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Volumn 58, Issue 5, 2011, Pages 1181-1200

Etiology and Treatment of Hypogonadism in Adolescents

Author keywords

Adolescents; Delayed puberty; Hypergonadotropic hypogonadism; Hypogonadotropic hypogonadism; Treatment

Indexed keywords

ANDRIO; ASPARAGINASE; CELL NUCLEUS RECEPTOR; CONJUGATED ESTROGEN; ESTRADIOL; ESTROGEN; ETHINYLESTRADIOL; LEPTIN; LEPTIN RECEPTOR; MEDROXYPROGESTERONE; MERCAPTOPURINE; METHOTREXATE; PIPERAZINE ESTRONE SULFATE; PREDNISOLONE; SEX HORMONE; TESTOPEL; TESTOSTERONE; TESTOSTERONE CIPIONATE; TESTOSTERONE ENANTATE; TESTOSTERONE ESTER; TESTOSTERONE UNDECANOATE; UNCLASSIFIED DRUG; VINCRISTINE;

EID: 80053596392     PISSN: 00313955     EISSN: 15578240     Source Type: Journal    
DOI: 10.1016/j.pcl.2011.07.009     Document Type: Review
Times cited : (56)

References (116)
  • 1
    • 0015518769 scopus 로고
    • Synchronization of augmented luteinizing hormone secretion with sleep during puberty
    • Boyar R., Finkelstein J., Roffwarg H., et al. Synchronization of augmented luteinizing hormone secretion with sleep during puberty. N Engl J Med 1972, 287(12):582-586.
    • (1972) N Engl J Med , vol.287 , Issue.12 , pp. 582-586
    • Boyar, R.1    Finkelstein, J.2    Roffwarg, H.3
  • 2
    • 0027538106 scopus 로고
    • Gonadotropin-releasing hormone pulse generator activity during pubertal transition in girls: pulsatile and diurnal patterns of circulating gonadotropins
    • Apter D., Butzow T.L., Laughlin G.A., et al. Gonadotropin-releasing hormone pulse generator activity during pubertal transition in girls: pulsatile and diurnal patterns of circulating gonadotropins. J Clin Endocrinol Metab 1993, 76(4):940-949.
    • (1993) J Clin Endocrinol Metab , vol.76 , Issue.4 , pp. 940-949
    • Apter, D.1    Butzow, T.L.2    Laughlin, G.A.3
  • 3
    • 0036280914 scopus 로고    scopus 로고
    • Delayed puberty: analysis of a large case series from an academic center
    • Sedlmeyer I.L., Palmert M.R. Delayed puberty: analysis of a large case series from an academic center. J Clin Endocrinol Metab 2002, 87(4):1613-1620.
    • (2002) J Clin Endocrinol Metab , vol.87 , Issue.4 , pp. 1613-1620
    • Sedlmeyer, I.L.1    Palmert, M.R.2
  • 4
    • 0026353138 scopus 로고
    • Constitutional delay of growth and puberty: do they really reach their target height?
    • von Kalckreuth G., Haverkamp F., Kessler M., et al. Constitutional delay of growth and puberty: do they really reach their target height?. Horm Res 1991, 35(6):222-225.
    • (1991) Horm Res , vol.35 , Issue.6 , pp. 222-225
    • von Kalckreuth, G.1    Haverkamp, F.2    Kessler, M.3
  • 5
    • 0029016324 scopus 로고
    • Long term treatment with low dose testosterone in constitutional delay of growth and puberty: effect on bone age maturation and pubertal progression
    • Bergada I., Bergada C. Long term treatment with low dose testosterone in constitutional delay of growth and puberty: effect on bone age maturation and pubertal progression. J Pediatr Endocrinol Metab 1995, 8(2):117-122.
    • (1995) J Pediatr Endocrinol Metab , vol.8 , Issue.2 , pp. 117-122
    • Bergada, I.1    Bergada, C.2
  • 6
    • 0035919206 scopus 로고    scopus 로고
    • Inherited disorders of the gonadotropin hormones
    • Achermann J.C., Weiss J., Lee E.J., et al. Inherited disorders of the gonadotropin hormones. Mol Cell Endocrinol 2001, 179(1-2):89-96.
    • (2001) Mol Cell Endocrinol , vol.179 , Issue.1-2 , pp. 89-96
    • Achermann, J.C.1    Weiss, J.2    Lee, E.J.3
  • 7
    • 38149046500 scopus 로고    scopus 로고
    • Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46, XY patients with severe underandrogenization but without adrenal insufficiency
    • Kohler B., Lin L., Ferraz-de-Souza B., et al. Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46, XY patients with severe underandrogenization but without adrenal insufficiency. Hum Mutat 2008, 29(1):59-64.
    • (2008) Hum Mutat , vol.29 , Issue.1 , pp. 59-64
    • Kohler, B.1    Lin, L.2    Ferraz-de-Souza, B.3
  • 8
    • 0033623571 scopus 로고    scopus 로고
    • Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency
    • Biason-Lauber A., Schoenle E.J. Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency. Am J Hum Genet 2000, 67(6):1563-1568.
    • (2000) Am J Hum Genet , vol.67 , Issue.6 , pp. 1563-1568
    • Biason-Lauber, A.1    Schoenle, E.J.2
  • 9
    • 0028598360 scopus 로고
    • Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
    • Muscatelli F., Strom T.M., Walker A.P., et al. Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature 1994, 372(6507):672-676.
    • (1994) Nature , vol.372 , Issue.6507 , pp. 672-676
    • Muscatelli, F.1    Strom, T.M.2    Walker, A.P.3
  • 10
    • 59449097715 scopus 로고    scopus 로고
    • Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene
    • Yang F., Hanaki K., Kinoshita T., et al. Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene. Eur J Pediatr 2009, 168:329-331.
    • (2009) Eur J Pediatr , vol.168 , pp. 329-331
    • Yang, F.1    Hanaki, K.2    Kinoshita, T.3
  • 11
    • 0029809471 scopus 로고    scopus 로고
    • Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalamic and pituitary defects in gonadotropin production
    • Habiby R.L., Boepple P., Nachtigall L., et al. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalamic and pituitary defects in gonadotropin production. J Clin Invest 1996, 98(4):1055-1062.
    • (1996) J Clin Invest , vol.98 , Issue.4 , pp. 1055-1062
    • Habiby, R.L.1    Boepple, P.2    Nachtigall, L.3
  • 12
    • 33744523194 scopus 로고    scopus 로고
    • DAX1 and X-linked adrenal hypoplasia congenita: clinical and molecular analysis in five patients
    • Mantovani G., De Menis E., Borretta G., et al. DAX1 and X-linked adrenal hypoplasia congenita: clinical and molecular analysis in five patients. Eur J Endocrinol 2006, 154(5):685-689.
    • (2006) Eur J Endocrinol , vol.154 , Issue.5 , pp. 685-689
    • Mantovani, G.1    De Menis, E.2    Borretta, G.3
  • 13
    • 0025938481 scopus 로고
    • A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
    • Franco B., Guioli S., Pragliola A., et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature 1991, 353(6344):529-536.
