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Volumn 24, Issue 2, 2011, Pages

Pubertal Delay, Hypokalemia, and Hypertension Caused by a Rare Form of Congenital Adrenal Hyperplasia

Author keywords

17alpha hydroxylase; Adrenal hyperplasia; Congenital; Pubertal delay

Indexed keywords

ALDOSTERONE; ANDROGEN; ANTIHYPERTENSIVE AGENT; CORTICOSTERONE; CORTICOTROPIN; DEOXYCORTICOSTERONE; ESTROGEN; FOLLITROPIN; GLUCOCORTICOID; HYDROCORTISONE; LUTEINIZING HORMONE; MINERALOCORTICOID; POTASSIUM; SEX HORMONE; SPIRONOLACTONE; STEROID 17,20 LYASE; STEROID 17ALPHA MONOOXYGENASE;

EID: 79952108015     PISSN: 10833188     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpag.2010.08.018     Document Type: Article
Times cited : (9)

References (7)
  • 2
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    • The genetics, pathophysiology, and management of human deficiencies of P450c17
    • Auchus R.J. The genetics, pathophysiology, and management of human deficiencies of P450c17. Endocrinol Metab Clin North Am 2001, 30:101.
    • (2001) Endocrinol Metab Clin North Am , vol.30 , pp. 101
    • Auchus, R.J.1
  • 4
    • 0842291524 scopus 로고    scopus 로고
    • Brazilian Congenital Adrenal Hyperplasia Multicenter Study Group: 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. Brazilian Congenital Adrenal Hyperplasia Multicenter Study Group: Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency. J Clin Endocrinol Metab 2004, 89:49.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 49
    • Costa-Santos, M.1    Kater, C.E.2    Auchus, R.J.3
  • 5
    • 33947531089 scopus 로고    scopus 로고
    • P450c17 deficiency: Clinical and molecular characterization of six patients
    • Rosa S., Duff C., Meyer M., et al. P450c17 deficiency: Clinical and molecular characterization of six patients. J Clin Endocrinol Metab 2007, 92:1000.
    • (2007) J Clin Endocrinol Metab , vol.92 , pp. 1000
    • Rosa, S.1    Duff, C.2    Meyer, M.3
  • 6
    • 0031648545 scopus 로고    scopus 로고
    • Molecular basis of hypokalemic myopathy caused by 17alpha-hydroxlyase/17,20-lyase deficiency
    • Satoh J., Kuroda Y., Nawata H., et al. Molecular basis of hypokalemic myopathy caused by 17alpha-hydroxlyase/17,20-lyase deficiency. Neurology 1998, 51:1748.
    • (1998) Neurology , vol.51 , pp. 1748
    • Satoh, J.1    Kuroda, Y.2    Nawata, H.3
  • 7
    • 77952133588 scopus 로고    scopus 로고
    • Delayed puberty
    • Kaplowitz P.B. Delayed puberty. Pediatr Rev 2010, 31:189.
    • (2010) Pediatr Rev , vol.31 , pp. 189
    • Kaplowitz, P.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.