Albright, F., Smith, P. H. & Fraser, R. A syndrome characterized by primary ovarian insufficiency and decreased stature: Report of 11 cases with a digression on hormonal control of axillary and pubic hair. Am. J. Med. Sci.204, 625–648 (1942). Article Google Scholar
Welt, C. K. Primary ovarian insufficiency: a more accurate term for premature ovarian failure. Clin. Endocrinol. (Oxf.)68, 499–509 (2008). Article Google Scholar
Persani, L., Rossetti, R. & Cacciatore, C. Genes involved in human premature ovarian failure. J. Mol. Endocrinol.45, 257–279 (2010). ArticleCASPubMed Google Scholar
Bakalov, V. K. et al. Autoimmune oophoritis as a mechanism of follicular dysfunction in women with 46,XX spontaneous premature ovarian failure. Fertil. Steril.84, 958–965 (2005). ArticlePubMed Google Scholar
Aittomäki, K. et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell82, 959–968 (1995). ArticlePubMed Google Scholar
Latronico, A. C. et al. Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene. N. Engl. J. Med.334, 507–512 (1996). ArticleCASPubMed Google Scholar
Araki, S. et al. Arrest of follicular development in a patient with 17 alpha-hydroxylase deficiency: folliculogenesis in association with a lack of estrogen synthesis in the ovaries. Fertil. Steril.47, 169–172 (1987). ArticleCASPubMed Google Scholar
Conte, F. A., Grumbach, M. M., Ito, Y., Fisher, C. R. & Simpson, E. R. A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom). J. Clin. Endocrinol. Metab.78, 1287–1292 (1994). CASPubMed Google Scholar
Nelson, L. M. et al. Development of luteinized graafian follicles in patients with karyotypically normal spontaneous premature ovarian failure. J. Clin. Endocrinol. Metab.79, 1470–1475 (1994). CASPubMed Google Scholar
Nelson, L. M., Covington, S. N. & Rebar, R. W. An update: spontaneous premature ovarian failure is not an early menopause. Fertil. Steril.83, 1327–1332 (2005). ArticlePubMed Google Scholar
Hubayter, Z. R. et al. A prospective evaluation of antral follicle function in women with 46, XX spontaneous primary ovarian insufficiency. Fertil. Steril.94, 1769–1774 (2010). ArticlePubMed Google Scholar
Karimov, C. B. et al. Increased frequency of occult fragile X-associated primary ovarian insufficiency in infertile women with evidence of impaired ovarian function. Hum. Reprod.26, 2077–2083 (2011). ArticleCASPubMed Google Scholar
Goswami, D. & Conway, G. S. Premature ovarian failure. Hum. Reprod. Update11, 391–410 (2005). ArticleCASPubMed Google Scholar
Skillern, A. & Rajkovic, A. Recent developments in identifying genetic determinants of premature ovarian failure. Sex. Dev.2, 228–243 (2008). ArticleCASPubMed Google Scholar
Knauff, E. A. et al. Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. Hum. Reprod.24, 2372–2378 (2009). ArticleCASPubMed Google Scholar
van Dooren, M. F., Bertoli-Avellab, A. M. & Oldenburg, R. A. Premature ovarian failure and gene polymorphisms. Curr. Opin. Obstet. Gynecol.21, 313–317 (2009). ArticlePubMed Google Scholar