    • (1991) Nature , vol.353 , Issue.6344 , pp. 529-536
    • Franco, B.1    Guioli, S.2    Pragliola, A.3
  • 14
    • 0028353887 scopus 로고
    • Kallman syndrome versus idiopathic hypogonadotropic hypogonadism at MR imaging
    • Vogl T.J., Stemmler J., Heye B., et al. Kallman syndrome versus idiopathic hypogonadotropic hypogonadism at MR imaging. Radiology 1994, 191(1):53-57.
    • (1994) Radiology , vol.191 , Issue.1 , pp. 53-57
    • Vogl, T.J.1    Stemmler, J.2    Heye, B.3
  • 15
    • 17744373868 scopus 로고    scopus 로고
    • The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics
    • Oliveira L.M., Seminara S.B., Beranova M., et al. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. J Clin Endocrinol Metab 2001, 86(4):1532-1538.
    • (2001) J Clin Endocrinol Metab , vol.86 , Issue.4 , pp. 1532-1538
    • Oliveira, L.M.1    Seminara, S.B.2    Beranova, M.3
  • 16
    • 12144288744 scopus 로고    scopus 로고
    • Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients
    • Sato N., Katsumata N., Kagami M., et al. Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients. J Clin Endocrinol Metab 2004, 89(3):1079-1088.
    • (2004) J Clin Endocrinol Metab , vol.89 , Issue.3 , pp. 1079-1088
    • Sato, N.1    Katsumata, N.2    Kagami, M.3
  • 17
    • 36849044530 scopus 로고    scopus 로고
    • Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
    • Pitteloud N., Zhang C., Pignatelli D., et al. Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc Natl Acad Sci U S A 2007, 104(44):17447-17452.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , Issue.44 , pp. 17447-17452
    • Pitteloud, N.1    Zhang, C.2    Pignatelli, D.3
  • 18
    • 0030698188 scopus 로고    scopus 로고
    • A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
    • de Roux N., Young J., Misrahi M., et al. A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor. N Engl J Med 1997, 337(22):1597-1602.
    • (1997) N Engl J Med , vol.337 , Issue.22 , pp. 1597-1602
    • de Roux, N.1    Young, J.2    Misrahi, M.3
  • 19
    • 0035919208 scopus 로고    scopus 로고
    • Inherited disorders of GnRH and gonadotropin receptors
    • de Roux N., Milgrom E. Inherited disorders of GnRH and gonadotropin receptors. Mol Cell Endocrinol 2001, 179(1-2):83-87.
    • (2001) Mol Cell Endocrinol , vol.179 , Issue.1-2 , pp. 83-87
    • de Roux, N.1    Milgrom, E.2
  • 20
    • 0141814637 scopus 로고    scopus 로고
    • Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
    • de Roux N., Genin E., Carel J.C., et al. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci U S A 2003, 100(19):10972-10976.
    • (2003) Proc Natl Acad Sci U S A , vol.100 , Issue.19 , pp. 10972-10976
    • de Roux, N.1    Genin, E.2    Carel, J.C.3
  • 21
    • 34548331152 scopus 로고    scopus 로고
    • Reversal of idiopathic hypogonadotropic hypogonadism
    • Raivio T., Falardeau J., Dwyer A., et al. Reversal of idiopathic hypogonadotropic hypogonadism. N Engl J Med 2007, 357(9):863-873.
    • (2007) N Engl J Med , vol.357 , Issue.9 , pp. 863-873
    • Raivio, T.1    Falardeau, J.2    Dwyer, A.3
  • 22
    • 0342905437 scopus 로고    scopus 로고
    • Combined pituitary hormone deficiency: role of Pit-1 and Prop-1
    • Pfaffle R.W., Blankenstein O., Wuller S., et al. Combined pituitary hormone deficiency: role of Pit-1 and Prop-1. Acta Paediatr Suppl 1999, 88(433):33-41.
    • (1999) Acta Paediatr Suppl , vol.88 , Issue.433 , pp. 33-41
    • Pfaffle, R.W.1    Blankenstein, O.2    Wuller, S.3
  • 23
    • 0345257809 scopus 로고    scopus 로고
    • PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family
    • Lazar L., Gat-Yablonski G., Kornreich L., et al. PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family. Horm Res 2003, 60(5):227-231.
    • (2003) Horm Res , vol.60 , Issue.5 , pp. 227-231
    • Lazar, L.1    Gat-Yablonski, G.2    Kornreich, L.3
  • 24
    • 0035576879 scopus 로고    scopus 로고
    • Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis
    • Dasen J.S., Barbera J.P., Herman T.S., et al. Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis. Genes Dev 2001, 15(23):3193-3207.
    • (2001) Genes Dev , vol.15 , Issue.23 , pp. 3193-3207
    • Dasen, J.S.1    Barbera, J.P.2    Herman, T.S.3
  • 25
    • 17344362762 scopus 로고    scopus 로고
    • Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
    • Dattani M.T., Martinez-Barbera J.P., Thomas P.Q., et al. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse. Nat Genet 1998, 19(2):125-133.
    • (1998) Nat Genet , vol.19 , Issue.2 , pp. 125-133
    • Dattani, M.T.1    Martinez-Barbera, J.P.2    Thomas, P.Q.3
  • 26
    • 27844470124 scopus 로고    scopus 로고
    • Hypopituitarism and neurodevelopmental abnormalities in relation to central nervous system structural defects in children with optic nerve hypoplasia
    • Haddad N.G., Eugster E.A. Hypopituitarism and neurodevelopmental abnormalities in relation to central nervous system structural defects in children with optic nerve hypoplasia. J Pediatr Endocrinol Metab 2005, 18(9):853-858.
    • (2005) J Pediatr Endocrinol Metab , vol.18 , Issue.9 , pp. 853-858
    • Haddad, N.G.1    Eugster, E.A.2
  • 27
    • 40849095909 scopus 로고    scopus 로고
    • Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies
    • Pfaeffle R.W., Hunter C.S., Savage J.J., et al. Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies. J Clin Endocrinol Metab 2008, 93(3):1062-1071.
    • (2008) J Clin Endocrinol Metab , vol.93 , Issue.3 , pp. 1062-1071
    • Pfaeffle, R.W.1    Hunter, C.S.2    Savage, J.J.3
  • 28
    • 33748298959 scopus 로고    scopus 로고
    • Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans
    • Kelberman D., Rizzoti K., Avilion A., et al. Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. J Clin Invest 2006, 116(9):2442-2455.
    • (2006) J Clin Invest , vol.116 , Issue.9 , pp. 2442-2455
    • Kelberman, D.1    Rizzoti, K.2    Avilion, A.3
  • 29
    • 0036800760 scopus 로고    scopus 로고
    • Beneficial effects of leptin on obesity, T cell hyporesponsiveness, and neuroendocrine/metabolic dysfunction of human congenital leptin deficiency
    • Farooqi I.S., Matarese G., Lord G.M., et al. Beneficial effects of leptin on obesity, T cell hyporesponsiveness, and neuroendocrine/metabolic dysfunction of human congenital leptin deficiency. J Clin Invest 2002, 110(8):1093-1103.
