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Volumn 43, Issue 5, 2006, Pages 419-423

Audit of care of patients with congenital adrenal hyperplasia due to 21-Hydroxylase deficiency in a referral hospital in South India

Author keywords

Ambiguous genitalia; Congenital adrenal hyperplasia

Indexed keywords

ARTICLE; BONE AGE; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; FOLLOW UP; HUMAN; INDIA; KARYOTYPE; MALE; PATIENT CARE; PRESCHOOL CHILD; SCHOOL CHILD; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 33744503974     PISSN: 00196061     EISSN: 00196061     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (11)
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  • 2
    • 0034454269 scopus 로고    scopus 로고
    • Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
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    • White, P.C.1    Speiser, P.W.2
  • 4
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    • Salt-wasting congenital adrenal hyperplasia: Detection of mutations in CYP21B gene in a Chilean population
    • Fardella CE, Poggi H, Pineda P, Soto J, Torrealba I, Cattani A, et al. Salt-wasting congenital adrenal hyperplasia: detection of mutations in CYP21B gene in a Chilean population. J Clin Endocrinol Metab1998; 83: 3357-3360.
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 3357-3360
    • Fardella, C.E.1    Poggi, H.2    Pineda, P.3    Soto, J.4    Torrealba, I.5    Cattani, A.6
  • 5
    • 0031788479 scopus 로고    scopus 로고
    • An update on the molecular genetics of congenital adrenal hyperplasia: Diagnostic and therapeutic aspects
    • Wedell A. An update on the molecular genetics of congenital adrenal hyperplasia: diagnostic and therapeutic aspects. J Pediatr Endocrinol Metab 1998;11:581-589.
    • (1998) J Pediatr Endocrinol Metab , vol.11 , pp. 581-589
    • Wedell, A.1
  • 6
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    • Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Pediatric Endocrinology
    • Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Pediatric Endocrinology. J Clin Endocrinol Metab 2002; 87: 4048-4053 .
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 4048-4053
  • 7
    • 0042466547 scopus 로고    scopus 로고
    • Medical Progress-Congenital adrenal hyperplasia
    • Speiser PW, White PC. Medical Progress-Congenital adrenal hyperplasia. N Engl J Med 2003; 349: 776-788.
    • (2003) N Engl J Med , vol.349 , pp. 776-788
    • Speiser, P.W.1    White, P.C.2
  • 9
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    • Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five niddle european countries
    • Kovacs.J, Votava F, Heize G, Solyom J, Lebl J, Pribilincova Z, et al. Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five niddle european countries. J Clin Endocrinol Metab 2001; 86: 2958-2964.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 2958-2964
    • Kovacs, J.1    Votava, F.2    Heize, G.3    Solyom, J.4    Lebl, J.5    Pribilincova, Z.6
  • 10
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    • (1997) Arch Dis Child , vol.77 , pp. 214-218
    • Silva, I.N.1    Kater, C.E.2    Cunha, C.F.3    Viana, M.B.4
  • 11
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    • Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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    • David, M.1    Sempe, M.2    Blanc, M.I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.