Oldenburg, R. A. et al. A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus. Hum. Reprod.23, 2835–2841 (2008). ArticleCASPubMed Google Scholar
Christin-Maitre, S. & Tachdjian, G. Genome-wide association study and premature ovarian failure. Ann. Endocrinol. (Paris)71, 218–221 (2010). ArticleCAS Google Scholar
Bondy, C. A. Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J. Clin. Endocrinol. Metab.92, 10–25 (2007). ArticleCASPubMed Google Scholar
Saenger, P. et al. Recommendations for the diagnosis and management of Turner syndrome. J. Clin. Endocrinol. Metab.86, 3061–3069 (2001). CASPubMed Google Scholar
Sherman, S. L. Premature ovarian failure in the fragile X syndrome. Am. J. Med. Genet.97, 189–194 (2000). ArticleCASPubMed Google Scholar
Verkerk, A. J. et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell65, 905–914 (1991). ArticleCASPubMed Google Scholar
Fu, Y. H. et al. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell67, 1047–1058 (1991). ArticleCASPubMed Google Scholar
Allingham-Hawkins, D. J. et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study—preliminary data. Am. J. Med. Genet.83, 322–325 (1999). ArticleCASPubMedPubMed Central Google Scholar
Conway, G. S., Payne, N. N., Webb, J., Murray, A. & Jacobs, P. A. Fragile X premutation screening in women with premature ovarian failure. Hum. Reprod.13, 1184–1187 (1998). ArticleCASPubMed Google Scholar
Conway, G. S., Kaltsas, G., Patel, A., Davies, M. C. & Jacobs, H. S. Characterization of idiopathic premature ovarian failure. Fertil. Steril.65, 337–341 (1996). ArticleCASPubMed Google Scholar
Novosad, J. A., Kalantaridou, S. N., Tong, Z. B. & Nelson, L. M. Ovarian antibodies as detected by indirect immunofluorescence are unreliable in the diagnosis of autoimmune premature ovarian failure: a controlled evaluation. BMC Womens Health3, 2 (2003). ArticlePubMedPubMed Central Google Scholar
La Marca, A. et al. Primary ovarian insufficiency: autoimmune causes. Curr. Opin. Obstet. Gynecol.22, 277–282 (2010). PubMed Google Scholar
Gatta, G., Capocaccia, R., Coleman, M. P., Ries, L. A. & Berrino, F. Childhood cancer survival in Europe and the United States. Cancer95, 1767–1772 (2002). ArticlePubMed Google Scholar
Gatta, G. et al. Childhood cancer survival trends in Europe: a EUROCARE Working Group study. J. Clin. Oncol.23, 3742–3751 (2005). ArticlePubMed Google Scholar
Edgar, A. B., Morris, E. M., Kelnar, C. J. & Wallace, W. H. Long-term follow-up of survivors of childhood cancer. Endocr. Dev.15, 159–180 (2009). ArticlePubMed Google Scholar
Bath, L. E., Wallace, W. H. & Critchley, H. O. Late effects of the treatment of childhood cancer on the female reproductive system and the potential for fertility preservation. BJOG109, 107–114 (2002). ArticlePubMed Google Scholar
van Dorp, W. et al. Long-term endocrine side effects of childhood Hodgkin's lymphoma treatment: a review. Hum. Reprod. Updatehttp://dx.doi.org/10.1093/humupd/dmr038.
