Bourdony CJ - Search Results

1

Identification of phthalate esters in the serum of young Puerto Rican girls with premature breast development.

Colón I, Caro D, Bourdony CJ, Rosario O. Colón I, et al. Among authors: bourdony cj. Environ Health Perspect. 2000 Sep;108(9):895-900. doi: 10.1289/ehp.108-2556932. Environ Health Perspect. 2000. PMID: 11017896 Free PMC article.

2

Natural history and incidence of premature thelarche in Puerto Rican girls aged 6 months to 8 years diagnosed between 1990 and 1995.

Larriuz-Serrano MC, Pérez-Cardona CM, Ramos-Valencia G, Bourdony CJ. Larriuz-Serrano MC, et al. Among authors: bourdony cj. P R Health Sci J. 2001 Mar;20(1):13-8. P R Health Sci J. 2001. PMID: 11394211

3

Secondary sexual characteristics and menses in young girls seen in office practice: a study from the Pediatric Research in Office Settings network.

Herman-Giddens ME, Slora EJ, Wasserman RC, Bourdony CJ, Bhapkar MV, Koch GG, Hasemeier CM. Herman-Giddens ME, et al. Among authors: bourdony cj. Pediatrics. 1997 Apr;99(4):505-12. doi: 10.1542/peds.99.4.505. Pediatrics. 1997. PMID: 9093289

4

Early puberty: a cautionary tale.

Herman-Giddens ME, Bourdony C, Slora E, Wasserman R. Herman-Giddens ME, et al. Pediatrics. 2001 Mar;107(3):609-10. doi: 10.1542/peds.107.3.609. Pediatrics. 2001. PMID: 11277110 No abstract available.

5

Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin.

Sandrini F, Farmakidis C, Kirschner LS, Wu SM, Tullio-Pelet A, Lyonnet S, Metzger DL, Bourdony CJ, Tiosano D, Chan WY, Stratakis CA. Sandrini F, et al. Among authors: bourdony cj. J Clin Endocrinol Metab. 2001 Nov;86(11):5433-7. doi: 10.1210/jcem.86.11.8037. J Clin Endocrinol Metab. 2001. PMID: 11701718

6

Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiency.

Wu SM, Stratakis CA, Chan CH, Hallermeier KM, Bourdony CJ, Rennert OM, Chan WY. Wu SM, et al. Among authors: bourdony cj. Mol Genet Metab. 1998 Aug;64(4):256-65. doi: 10.1006/mgme.1998.2724. Mol Genet Metab. 1998. PMID: 9758716 Free article.

7

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers.

Stratakis CA, Lin JP, Pras E, Rennert OM, Bourdony CJ, Chan WY. Stratakis CA, et al. Among authors: bourdony cj. Proc Assoc Am Physicians. 1997 Sep;109(5):478-82. Proc Assoc Am Physicians. 1997. PMID: 9285947

8

Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia.

Laue LL, Wu SM, Kudo M, Bourdony CJ, Cutler GB Jr, Hsueh AJ, Chan WY. Laue LL, et al. Among authors: bourdony cj. Mol Endocrinol. 1996 Aug;10(8):987-97. doi: 10.1210/mend.10.8.8843415. Mol Endocrinol. 1996. PMID: 8843415

9

Absence of molecular defect in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3 beta-HSD activity.

Chang YT, Zhang L, Alkaddour HS, Mason JI, Lin K, Yang X, Garibaldi LR, Bourdony CJ, Dolan LM, Donaldson DL, et al. Chang YT, et al. Among authors: bourdony cj. Pediatr Res. 1995 Jun;37(6):820-4. doi: 10.1203/00006450-199506000-00024. Pediatr Res. 1995. PMID: 7651769

10

Pain and suffering revised.

Bourdony CJ. Bourdony CJ. Bol Asoc Med P R. 1986 Feb;78(2):64. Bol Asoc Med P R. 1986. PMID: 3458472 No abstract available.

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