    • (2002) J Clin Invest , vol.110 , Issue.8 , pp. 1093-1103
    • Farooqi, I.S.1    Matarese, G.2    Lord, G.M.3
  • 30
    • 33846409122 scopus 로고    scopus 로고
    • Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor
    • Farooqi I.S., Wangensteen T., Collins S., et al. Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor. N Engl J Med 2007, 356(3):237-247.
    • (2007) N Engl J Med , vol.356 , Issue.3 , pp. 237-247
    • Farooqi, I.S.1    Wangensteen, T.2    Collins, S.3
  • 31
    • 0030458344 scopus 로고    scopus 로고
    • Genetic and clinical advances in Prader-Willi syndrome
    • Wharton R.H., Loechner K.J. Genetic and clinical advances in Prader-Willi syndrome. Curr Opin Pediatr 1996, 8(6):618-624.
    • (1996) Curr Opin Pediatr , vol.8 , Issue.6 , pp. 618-624
    • Wharton, R.H.1    Loechner, K.J.2
  • 33
    • 0038631972 scopus 로고    scopus 로고
    • Hypogonadism and pubertal development in Prader-Willi syndrome
    • Crino A., Schiaffini R., Ciampalini P., et al. Hypogonadism and pubertal development in Prader-Willi syndrome. Eur J Pediatr 2003, 162(5):327-333.
    • (2003) Eur J Pediatr , vol.162 , Issue.5 , pp. 327-333
    • Crino, A.1    Schiaffini, R.2    Ciampalini, P.3
  • 34
    • 0035063385 scopus 로고    scopus 로고
    • Fertility in Prader-Willi syndrome: a case report with Angelman syndrome in the offspring
    • Schulze A., Mogensen H., Hamborg-Petersen B., et al. Fertility in Prader-Willi syndrome: a case report with Angelman syndrome in the offspring. Acta Paediatr 2001, 90(4):455-459.
    • (2001) Acta Paediatr , vol.90 , Issue.4 , pp. 455-459
    • Schulze, A.1    Mogensen, H.2    Hamborg-Petersen, B.3
  • 35
    • 0032760438 scopus 로고    scopus 로고
    • A woman with Prader-Willi syndrome gives birth to a healthy baby girl
    • Akefeldt A., Tornhage C.J., Gillberg C. A woman with Prader-Willi syndrome gives birth to a healthy baby girl. Dev Med Child Neurol 1999, 41(11):789-790.
    • (1999) Dev Med Child Neurol , vol.41 , Issue.11 , pp. 789-790
    • Akefeldt, A.1    Tornhage, C.J.2    Gillberg, C.3
  • 36
    • 84907706418 scopus 로고
    • Psychosocial and emotional sequelae of individuals with traumatic brain injury: a literature review and recommendations
    • Morton M.V., Wehman P. Psychosocial and emotional sequelae of individuals with traumatic brain injury: a literature review and recommendations. Brain Inj 1995, 9(1):81-92.
    • (1995) Brain Inj , vol.9 , Issue.1 , pp. 81-92
    • Morton, M.V.1    Wehman, P.2
  • 37
    • 0034433921 scopus 로고    scopus 로고
    • Hypopituitarism following traumatic brain injury and aneurysmal subarachnoid hemorrhage: a preliminary report
    • Kelly D.F., Gonzalo I.T., Cohan P., et al. Hypopituitarism following traumatic brain injury and aneurysmal subarachnoid hemorrhage: a preliminary report. J Neurosurg 2000, 93(5):743-752.
    • (2000) J Neurosurg , vol.93 , Issue.5 , pp. 743-752
    • Kelly, D.F.1    Gonzalo, I.T.2    Cohan, P.3
  • 38
    • 0034966943 scopus 로고    scopus 로고
    • Prevalence of neuroendocrine dysfunction in patients recovering from traumatic brain injury
    • Lieberman S.A., Oberoi A.L., Gilkison C.R., et al. Prevalence of neuroendocrine dysfunction in patients recovering from traumatic brain injury. J Clin Endocrinol Metab 2001, 86(6):2752-2756.
    • (2001) J Clin Endocrinol Metab , vol.86 , Issue.6 , pp. 2752-2756
    • Lieberman, S.A.1    Oberoi, A.L.2    Gilkison, C.R.3
  • 39
    • 85047681972 scopus 로고    scopus 로고
    • Clinical review 113: hypopituitarism secondary to head trauma
    • Benvenga S., Campenni A., Ruggeri R.M., et al. Clinical review 113: hypopituitarism secondary to head trauma. J Clin Endocrinol Metab 2000, 85(4):1353-1361.
    • (2000) J Clin Endocrinol Metab , vol.85 , Issue.4 , pp. 1353-1361
    • Benvenga, S.1    Campenni, A.2    Ruggeri, R.M.3
  • 40
    • 33744950951 scopus 로고    scopus 로고
    • High risk of hypopituitarism after traumatic brain injury: a prospective investigation of anterior pituitary function in the acute phase and 12 months after trauma
    • Tanriverdi F., Senyurek H., Unluhizarci K., et al. High risk of hypopituitarism after traumatic brain injury: a prospective investigation of anterior pituitary function in the acute phase and 12 months after trauma. J Clin Endocrinol Metab 2006, 91(6):2105-2111.
    • (2006) J Clin Endocrinol Metab , vol.91 , Issue.6 , pp. 2105-2111
    • Tanriverdi, F.1    Senyurek, H.2    Unluhizarci, K.3
  • 41
    • 0036719859 scopus 로고    scopus 로고
    • Preirradiation endocrinopathies in pediatric brain tumor patients determined by dynamic tests of endocrine function
    • Merchant T.E., Williams T., Smith J.M., et al. Preirradiation endocrinopathies in pediatric brain tumor patients determined by dynamic tests of endocrine function. Int J Radiat Oncol Biol Phys 2002, 54(1):45-50.
    • (2002) Int J Radiat Oncol Biol Phys , vol.54 , Issue.1 , pp. 45-50
    • Merchant, T.E.1    Williams, T.2    Smith, J.M.3
  • 42
    • 4644331838 scopus 로고    scopus 로고
    • Endocrinological outcome of different treatment options in children with craniopharyngioma: a retrospective analysis of 66 cases
    • Gonc E.N., Yordam N., Ozon A., et al. Endocrinological outcome of different treatment options in children with craniopharyngioma: a retrospective analysis of 66 cases. Pediatr Neurosurg 2004, 40(3):112-119.
    • (2004) Pediatr Neurosurg , vol.40 , Issue.3 , pp. 112-119
    • Gonc, E.N.1    Yordam, N.2    Ozon, A.3
  • 43
    • 0031438472 scopus 로고    scopus 로고
    • Menarche in a cohort of 188 long-term survivors of acute lymphoblastic leukemia
    • Mills J.L., Fears T.R., Robison L.L., et al. Menarche in a cohort of 188 long-term survivors of acute lymphoblastic leukemia. J Pediatr 1997, 131(4):598-602.
    • (1997) J Pediatr , vol.131 , Issue.4 , pp. 598-602
    • Mills, J.L.1    Fears, T.R.2    Robison, L.L.3
  • 44
    • 0027080051 scopus 로고
    • Hypothalamic-pituitary dysfunction after radiation for brain tumors
    • Constine L.S., Woolf P.D., Cann D., et al. Hypothalamic-pituitary dysfunction after radiation for brain tumors. N Engl J Med 1993, 328(2):87-94.
