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Premature sexual development in individuals with neurodevelopmental disabilities.
Siddiqi SU, Van Dyke DC, Donohoue P, McBrien DM. Siddiqi SU, et al. Dev Med Child Neurol. 1999 Jun;41(6):392-5. doi: 10.1017/s0012162299000857. Dev Med Child Neurol. 1999. PMID: 10400173
E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Kirby-Keyser L, Porter CC, Donohoue PA. Kirby-Keyser L, et al. Hum Mutat. 1997;9(2):181-2. doi: 10.1002/(SICI)1098-1004(1997)9:2<181::AID-HUMU12>3.0.CO;2-Z. Hum Mutat. 1997. PMID: 9067760 No abstract available.
Phenotypic evolution of classic 21-hydroxylase deficiency.
Hoffman WH, Shin MY, Donohoue PA, Helman SW, Brown SL, Rosculet G, Mahesh VB. Hoffman WH, et al. Clin Endocrinol (Oxf). 1996 Jul;45(1):103-9. Clin Endocrinol (Oxf). 1996. PMID: 8796146
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
Vallette-Kasic S, Brue T, Pulichino AM, Gueydan M, Barlier A, David M, Nicolino M, Malpuech G, D├ęchelotte P, Deal C, Van Vliet G, De Vroede M, Riepe FG, Partsch CJ, Sippell WG, Berberoglu M, Atasay B, de Zegher F, Beckers D, Kyllo J, Donohoue P, Fassnacht M, Hahner S, Allolio B, Noordam C, Dunkel L, Hero M, Pigeon B, Weill J, Yigit S, Brauner R, Heinrich JJ, Cummings E, Riddell C, Enjalbert A, Drouin J. Vallette-Kasic S, et al. J Clin Endocrinol Metab. 2005 Mar;90(3):1323-31. doi: 10.1210/jc.2004-1300. Epub 2004 Dec 21. J Clin Endocrinol Metab. 2005. PMID: 15613420
Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita.
Reutens AT, Achermann JC, Ito M, Ito M, Gu WX, Habiby RL, Donohoue PA, Pang S, Hindmarsh PC, Jameson JL. Reutens AT, et al. J Clin Endocrinol Metab. 1999 Feb;84(2):504-11. doi: 10.1210/jcem.84.2.5468. J Clin Endocrinol Metab. 1999. PMID: 10022408
Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms.
Kyllo JH, Collins MM, Vetter KL, Cuttler L, Rosenfield RL, Donohoue PA. Kyllo JH, et al. Am J Med Genet. 1996 Mar 29;62(3):262-7. doi: 10.1002/(SICI)1096-8628(19960329)62:3<262::AID-AJMG11>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8882784
Rat adipose ob mRNA levels in states of altered circulating glucose and insulin.
Sivitz WI, Bailey HL, Donohoue P. Sivitz WI, et al. Biochem Biophys Res Commun. 1996 Mar 27;220(3):520-5. doi: 10.1006/bbrc.1996.0437. Biochem Biophys Res Commun. 1996. PMID: 8607798
Plasma leptin in diabetic and insulin-treated diabetic and normal rats.
Sivitz WI, Walsh S, Morgan D, Donohoue P, Haynes W, Leibel RL. Sivitz WI, et al. Metabolism. 1998 May;47(5):584-91. doi: 10.1016/s0026-0495(98)90244-x. Metabolism. 1998. PMID: 9591751
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