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

Year Number of Results
1946 1
1952 1
1954 1
1957 3
1959 2
1960 1
1961 2
1962 3
1964 1
1965 1
1967 1
1974 1
1978 1
1982 1
1984 1
1989 1
1992 2
1994 1
1996 1
1997 1
1998 3
1999 1
2000 1
2002 4
2003 4
2004 2
2005 1
2006 7
2007 2
2008 2
2009 2
2010 10
2011 11
2012 12
2013 8
2014 4
2015 11
2016 1
2017 3
2018 1
2019 3
2020 0
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Article attribute
Article type
Publication date

Similar Articles for PMID: 23760708

110 results
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Page 1
Clinically relevant genetic advances in endocrinology.
Rogers A, Thakker RV. Rogers A, et al. Clin Med (Lond). 2013 Jun;13(3):299-305. doi: 10.7861/clinmedicine.13-3-299. Clin Med (Lond). 2013. PMID: 23760708 Free PMC article. No abstract available.
[A pedigree with X-linked congenital adrenal dysplasia].
Yuan W, Fu J, Liang L, Huang K. Yuan W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):123-5. doi: 10.3760/cma.j.issn.1003-9406.2013.01.030. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450496 Chinese. No abstract available.
Congenital adrenal hypoplasia and hypogonadotropic hypogonadism: phenotypic variability of the DAX-1 gene R267P mutation.
Sánchez-Pacheco M, Moreno-Pérez O, Sánchez-Ortiga R, Picó A, Moreno F. Sánchez-Pacheco M, et al. Endocrinol Nutr. 2012 Feb;59(2):140-2. doi: 10.1016/j.endonu.2011.05.016. Epub 2011 Sep 16. Endocrinol Nutr. 2012. PMID: 21925982 English, Spanish. No abstract available.
Primary adrenal insufficiency caused by a novel mutation in DAX1 gene.
Evliyaoğlu O, Dokurel İ, Bucak F, Özcabı B, Ercan Ö, Ceylaner S. Evliyaoğlu O, et al. J Clin Res Pediatr Endocrinol. 2013;5(1):55-7. doi: 10.4274/Jcrpe.895. J Clin Res Pediatr Endocrinol. 2013. PMID: 23367499 Free PMC article.
NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding.
Rojek A, Obara-Moszynska M, Malecka E, Slomko-Jozwiak M, Niedziela M. Rojek A, et al. J Appl Genet. 2013 May;54(2):225-30. doi: 10.1007/s13353-013-0135-3. Epub 2013 Feb 2. J Appl Genet. 2013. PMID: 23378245 No abstract available.
Gain of function in CDKN1C.
Riccio A, Cubellis MV. Riccio A, et al. Nat Genet. 2012 Jun 27;44(7):737-8. doi: 10.1038/ng.2336. Nat Genet. 2012. PMID: 22735584 No abstract available.
Genetic forms of adrenal insufficiency.
Brett EM, Auchus RJ. Brett EM, et al. Endocr Pract. 2015 Apr;21(4):395-9. doi: 10.4158/EP14503.RA. Epub 2015 Feb 9. Endocr Pract. 2015. PMID: 25667374 Review.
Two novel DAX1 gene mutations in Chinese patients with X-linked adrenal hypoplasia congenita: clinical, hormonal and genetic analysis.
Wu CM, Zhang HB, Zhou Q, Wan L, Jin J, Ni L, Pan YJ, Wu XY, Ruan LY. Wu CM, et al. J Endocrinol Invest. 2011 Sep;34(8):e235-9. doi: 10.3275/7484. Epub 2011 Jan 26. J Endocrinol Invest. 2011. PMID: 21270512
Foreword.
[No authors listed] [No authors listed] J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):1. doi: 10.1016/j.jsbmb.2016.11.007. J Steroid Biochem Mol Biol. 2017. PMID: 27890074 No abstract available.
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