    • (1993) N Engl J Med , vol.328 , Issue.2 , pp. 87-94
    • Constine, L.S.1    Woolf, P.D.2    Cann, D.3
  • 45
    • 0020414193 scopus 로고
    • Effect of hypothalamic and pituitary irradiation on pubertal development in children with cranial tumors
    • Rappaport R., Brauner R., Czernichow P., et al. Effect of hypothalamic and pituitary irradiation on pubertal development in children with cranial tumors. J Clin Endocrinol Metab 1982, 54(6):1164-1168.
    • (1982) J Clin Endocrinol Metab , vol.54 , Issue.6 , pp. 1164-1168
    • Rappaport, R.1    Brauner, R.2    Czernichow, P.3
  • 46
    • 38349009219 scopus 로고    scopus 로고
    • Endocrine late effects of childhood cancer therapy: a report from the Children's Oncology Group
    • Nandagopal R., Laverdiere C., Mulrooney D., et al. Endocrine late effects of childhood cancer therapy: a report from the Children's Oncology Group. Horm Res 2008, 69(2):65-74.
    • (2008) Horm Res , vol.69 , Issue.2 , pp. 65-74
    • Nandagopal, R.1    Laverdiere, C.2    Mulrooney, D.3
  • 47
    • 21844471790 scopus 로고    scopus 로고
    • Role of leptin in energy-deprivation states: normal human physiology and clinical implications for hypothalamic amenorrhoea and anorexia nervosa
    • Chan J.L., Mantzoros C.S. Role of leptin in energy-deprivation states: normal human physiology and clinical implications for hypothalamic amenorrhoea and anorexia nervosa. Lancet 2005, 366(9479):74-85.
    • (2005) Lancet , vol.366 , Issue.9479 , pp. 74-85
    • Chan, J.L.1    Mantzoros, C.S.2
  • 48
    • 4344690525 scopus 로고    scopus 로고
    • Recombinant human leptin in women with hypothalamic amenorrhea
    • Welt C.K., Chan J.L., Bullen J., et al. Recombinant human leptin in women with hypothalamic amenorrhea. N Engl J Med 2004, 351(10):987-997.
    • (2004) N Engl J Med , vol.351 , Issue.10 , pp. 987-997
    • Welt, C.K.1    Chan, J.L.2    Bullen, J.3
  • 49
    • 0025921769 scopus 로고
    • Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark
    • Nielsen J., Wohlert M. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet 1991, 87(1):81-83.
    • (1991) Hum Genet , vol.87 , Issue.1 , pp. 81-83
    • Nielsen, J.1    Wohlert, M.2
  • 50
    • 33846055706 scopus 로고    scopus 로고
    • Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group
    • Bondy C.A. Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J Clin Endocrinol Metab 2007, 92(1):10-25.
    • (2007) J Clin Endocrinol Metab , vol.92 , Issue.1 , pp. 10-25
    • Bondy, C.A.1
  • 51
    • 0031156671 scopus 로고    scopus 로고
    • Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome
    • Pasquino A.M., Passeri F., Pucarelli I., et al. Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome. J Clin Endocrinol Metab 1997, 82(6):1810-1813.
    • (1997) J Clin Endocrinol Metab , vol.82 , Issue.6 , pp. 1810-1813
    • Pasquino, A.M.1    Passeri, F.2    Pucarelli, I.3
  • 52
    • 0032897663 scopus 로고    scopus 로고
    • Pregnancies in women with Turner's syndrome
    • Hovatta O. Pregnancies in women with Turner's syndrome. Ann Med 1999, 31(2):106-110.
    • (1999) Ann Med , vol.31 , Issue.2 , pp. 106-110
    • Hovatta, O.1
  • 53
    • 33845508061 scopus 로고    scopus 로고
    • Differences in follicle-stimulating hormone secretion between 45, X monosomy Turner syndrome and 45, X/46, XX mosaicism are evident at an early age
    • Fechner P.Y., Davenport M.L., Qualy R.L., et al. Differences in follicle-stimulating hormone secretion between 45, X monosomy Turner syndrome and 45, X/46, XX mosaicism are evident at an early age. J Clin Endocrinol Metab 2006, 91(12):4896-4902.
    • (2006) J Clin Endocrinol Metab , vol.91 , Issue.12 , pp. 4896-4902
    • Fechner, P.Y.1    Davenport, M.L.2    Qualy, R.L.3
  • 54
    • 0037326103 scopus 로고    scopus 로고
    • Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study
    • Bojesen A., Juul S., Gravholt C.H. Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab 2003, 88(2):622-626.
    • (2003) J Clin Endocrinol Metab , vol.88 , Issue.2 , pp. 622-626
    • Bojesen, A.1    Juul, S.2    Gravholt, C.H.3
  • 55
    • 0032881765 scopus 로고    scopus 로고
    • Mosaic Turner syndrome: cytogenetics versus FISH
    • Abulhasan S.J., Tayel S.M., al-Awadi S.A. Mosaic Turner syndrome: cytogenetics versus FISH. Ann Hum Genet 1999, 63(Pt 3):199-206.
    • (1999) Ann Hum Genet , vol.63 , Issue.PART 3 , pp. 199-206
    • Abulhasan, S.J.1    Tayel, S.M.2    al-Awadi, S.A.3
  • 56
    • 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(6):1477-1483.
    • (2006) Hum Reprod , vol.21 , Issue.6 , pp. 1477-1483
    • Rizzolio, F.1    Bione, S.2    Sala, C.3
  • 57
    • 0023802274 scopus 로고
    • 47, XXX: what is the prognosis?
    • Linden M.G., Bender B.G., Harmon R.J., et al. 47, XXX: what is the prognosis?. Pediatrics 1988, 82(4):619-630.
    • (1988) Pediatrics , vol.82 , Issue.4 , pp. 619-630
    • Linden, M.G.1    Bender, B.G.2    Harmon, R.J.3
  • 58
    • 0027450295 scopus 로고
    • Exstrophy of the cloaca in a 47, XXX child: review of genitourinary malformations in triple-X patients
    • Lin H.J., Ndiforchu F., Patell S. Exstrophy of the cloaca in a 47, XXX child: review of genitourinary malformations in triple-X patients. Am J Med Genet 1993, 45(6):761-763.
    • (1993) Am J Med Genet , vol.45 , Issue.6 , pp. 761-763
    • Lin, H.J.1    Ndiforchu, F.2    Patell, S.3
  • 59
    • 0034880096 scopus 로고    scopus 로고
    • 47, XXX in an adolescent with premature ovarian failure and autoimmune disease
    • Holland C.M. 47, XXX in an adolescent with premature ovarian failure and autoimmune disease. J Pediatr Adolesc Gynecol 2001, 14(2):77-80.
    • (2001) J Pediatr Adolesc Gynecol , vol.14 , Issue.2 , pp. 77-80
    • Holland, C.M.1
  • 60
    • 0027324274 scopus 로고
    • Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone
    • Matthews C.H., Borgato S., Beck-Peccoz P., et al. Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone. Nat Genet 1993, 5(1):83-86.
