Witchel SF - Search Results

1

Oocyte Cryopreservation in a Transgender Male Adolescent.

Rothenberg SS, Witchel SF, Menke MN. Rothenberg SS, et al. Among authors: witchel sf. N Engl J Med. 2019 Feb 28;380(9):886-887. doi: 10.1056/NEJMc1813275. N Engl J Med. 2019. PMID: 30811918 No abstract available.

2

Leptin concentrations in precocious puberty or untimely puberty with and without GnRH analogue therapy.

Witchel SF, Arslanian S, Lee PA. Witchel SF, et al. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):839-45. doi: 10.1515/jpem.1999.12.6.839. J Pediatr Endocrinol Metab. 1999. PMID: 10614541

3

Disorders of Puberty: Take a Good History!

Witchel SF. Witchel SF. J Clin Endocrinol Metab. 2016 Jul;101(7):2643-6. doi: 10.1210/jc.2016-2116. J Clin Endocrinol Metab. 2016. PMID: 27381960 No abstract available.

4

Genetics, Genome-Wide Association Studies, and Menarche.

Witchel SF. Witchel SF. Semin Reprod Med. 2016 Jul;34(4):205-14. doi: 10.1055/s-0036-1585405. Epub 2016 Aug 11. Semin Reprod Med. 2016. PMID: 27513021 Review.

5

Polycystic ovary syndrome in adolescent girls.

Baldauff NH, Witchel SF. Baldauff NH, et al. Among authors: witchel sf. Curr Opin Endocrinol Diabetes Obes. 2017 Feb;24(1):56-66. doi: 10.1097/MED.0000000000000309. Curr Opin Endocrinol Diabetes Obes. 2017. PMID: 27906711 Review.

6

Non-classic congenital adrenal hyperplasia.

Witchel SF. Witchel SF. Steroids. 2013 Aug;78(8):747-50. doi: 10.1016/j.steroids.2013.04.010. Epub 2013 Apr 28. Steroids. 2013. PMID: 23632099 Review.

7

Treatment of central precocious puberty: comparison of urinary gonadotropin excretion and gonadotropin-releasing hormone (GnRH) stimulation tests in monitoring GnRH analog therapy.

Witchel SF, Baens-Bailon RG, Lee PA. Witchel SF, et al. J Clin Endocrinol Metab. 1996 Apr;81(4):1353-6. doi: 10.1210/jcem.81.4.8636332. J Clin Endocrinol Metab. 1996. PMID: 8636332

8

Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Witchel SF, Bhamidipati DK, Hoffman EP, Cohen JB. Witchel SF, et al. J Clin Endocrinol Metab. 1996 Nov;81(11):4081-8. doi: 10.1210/jcem.81.11.8923864. J Clin Endocrinol Metab. 1996. PMID: 8923864

9

Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22).

Witchel SF, Wenger SL, Hoffman EP. Witchel SF, et al. J Pediatr Adolesc Gynecol. 1997 May;10(2):78-82. doi: 10.1016/s1083-3188(97)70055-x. J Pediatr Adolesc Gynecol. 1997. PMID: 9179806

10

Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Witchel SF, Lee PA, Suda-Hartman M, Trucco M, Hoffman EP. Witchel SF, et al. J Clin Endocrinol Metab. 1997 Jul;82(7):2097-101. doi: 10.1210/jcem.82.7.4086. J Clin Endocrinol Metab. 1997. PMID: 9215278

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