-
1
-
-
77957850956
-
The surgical challenges of disorders of sex development DSD
-
Gorduza D, Vidal I, Birraux J, et al. The surgical challenges of disorders of sex development (DSD). Arch Esp Urol 2010; 63:495-504.
-
(2010)
Arch. Esp. Urol.
, vol.63
, pp. 495-504
-
-
Gorduza, D.1
Vidal, I.2
Birraux, J.3
-
2
-
-
84860188557
-
Consensus in guidelines for evaluation of dsd by the texas childrens hospital multidisciplinary gender medicine team
-
ID 919707: 10.1155/2010/919707.
-
Douglas G, Axelrad ME, Brandt ML, et al. Consensus in guidelines for evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team. Int J Pediatr Endocrinol 2010; article ID 919707, 17 pp. doi: 10.1155/2010/919707.
-
(2010)
Int. J. Pediatr. Endocrinol.
, pp. 17
-
-
Douglas, G.1
Axelrad, M.E.2
Brandt, M.L.3
-
5
-
-
78049251776
-
Disorders of sex development network working group psychological adjustment and sexual development of adolescents with disorders of sex development
-
Kleinemeier E, Jürgensen M, Lux A, et al., Disorders of Sex Development Network Working Group. Psychological adjustment and sexual development of adolescents with disorders of sex development. J Adolesc Health 2010; 47:463-471.
-
(2010)
J. Adolesc. Health
, vol.47
, pp. 463-471
-
-
Kleinemeier, E.1
Jürgensen, M.2
Lux, A.3
-
6
-
-
77957804691
-
Approach to assigning gender in 46 XX congenital adrenal hyperplasia with male external genitalia: Replacing dogmatism with pragmatism
-
Houk CP, Lee PA. Approach to assigning gender in 46,XX congenital adrenal hyperplasia with male external genitalia: replacing dogmatism with pragmatism. J Clin Endocrinol Metab 2010; 95:4501-4508.
-
(2010)
J. Clin. Endocrinol. Metab.
, vol.95
, pp. 4501-4508
-
-
Houk, C.P.1
Lee, P.A.2
-
7
-
-
79958803288
-
UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development
-
10.1111/j.1365-2265.2011.04076.x.
-
Ahmed SF, Achermann JC, Arlt W, et al. UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development. Clin Endocrinol 2011; 75:12-26. doi: 10.1111/j.1365-2265.2011. 04076.x.
-
(2011)
Clin. Endocrinol.
, vol.75
, pp. 12-26
-
-
Ahmed, S.F.1
Achermann, J.C.2
Arlt, W.3
-
8
-
-
79958768847
-
Factors that influence the decision to perform a karyotype in suspected disorders of sex development: Lessons from the Scottish genital anomaly network register
-
10.1159/000326815.
-
Rodie M, McGowan R, Mayo A, et al. Factors that influence the decision to perform a karyotype in suspected disorders of sex development: lessons from the Scottish genital anomaly network register. Sex Dev 2011; 5:103-108; doi: 10.1159/000326815.
-
(2011)
Sex. Dev.
, vol.5
, pp. 103-108
-
-
Rodie, M.1
McGowan, R.2
Mayo, A.3
-
9
-
-
79957835106
-
Disorders of sex development - When and how to tell the patient
-
Austin J, Tamar-Mattis A, Mazur T, et al. Disorders of sex development - when and how to tell the patient. Pediatr Endocrinol Rev 2011; 8:213-217.
-
(2011)
Pediatr. Endocrinol. Rev.
, vol.8
, pp. 213-217
-
-
Austin, J.1
Tamar-Mattis, A.2
Mazur, T.3
-
10
-
-
79960943028
-
Gonadal development and tumor formation at the crossroads of male and female sex determination
-
Cools M, Wolffenbuttel KP, Drop SL, et al. Gonadal development and tumor formation at the crossroads of male and female sex determination. Sex Dev 2011; 5:167-180.
-
(2011)
Sex. Dev.
, vol.5
, pp. 167-180
-
-
Cools, M.1
Wolffenbuttel, K.P.2
Drop, S.L.3
-
11
-
-
84873061531
-
Normal sex differences in prenatal growth and abnormal prenatal growth retardation associated with 46 XY disorders of sex development are absent in newborns with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Chalmers LJ, Doherty P, Migeon CJ, et al. Normal sex differences in prenatal growth and abnormal prenatal growth retardation associated with 46,XY disorders of sex development are absent in newborns with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Biol Sex Differences 2011; 2:5; http://www.bsd-journal.com/content/2/1/5.