    • (1993) Nat Genet , vol.5 , Issue.1 , pp. 83-86
    • Matthews, C.H.1    Borgato, S.2    Beck-Peccoz, P.3
  • 61
    • 0030744037 scopus 로고    scopus 로고
    • Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene
    • Layman L.C., Lee E.J., Peak D.B., et al. Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene. N Engl J Med 1997, 337(9):607-611.
    • (1997) N Engl J Med , vol.337 , Issue.9 , pp. 607-611
    • Layman, L.C.1    Lee, E.J.2    Peak, D.B.3
  • 62
    • 0031712880 scopus 로고    scopus 로고
    • Follitropin (FSH) deficiency in an infertile male due to FSHbeta gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations
    • Lindstedt G., Nystrom E., Matthews C., et al. Follitropin (FSH) deficiency in an infertile male due to FSHbeta gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations. Clin Chem Lab Med 1998, 36(8):663-665.
    • (1998) Clin Chem Lab Med , vol.36 , Issue.8 , pp. 663-665
    • Lindstedt, G.1    Nystrom, E.2    Matthews, C.3
  • 63
    • 0026335545 scopus 로고
    • Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone
    • Weiss J., Axelrod L., Whitcomb R.W., et al. Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. N Engl J Med 1992, 326(3):179-183.
    • (1992) N Engl J Med , vol.326 , Issue.3 , pp. 179-183
    • Weiss, J.1    Axelrod, L.2    Whitcomb, R.W.3
  • 64
    • 84995842414 scopus 로고
    • Identification of two point mutations in the gene coding luteinizing hormone (LH) beta-subunit, associated with immunologically anomalous LH variants
    • Furui K., Suganuma N., Tsukahara S., et al. Identification of two point mutations in the gene coding luteinizing hormone (LH) beta-subunit, associated with immunologically anomalous LH variants. J Clin Endocrinol Metab 1994, 78(1):107-113.
    • (1994) J Clin Endocrinol Metab , vol.78 , Issue.1 , pp. 107-113
    • Furui, K.1    Suganuma, N.2    Tsukahara, S.3
  • 65
    • 0028835899 scopus 로고
    • Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene
    • Kremer H., Kraaij R., Toledo S.P., et al. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nat Genet 1995, 9(2):160-164.
    • (1995) Nat Genet , vol.9 , Issue.2 , pp. 160-164
    • Kremer, H.1    Kraaij, R.2    Toledo, S.P.3
  • 66
    • 0030025051 scopus 로고    scopus 로고
    • Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene
    • Latronico A.C., Anasti J., Arnhold I.J., 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 1996, 334(8):507-512.
    • (1996) N Engl J Med , vol.334 , Issue.8 , pp. 507-512
    • Latronico, A.C.1    Anasti, J.2    Arnhold, I.J.3
  • 67
    • 0033393223 scopus 로고    scopus 로고
    • Clinical features of women with resistance to luteinizing hormone
    • Arnhold I.J., Latronico A.C., Batista M.C., et al. Clinical features of women with resistance to luteinizing hormone. Clin Endocrinol (Oxf) 1999, 51(6):701-707.
    • (1999) Clin Endocrinol (Oxf) , vol.51 , Issue.6 , pp. 701-707
    • Arnhold, I.J.1    Latronico, A.C.2    Batista, M.C.3
  • 68
    • 0028329869 scopus 로고
    • The genetics of XX gonadal dysgenesis
    • Aittomaki K. The genetics of XX gonadal dysgenesis. Am J Hum Genet 1994, 54(5):844-851.
    • (1994) Am J Hum Genet , vol.54 , Issue.5 , pp. 844-851
    • Aittomaki, K.1
  • 69
    • 0028924164 scopus 로고
    • Endocrinology of the carbohydrate-deficient glycoprotein syndrome type 1 from birth through adolescence
    • de Zegher F., Jaeken J. Endocrinology of the carbohydrate-deficient glycoprotein syndrome type 1 from birth through adolescence. Pediatr Res 1995, 37(4 Pt 1):395-401.
    • (1995) Pediatr Res , vol.37 , Issue.4 PART 1 , pp. 395-401
    • de Zegher, F.1    Jaeken, J.2
  • 70
    • 33751399421 scopus 로고    scopus 로고
    • Presentation and clinical progression of pseudohypoparathyroidism with multi-hormone resistance and Albright hereditary osteodystrophy: a case series
    • Gelfand I.M., Eugster E.A., DiMeglio L.A. Presentation and clinical progression of pseudohypoparathyroidism with multi-hormone resistance and Albright hereditary osteodystrophy: a case series. J Pediatr 2006, 149(6):877-880.
    • (2006) J Pediatr , vol.149 , Issue.6 , pp. 877-880
    • Gelfand, I.M.1    Eugster, E.A.2    DiMeglio, L.A.3
  • 71
    • 33748439007 scopus 로고    scopus 로고
    • Consensus statement on management of intersex disorders. International Consensus Conference on Intersex
    • Lee P.A., Houk C.P., Ahmed S.F., et al. Consensus statement on management of intersex disorders. International Consensus Conference on Intersex. Pediatrics 2006, 118(2):e488-e500.
    • (2006) Pediatrics , vol.118 , Issue.2
    • Lee, P.A.1    Houk, C.P.2    Ahmed, S.F.3
  • 72
    • 41949111680 scopus 로고    scopus 로고
    • Swyer syndrome: presentation and outcomes
    • Michala L., Goswami D., Creighton S.M., et al. Swyer syndrome: presentation and outcomes. BJOG May 2008, 115(6):737-741.
    • (2008) BJOG , vol.115 , Issue.6 , pp. 737-741
    • Michala, L.1    Goswami, D.2    Creighton, S.M.3
  • 73
    • 34848847445 scopus 로고    scopus 로고
    • Tumors of dysgenetic gonads in Swyer syndrome
    • Zielinska D., Zajaczek S., Rzepka-Gorska I. Tumors of dysgenetic gonads in Swyer syndrome. J Pediatr Surg 2007, 42(10):1721-1724.
    • (2007) J Pediatr Surg , vol.42 , Issue.10 , pp. 1721-1724
    • Zielinska, D.1    Zajaczek, S.2    Rzepka-Gorska, I.3
  • 74
    • 57049125097 scopus 로고    scopus 로고
    • Complete androgen insensitivity syndrome-a review
    • Oakes M.B., Eyvazzadeh A.D., Quint E., et al. Complete androgen insensitivity syndrome-a review. J Pediatr Adolesc Gynecol 2008, 21(6):305-310.
    • (2008) J Pediatr Adolesc Gynecol , vol.21 , Issue.6 , pp. 305-310
    • Oakes, M.B.1    Eyvazzadeh, A.D.2    Quint, E.3
  • 75
    • 12444296564 scopus 로고    scopus 로고
    • The incidence of complete androgen insensitivity in girls with inguinal hernias and assessment of screening by vaginal length measurement
    • [discussion: 136-7]
    • Sarpel U., Palmer S.K., Dolgin S.E. The incidence of complete androgen insensitivity in girls with inguinal hernias and assessment of screening by vaginal length measurement. J Pediatr Surg 2005, 40(1):133-136. [discussion: 136-7].
