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Diabetes Care|November 6, 2008
Pitfalls in the measurement of the nocturnal blood pressure dip in adolescents with type 1 diabetesAngela Delaney, Margaret Pellizzari, Phyllis W Speiser, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
Novel P450c17 mutation H373D causing combined 17alpha-hydroxylase/17,20-lyase deficiencyTaninee Sahakitrungruang, Meng Kian Tee, Phyllis W Speiser, et al.
The Journal of Clinical Endocrinology and Metabolism|October 14, 2017
Iatrogenic Cushing Syndrome in a Child With Congenital Adrenal Hyperplasia: Erroneous Compounding of HydrocortisoneJulia E Barillas, Daniel Eichner, Ryan Van Wagoner, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2011
Presentation of primary adrenal insufficiency in childhoodSusan Hsieh, Perrin C White
Clinical Endocrinology|February 14, 2017
Risk factors for hospitalization of children with congenital adrenal hyperplasiaMing Yang, Perrin C White
The Journal of Clinical Endocrinology and Metabolism|January 21, 2025
Genetics and Pathophysiology of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase DeficiencyMing Yang, Perrin C White
The Journal of Clinical Endocrinology and Metabolism|October 2, 2018
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice GuidelinePhyllis W Speiser, Wiebke Arlt, Richard J Auchus, et al.
Pediatric Endocrinology Reviews : PER|February 4, 2006
Safety of medications and hormones used in pediatric endocrinology: adrenalGraeme R Frank, Phyllis W Speiser, Kurt J Griffin, et al.
International Journal of Pediatric Endocrinology|October 29, 2010
A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase DeficiencyPhyllis W Speiser, Ricardo Azziz, Laurence S Baskin, et al.
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