Brougham, M. F. & Wallace, W. H. Subfertility in children and young people treated for solid and haematological malignancies. Br. J. Haematol.131, 143–155 (2005). PubMed Google Scholar
Josso, N. et al. Anti-müllerian hormone: the Jost factor. Recent Prog. Horm. Res.48, 1–59 (1993). CASPubMed Google Scholar
Lee, M. M. & Donahoe, P. K. Müllerian inhibiting substance: a gonadal hormone with multiple functions. Endocr. Rev.14, 152–164 (1993). CASPubMed Google Scholar
Josso, N., Picard, J. Y. & Tran, D. The anti-Müllerian hormone. Birth Defects Orig. Artic. Ser.13, 59–84 (1977). CASPubMed Google Scholar
Durlinger, A. L., Visser, J. A. & Themmen, A. P. Regulation of ovarian function: the role of anti-Müllerian hormone. Reproduction124, 601–609 (2002). ArticleCASPubMed Google Scholar
Rajpert-De Meyts, E. et al. Expression of anti-Müllerian hormone during normal and pathological gonadal development: association with differentiation of Sertoli and granulosa cells. J. Clin. Endocrinol. Metab.84, 3836–3844 (1999). PubMed Google Scholar
Weenen, C. et al. Anti-Müllerian hormone expression pattern in the human ovary: potential implications for initial and cyclic follicle recruitment. Mol. Hum. Reprod.10, 77–83 (2004). ArticleCASPubMed Google Scholar
Shi, J. et al. Bone morphogenetic protein-6 stimulates gene expression of follicle-stimulating hormone receptor, inhibin/activin beta subunits, and anti-Müllerian hormone in human granulosa cells. Fertil. Steril.92, 1794–1798 (2009). ArticlePubMed Google Scholar
Salmon, N. A., Handyside, A. H. & Joyce, I. M. Oocyte regulation of anti-Müllerian hormone expression in granulosa cells during ovarian follicle development in mice. Dev. Biol.266, 201–208 (2004). ArticleCASPubMed Google Scholar
Grøndahl, M. L. et al. Anti-Müllerian hormone remains highly expressed in human cumulus cells during the final stages of folliculogenesis. Reprod. Biomed. Online22, 389–398 (2011). ArticleCASPubMed Google Scholar
McGee, E. A. & Hsueh, A. J. Initial and cyclic recruitment of ovarian follicles. Endocr. Rev.21, 200–214 (2000). CASPubMed Google Scholar
Durlinger, A. L. L. et al. Control of primordial follicle recruitment by anti-Müllerian hormone in the mouse ovary. Endocrinology140, 5789–5796 (1999). ArticleCASPubMed Google Scholar
Carlsson, I. B. et al. Anti-Müllerian hormone inhibits initiation of growth of human primordial ovarian follicles in vitro. Hum. Reprod.21, 2223–2227 (2006). ArticleCASPubMed Google Scholar
Durlinger, A. L. L. et al. Anti-Müllerian hormone inhibits initiation of primordial follicle growth in the mouse ovary. Endocrinology143, 1076–1084 (2002). ArticleCASPubMed Google Scholar
Gigli, I., Cushman, R. A., Wahl, C. M. & Fortune, J. E. Evidence for a role for anti-Müllerian hormone in the suppression of follicle activation in mouse ovaries and bovine ovarian cortex grafted beneath the chick chorioallantoic membrane. Mol. Reprod. Dev.71, 480–488 (2005). ArticleCASPubMed Google Scholar
Kevenaar, M. E. et al. A polymorphism in the AMH type II receptor gene is associated with age at menopause in interaction with parity. Hum. Reprod.22, 2382–2388 (2007). ArticleCASPubMed Google Scholar
Durlinger, A. L. L. et al. Anti-Müllerian hormone attenuates the effects of FSH on follicle development in the mouse ovary. Endocrinology142, 4891–4899 (2001). ArticleCASPubMed Google Scholar
Visser, J. A. et al. Increased oocyte degeneration and follicular atresia during the estrous cycle in anti-Müllerian hormone null mice. Endocrinology148, 2301–2308 (2007). ArticleCASPubMed Google Scholar