    • (2005) J Pediatr Surg , vol.40 , Issue.1 , pp. 133-136
    • Sarpel, U.1    Palmer, S.K.2    Dolgin, S.E.3
  • 76
    • 0842291524 scopus 로고    scopus 로고
    • Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency
    • Costa-Santos M., Kater C.E., Auchus R.J. Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency. J Clin Endocrinol Metab 2004, 89(1):49-60.
    • (2004) J Clin Endocrinol Metab , vol.89 , Issue.1 , pp. 49-60
    • Costa-Santos, M.1    Kater, C.E.2    Auchus, R.J.3
  • 77
    • 33748742537 scopus 로고    scopus 로고
    • Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene
    • Yang J., Cui B., Sun S., et al. Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene. J Clin Endocrinol Metab 2006, 91(9):3619-3625.
    • (2006) J Clin Endocrinol Metab , vol.91 , Issue.9 , pp. 3619-3625
    • Yang, J.1    Cui, B.2    Sun, S.3
  • 78
    • 33747651019 scopus 로고    scopus 로고
    • Homozygous mutation of P450 side-chain cleavage enzyme gene (CYP11A1) in 46, XY patient with adrenal insufficiency, complete sex reversal, and agenesis of corpus callosum
    • al Kandari H., Katsumata N., Alexander S., et al. Homozygous mutation of P450 side-chain cleavage enzyme gene (CYP11A1) in 46, XY patient with adrenal insufficiency, complete sex reversal, and agenesis of corpus callosum. J Clin Endocrinol Metab 2006, 91(8):2821-2826.
    • (2006) J Clin Endocrinol Metab , vol.91 , Issue.8 , pp. 2821-2826
    • al Kandari, H.1    Katsumata, N.2    Alexander, S.3
  • 79
    • 33845504474 scopus 로고    scopus 로고
    • Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia
    • Baker B.Y., Lin L., Kim C.J., et al. Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia. J Clin Endocrinol Metab 2006, 91(12):4781-4785.
    • (2006) J Clin Endocrinol Metab , vol.91 , Issue.12 , pp. 4781-4785
    • Baker, B.Y.1    Lin, L.2    Kim, C.J.3
  • 80
    • 0030901671 scopus 로고    scopus 로고
    • Spontaneous puberty in 46, XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene
    • Fujieda K., Tajima T., Nakae J., et al. Spontaneous puberty in 46, XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene. J Clin Invest 1997, 99(6):1265-1271.
    • (1997) J Clin Invest , vol.99 , Issue.6 , pp. 1265-1271
    • Fujieda, K.1    Tajima, T.2    Nakae, J.3
  • 81
    • 0019514933 scopus 로고
    • Hypergonadotropic hypogonadism in female patients with galactosemia
    • Kaufman F.R., Kogut M.D., Donnell G.N., et al. Hypergonadotropic hypogonadism in female patients with galactosemia. N Engl J Med 1981, 304(17):994-998.
    • (1981) N Engl J Med , vol.304 , Issue.17 , pp. 994-998
    • Kaufman, F.R.1    Kogut, M.D.2    Donnell, G.N.3
  • 82
    • 0031015317 scopus 로고    scopus 로고
    • Altered follicle stimulating hormone isoforms in female galactosaemia patients
    • Prestoz L.L., Couto A.S., Shin Y.S., et al. Altered follicle stimulating hormone isoforms in female galactosaemia patients. Eur J Pediatr 1997, 156(2):116-120.
    • (1997) Eur J Pediatr , vol.156 , Issue.2 , pp. 116-120
    • Prestoz, L.L.1    Couto, A.S.2    Shin, Y.S.3
  • 83
    • 0025886416 scopus 로고
    • Testicular regression syndrome-a pathological study of 77 cases
    • Smith N.M., Byard R.W., Bourne A.J. Testicular regression syndrome-a pathological study of 77 cases. Histopathology 1991, 19(3):269-272.
    • (1991) Histopathology , vol.19 , Issue.3 , pp. 269-272
    • Smith, N.M.1    Byard, R.W.2    Bourne, A.J.3
  • 84
    • 33747617150 scopus 로고    scopus 로고
    • Histopathological features of testicular regression syndrome: relation to patient age and implications for management
    • Law H., Mushtaq I., Wingrove K., et al. Histopathological features of testicular regression syndrome: relation to patient age and implications for management. Fetal Pediatr Pathol 2006, 25(2):119-129.
    • (2006) Fetal Pediatr Pathol , vol.25 , Issue.2 , pp. 119-129
    • Law, H.1    Mushtaq, I.2    Wingrove, K.3
  • 85
    • 0028942092 scopus 로고
    • Testicular degeneration in three patients with the persistent mullerian duct syndrome
    • Imbeaud S., Rey R., Berta P., et al. Testicular degeneration in three patients with the persistent mullerian duct syndrome. Eur J Pediatr 1995, 154(3):187-190.
    • (1995) Eur J Pediatr , vol.154 , Issue.3 , pp. 187-190
    • Imbeaud, S.1    Rey, R.2    Berta, P.3
  • 86
    • 10344233163 scopus 로고    scopus 로고
    • An analysis of the genetic factors involved in testicular descent in a cohort of 14 male patients with anorchia
    • Vinci G., Anjot M.N., Trivin C., et al. An analysis of the genetic factors involved in testicular descent in a cohort of 14 male patients with anorchia. J Clin Endocrinol Metab 2004, 89(12):6282-6285.
    • (2004) J Clin Endocrinol Metab , vol.89 , Issue.12 , pp. 6282-6285
    • Vinci, G.1    Anjot, M.N.2    Trivin, C.3
  • 87
    • 0037250894 scopus 로고    scopus 로고
    • The radiosensitivity of the human oocyte
    • Wallace W.H., Thomson A.B., Kelsey T.W. The radiosensitivity of the human oocyte. Hum Reprod 2003, 18(1):117-121.
    • (2003) Hum Reprod , vol.18 , Issue.1 , pp. 117-121
    • Wallace, W.H.1    Thomson, A.B.2    Kelsey, T.W.3
  • 88
    • 10744220220 scopus 로고    scopus 로고
    • Reduced ovarian function in long-term survivors of radiation- and chemotherapy-treated childhood cancer
    • Larsen E.C., Muller J., Schmiegelow K., et al. Reduced ovarian function in long-term survivors of radiation- and chemotherapy-treated childhood cancer. J Clin Endocrinol Metab 2003, 88(11):5307-5314.
    • (2003) J Clin Endocrinol Metab , vol.88 , Issue.11 , pp. 5307-5314
    • Larsen, E.C.1    Muller, J.2    Schmiegelow, K.3
  • 89
    • 0343415080 scopus 로고    scopus 로고
    • Persistent altered spermatogenesis in long-term childhood cancer survivors
    • Lopez Andreu J.A., Fernandez P.J., Ferris i Tortajada J., et al. Persistent altered spermatogenesis in long-term childhood cancer survivors. Pediatr Hematol Oncol 2000, 17(1):21-30.
