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Volumn 67, Issue 6, 2006, Pages 557-566

Premature ovarian failure;L'insuffisance ovarienne prématurée

Author keywords

FMR1; Ovary; Premature ovarian failure; X chromosome

Indexed keywords

BONE MORPHOGENETIC PROTEIN 15; GONADOTROPIN; GROWTH DIFFERENTIATION FACTOR 9; STEROID 17ALPHA MONOOXYGENASE;

EID: 33845962386     PISSN: 00034266     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0003-4266(06)73007-4     Document Type: Review
Times cited : (20)

References (80)
  • 1
    • 0024444574 scopus 로고
    • Pregnancy in women with premature ovarian failure using tubal and intrauterine transfer of cryopreserved zygotes
    • Abdalla HI, Baber RJ, Kirkland A, Leonard T, Studd JW. Pregnancy in women with premature ovarian failure using tubal and intrauterine transfer of cryopreserved zygotes. Br J Obstet Gynaecol 1989 ; 96 : 1071-5.
    • (1989) Br J Obstet Gynaecol , vol.96 , pp. 1071-1075
    • Abdalla, H.I.1    Baber, R.J.2    Kirkland, A.3    Leonard, T.4    Studd, J.W.5
  • 2
    • 0025295238 scopus 로고
    • Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
    • Ahonen P, Myllarniemi S, Sipila I, Perheentupa J. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med 1990 ; 322 : 1829-36.
    • (1990) N Engl J Med , vol.322 , pp. 1829-1836
    • Ahonen, P.1    Myllarniemi, S.2    Sipila, I.3    Perheentupa, J.4
  • 3
    • 0029838761 scopus 로고    scopus 로고
    • Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene
    • Aittomaki K, Herva R, Stenman UH, et al. Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene. J Clin Endocrinol Metab 1996 ; 81 : 3722-6.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 3722-3726
    • Aittomaki, K.1    Herva, R.2    Stenman, U.H.3
  • 4
    • 0029118115 scopus 로고
    • Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
    • Aittomaki K, Lucena JL, Pakarinen P, et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 1995 ; 82 : 959-68.
    • (1995) Cell , vol.82 , pp. 959-968
    • Aittomaki, K.1    Lucena, J.L.2    Pakarinen, P.3
  • 5
    • 0033515496 scopus 로고    scopus 로고
    • Fragile X premutation is a significant risk factor for premature ovarian failure: The International Collaborative POF in Fragile X study-preliminary data
    • Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, 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 1999 ; 83 : 322-5.
    • (1999) Am J Med Genet , vol.83 , pp. 322-325
    • Allingham-Hawkins, D.J.1    Babul-Hirji, R.2    Chitayat, D.3
  • 6
    • 0029864808 scopus 로고    scopus 로고
    • A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23
    • Amati P, Gasparini P, Zlotogora J, et al. A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23. Am J Hum Genet 1996 ; 58 : 1089-92.
    • (1996) Am J Hum Genet , vol.58 , pp. 1089-1092
    • Amati, P.1    Gasparini, P.2    Zlotogora, J.3
  • 8
    • 0032190476 scopus 로고    scopus 로고
    • A novel phenotype related to partial loss of function mutations of the FSH receptor
    • Beau I, Touraine P, Meduri G, Gougeon A, Desroches A, et al. A novel phenotype related to partial loss of function mutations of the FSH receptor. J Clin Invest 1998 ; 102 : 1352-9.
    • (1998) J Clin Invest , vol.102 , pp. 1352-1359
    • Beau, I.1    Touraine, P.2    Meduri, G.3    Gougeon, A.4    Desroches, A.5
  • 9
    • 13544266419 scopus 로고    scopus 로고
    • Clinical and hormonal features of selective follicle-stimulating hormone (FSH) deficiency due to FSH beta-subunit gene mutations in both sexes
    • Berger K, Souza H, Brito VN, d'Alva CB, Mendonca BB, Latronico AC. Clinical and hormonal features of selective follicle-stimulating hormone (FSH) deficiency due to FSH beta-subunit gene mutations in both sexes. Fertil Steril 2005 ; 83 : 466-70.