di Clemente, N. et al. Inhibitory effect of AMH upon the expression of aromatase and LH receptors of granulosa cells of rat and porcine immature ovaries. Endocrine2, 553–558 (1994). CAS Google Scholar
Grossman, M. P., Nakajima, S. T., Fallat, M. E. & Siow, Y. Müllerian-inhibiting substance inhibits cytochrome P450 aromatase activity in human granulosa lutein cell culture. Fertil. Steril.89, 1364–1370 (2008). ArticleCASPubMed Google Scholar
Andersen, C. Y. & Byskov, A. G. Estradiol and regulation of anti-Müllerian hormone, inhibin-A, and inhibin-B secretion: analysis of small antral and preovulatory human follicles' fluid. J. Clin. Endocrinol. Metab.91, 4064–4069 (2006). ArticleCASPubMed Google Scholar
Kevenaar, M. E. et al. Anti-Müllerian hormone and anti-Müllerian hormone type II receptor polymorphisms are associated with follicular phase estradiol levels in normo-ovulatory women. Hum. Reprod.22, 1547–1554 (2007). ArticleCASPubMed Google Scholar
te Velde, E. R., Scheffer, G. J., Dorland, M., Broekmans, F. J. & Fauser, B. C. Developmental and endocrine aspects of normal ovarian aging. Mol. Cell. Endocrinol.145, 67–73 (1998). ArticleCASPubMed Google Scholar
Scheffer, G. J. et al. Antral follicle counts by transvaginal ultrasonography are related to age in women with proven natural fertility. Fertil. Steril.72, 845–851 (1999). ArticleCASPubMed Google Scholar
Bergada, I. et al. Time course of the serum gonadotropin surge, inhibins, and anti-Müllerian hormone in normal newborn males during the first month of life. J. Clin. Endocrinol. Metab.91, 4092–4098 (2006). ArticleCASPubMed Google Scholar
Guibourdenche, J. et al. Anti-Müllerian hormone levels in serum from human foetuses and children: pattern and clinical interest. Mol. Cell. Endocrinol.211, 55–63 (2003). ArticleCASPubMed Google Scholar
Hagen, C. P. et al. Serum levels of anti-Müllerian hormone as a marker of ovarian function in 926 healthy females from birth to adulthood and in 172 Turner syndrome patients. J. Clin. Endocrinol. Metab.95, 5003–5010 (2010). ArticleCASPubMed Google Scholar
Lee, M. M. et al. Mullerian inhibiting substance in humans: normal levels from infancy to adulthood. J. Clin. Endocrinol. Metab.81, 571–576 (1996). CASPubMed Google Scholar
van Rooij, I. A. et al. Anti-müllerian hormone is a promising predictor for the occurrence of the menopausal transition. Menopause11, 601–606 (2004). ArticlePubMed Google Scholar
van Rooij, I. A. et al. Serum antimullerian hormone levels best reflect the reproductive decline with age in normal women with proven fertility: A longitudinal study. Fertil. Steril.83, 979–987 (2005). ArticleCASPubMed Google Scholar
de Vet, A., Laven, J. S., de Jong, F. H., Themmen, A. P. N. & Fauser, B. C. Antimüllerian hormone serum levels: a putative marker for ovarian aging. Fertil. Steril.77, 357–362 (2002). ArticlePubMed Google Scholar
Fanchin, R. 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. Hum. Reprod.18, 323–327 (2003). ArticleCASPubMed Google Scholar
van Rooij, I. A. et al. Serum anti-Müllerian hormone levels: a novel measure of ovarian reserve. Hum. Reprod.17, 3065–3071 (2002). ArticleCASPubMed Google Scholar
Hansen, K. R., Hodnett, G. M., Knowlton, N. & Craig, L. B. Correlation of ovarian reserve tests with histologically determined primordial follicle number. Fertil. Steril.95, 170–175 (2011). ArticlePubMed Google Scholar
Kevenaar, M. E. et al. Serum anti-mullerian hormone levels reflect the size of the primordial follicle pool in mice. Endocrinology147, 3228–3234 (2006). ArticleCASPubMed Google Scholar
