Similar articles for PMID: 16544037

Year	Number of Results
1978	1
1980	1
1992	4
1993	2
1994	3
1995	4
1996	3
1997	3
1998	6
1999	2
2000	1
2001	4
2002	1
2003	5
2004	2
2005	5
2006	5
2007	3
2008	1
2009	2
2010	3
2011	3
2012	3
2013	5
2014	4
2015	3
2016	6
2017	8
2018	4
2019	4
2020	3
2022	4
2024	0

1

[XX male: 3 case reports during childhood].

Damiani D, Guedes DR, Damiani D, Dichtchekenian V, Coelho Neto JR, Maciel-Guerra AT, Guerra-Júnior G, Mello MP, Setian N. Damiani D, et al. Arq Bras Endocrinol Metabol. 2005 Feb;49(1):79-82. doi: 10.1590/s0004-27302005000100010. Epub 2006 Mar 16. Arq Bras Endocrinol Metabol. 2005. PMID: 16544037 Portuguese.

2

Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis.

Grigorescu-Sido A, Heinrich U, Grigorescu-Sido P, Jauch A, Hager HD, Vogt PH, Duncea I, Bettendorf M. Grigorescu-Sido A, et al. J Pediatr Endocrinol Metab. 2005 Feb;18(2):197-203. doi: 10.1515/jpem.2005.18.2.197. J Pediatr Endocrinol Metab. 2005. PMID: 15751609

3

Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature.

Ergun-Longmire B, Vinci G, Alonso L, Matthew S, Tansil S, Lin-Su K, McElreavey K, New MI. Ergun-Longmire B, et al. J Pediatr Endocrinol Metab. 2005 Aug;18(8):739-48. doi: 10.1515/jpem.2005.18.8.739. J Pediatr Endocrinol Metab. 2005. PMID: 16200839

4

True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: clinical features, cytogenetic findings, and literature review.

Modan-Moses D, Litmanovitch T, Rienstein S, Meyerovitch J, Goldman B, Aviram-Goldring A. Modan-Moses D, et al. Am J Med Genet A. 2003 Jan 30;116A(3):300-3. doi: 10.1002/ajmg.a.10869. Am J Med Genet A. 2003. PMID: 12503111 Review.

5

A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia.

Ellaithi M, Gisselsson D, Nilsson T, Abd El-Fatah S, Ali T, Elagib A, Ibrahim ME, Fadl-Elmula I. Ellaithi M, et al. BMC Pediatr. 2006 Apr 4;6:11. doi: 10.1186/1471-2431-6-11. BMC Pediatr. 2006. PMID: 16594994 Free PMC article.

6

[Analysis of clinical features and related genes variation in five patients with 46, XX male syndrome].

Qin XY, Dong WK, Wang W, Dong ZY, Xiao Y, Lu WL, Wang DF. Qin XY, et al. Zhonghua Er Ke Za Zhi. 2016 Nov 2;54(11):840-843. doi: 10.3760/cma.j.issn.0578-1310.2016.11.010. Zhonghua Er Ke Za Zhi. 2016. PMID: 27806792 Chinese.

7

True hermaphroditism: genetic variants and clinical management.

Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M, Nihoul-Fékété C, Rappaport R. Hadjiathanasiou CG, et al. J Pediatr. 1994 Nov;125(5 Pt 1):738-44. doi: 10.1016/s0022-3476(94)70067-2. J Pediatr. 1994. PMID: 7965425 Clinical Trial.

8

Clinical and molecular analysis of XX sex reversed patients.

Kolon TF, Ferrer FA, McKenna PH. Kolon TF, et al. J Urol. 1998 Sep;160(3 Pt 2):1169-72; discussion 1178. doi: 10.1097/00005392-199809020-00057. J Urol. 1998. PMID: 9719302

9

46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature.

Li TF, Wu QY, Zhang C, Li WW, Zhou Q, Jiang WJ, Cui YX, Xia XY, Shi YC. Li TF, et al. BMC Urol. 2014 Dec 22;14:104. doi: 10.1186/1471-2490-14-104. BMC Urol. 2014. PMID: 25529318 Free PMC article. Review.

10

46,XX male disorder of sexual development:a case report.

Anık A, Çatlı G, Abacı A, Böber E. Anık A, et al. J Clin Res Pediatr Endocrinol. 2013;5(4):258-60. doi: 10.4274/Jcrpe.1098. J Clin Res Pediatr Endocrinol. 2013. PMID: 24379036 Free PMC article.

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