Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

[1]  S. Witchel Management of CAH during pregnancy: optimizing outcomes , 2012, Current opinion in endocrinology, diabetes, and obesity.

[2]  H. Falhammar,et al.  Fertility, sexuality and testicular adrenal rest tumors in adult males with congenital adrenal hyperplasia , 2011, European journal of endocrinology.

[3]  A. Nordenström Adult women with 21-hydroxylase deficient congenital adrenal hyperplasia, surgical and psychological aspects , 2011, Current opinion in pediatrics.

[4]  N. Krone,et al.  Health Problems in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency , 2011, Hormone Research in Paediatrics.

[5]  P. Hindmarsh,et al.  Prenatal hormones and childhood sex segregation: Playmate and play style preferences in girls with congenital adrenal hyperplasia , 2011, Hormones and Behavior.

[6]  V. Montori,et al.  Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. , 2010, The Journal of clinical endocrinology and metabolism.

[7]  R. Azziz,et al.  Nonclassic Congenital Adrenal Hyperplasia , 2010, International journal of pediatric endocrinology.

[8]  J. Golmard,et al.  Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 2010, The Journal of clinical endocrinology and metabolism.

[9]  G. Conway,et al.  Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): normal pregnancy rate but reduced fertility rate , 2009, Clinical endocrinology.

[10]  F. Beuschlein,et al.  High prevalence of reduced fecundity in men with congenital adrenal hyperplasia. , 2009, The Journal of clinical endocrinology and metabolism.

[11]  F. Sweep,et al.  Testicular adrenal rest tumours in congenital adrenal hyperplasia. , 2009, Best practice & research. Clinical endocrinology & metabolism.

[12]  N. Jørgensen,et al.  Improvement of semen quality in an infertile man with 21-hydroxylase deficiency, suppressed serum gonadotropins and testicular adrenal rest tumours. , 2009, International journal of andrology.

[13]  H. Falhammar,et al.  Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 2008, Human reproduction.

[14]  S. Kliesch,et al.  [Semen analysis: spermiogram according to WHO criteria]. , 2008 .

[15]  G. Conway,et al.  Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia. , 2008, The Journal of urology.

[16]  J. Llor,et al.  [Polycystic ovary syndrome and congenital adrenal hyperplasia: a different entity for comparable phenotypes?]. , 2007, Revue medicale suisse.

[17]  C. Bouvattier,et al.  Impaired sexual and reproductive outcomes in women with classical forms of congenital adrenal hyperplasia. , 2007, The Journal of clinical endocrinology and metabolism.

[18]  R. Azziz,et al.  Diagnosis of Polycystic Ovary Syndrome , 2007, Clinical obstetrics and gynecology.

[19]  Gerard Conway,et al.  Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. , 2003, The Journal of clinical endocrinology and metabolism.

[20]  R. Fanchin,et al.  Serum anti-Müllerian hormone is more strongly related to ovarian follicular status than serum inhibin B, estradiol, FSH and LH on day 3. , 2003, Human reproduction.

[21]  P. White,et al.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 2000, Endocrine reviews.

[22]  J. Honour,et al.  Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency , 1995, Clinical endocrinology.

[23]  M. Kim,et al.  Hirsutism: implications, etiology, and management. , 1981, American journal of obstetrics and gynecology.