Seifer, D. B., Baker, V. L. & Leader, B. Age-specific serum anti-Müllerian hormone values for 17,120 women presenting to fertility centers within the United States. Fertil. Steril.95, 747–750 (2011). ArticleCASPubMed Google Scholar
Kelsey, T. W., Wright, P., Nelson, S. M., Anderson, R. A. & Wallace, W. H. A validated model of serum anti-müllerian hormone from conception to menopause. PLoS ONE6, e22024 (2011). ArticleCASPubMedPubMed Central Google Scholar
Nelson, S. M. et al. External validation of nomogram for the decline in serum anti-Müllerian hormone in women: a population study of 15,834 infertility patients. Reprod. Biomed. Online23, 204–206 (2011). ArticlePubMed Google Scholar
Hehenkamp, W. J. et al. Anti-Müllerian hormone levels in the spontaneous menstrual cycle do not show substantial fluctuation. J. Clin. Endocrinol. Metab.91, 4057–4063 (2006). ArticleCASPubMed Google Scholar
La Marca, A., Stabile, G., Artenisio, A. C. & Volpe, A. Serum anti-Müllerian hormone throughout the human menstrual cycle. Hum. Reprod.21, 3103–3107 (2006). ArticleCASPubMed Google Scholar
Streuli, I. et al. Serum antimüllerian hormone levels remain stable throughout the menstrual cycle and after oral or vaginal administration of synthetic sex steroids. Fertil. Steril.90, 395–400 (2008). ArticleCASPubMed Google Scholar
Tsepelidis, S. et al. Stable serum levels of anti-Müllerian hormone during the menstrual cycle: a prospective study in normo-ovulatory women. Hum. Reprod.22, 1837–1840 (2007). ArticleCASPubMed Google Scholar
Robertson, D. M., Hale, G. E., Fraser, I. S., Hughes, C. L. & Burger, H. G. Changes in serum antimüllerian hormone levels across the ovulatory menstrual cycle in late reproductive age. Menopause18, 521–524 (2011). ArticlePubMed Google Scholar
Sowers, M. et al. Anti-Müllerian hormone and inhibin B variability during normal menstrual cycles. Fertil. Steril.94, 1482–1486 (2010). ArticleCASPubMed Google Scholar
Streuli, I. et al. Clinical uses of anti-Müllerian hormone assays: pitfalls and promises. Fertil. Steril.91, 226–230 (2009). ArticleCASPubMed Google Scholar
Wunder, D. M., Bersinger, N. A., Yared, M., Kretschmer, R. & Birkhäuser, M. H. Statistically significant changes of antimüllerian hormone and inhibin levels during the physiologic menstrual cycle in reproductive age women. Fertil. Steril.89, 927–933 (2008). ArticleCASPubMed Google Scholar
Fanchin, R. et al. High reproducibility of serum anti-Mullerian hormone measurements suggests a multi-staged follicular secretion and strengthens its role in the assessment of ovarian follicular status. Hum. Reprod.20, 923–927 (2005). ArticleCASPubMed Google Scholar
Sowers, M. R. et al. Anti-mullerian hormone and inhibin B in the definition of ovarian aging and the menopause transition. J. Clin. Endocrinol. Metab.93, 3478–3483 (2008). ArticleCASPubMedPubMed Central Google Scholar
van Disseldorp, J. et al. Relationship of serum antimüllerian hormone concentration to age at menopause. J. Clin. Endocrinol. Metab.93, 2129–2134 (2008). ArticleCASPubMed Google Scholar
Broer, S. L. et al. Anti-mullerian hormone predicts menopause: a long-term follow-up study in normoovulatory women. J. Clin. Endocrinol. Metab.96, 2532–2539 (2011). ArticleCASPubMed Google Scholar
Tehrani, F. R., Shakeri, N., Solaymani-Dodaran, M. & Azizi, F. Predicting age at menopause from serum antimüllerian hormone concentration. Menopause18, 766–770 (2011). ArticlePubMed Google Scholar
Tehrani, F. R., Solaymani-Dodaran, M. & Azizi, F. A single test of antimullerian hormone in late reproductive-aged women is a good predictor of menopause. Menopause16, 797–802 (2009). ArticlePubMed Google Scholar