    • (2005) Fertil Steril , vol.83 , pp. 466-470
    • Berger, K.1    Souza, H.2    Brito, V.N.3    d'Alva, C.B.4    Mendonca, B.B.5    Latronico, A.C.6
  • 10
    • 17344369363 scopus 로고    scopus 로고
    • A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: Evidence for conserved function in oogenesis and implications for human sterility
    • Bione S, Sala C, Manzini C, et al. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. Am J Hum Genet 1998 ; 62 : 533-41.
    • (1998) Am J Hum Genet , vol.62 , pp. 533-541
    • Bione, S.1    Sala, C.2    Manzini, C.3
  • 11
    • 0029855881 scopus 로고    scopus 로고
    • The pathophysiology and genetics of congenital lipoid adrenal hyperplasia. International Congenital Lipoid Adrenal Hyperplasia Consortium
    • Bose HS, Sugawara T, Strauss JF, Miller WL. The pathophysiology and genetics of congenital lipoid adrenal hyperplasia. International Congenital Lipoid Adrenal Hyperplasia Consortium. N Engl J Med 1996 ; 335 : 1870-8
    • (1996) N Engl J Med , vol.335 , pp. 1870-1878
    • Bose, H.S.1    Sugawara, T.2    Strauss, J.F.3    Miller, W.L.4
  • 12
    • 0031809893 scopus 로고    scopus 로고
    • Fragile X premutation screening in women with premature ovarian failure
    • Conway GS, Payne NN, Webb J, Murray A, Jacobs PA. Fragile X premutation screening in women with premature ovarian failure. Hum Reprod 1998 ; 13 : 1184-7.
    • (1998) Hum Reprod , vol.13 , pp. 1184-1187
    • Conway, G.S.1    Payne, N.N.2    Webb, J.3    Murray, A.4    Jacobs, P.A.5
  • 13
    • 0034508805 scopus 로고    scopus 로고
    • Premature ovarian failure
    • Conway GS. Premature ovarian failure. Br Med Bull 2000 ; 56 : 643-9.
    • (2000) Br Med Bull , vol.56 , pp. 643-649
    • Conway, G.S.1
  • 15
    • 0030059908 scopus 로고    scopus 로고
    • Predicting age at menopause
    • Cramer DW, Xu H. Predicting age at menopause. Maturitas 1996 ; 23 : 319-26.
    • (1996) Maturitas , vol.23 , pp. 319-326
    • Cramer, D.W.1    Xu, H.2
  • 16
    • 0029127258 scopus 로고
    • Family history as a predictor of early menopause
    • Cramer DW, Xu H, Harlow BL. Family history as a predictor of early menopause. Fertil Steril 1995 ; 64 : 740-5.
    • (1995) Fertil Steril , vol.64 , pp. 740-745
    • Cramer, D.W.1    Xu, H.2    Harlow, B.L.3
  • 17
    • 0035131812 scopus 로고    scopus 로고
    • The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
    • Crisponi L, Deiana M, Loi A, et al. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet 2001 ; 27 : 159-66.
    • (2001) Nat Genet , vol.27 , pp. 159-166
    • Crisponi, L.1    Deiana, M.2    Loi, A.3
  • 18
    • 20444365482 scopus 로고    scopus 로고
    • Premature ovarian failure and forkhead transcription factor FOXL2: Blepharophimosis-ptosis- epicantus inversus syndrome and ovarian dysfunction
    • de Baere E, Copelli S, Caburet S, Laissue P, Beysen D et al. Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis- epicantus inversus syndrome and ovarian dysfunction. Pediatr Endocrinol Rev 2005 ; 2 : 653-60.