    • (2000) Pediatr Hematol Oncol , vol.17 , Issue.1 , pp. 21-30
    • Lopez Andreu, J.A.1    Fernandez, P.J.2    Ferris i Tortajada, J.3
  • 90
    • 0024555619 scopus 로고
    • Vulnerability of the human Leydig cell to radiation damage is dependent upon age
    • Shalet S.M., Tsatsoulis A., Whitehead E., et al. Vulnerability of the human Leydig cell to radiation damage is dependent upon age. J Endocrinol 1989, 120(1):161-165.
    • (1989) J Endocrinol , vol.120 , Issue.1 , pp. 161-165
    • Shalet, S.M.1    Tsatsoulis, A.2    Whitehead, E.3
  • 91
    • 54049105397 scopus 로고    scopus 로고
    • Endocrine and metabolic disorders in young adult survivors of childhood acute lymphoblastic leukaemia (ALL) or non-Hodgkin lymphoma (NHL)
    • Steffens M., Beauloye V., Brichard B., et al. Endocrine and metabolic disorders in young adult survivors of childhood acute lymphoblastic leukaemia (ALL) or non-Hodgkin lymphoma (NHL). Clin Endocrinol (Oxf) 2008, 69(5):819-827.
    • (2008) Clin Endocrinol (Oxf) , vol.69 , Issue.5 , pp. 819-827
    • Steffens, M.1    Beauloye, V.2    Brichard, B.3
  • 92
    • 38149108467 scopus 로고    scopus 로고
    • Unexpected recovery of ovarian function many years after bone marrow transplantation
    • Rahhal S.N., Eugster E.A. Unexpected recovery of ovarian function many years after bone marrow transplantation. J Pediatr 2008, 152(2):289-290.
    • (2008) J Pediatr , vol.152 , Issue.2 , pp. 289-290
    • Rahhal, S.N.1    Eugster, E.A.2
  • 93
    • 0030948610 scopus 로고    scopus 로고
    • Systematic approach for detection of endocrine disorders in children treated for brain tumors
    • Meacham L.R., Ghim T.T., Crocker I.R., et al. Systematic approach for detection of endocrine disorders in children treated for brain tumors. Med Pediatr Oncol 1997, 29(2):86-91.
    • (1997) Med Pediatr Oncol , vol.29 , Issue.2 , pp. 86-91
    • Meacham, L.R.1    Ghim, T.T.2    Crocker, I.R.3
  • 94
    • 0035985901 scopus 로고    scopus 로고
    • Autoimmune polyglandular syndrome. II: clinical syndrome and treatment
    • Schatz D.A., Winter W.E. Autoimmune polyglandular syndrome. II: clinical syndrome and treatment. Endocrinol Metab Clin North Am 2002, 31(2):339-352.
    • (2002) Endocrinol Metab Clin North Am , vol.31 , Issue.2 , pp. 339-352
    • Schatz, D.A.1    Winter, W.E.2
  • 95
    • 33846990524 scopus 로고    scopus 로고
    • Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene
    • Wolff A.S., Erichsen M.M., Meager A., et al. Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene. J Clin Endocrinol Metab 2007, 92(2):595-603.
    • (2007) J Clin Endocrinol Metab , vol.92 , Issue.2 , pp. 595-603
    • Wolff, A.S.1    Erichsen, M.M.2    Meager, A.3
  • 96
    • 0023138282 scopus 로고
    • Adrenal and steroidal cell antibodies in patients with autoimmune polyglandular disease type I and risk of adrenocortical and ovarian failure
    • Ahonen P., Miettinen A., Perheentupa J. Adrenal and steroidal cell antibodies in patients with autoimmune polyglandular disease type I and risk of adrenocortical and ovarian failure. J Clin Endocrinol Metab 1987, 64(3):494-500.
    • (1987) J Clin Endocrinol Metab , vol.64 , Issue.3 , pp. 494-500
    • Ahonen, P.1    Miettinen, A.2    Perheentupa, J.3
  • 97
    • 84995870568 scopus 로고
    • Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease
    • Uibo R., Aavik E., Peterson P., et al. Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease. J Clin Endocrinol Metab 1994, 78(2):323-328.
    • (1994) J Clin Endocrinol Metab , vol.78 , Issue.2 , pp. 323-328
    • Uibo, R.1    Aavik, E.2    Peterson, P.3
  • 98
    • 0031049942 scopus 로고    scopus 로고
    • Premature ovarian failure and ovarian autoimmunity
    • Hoek A., Schoemaker J., Drexhage H.A. Premature ovarian failure and ovarian autoimmunity. Endocr Rev 1997, 18(1):107-134.
    • (1997) Endocr Rev , vol.18 , Issue.1 , pp. 107-134
    • Hoek, A.1    Schoemaker, J.2    Drexhage, H.A.3
  • 99
    • 0037961060 scopus 로고    scopus 로고
    • Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria?
    • Buzi F., Badolato R., Mazza C., et al. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria?. J Clin Endocrinol Metab 2003, 88(7):3146-3148.
    • (2003) J Clin Endocrinol Metab , vol.88 , Issue.7 , pp. 3146-3148
    • Buzi, F.1    Badolato, R.2    Mazza, C.3
  • 100
    • 0033772333 scopus 로고    scopus 로고
    • Organ-specific and non-organ-specific autoantibodies in children and young adults with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
    • Perniola R., Falorni A., Clemente M.G., et al. Organ-specific and non-organ-specific autoantibodies in children and young adults with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). Eur J Endocrinol 2000, 143(4):497-503.
    • (2000) Eur J Endocrinol , vol.143 , Issue.4 , pp. 497-503
    • Perniola, R.1    Falorni, A.2    Clemente, M.G.3
  • 101
    • 0030949954 scopus 로고    scopus 로고
    • Antisperm antibodies in prepubertal boys treated with chemotherapy for malignant or non-malignant diseases and in boys with genital tract abnormalities
    • Sinisi A.A., D'Apuzzo A., Pasquali D., et al. Antisperm antibodies in prepubertal boys treated with chemotherapy for malignant or non-malignant diseases and in boys with genital tract abnormalities. Int J Androl 1997, 20(1):23-28.
    • (1997) Int J Androl , vol.20 , Issue.1 , pp. 23-28
    • Sinisi, A.A.1    D'Apuzzo, A.2    Pasquali, D.3
  • 102
    • 0027295389 scopus 로고
    • Potential of gonadotropin-releasing hormone agonists in the diagnosis of pubertal disorders in girls
    • Goodpasture J.C., Ghai K., Cara J.F., et al. Potential of gonadotropin-releasing hormone agonists in the diagnosis of pubertal disorders in girls. Clin Obstet Gynecol 1993, 36(3):773-785.
    • (1993) Clin Obstet Gynecol , vol.36 , Issue.3 , pp. 773-785
    • Goodpasture, J.C.1    Ghai, K.2    Cara, J.F.3
  • 103
    • 0031926873 scopus 로고    scopus 로고
    • Optimizing estrogen replacement treatment in Turner syndrome
    • Rosenfield R.L., Perovic N., Devine N., et al. Optimizing estrogen replacement treatment in Turner syndrome. Pediatrics 1998, 102(2 Pt 3):486-488.