Hendriks, D. J., Mol, B. W., Bancsi, L. F., Te Velde, E. R. & Broekmans, F. J. Antral follicle count in the prediction of poor ovarian response and pregnancy after in vitro fertilization: a meta-analysis and comparison with basal follicle-stimulating hormone level. Fertil. Steril.83, 291–301 (2005). ArticlePubMed Google Scholar
Seifer, D. B., MacLaughlin, D. T., Christian, B. P., Feng, B. & Shelden, R. M. Early follicular serum müllerian-inhibiting substance levels are associated with ovarian response during assisted reproductive technology cycles. Fertil. Steril.77, 468–471 (2002). ArticlePubMed Google Scholar
La Marca, A. et al. Anti-Müllerian hormone measurement on any day of the menstrual cycle strongly predicts ovarian response in assisted reproductive technology. Hum. Reprod.22, 766–771 (2007). ArticleCASPubMed Google Scholar
Nelson, S. M., Yates, R. W. & Fleming, R. Serum anti-Müllerian hormone and FSH: prediction of live birth and extremes of response in stimulated cycles—implications for individualization of therapy. Hum. Reprod.22, 2414–2421 (2007). ArticleCASPubMed Google Scholar
Nelson, S. M. et al. Anti-Müllerian hormone-based approach to controlled ovarian stimulation for assisted conception. Hum. Reprod.24, 867–875 (2009). ArticleCASPubMed Google Scholar
Broer, S. L. et al. AMH and AFC as predictors of excessive response in controlled ovarian hyperstimulation: a meta-analysis. Hum. Reprod. Update17, 46–54 (2011). ArticleCASPubMed Google Scholar
Broer, S. L., Mol, B., Dolleman, M., Fauser, B. C. & Broekmans, F. J. The role of anti-Müllerian hormone assessment in assisted reproductive technology outcome. Curr. Opin. Obstet. Gynecol.22, 193–201 (2010). ArticlePubMed Google Scholar
Broer, S. L., Mol, B. W., Hendriks, D. & Broekmans, F. J. The role of antimüllerian hormone in prediction of outcome after IVF: comparison with the antral follicle count. Fertil. Steril.91, 705–714 (2009). ArticleCASPubMed Google Scholar
Fadini, R. et al. Anti-mullerian hormone as a predictive marker for the selection of women for oocyte in vitro maturation treatment. J. Assist. Reprod. Genet.28, 501–508 (2011). ArticlePubMedPubMed Central Google Scholar
Gnoth, C. et al. Relevance of anti-Müllerian hormone measurement in a routine IVF program. Hum. Reprod.23, 1359–1365 (2008). ArticleCASPubMed Google Scholar
Lie Fong, S. et al. Anti-Müllerian hormone: a marker for oocyte quantity, oocyte quality and embryo quality? Reprod. Biomed. Online16, 664–670 (2008). ArticleCASPubMed Google Scholar
Smeenk, J. M. et al. Antimüllerian hormone predicts ovarian responsiveness, but not embryo quality or pregnancy, after in vitro fertilization or intracyoplasmic sperm injection. Fertil. Steril.87, 223–226 (2007). ArticleCASPubMed Google Scholar
La Marca, A. et al. Serum anti-müllerian hormone levels in women with secondary amenorrhea. Fertil. Steril.85, 1547–1549 (2006). ArticleCASPubMed Google Scholar
Méduri, G. et al. Serum anti-Müllerian hormone expression in women with premature ovarian failure. Hum. Reprod.22, 117–123 (2007). ArticleCASPubMed Google Scholar
Bachelot, A. et al. Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure. Eur. J. Endocrinol.161, 179–187 (2009). ArticleCASPubMed Google Scholar
Knauff, E. A. et al. Anti-Müllerian hormone, inhibin B, and antral follicle count in young women with ovarian failure. J. Clin. Endocrinol. Metab.94, 786–792 (2009). ArticleCASPubMed Google Scholar