    • (2005) Pediatr Endocrinol Rev , vol.2 , pp. 653-660
    • de Baere, E.1    Copelli, S.2    Caburet, S.3    Laissue, P.4    Beysen, D.5
  • 19
    • 0034815279 scopus 로고    scopus 로고
    • The role of genetic factors in age at natural menopause
    • de Bruin JP, Bovenhuis H, Van Noord PA et al. The role of genetic factors in age at natural menopause. Hum Reprod 2001 ; 16 : 2014-8.
    • (2001) Hum Reprod , vol.16 , pp. 2014-2018
    • de Bruin, J.P.1    Bovenhuis, H.2    Van Noord, P.A.3
  • 20
    • 3042601976 scopus 로고    scopus 로고
    • Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene
    • Di Pasquale E, Beck-Peccoz P, Persani L. Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene. Am J Hum Genet 2004 ; 75 : 106-11.
    • (2004) Am J Hum Genet , vol.75 , pp. 106-111
    • Di Pasquale, E.1    Beck-Peccoz, P.2    Persani, L.3
  • 21
    • 33646389819 scopus 로고    scopus 로고
    • Identification of new variants of human BMP15 in a large cohort with premature ovarian failure
    • di Pasquale Rossetti R, Marozzi A et al. Identification of new variants of human BMP15 in a large cohort with premature ovarian failure. J Clin Endocrinol Metab 2006 ; 91 : 1976-9.
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 1976-1979
    • di Pasquale Rossetti, R.1    Marozzi, A.2
  • 22
    • 27944490382 scopus 로고    scopus 로고
    • Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure
    • Dixit H, Rao LK, Padmalatha V, et al. Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure. Menopause 2005 ; 12 : 749-54.
    • (2005) Menopause , vol.12 , pp. 749-754
    • Dixit, H.1    Rao, L.K.2    Padmalatha, V.3
  • 23
    • 5144225480 scopus 로고    scopus 로고
    • Livebirth after orthotopic transplantation of cryopreserved ovarian tissue
    • Donnez J, Dolmans MM. Livebirth after orthotopic transplantation of cryopreserved ovarian tissue. Lancet 2004 : 364 : 2092-3.
    • (2004) Lancet , vol.364 , pp. 2092-2093
    • Donnez, J.1    Dolmans, M.M.2
  • 25
    • 0027064693 scopus 로고
    • Accelerated disappearance of ovarian follicles in mid-life: Implications for forecasting menopause
    • Faddy MJ, Gosden RG, Gougeon A, Richardson SJ, Nelson JF. Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Hum Reprod 1992 ; 7 : 1342-6.
    • (1992) Hum Reprod , vol.7 , pp. 1342-1346
    • Faddy, M.J.1    Gosden, R.G.2    Gougeon, A.3    Richardson, S.J.4    Nelson, J.F.5
  • 26
    • 2642617816 scopus 로고    scopus 로고
    • Prevalence, specificity, significance of ovarian antibodies during spontaneous premature ovarian failure
    • Fenichel P. Prevalence, specificity, significance of ovarian antibodies during spontaneous premature ovarian failure. Hum Reprod 1997 ; 12 : 2623-28.
    • (1997) Hum Reprod , vol.12 , pp. 2623-2628
    • Fenichel, P.1
  • 28
    • 0038677908 scopus 로고    scopus 로고
    • Fertility in young women after chemotherapy with alkylating agents for Hodgkin and non-Hodgkin lymphomas
    • Franchi-Razgui P, Rousselot P, Espie M et al. Fertility in young women after chemotherapy with alkylating agents for Hodgkin and non-Hodgkin lymphomas. Hematol J 2003 ; 4 : 116-20.
    • (2003) Hematol J , vol.4 , pp. 116-120
    • Franchi-Razgui, P.1    Rousselot, P.2    Espie, M.3
  • 29
    • 0033917569 scopus 로고    scopus 로고
    • Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner
    • Galloway SM, Mcnatty KP, Cambridge LM et al. Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nat Genet 2000 ; 25 : 279-83.
