012. PMID: 22908070 Free article.
A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.
Hersmus R, van der Zwan YG, Stoop H, Bernard P, Sreenivasan R, Oosterhuis JW, Brüggenwirth HT, de Boer S, White S, Wolffenbuttel KP, Alders M, McElreavy K, Drop SL, Harley VR, Looijenga LH. Hersmus R, et al. PLoS One. 2012;7(7):e40858. doi: 10.1371/journal.pone.0040858. Epub 2012 Jul 18. PLoS One. 2012. PMID: 22815844 Free PMC article.
[Pure 46,XY gonadal dysgenesis].
Ságodi L, Ladányi E, Kiss Á, Tar A, Lukács V, Minik K, Vámosi I. Ságodi L, et al. Orv Hetil. 2010 Nov 28;151(48):1991-5. doi: 10.1556/OH.2010.28960. Orv Hetil. 2010. PMID: 21084251 Hungarian.
130 results