Sullivan, A. K. et al. Association of FMR1 repeat size with ovarian dysfunction. Hum. Reprod.20, 402–412 (2005). ArticleCASPubMed Google Scholar
Rohr, J. et al. Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study. Hum. Reprod.23, 1220–1225 (2008). ArticleCASPubMed Google Scholar
Spath, M. A. et al. Intra-individual stability over time of standardized anti-Müllerian hormone in FMR1 premutation carriers. Hum. Reprod.26, 2185–2191 (2011). ArticleCASPubMedPubMed Central Google Scholar
Gleicher, N., Weghofer, A., Oktay, K. & Barad, D. H. Correlation of triple repeats on the FMR1 (fragile X) gene to ovarian reserve: a new infertility test? Acta Obstet. Gynecol. Scand.88, 1024–1030 (2009). ArticleCASPubMed Google Scholar
Gleicher, N., Weghofer, A., Oktay, K. & Barad, D. Relevance of triple CGG repeats in the FMR1 gene to ovarian reserve. Reprod. Biomed. Online19, 385–390 (2009). ArticleCASPubMed Google Scholar
Gleicher, N., Weghofer, A. & Barad, D. H. A pilot study of premature ovarian senescence: I. Correlation of triple CGG repeats on the FMR1 gene to ovarian reserve parameters FSH and anti-Müllerian hormone. Fertil. Steril.91, 1700–1706 (2009). ArticleCASPubMed Google Scholar
Bennett, C. E., Conway, G. S., Macpherson, J. N., Jacobs, P. A. & Murray, A. Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure. Hum. Reprod.25, 1335–1338 (2010). ArticleCASPubMedPubMed Central Google Scholar
Abir, R. et al. Turner's syndrome and fertility: current status and possible putative prospects. Hum. Reprod. Update7, 603–610 (2001). ArticleCASPubMed Google Scholar
Toniolo, D. & Rizzolio, F. X chromosome and ovarian failure. Semin. Reprod. Med.25, 264–271 (2007). ArticleCASPubMed Google Scholar
Borgström, B. et al. Fertility preservation in girls with turner syndrome: prognostic signs of the presence of ovarian follicles. J. Clin. Endocrinol. Metab.94, 74–80 (2009). ArticleCASPubMed Google Scholar
Purushothaman, R., Lazareva, O., Oktay, K. & Ten, S. Markers of ovarian reserve in young girls with Turner's syndrome. Fertil. Steril.94, 1557–1559 (2010). ArticlePubMed Google Scholar
Tsigkou, A. et al. High serum inhibin concentration discriminates autoimmune oophoritis from other forms of primary ovarian insufficiency. J. Clin. Endocrinol. Metab.93, 1263–1269 (2008). ArticleCASPubMed Google Scholar
La Marca, A. et al. Primary ovarian insufficiency due to steroidogenic cell autoimmunity is associated with a preserved pool of functioning follicles. J. Clin. Endocrinol. Metab.94, 3816–3823 (2009). ArticleCASPubMed Google Scholar
Gleicher, N., Weghofer, A. & Barad, D. H. A pilot study of premature ovarian senescence: II. Different genotype and phenotype for genetic and autoimmune etiologies. Fertil. Steril.91, 1707–1711 (2009). ArticleCASPubMed Google Scholar
Clowse, M. E. et al. Ovarian preservation by GnRH agonists during chemotherapy: a meta-analysis. J. Womens Health18, 311–319 (2009). Article Google Scholar
Nitzschke, M. et al. GnRH analogs do not protect ovaries from chemotherapy-induced ultrastructural injury in Hodgkin's lymphoma patients. Arch. Gynecol. Obstet.282, 83–88 (2010). ArticleCASPubMed Google Scholar
Sánchez-Serrano, M. et al. Twins born after transplantation of ovarian cortical tissue and oocyte vitrification. Fertil. Steril.93, 268.e11–268.e13 (2010). Article Google Scholar
Meirow, D. et al. Monitoring the ovaries after autotransplantation of cryopreserved ovarian tissue: endocrine studies, in vitro fertilization cycles, and live birth. Fertil. Steril.87, 418.e7–418.e15 (2007). Article Google Scholar
