Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

208 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Congenital adrenal hyperplasia: an update in children.
Trapp CM, Speiser PW, Oberfield SE. Trapp CM, et al. Curr Opin Endocrinol Diabetes Obes. 2011 Jun;18(3):166-70. doi: 10.1097/MED.0b013e328346938c. Curr Opin Endocrinol Diabetes Obes. 2011. PMID: 21494138 Free PMC article. Review.
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC; Endocrine Society. Speiser PW, et al. Among authors: oberfield se. J Clin Endocrinol Metab. 2010 Sep;95(9):4133-60. doi: 10.1210/jc.2009-2631. J Clin Endocrinol Metab. 2010. PMID: 20823466 Free PMC article.
A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency.
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC. Speiser PW, et al. Among authors: oberfield se. Int J Pediatr Endocrinol. 2010;2010:494173. doi: 10.1155/2010/494173. Epub 2010 Jun 30. Int J Pediatr Endocrinol. 2010. PMID: 20981249 Free PMC article.
Childhood hypertension due to adrenocortical disorders.
Oberfield SE, Levine LS, New MI. Oberfield SE, et al. Pediatr Ann. 1982 Jul;11(7):623-6, 628. doi: 10.3928/0090-4481-19820701-12. Pediatr Ann. 1982. PMID: 6287390 Review. No abstract available.
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: oberfield s. J Clin Endocrinol Metab. 1980 Dec;51(6):1316-24. doi: 10.1210/jcem-51-6-1316. J Clin Endocrinol Metab. 1980. PMID: 6449518
208 results