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Volumn 61, Issue 5, 2004, Pages 242-245

Transient hyper-17-OHPnemia unrelated to cross-reactions with residual fetal adrenal cortex products

Author keywords

21 Hydroxylase; Gas chromatography mass spectrometry; High performance liquid chromatography radioimmunoassay; Hyper 17 hydroxyprogesteronemia; Transient hyper 17 OHPnemia

Indexed keywords

HYDROXYPROGESTERONE; PREGNANETRIOLONE; SEX HORMONE; STEROID 21 MONOOXYGENASE; UNCLASSIFIED DRUG;

EID: 1842851860     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000076961     Document Type: Article
Times cited : (3)

References (12)
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  • 2
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    • 450 17α-hydroxylase/17,20-lyase, and 3β-hydroxysteroid dehydrogenase isomerase steroidogenic enzymes in human and rhesus monkey fetal adrenal glands: Reappraisal of functional zonation
    • 450 17α-hydroxylase/17,20-lyase, and 3β-hydroxysteroid dehydrogenase isomerase steroidogenic enzymes in human and rhesus monkey fetal adrenal glands: Reappraisal of functional zonation. J Clin Endocrinol Metab 1993;77:1184-1189.
    • (1993) J Clin Endocrinol Metab , vol.77 , pp. 1184-1189
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    • Serum profile of steroid hormone in patients with Cushing's syndrome determined by new HPLC/RIA method
    • Ueshiba H, Segawa M, Hayashi T, Miyachi Y, Irie M: Serum profile of steroid hormone in patients with Cushing's syndrome determined by new HPLC/RIA method. Clin Chem 1991;37:1329-1333.
    • (1991) Clin Chem , vol.37 , pp. 1329-1333
    • Ueshiba, H.1    Segawa, M.2    Hayashi, T.3    Miyachi, Y.4    Irie, M.5
  • 7
    • 0036075210 scopus 로고    scopus 로고
    • Genetic analysis of Japanese patients with 21-hydroxylase deficiency: Identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21
    • Koyama S, Toyoura T, Saisyo S, Shimozawa K, Yata J: Genetic analysis of Japanese patients with 21-hydroxylase deficiency: Identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21. J Clin Endocrinol Metab 2002;87:2668-2679.
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 2668-2679
    • Koyama, S.1    Toyoura, T.2    Saisyo, S.3    Shimozawa, K.4    Yata, J.5
  • 9
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    • 17-OH-progesterone concentration in newborn infants
    • Hughes IA, Riad-Fahmy D, Griffiths, K: 17-OH-progesterone concentration in newborn infants. Arch Dis Child 1979;54:347-349.
    • (1979) Arch Dis Child , vol.54 , pp. 347-349
    • Hughes, I.A.1    Riad-Fahmy, D.2    Griffiths, K.3
  • 11
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    • The interpretation of blood spot 17α-hydroxyprogesterone levels in term and pre-term neonates
    • Berry J, Betts P, Wood PJ: The interpretation of blood spot 17α-hydroxyprogesterone levels in term and pre-term neonates. Ann Clin Biochem 1986;23:546-551.
    • (1986) Ann Clin Biochem , vol.23 , pp. 546-551
    • Berry, J.1    Betts, P.2    Wood, P.J.3
  • 12
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    • Analysis of blood spot 17α-hydroxyprogesterone concentration in premature infants-proposal for cut-off limits in screening for congenital adrenal hyperplasia
    • Ohkubo S, Shimozawa K, Matsumoto M, Kitagawa T: Analysis of blood spot 17α-hydroxyprogesterone concentration in premature infants-proposal for cut-off limits in screening for congenital adrenal hyperplasia. Acta Pediatr Jpn 1992;34:126-133.
    • (1992) Acta Pediatr Jpn , vol.34 , pp. 126-133
    • Ohkubo, S.1    Shimozawa, K.2    Matsumoto, M.3    Kitagawa, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.