    • (2000) Nat Genet , vol.25 , pp. 279-283
    • Galloway, S.M.1    Mcnatty, K.P.2    Cambridge, L.M.3
  • 31
    • 20444446397 scopus 로고    scopus 로고
    • Assessing the emotional needs of women with spontaneous premature ovarian failure
    • Groff AA, Covington SN, Halverson LR et al. Assessing the emotional needs of women with spontaneous premature ovarian failure. Fertil Steril 2005 ; 83 : 1734-41.
    • (2005) Fertil Steril , vol.83 , pp. 1734-1741
    • Groff, A.A.1    Covington, S.N.2    Halverson, L.R.3
  • 32
    • 32144433506 scopus 로고    scopus 로고
    • INHA promoter polymorphisms are associated with premature ovarian failure
    • Harris SE, Chand AL, Winship IM et al. INHA promoter polymorphisms are associated with premature ovarian failure. Mol Hum Reprod 2005 ; 11 : 779-84.
    • (2005) Mol Hum Reprod , vol.11 , pp. 779-784
    • Harris, S.E.1    Chand, A.L.2    Winship, I.M.3
  • 33
    • 30544431725 scopus 로고    scopus 로고
    • Bilateral oophorectomy and premature menopause
    • Hendrix SL. Bilateral oophorectomy and premature menopause. Am J Med 2005 ; 118 : 131-5.
    • (2005) Am J Med , vol.118 , pp. 131-135
    • Hendrix, S.L.1
  • 34
    • 24644461526 scopus 로고    scopus 로고
    • Mutations in human gonadotropin and gonadotropin-receptor genes
    • Huhtaniemi IT, Themmen AP. Mutations in human gonadotropin and gonadotropin-receptor genes. Endocrine 2005 ; 26 : 207-17.
    • (2005) Endocrine , vol.26 , pp. 207-217
    • Huhtaniemi, I.T.1    Themmen, A.P.2
  • 35
    • 0000549995 scopus 로고    scopus 로고
    • Jacobs PA, Baikie AG, Brown WM, Macgregor TN, Maclean N, Harnden DG. Evidence for the existence of the human super female. Lancet 1959 ; 2 : 423-5.
    • Jacobs PA, Baikie AG, Brown WM, Macgregor TN, Maclean N, Harnden DG. Evidence for the existence of the human "super female". Lancet 1959 ; 2 : 423-5.
  • 36
    • 1642349298 scopus 로고    scopus 로고
    • Germline stem cells and follicular renewal in the postnatal mammalian ovary
    • Johnson J, Canning J, Kaneko T, Pru JK, Tilly JL. Germline stem cells and follicular renewal in the postnatal mammalian ovary. Nature 2004 ; 428 : 145-50.
    • (2004) Nature , vol.428 , pp. 145-150
    • Johnson, J.1    Canning, J.2    Kaneko, T.3    Pru, J.K.4    Tilly, J.L.5
  • 37
    • 28744434744 scopus 로고    scopus 로고
    • A pilot study of an investigational testosterone transdermal patch system in young women with spontaneous premature ovarian failure
    • Kalantaridou SN, Calis KA, Mazer NA, Godoy H, Nelson LM. A pilot study of an investigational testosterone transdermal patch system in young women with spontaneous premature ovarian failure. J Clin Endocrinol Metab 2005 ; 90 : 6549-52.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 6549-6552
    • Kalantaridou, S.N.1    Calis, K.A.2    Mazer, N.A.3    Godoy, H.4    Nelson, L.M.5
  • 40
    • 0032715145 scopus 로고    scopus 로고
    • Premature ovarian failure: A systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy
    • Van Kasteren YM, Schoemaker J. Premature ovarian failure: a systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy. Hum Reprod Update 1999 ; 5 : 483-92.
