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Volumn 90, Issue 6, 2007, Pages 1239-1243

Septo-optic dysplasia associated with abnormal pubertal development

Author keywords

Blindness; Magnetic resonance imaging; Primary amenorrhea; Septo optic dysplasia (SOD)

Indexed keywords

CALCIUM; ESTRADIOL; ESTROGEN; HORMONE; PROGESTERONE;

EID: 34347338499     PISSN: 01252208     EISSN: 01252208     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (2)

References (12)
  • 4
    • 20444416220 scopus 로고    scopus 로고
    • Novel insights into the aetiology and pathogenesis of hypopituitarism
    • Dattani MT. Novel insights into the aetiology and pathogenesis of hypopituitarism. Horm Res 2004; 62(Suppl 3): 1-13.
    • (2004) Horm Res , vol.62 , Issue.SUPPL. 3 , pp. 1-13
    • Dattani, M.T.1
  • 5
    • 0033866207 scopus 로고    scopus 로고
    • Septo-optic dysplasia in combination with a pigmented skin lesion: A case report with nosological discussion
    • De Smedt S, Demaerel P, Casaer P, Casteels I. Septo-optic dysplasia in combination with a pigmented skin lesion: a case report with nosological discussion. Eur J Paediatr Neurol 2000; 4: 189-93.
    • (2000) Eur J Paediatr Neurol , vol.4 , pp. 189-193
    • De Smedt, S.1    Demaerel, P.2    Casaer, P.3    Casteels, I.4
  • 6
    • 13444254372 scopus 로고    scopus 로고
    • Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia
    • Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, et al. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Clin Endocrinol (Oxf) 2005; 62: 163-8.
    • (2005) Clin Endocrinol (Oxf) , vol.62 , pp. 163-168
    • Rainbow, L.A.1    Rees, S.A.2    Shaikh, M.G.3    Shaw, N.J.4    Cole, T.5    Barrett, T.G.6
  • 7
    • 0036190989 scopus 로고    scopus 로고
    • Endocrinopathies associated with midline cerebral and cranial malformations
    • Traggiai C, Stanhope R. Endocrinopathies associated with midline cerebral and cranial malformations. J Pediatr 2002; 140: 252-5.
    • (2002) J Pediatr , vol.140 , pp. 252-255
    • Traggiai, C.1    Stanhope, R.2
  • 11
    • 0037238607 scopus 로고    scopus 로고
    • Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient
    • Tajima T, Hattorri T, Nakajima T, Okuhara K, Sato K, Abe S, et al. Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient. J Clin Endocrinol Metab 2003; 88: 45-50.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 45-50
    • Tajima, T.1    Hattorri, T.2    Nakajima, T.3    Okuhara, K.4    Sato, K.5    Abe, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.