    • (1998) Pediatrics , vol.102 , Issue.2 PART 3 , pp. 486-488
    • Rosenfield, R.L.1    Perovic, N.2    Devine, N.3
  • 104
    • 33744811403 scopus 로고    scopus 로고
    • Optimising management in Turner syndrome: from infancy to adult transfer
    • Donaldson M.D., Gault E.J., Tan K.W., et al. Optimising management in Turner syndrome: from infancy to adult transfer. Arch Dis Child 2006, 91(6):513-520.
    • (2006) Arch Dis Child , vol.91 , Issue.6 , pp. 513-520
    • Donaldson, M.D.1    Gault, E.J.2    Tan, K.W.3
  • 105
    • 35948950716 scopus 로고    scopus 로고
    • Metabolic effects of oral versus transdermal estrogen in growth hormone-treated girls with turner syndrome
    • Mauras N., Shulman D., Hsiang H.Y., et al. Metabolic effects of oral versus transdermal estrogen in growth hormone-treated girls with turner syndrome. J Clin Endocrinol Metab 2007, 92(11):4154-4160.
    • (2007) J Clin Endocrinol Metab , vol.92 , Issue.11 , pp. 4154-4160
    • Mauras, N.1    Shulman, D.2    Hsiang, H.Y.3
  • 106
    • 0034919022 scopus 로고    scopus 로고
    • Nocturnal application of transdermal estradiol patches produces levels of estradiol that mimic those seen at the onset of spontaneous puberty in girls
    • Ankarberg-Lindgren C., Elfving M., Wikland K.A., et al. Nocturnal application of transdermal estradiol patches produces levels of estradiol that mimic those seen at the onset of spontaneous puberty in girls. J Clin Endocrinol Metab 2001, 86(7):3039-3044.
    • (2001) J Clin Endocrinol Metab , vol.86 , Issue.7 , pp. 3039-3044
    • Ankarberg-Lindgren, C.1    Elfving, M.2    Wikland, K.A.3
  • 107
    • 0022620053 scopus 로고
    • Biologic effects of transdermal estradiol
    • Chetkowski R.J., Meldrum D.R., Steingold K.A., et al. Biologic effects of transdermal estradiol. N Engl J Med 1986, 314(25):1615-1620.
    • (1986) N Engl J Med , vol.314 , Issue.25 , pp. 1615-1620
    • Chetkowski, R.J.1    Meldrum, D.R.2    Steingold, K.A.3
  • 108
    • 66749175804 scopus 로고    scopus 로고
    • Oral versus transdermal estrogen replacement in girls with Turner syndrome: a pilot comparative study
    • Nabhan Z.M., DiMeglio L.A., Qi R., et al. Oral versus transdermal estrogen replacement in girls with Turner syndrome: a pilot comparative study. J Clin Endocrinol Metab 2009, 94(6):2009-2014.
    • (2009) J Clin Endocrinol Metab , vol.94 , Issue.6 , pp. 2009-2014
    • Nabhan, Z.M.1    DiMeglio, L.A.2    Qi, R.3
  • 109
    • 3242707445 scopus 로고    scopus 로고
    • Use of percutaneous estrogen gel for induction of puberty in girls with Turner syndrome
    • Piippo S., Lenko H., Kainulainen P., et al. Use of percutaneous estrogen gel for induction of puberty in girls with Turner syndrome. J Clin Endocrinol Metab 2004, 89(7):3241-3247.
    • (2004) J Clin Endocrinol Metab , vol.89 , Issue.7 , pp. 3241-3247
    • Piippo, S.1    Lenko, H.2    Kainulainen, P.3
  • 110
    • 0024234570 scopus 로고
    • Testosterone treatment in adolescent boys with constitutional delay in growth and development
    • Richman R.A., Kirsch L.R. Testosterone treatment in adolescent boys with constitutional delay in growth and development. N Engl J Med 1988, 319(24):1563-1567.
    • (1988) N Engl J Med , vol.319 , Issue.24 , pp. 1563-1567
    • Richman, R.A.1    Kirsch, L.R.2
  • 111
    • 0029143604 scopus 로고
    • Testosterone treatment in adolescent boys with constitutional delay of growth and development
    • Soliman A.T., Khadir M.M., Asfour M. Testosterone treatment in adolescent boys with constitutional delay of growth and development. Metabolism 1995, 44(8):1013-1015.
    • (1995) Metabolism , vol.44 , Issue.8 , pp. 1013-1015
    • Soliman, A.T.1    Khadir, M.M.2    Asfour, M.3
  • 112
    • 0030953347 scopus 로고    scopus 로고
    • Testosterone treatment in adolescents with delayed puberty: changes in body composition, protein, fat, and glucose metabolism
    • Arslanian S., Suprasongsin C. Testosterone treatment in adolescents with delayed puberty: changes in body composition, protein, fat, and glucose metabolism. J Clin Endocrinol Metab 1997, 82(10):3213-3220.
    • (1997) J Clin Endocrinol Metab , vol.82 , Issue.10 , pp. 3213-3220
    • Arslanian, S.1    Suprasongsin, C.2
  • 113
    • 16344365270 scopus 로고    scopus 로고
    • Pubertal androgen therapy in boys
    • Rogol A.D. Pubertal androgen therapy in boys. Pediatr Endocrinol Rev 2005, 2(3):383-390.
    • (2005) Pediatr Endocrinol Rev , vol.2 , Issue.3 , pp. 383-390
    • Rogol, A.D.1
  • 114
    • 0026548945 scopus 로고
    • The short-term effect of testosterone on growth in boys on hemodialysis
    • Kassmann K., Rappaport R., Broyer M. The short-term effect of testosterone on growth in boys on hemodialysis. Clin Nephrol 1992, 37(3):148-154.
    • (1992) Clin Nephrol , vol.37 , Issue.3 , pp. 148-154
    • Kassmann, K.1    Rappaport, R.2    Broyer, M.3
  • 115
    • 1442327777 scopus 로고    scopus 로고
    • Transdermal testosterone application: pharmacokinetics and effects on pubertal status, short-term growth, and bone turnover
    • Mayo A., Macintyre H., Wallace A.M., et al. Transdermal testosterone application: pharmacokinetics and effects on pubertal status, short-term growth, and bone turnover. J Clin Endocrinol Metab 2004, 89(2):681-687.
    • (2004) J Clin Endocrinol Metab , vol.89 , Issue.2 , pp. 681-687
    • Mayo, A.1    Macintyre, H.2    Wallace, A.M.3
  • 116
    • 35248881204 scopus 로고    scopus 로고
    • Clinical effects of treatment for hypogonadism in male adolescents with Prader-Labhart-Willi syndrome
    • Eiholzer U., Grieser J., Schlumpf M., et al. Clinical effects of treatment for hypogonadism in male adolescents with Prader-Labhart-Willi syndrome. Horm Res 2007, 68(4):178-184.
    • (2007) Horm Res , vol.68 , Issue.4 , pp. 178-184
    • Eiholzer, U.1    Grieser, J.2    Schlumpf, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.