    • (1999) Hum Reprod Update , vol.5 , pp. 483-492
    • Van Kasteren, Y.M.1    Schoemaker, J.2
  • 42
    • 0024160813 scopus 로고
    • Spontaneous and pharmacologically induced remissions in patients with premature ovarian failure
    • Kreiner D, Droesch K, Navot D, Scott R, Rosenwaks Z. Spontaneous and pharmacologically induced remissions in patients with premature ovarian failure. Obstet Gynecol 1988 ; 72 : 926-8.
    • (1988) Obstet Gynecol , vol.72 , pp. 926-928
    • Kreiner, D.1    Droesch, K.2    Navot, D.3    Scott, R.4    Rosenwaks, Z.5
  • 43
    • 33744519199 scopus 로고    scopus 로고
    • mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure
    • Laissue P, Christin-Maitre S, Touraine P, Kuttenn F et al. mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. Eur J Endocrinol 2006 ; 154 : 1-6.
    • (2006) Eur J Endocrinol , vol.154 , pp. 1-6
    • Laissue, P.1    Christin-Maitre, S.2    Touraine, P.3    Kuttenn, F.4
  • 45
    • 0037248189 scopus 로고    scopus 로고
    • Premature menopause in a muti-ethnic population study of the menopause transition
    • Luborsky JL, Meyer P, Sowers MF, Gold EB, Santoro N. Premature menopause in a muti-ethnic population study of the menopause transition. Hum Reprod 2003 ; 18 : 199-206.
    • (2003) Hum Reprod , vol.18 , pp. 199-206
    • Luborsky, J.L.1    Meyer, P.2    Sowers, M.F.3    Gold, E.B.4    Santoro, N.5
  • 46
    • 0030806302 scopus 로고    scopus 로고
    • Zfx mutation results in small animal size and reduced germ cell number in male and female mice
    • Luoh SW, Bain PA, Polakiewicz RD, et al. Zfx mutation results in small animal size and reduced germ cell number in male and female mice. Development 1997 ; 124 : 2275-84.
    • (1997) Development , vol.124 , pp. 2275-2284
    • Luoh, S.W.1    Bain, P.A.2    Polakiewicz, R.D.3
  • 48
    • 0036150943 scopus 로고    scopus 로고
    • Ligand activation of the aromatic hydrocarbon receptor transcription factor drives Bax-dependent apoptosis in developing fetal ovarian germ cells
    • Matikainen TM, Moriyama T, Morita Y et al. Ligand activation of the aromatic hydrocarbon receptor transcription factor drives Bax-dependent apoptosis in developing fetal ovarian germ cells. Endocrinology 2002 ; 143 : 615-20.
    • (2002) Endocrinology , vol.143 , pp. 615-620
    • Matikainen, T.M.1    Moriyama, T.2    Morita, Y.3
  • 49
    • 0029896535 scopus 로고    scopus 로고
    • The normal menopause transition: An overview
    • Mckinlay SM. The normal menopause transition: an overview. Maturitas 1996 ; 23 : 137-45.
    • (1996) Maturitas , vol.23 , pp. 137-145
    • Mckinlay, S.M.1
  • 50
    • 0042384795 scopus 로고    scopus 로고
    • Delayed puberty and primary amenorrhea associated with a novel mutation of the human follicle-stimulating hormone receptor: Clinical, histological, and molecular studies
    • Meduri G, Touraine P, Beau I et al. Delayed puberty and primary amenorrhea associated with a novel mutation of the human follicle-stimulating hormone receptor: clinical, histological, and molecular studies. J Clin Endocrinol Metab 2003 ; 88 : 3491-8.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 3491-3498
    • Meduri, G.1    Touraine, P.2    Beau, I.3
  • 51
    • 0029946572 scopus 로고    scopus 로고
    • Gonadal (ovarian) dysgenesis in 46, XX individuals: Frequency of the autosomal recessive form
    • Meyers CM, Boughman JA, Rivas M, Wilroy RS, Simpson JL. Gonadal (ovarian) dysgenesis in 46, XX individuals: frequency of the autosomal recessive form. Am J Med Genet 1996 ; 63 : 518-24.
