-
1
-
-
0033607164
-
Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess
-
New MI, Wilson RC. Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess. PNAS 1999; 22: 2790-2797.
-
(1999)
PNAS
, vol.22
, pp. 2790-2797
-
-
New, M.I.1
Wilson, R.C.2
-
2
-
-
0034454269
-
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
-
White PC, Speiser PW. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Endocrine Rev 2000; 21: 245-291.
-
(2000)
Endocrine Rev
, vol.21
, pp. 245-291
-
-
White, P.C.1
Speiser, P.W.2
-
3
-
-
0020556434
-
Genotyping 21-hydroxylase deficiency: Hormonal reference data
-
New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, et al. Genotyping 21-hydroxylase deficiency: Hormonal reference data. J Clin Endocrinol Metab 1983; 57: 320-326.
-
(1983)
J Clin Endocrinol Metab
, vol.57
, pp. 320-326
-
-
New, M.I.1
Lorenzen, F.2
Lerner, A.J.3
Kohn, B.4
Oberfield, S.E.5
Pollack, M.S.6
-
4
-
-
0031772706
-
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
-
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
-
-
0036726640
-
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
-
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
-
-
0034917140
-
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
-
-
0030820133
-
Randomised controlled trial of growth effect of hydrocortisone in congenital adrenal hyperplasia
-
Silva IN, Kater CE, Cunha CF, Viana MB. Randomised controlled trial of growth effect of hydrocortisone in congenital adrenal hyperplasia. Arch Dis Child 1997; 77: 214 -218.
-
(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
-
-
0028348383
-
Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
David M, Sempe M, Blanc MI. Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Arch Pediatr 1994; 1: 363-367.
-
(1994)
Arch Pediatr
, vol.1
, pp. 363-367
-
-
David, M.1
Sempe, M.2
Blanc, M.I.3
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