-
(2011)
Biol. Sex. Differences
, vol.2
, pp. 5
-
-
Chalmers, L.J.1
Doherty, P.2
Migeon, C.J.3
-
12
-
-
79952333478
-
Copy number variation in patients with disorders of sex development due to 46 XY gonadal dysgenesis
-
10.1371/journal.pone.0017793.
-
White S, Ohnesorg T, Notini A, et al. Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis. PLoS One 2011; 6:e17793. doi: 10.1371/journal.pone.0017793.
-
(2011)
PLoS One
, vol.6
-
-
White, S.1
Ohnesorg, T.2
Notini, A.3
-
13
-
-
79958023683
-
WT1 mutation as a cause of 46 XY DSD and wilms tumor: A case report and literature review
-
10.1111/j.1651-2227.2011.02167.x
-
Dai YL, Fu JF, Hong F, et al. WT1 mutation as a cause of 46 XY DSD and Wilm's tumor: a case report and literature review. Acta Paediatr 2011; 100:e39-e42; doi: 10.1111/j.1651-2227.2011.02167.x.
-
(2011)
Acta. Paediatr.
, vol.100
-
-
Dai, Y.L.1
Fu, J.F.2
Hong, F.3
-
14
-
-
79960082053
-
Analysis of the wilms tumor suppressor gene WT1 in patients 46 XY disorders of sex development
-
Köhler B, Biebermann H, Friedsam V, et al. Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex development. J Clin Endocrinol Metab 2011; 96:E1131-E1136.
-
(2011)
J. Clin. Endocrinol. Metab.
, vol.96
-
-
Köhler, B.1
Biebermann, H.2
Friedsam, V.3
-
15
-
-
79952987603
-
Predominant sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father
-
Philibert P, Polak M, Colmenares A, et al. Predominant sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father. Fertil Steril 2011; 95:1788.e5-1788.e9.
-
(2011)
Fertil. Steril.
, vol.95
-
-
Philibert, P.1
Polak, M.2
Colmenares, A.3
-
16
-
-
79151484625
-
Three new SF-1 NR5A1 gene mutations in two unrelated families with multiple affected members: Withinfamily variability in 46 XY subjects and low ovarian reserve in fertile 46 XX subjects
-
Warman DM, Costanzo M, Marino R, et al. Three new SF-1 (NR5A1) gene mutations in two unrelated families with multiple affected members: withinfamily variability in 46,XY subjects and low ovarian reserve in fertile 46,XX subjects. Horm Res Paediatr 2011; 75:70-77.
-
(2011)
Horm. Res. Paediatr.
, vol.75
, pp. 70-77
-
-
Warman, D.M.1
Costanzo, M.2
Marino, R.3
-
17
-
-
81455135440
-
SRD5A2 gene mutations and polymorphisms in Spanish 46 XY patients with a disorder of sex differentiation
-
10.1111/j.1365-2605.2010.01136.x. Epub ahead of print]
-
Fernández-Cancio M, Audí L, Andaluz P, et al. SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation. Int J Androl 2011. doi: 10.1111/j.1365-2605.2010.01136.x. [Epub ahead of print]
-
(2011)
Int. J. Androl.
-
-
Fernández-Cancio, M.1
Audí, L.2
Andaluz, P.3
-
18
-
-
79957767768
-
Recognition of 5a-reductase-2 deficiency in an adult female 46XY DSD clinic
-
Berra M, Williams EL, Muroni B, et al. Recognition of 5a-reductase-2 deficiency in an adult female 46XY DSD clinic. Eur J Endocrinol 2011; 164:1019-1025.
-
(2011)
Eur. J. Endocrinol.
, vol.164
, pp. 1019-1025
-
-
Berra, M.1
Williams, E.L.2
Muroni, B.3
-
19
-
-
84873074517
-
Long-term biochemical evaluation of the androgen receptor pathway in males with disorders of sex development
-
Epub ahead of print
-
Schwentner C, Czyz J, Seibold J, et al. Long-term biochemical evaluation of the androgen receptor pathway in males with disorders of sex development. World J Urol 2010 [Epub ahead of print].
-
(2010)
World J. Urol.
-
-
Schwentner, C.1
Czyz, J.2
Seibold, J.3
-
21
-
-
80053555736
-
Idiopathic partial androgen insensitivity syndrome in 28 newborn and infant males: Impact of prenatal exposure to environmental endocrine-disruptor chemicals
-
Epub ahead of print
-
Gaspari L, Paris F, Philibert P, et al. 'Idiopathic' partial androgen insensitivity syndrome in 28 newborn and infant males: impact of prenatal exposure to environmental endocrine-disruptor chemicals? Eur J Endocrinol 2011 [Epub ahead of print].
-
(2011)
Eur. J. Endocrinol.
-
-
Gaspari, L.1
Paris, F.2
Philibert, P.3
|