    • (1996) Am J Med Genet , vol.63 , pp. 518-524
    • Meyers, C.M.1    Boughman, J.A.2    Rivas, M.3    Wilroy, R.S.4    Simpson, J.L.5
  • 52
    • 0028792229 scopus 로고
    • Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens
    • Morishima A, Grumbach MM, Simpson ER, Fisher C, QIN K. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. J Clin Endocrinol Metab 1995 ; 80 : 3689-98.
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 3689-3698
    • Morishima, A.1    Grumbach, M.M.2    Simpson, E.R.3    Fisher, C.4    QIN, K.5
  • 53
    • 0032826352 scopus 로고    scopus 로고
    • Microdeletions in FMR2 may be a significant cause of premature ovarian failure
    • Murray A, Webb J, Dennis N, Conway G, Morton N. Microdeletions in FMR2 may be a significant cause of premature ovarian failure. J Med Genet 1999 ; 36 : 767-70.
    • (1999) J Med Genet , vol.36 , pp. 767-770
    • Murray, A.1    Webb, J.2    Dennis, N.3    Conway, G.4    Morton, N.5
  • 54
    • 0031857007 scopus 로고    scopus 로고
    • Studies of FRAXA and FRAXE in women with premature ovarian failure
    • Murray A, Webb J, Grimley S, Conway G, Jacobs P. Studies of FRAXA and FRAXE in women with premature ovarian failure. J Med Genet 1998 ; 35 : 637-40.
    • (1998) J Med Genet , vol.35 , pp. 637-640
    • Murray, A.1    Webb, J.2    Grimley, S.3    Conway, G.4    Jacobs, P.5
  • 55
    • 16944367194 scopus 로고    scopus 로고
    • Positional cloning of the APECED gene
    • Nagamine K, Peterson P, Scott HS et al. Positional cloning of the APECED gene. Nat Genet 1997 ; 17 : 393-8.
    • (1997) Nat Genet , vol.17 , pp. 393-398
    • Nagamine, K.1    Peterson, P.2    Scott, H.S.3
  • 56
    • 85058720212 scopus 로고    scopus 로고
    • Livebirth after orthotopic transplantation of ovarian tissue
    • Oktay K, Tilly J. Livebirth after orthotopic transplantation of ovarian tissue. Lancet 2004 ; 364 : 2091-2.
    • (2004) Lancet , vol.364 , pp. 2091-2092
    • Oktay, K.1    Tilly, J.2
  • 57
    • 0028087750 scopus 로고
    • Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature
    • Powell CM, Taggart RT, Drumheller TC et al. Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature. Am J Med Genet 1994 ; 52 : 19-26.
    • (1994) Am J Med Genet , vol.52 , pp. 19-26
    • Powell, C.M.1    Taggart, R.T.2    Drumheller, T.C.3
  • 58
    • 0037221590 scopus 로고    scopus 로고
    • frequency and risk factors among women attending a network of menopause clinics in Italy. B
    • Progetto Menopausa Italia Study Group Premature ovarian failure
    • Progetto Menopausa Italia Study Group Premature ovarian failure: frequency and risk factors among women attending a network of menopause clinics in Italy. B J Obstet Gynecol 2003 ; 110 : 59-63.
    • (2003) J Obstet Gynecol , vol.110 , pp. 59-63
  • 59
    • 0033934014 scopus 로고    scopus 로고
    • Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene
    • Prueitt RL, Ross JL, Zinn AR. Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene. Cytogenet Cell Genet 2000 ; 89 : 44-50.
    • (2000) Cytogenet Cell Genet , vol.89 , pp. 44-50
    • Prueitt, R.L.1    Ross, J.L.2    Zinn, A.R.3
  • 60
    • 0026582201 scopus 로고
    • Pseudoautosomal repeat displays higher variability in blacks than in Caucasians
    • Rappold GA, Henke A, Pohlschmid M, Huisman TH. Pseudoautosomal repeat displays higher variability in blacks than in Caucasians. Hum Genet 1992 ; 88 : 573-8.