Janse, F. et al. Limited value of ovarian function markers following orthotopic transplantation of ovarian tissue after gonadotoxic treatment. J. Clin. Endocrinol. Metab.96, 1136–1144 (2011). ArticleCASPubMed Google Scholar
Schmidt, K. T. et al. Autotransplantation of cryopreserved ovarian tissue in 12 women with chemotherapy-induced premature ovarian failure: the Danish experience. Fertil. Steril.95, 695–701 (2011). ArticlePubMed Google Scholar
Lie Fong, S. et al. Assessment of ovarian reserve in adult childhood cancer survivors using anti-Müllerian hormone. Hum. Reprod.24, 982–990 (2009). ArticleCASPubMed Google Scholar
Rosendahl, M. et al. Ovarian function after removal of an entire ovary for cryopreservation of pieces of cortex prior to gonadotoxic treatment: a follow-up study. Hum. Reprod.23, 2475–2483 (2008). ArticlePubMed Google Scholar
van Beek, R. D. et al. Anti-Mullerian hormone is a sensitive serum marker for gonadal function in women treated for Hodgkin's lymphoma during childhood. J. Clin. Endocrinol. Metab.92, 3869–3874 (2007). ArticleCASPubMed Google Scholar
Bath, L. E., Wallace, W. H., Shaw, M. P., Fitzpatrick, C. & Anderson, R. A. Depletion of ovarian reserve in young women after treatment for cancer in childhood: detection by anti-Müllerian hormone, inhibin B and ovarian ultrasound. Hum. Reprod.18, 2368–2374 (2003). ArticleCASPubMed Google Scholar
Lie Fong, S. et al. Anti-müllerian hormone as a marker of ovarian function in women after chemotherapy and radiotherapy for haematological malignancies. Hum. Reprod.23, 674–678 (2008). ArticleCASPubMed Google Scholar
Su, H. I. et al. Antimullerian hormone and inhibin B are hormone measures of ovarian function in late reproductive-aged breast cancer survivors. Cancer116, 592–599 (2010). ArticleCASPubMed Google Scholar
Partridge, A. H. et al. Ovarian reserve in women who remain premenopausal after chemotherapy for early stage breast cancer. Fertil. Steril.94, 638–644 (2010). ArticlePubMed Google Scholar
Anderson, R. A., Themmen, A. P., Al-Qahtani, A., Groome, N. P. & Cameron, D. A. The effects of chemotherapy and long-term gonadotrophin suppression on the ovarian reserve in premenopausal women with breast cancer. Hum. Reprod.21, 2583–2592 (2006). ArticleCASPubMed Google Scholar
Yu, B. et al. Changes in markers of ovarian reserve and endocrine function in young women with breast cancer undergoing adjuvant chemotherapy. Cancer116, 2099–2105 (2010). CASPubMed Google Scholar
Rosendahl, M. et al. Dynamics and mechanisms of chemotherapy-induced ovarian follicular depletion in women of fertile age. Fertil. Steril.94, 156–166 (2010). ArticleCASPubMed Google Scholar
Anders, C. et al. A pilot study of predictive markers of chemotherapy-related amenorrhea among premenopausal women with early stage breast cancer. Cancer Invest.26, 286–295 (2008). ArticleCASPubMedPubMed Central Google Scholar
Anderson, R. A. & Cameron, D. A. Pretreatment serum anti-müllerian hormone predicts long-term ovarian function and bone mass after chemotherapy for early breast cancer. J. Clin. Endocrinol. Metab.96, 1336–1343 (2011). ArticleCASPubMed Google Scholar
Kaipia, A. & Hsueh, A. J. Regulation of ovarian follicle atresia. Annu. Rev. Physiol.59, 349–363 (1997). ArticleCASPubMed Google Scholar
Visser, J. A. AMH signaling: from receptor to target gene. Mol. Cell. Endocrinol.211, 65–73 (2003). ArticleCASPubMed Google Scholar
Erickson, G. F. & Shimasaki, S. The spatiotemporal expression pattern of the bone morphogenetic protein family in rat ovary cell types during the estrous cycle. Reprod. Biol. Endocrinol.1, 9 (2003). ArticlePubMedPubMed Central Google Scholar