-
1
-
-
0017179271
-
The application of serum 17-OH-progesterone radioimmunoassay to the diagnosis management of congenital adrenal hyperplasia
-
Hughes IA, Winter JSD: The application of serum 17-OH-progesterone radioimmunoassay to the diagnosis management of congenital adrenal hyperplasia. J Pediatr 1976;88:766-773.
-
(1976)
J Pediatr
, vol.88
, pp. 766-773
-
-
Hughes, I.A.1
Winter, J.S.D.2
-
2
-
-
0027423246
-
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
-
-
Mesiano, S.1
Coulter, C.L.2
Jaffe, R.B.3
-
3
-
-
0028057326
-
Adrenal steroidogenesis in very low birth weight preterm infants
-
Hingre RV, Gross SJ, Hingre KS, Mayes DM, Richman RA: Adrenal steroidogenesis in very low birth weight preterm infants. J Clin Endocrinol Metab 1994;78:266-270.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 266-270
-
-
Hingre, R.V.1
Gross, S.J.2
Hingre, K.S.3
Mayes, D.M.4
Richman, R.A.5
-
4
-
-
0025995697
-
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
-
5
-
-
0036345166
-
The diagnosis of congenital adrenal hyperplasia in newborn by gas chromatography/mass spectrometry analysis of random urine specimens
-
Caulfield MP, Lynn T, Gottschalk ME, Jones KL, Taylor NF, Malunowicz EM, Shackleton CH, Reitz RE, Fisher DA: The diagnosis of congenital adrenal hyperplasia in newborn by gas chromatography/mass spectrometry analysis of random urine specimens. J Clin Endocrinol Metab 2002;87:3682-3690.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 3682-3690
-
-
Caulfield, M.P.1
Lynn, T.2
Gottschalk, M.E.3
Jones, K.L.4
Taylor, N.F.5
Malunowicz, E.M.6
Shackleton, C.H.7
Reitz, R.E.8
Fisher, D.A.9
-
6
-
-
0942298678
-
Reference values for urinary steroids in newborn infants: Gas chromatography/mass spectrometry in selected ion monitoring
-
Homma K, Hasegawa T, Masumoto M, Takeshita E, Watanabe K, Chiba H, Kurosawa T, Takahashi T, Matsuo N: Reference values for urinary steroids in newborn infants: Gas chromatography/mass spectrometry in selected ion monitoring. Endocr J 2003;50:783-792.
-
(2003)
Endocr J
, vol.50
, pp. 783-792
-
-
Homma, K.1
Hasegawa, T.2
Masumoto, M.3
Takeshita, E.4
Watanabe, K.5
Chiba, H.6
Kurosawa, T.7
Takahashi, T.8
Matsuo, N.9
-
7
-
-
0036075210
-
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
-
8
-
-
0020556434
-
Genotyping steroid 21-hydroxylase deficiency: Hormonal reference data
-
New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS: Genotyping steroid 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
Dupont, B.7
Stoner, E.8
Levy, D.J.9
Pang, S.10
Levine, L.S.11
-
10
-
-
0021034930
-
Neonatal screening for congenital adrenal hyperplasia
-
Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, Paolini M: Neonatal screening for congenital adrenal hyperplasia. Arch Dis Child 1983;58:803-806.
-
(1983)
Arch Dis Child
, vol.58
, pp. 803-806
-
-
Cacciari, E.1
Balsamo, A.2
Cassio, A.3
Piazzi, S.4
Bernardi, F.5
Salardi, S.6
Cicognani, A.7
Pirazzoli, P.8
Zappulla, F.9
Capelli, M.10
Paolini, M.11
-
11
-
-
0022548502
-
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
-
-
0026734638
-
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
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