    • (1992) Hum Genet , vol.88 , pp. 573-578
    • Rappold, G.A.1    Henke, A.2    Pohlschmid, M.3    Huisman, T.H.4
  • 61
    • 33646496697 scopus 로고    scopus 로고
    • Chromosomal rearrangements in Xq and premature ovarian failure: Mapping of 25 new cases and review of the literature
    • Rizzolio F, Bione S, Sala C et al. Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature. Hum Reprod 2006 ; 21 : 1477-83.
    • (2006) Hum Reprod , vol.21 , pp. 1477-1483
    • Rizzolio, F.1    Bione, S.2    Sala, C.3
  • 62
    • 0035993342 scopus 로고    scopus 로고
    • Growth and ovarian function in girls with 48, XXXX karyotype - patient report and review of the literature
    • Rooman RP, Van Driessche K, Du Caju MV. Growth and ovarian function in girls with 48, XXXX karyotype - patient report and review of the literature. J Pediatr Endocrinol Metab 2002 ; 15 : 1051-5.
    • (2002) J Pediatr Endocrinol Metab , vol.15 , pp. 1051-1055
    • Rooman, R.P.1    Van Driessche, K.2    Du Caju, M.V.3
  • 63
    • 0031568876 scopus 로고    scopus 로고
    • Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21
    • Sala C, Arrigo G, Torri G et al. Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21. Genomics 1997 ; 40 : 123-31.
    • (1997) Genomics , vol.40 , pp. 123-131
    • Sala, C.1    Arrigo, G.2    Torri, G.3
  • 64
    • 0034534985 scopus 로고    scopus 로고
    • Inhibin: A candidate gene for premature ovarian failure
    • Shelling AN, Burton KA, Chand AL et al. Inhibin: a candidate gene for premature ovarian failure. Hum Reprod 2000 ; 15 : 2644-9.
    • (2000) Hum Reprod , vol.15 , pp. 2644-2649
    • Shelling, A.N.1    Burton, K.A.2    Chand, A.L.3
  • 65
    • 21744449936 scopus 로고    scopus 로고
    • Woman gives birth after receiving transplant of her own ovarian tissue
    • Siegel-Itzkovich J. Woman gives birth after receiving transplant of her own ovarian tissue. BMJ 2005 ; 331 : 70.
    • (2005) BMJ , vol.331 , pp. 70
    • Siegel-Itzkovich, J.1
  • 66
    • 0033616191 scopus 로고    scopus 로고
    • Ovarian differentiation and gonadal failure
    • Simpson JL, Rajkovic A. Ovarian differentiation and gonadal failure. Am J Med Genet 1999 ; 89 : 186-200.
    • (1999) Am J Med Genet , vol.89 , pp. 186-200
    • Simpson, J.L.1    Rajkovic, A.2
  • 67
    • 0013925220 scopus 로고
    • The anatomy and histology of XO human embryos and fetuses
    • Singh RP, Carr DH. The anatomy and histology of XO human embryos and fetuses. Anat Rec 1966 ; 155 : 369-83.
    • (1966) Anat Rec , vol.155 , pp. 369-383
    • Singh, R.P.1    Carr, D.H.2
  • 68
    • 0031760136 scopus 로고    scopus 로고
    • Genes control the cessation of a woman's reproductive life: A twin study of hysterectomy and age at menopause
    • Snieder H, Mac Gregor AJ, Spector TD. Genes control the cessation of a woman's reproductive life: a twin study of hysterectomy and age at menopause. J Clin Endocrinol Metab 1998 ; 83 : 1875-80.
