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108 related items for PubMed ID: 2552757
1. A chemiluminescent method for the measurement of pregnanetriol-3 alpha-glucuronide in human diluted urine. Pinzani P, Magini A, Franceschetti F, Messeri G, Pazzagli M. J Biolumin Chemilumin; 1989 Jul; 4(1):580-6. PubMed ID: 2552757 [Abstract] [Full Text] [Related]
2. A chemiluminescent immunoassay for the direct measurement of urinary 5 alpha-androstane-3 alpha, 17 beta-diol-glucuronide in urine. Pinzani P, Franceschetti F, Magini A, Orlandini A, Pazzagli M. J Biolumin Chemilumin; 1989 Jul; 4(1):575-9. PubMed ID: 2801242 [Abstract] [Full Text] [Related]
3. [Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography]. Hikita Y. Nihon Naibunpi Gakkai Zasshi; 1985 Mar 20; 61(3):197-219. PubMed ID: 3874793 [Abstract] [Full Text] [Related]
4. The radioimmunoassay of pregnanetriol 3 alpha-glucuronide. Samarajeewa P, Kellie AE. J Steroid Biochem; 1985 Jun 20; 22(6):843-9. PubMed ID: 4021487 [Abstract] [Full Text] [Related]
5. Molecular characterization of a Leydig cell tumor presenting as congenital adrenal hyperplasia. Solish SB, Goldsmith MA, Voutilainen R, Miller WL. J Clin Endocrinol Metab; 1989 Dec 20; 69(6):1148-52. PubMed ID: 2555382 [Abstract] [Full Text] [Related]
6. Diagnosis of adrenal cortical dysfunction by liquid chromatography-tandem mass spectrometry. Kao PC, Machacek DA, Magera MJ, Lacey JM, Rinaldo P. Ann Clin Lab Sci; 2001 Apr 20; 31(2):199-204. PubMed ID: 11337910 [Abstract] [Full Text] [Related]
7. Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates. Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, Toyoura T, Jinno K, Ohashi T, Hamajima T, Takahashi Y, Takahashi T, Matsuo N. J Clin Endocrinol Metab; 2004 Dec 20; 89(12):6087-91. PubMed ID: 15579762 [Abstract] [Full Text] [Related]
8. Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots. Lai CC, Tsai CH, Tsai FJ, Lee CC, Lin WD. Rapid Commun Mass Spectrom; 2001 Dec 20; 15(22):2145-51. PubMed ID: 11746879 [Abstract] [Full Text] [Related]
9. Urinary excretion of pregnanetriol and 5 -pregnenetriol in two forms of congenital adrenal hyperplasia. Bongiovanni AM, Eberlein WR, Moshang T. J Clin Invest; 1971 Dec 20; 50(12):2751-4. PubMed ID: 5129323 [Abstract] [Full Text] [Related]
10. [Pregnanetriolone excretion after stimulation with ACTH as a test on presumably heterozygous carriers of a 21-hydroxylase-deficiency (author's transl)]. Gleispach H, Berger H, Glatzl J, Rössler H. Padiatr Padol; 1974 Dec 20; 9(3):204-8. PubMed ID: 4369650 [No Abstract] [Full Text] [Related]
11. Lipid cell tumor of the ovary in reference to adult-onset congenital adrenal hyperplasia and polycystic ovary syndrome. A case report. Rosenfield RL, Cohen RM, Talerman A. J Reprod Med; 1987 May 20; 32(5):363-9. PubMed ID: 3598985 [Abstract] [Full Text] [Related]
12. [A case of congenital adrenogenital syndrome]. Sumiya H, Kawamura K, Kataumi Z, Fuse H, Ito H, Shimazaki J. Hinyokika Kiyo; 1985 Aug 20; 31(8):1433-9. PubMed ID: 3878668 [Abstract] [Full Text] [Related]
13. Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms. Kamrath C, Hartmann MF, Boettcher C, Wudy SA. J Pediatr; 2014 Aug 20; 165(2):280-4. PubMed ID: 24862381 [Abstract] [Full Text] [Related]
14. [Determination of urinary 17 alpha-hydroxyprogesterone excretion using ELISA--evaluation of normal subjects and patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. Shibata Y. Nihon Naibunpi Gakkai Zasshi; 1991 Aug 20; 67(8):819-39. PubMed ID: 1813324 [Abstract] [Full Text] [Related]
15. Detection of late-onset adrenal hyperplasia in girls with peripubertal virilization. Sólyom J, Gács G, Keszei K, Láng K, Orley J, Petheö I, Ságodi L. Acta Endocrinol (Copenh); 1987 Jul 20; 115(3):413-8. PubMed ID: 3039770 [Abstract] [Full Text] [Related]
16. Urinary 17 alpha-hydroxyprogesterone in management of 21-hydroxylase deficiency. Lim YJ, Yong AB, Warne GL, Montalto J. J Paediatr Child Health; 1995 Feb 20; 31(1):47-50. PubMed ID: 7748691 [Abstract] [Full Text] [Related]
17. Congenital adrenal hyperplasia family studies using the short ACTH test. Kreutzmann DJ, Cowell CT, Howard NJ, De Souza M, Silink M. Aust Paediatr J; 1989 Dec 20; 25(6):340-5. PubMed ID: 2619637 [Abstract] [Full Text] [Related]
18. [Evaluation of salivary 17-hydroxyprogesterone and its clinical usefulness in the study of hirsutism and the partial deficiency of 21-hydroxylase]. Bonnín MR, Machuca I, Villabona C, González A, Soler J, Navarro MA. Med Clin (Barc); 1994 Feb 12; 102(5):169-71. PubMed ID: 8127165 [Abstract] [Full Text] [Related]
19. [Strategies in screening of nonclassical forms of congenital adrenal hyperplasia caused by P450c21 deficiency in hyperandrogenic women]. Rodríguez Espinosa J, Calaf Alsina J. Med Clin (Barc); 1994 Nov 19; 103(17):645-51. PubMed ID: 7808062 [Abstract] [Full Text] [Related]
20. 17-Hydroxyprogesterone in normal children and congenital adrenal hyperplasia. Measurement in serum by radioimmunoassay after thin-layer chromatography. Petersen KE, Christensen T. Acta Paediatr Scand; 1979 Mar 19; 68(2):205-11. PubMed ID: 217232 [Abstract] [Full Text] [Related] Page: [Next] [New Search]