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Congenital adrenal hyperplasia.
Speiser PW, White PC. Speiser PW, et al. N Engl J Med. 2003 Aug 21;349(8):776-88. doi: 10.1056/NEJMra021561. N Engl J Med. 2003. PMID: 12930931 Review. No abstract available.
Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency.
Speiser PW, Serrat J, New MI, Gertner JM. Speiser PW, et al. J Clin Endocrinol Metab. 1992 Dec;75(6):1421-4. doi: 10.1210/jcem.75.6.1464643. J Clin Endocrinol Metab. 1992. PMID: 1464643
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Speiser PW, New MI, Tannin GM, Pickering D, Yang SY, White PC. Speiser PW, et al. Hum Genet. 1992 Mar;88(6):647-8. doi: 10.1007/BF02265290. Hum Genet. 1992. PMID: 1551668
Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia).
Karaviti LP, Mercado AB, Mercado MB, Speiser PW, Buegeleisen M, Crawford C, Antonian L, White PC, New MI. Karaviti LP, et al. Among authors: speiser pw. J Steroid Biochem Mol Biol. 1992 Mar;41(3-8):445-51. doi: 10.1016/0960-0760(92)90370-x. J Steroid Biochem Mol Biol. 1992. PMID: 1562517 Clinical Trial.
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Speiser PW, Dupont J, Zhu D, Serrat J, Buegeleisen M, Tusie-Luna MT, Lesser M, New MI, White PC. Speiser PW, et al. J Clin Invest. 1992 Aug;90(2):584-95. doi: 10.1172/JCI115897. J Clin Invest. 1992. PMID: 1644925 Free PMC article.
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E, et al. Speiser PW, et al. J Clin Endocrinol Metab. 1990 Apr;70(4):838-48. doi: 10.1210/jcem-70-4-838. J Clin Endocrinol Metab. 1990. PMID: 1969421 Review.
Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase.
Speiser PW, Agdere L, Ueshiba H, White PC, New MI. Speiser PW, et al. N Engl J Med. 1991 Jan 17;324(3):145-9. doi: 10.1056/NEJM199101173240302. N Engl J Med. 1991. PMID: 1984191
Bilateral adrenal uptake of gallium-67 citrate in a patient with congenital adrenal hyperplasia.
Lorberboym M, Sarkar SD, Speiser P, Tannen G, New MI. Lorberboym M, et al. Among authors: speiser p. Clin Nucl Med. 1990 Nov;15(11):849. doi: 10.1097/00003072-199011000-00021. Clin Nucl Med. 1990. PMID: 2292164 No abstract available.
Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
Speiser PW, New MI, White PC. Speiser PW, et al. N Engl J Med. 1988 Jul 7;319(1):19-23. doi: 10.1056/NEJM198807073190104. N Engl J Med. 1988. PMID: 3260007
Splicing mutation in CYP21 associated with delayed presentation of salt-wasting congenital adrenal hyperplasia.
Kohn B, Day D, Alemzadeh R, Enerio D, Patel SV, Pelczar JV, Speiser PW. Kohn B, et al. Among authors: speiser pw. Am J Med Genet. 1995 Jul 3;57(3):450-4. doi: 10.1002/ajmg.1320570318. Am J Med Genet. 1995. PMID: 7677150
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