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 1875-1880
    • Snieder, H.1    Mac Gregor, A.J.2    Spector, T.D.3
  • 69
    • 33645813159 scopus 로고    scopus 로고
    • Controversial role of inhibin alpha-subunit gene in the aetiology of premature ovarian failure
    • Sundblad V, Chiauzzi VA, Andreone L, Campo S, Charreau EH, Dain L. Controversial role of inhibin alpha-subunit gene in the aetiology of premature ovarian failure. Hum Reprod 2006 ; 21 : 1154-60.
    • (2006) Hum Reprod , vol.21 , pp. 1154-1160
    • Sundblad, V.1    Chiauzzi, V.A.2    Andreone, L.3    Campo, S.4    Charreau, E.H.5    Dain, L.6
  • 70
    • 0026865445 scopus 로고
    • Characterisation of a new rare fragile site easily confused with the fragile X
    • Sutherland GR, Baker E. Characterisation of a new rare fragile site easily confused with the fragile X. Hum Mol Genet 1992 ; 1 : 111-3.
    • (1992) Hum Mol Genet , vol.1 , pp. 111-113
    • Sutherland, G.R.1    Baker, E.2
  • 72
    • 0027440971 scopus 로고
    • Deletion (X) (q26.1→q28) in a proband and her mother: Molecular characterization and phenotypic-karyotypic deductions
    • Tharapel AT, Anderson KP, Simpson JL et al. Deletion (X) (q26.1→q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. Am J Hum Genet 1993 ; 52 : 463-71.
    • (1993) Am J Hum Genet , vol.52 , pp. 463-471
    • Tharapel, A.T.1    Anderson, K.P.2    Simpson, J.L.3
  • 73
    • 0025092789 scopus 로고
    • The critical region on the human Xq
    • Therman E, Laxova R, Susman B. The critical region on the human Xq. Hum Genet 1990 ; 85 : 455-61.
    • (1990) Hum Genet , vol.85 , pp. 455-461
    • Therman, E.1    Laxova, R.2    Susman, B.3
  • 75
    • 0033305435 scopus 로고    scopus 로고
    • New natural inactivating mutations of the follicle-stimulating hormone receptor: Correlations between receptor function and phenotype
    • Touraine P, Beau I, Gougeon A, et al. New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype. Mol Endocrinol 1999 ; 13 : 1844-54.
    • (1999) Mol Endocrinol , vol.13 , pp. 1844-1854
    • Touraine, P.1    Beau, I.2    Gougeon, A.3
  • 76
    • 0032480627 scopus 로고    scopus 로고
    • Genetic influences on the age at menopause
    • Treloar SA, Do KA, Martin NG. Genetic influences on the age at menopause. Lancet 1998 ; 352 : 1084-5.
    • (1998) Lancet , vol.352 , pp. 1084-1085
    • Treloar, S.A.1    Do, K.A.2    Martin, N.G.3
  • 78
    • 0025648036 scopus 로고
    • Long-term prognosis in galactosaemia: Results of a survey of 350 cases
    • Waggoner DD, Buist NR, Donnell GN. Long-term prognosis in galactosaemia: results of a survey of 350 cases. J Inherit Metab Dis 1990 ; 13 : 802-18.
    • (1990) J Inherit Metab Dis , vol.13 , pp. 802-818
    • Waggoner, D.D.1    Buist, N.R.2    Donnell, G.N.3
  • 79
    • 0016671640 scopus 로고
    • Mumps and the menopause
    • Wood C. Mumps and the menopause. Br J Sex Med 1975 ; 2 : 19.
    • (1975) Br J Sex Med , vol.2 , pp. 19
    • Wood, C.1
  • 80
    • 0032103696 scopus 로고    scopus 로고
    • Turner syndrome and haploinsufficiency
    • Zinn AR, Ross JL. Turner syndrome and haploinsufficiency. Curr Opin Genet Dev 1998 ; 8 : 322-7.
    • (1998) Curr Opin Genet Dev , vol.8 , pp. 322-327
    • Zinn, A.R.1    Ross, J.L.2


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