Speiser, Phyllis W.

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society Clinical Practice Guideline.

Speiser, P. W., Azziz, R., Baskin, L. S., Ghizzoni, L., Hensle, T. W., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Montori, V. M., Oberfield, S. E., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,468

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency*

White, P. C., & Speiser, P. W. (2000) · Endocrine Reviews

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,432

Congenital adrenal hyperplasia

Speiser, P. W., & White, P. C. (2003) · New England Journal of Medicine

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,405

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline

Speiser, P. W., Arlt, W., Auchus, R. J., Baskin, L. S., Conway, G. S., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Murad, M. H., Oberfield, S. E., et al. (2018) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,234

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Speiser, P. W., Dupont, J., Zhu, D., Serrat, J., Buegeleisen, M., Tusie-Luna, M. T., Lesser, M., New, M. I., & White, P. C. (1992) · Journal of Clinical Investigation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 572

Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management

Claahsen - van der Grinten, H. L., Speiser, P. W., Ahmed, S. F., Arlt, W., Auchus, R. J., Falhammar, H., Flück, C. E., Guasti, L., Huebner, A., Kortmann, B. B. M., et al. (2022) · Endocrine Reviews

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 556

High frequency of nonclassical steroid 21-hydroxylase deficiency

SPEISER, P. W., DUPONT, B. O., RUBINSTEIN, P., PIAZZA, A., KASTELAN, A., & NEW, M. I. (1986) · Obstetrical & Gynecological Survey

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 523

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2.

Pascoe, L., Curnow, K. M., Slutsker, L., Connell, J. M., Speiser, P. W., New, M. I., & White, P. C. (1992) · Proceedings of the National Academy of Sciences

Hormonal Regulation and HypertensionRenin-Angiotensin System Studies

Cited by 271

Mutations in Prokineticin 2 and Prokineticin receptor 2 genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

Cole, L. W., Sidis, Y., Zhang, C., Quinton, R., Plummer, L., Pignatelli, D., Hughes, V. A., Dwyer, A. A., Raivio, T., Hayes, F. J., et al. (2008) · The Journal of Clinical Endocrinology & Metabolism

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 208

Molecular Genetic Analysis of Nonclassic Steroid 21-Hydroxylase Deficiency Associated with HLA-B14,DR1

Speiser, P. W., New, M. I., & White, P. C. (1988) · New England Journal of Medicine

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 205

21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: a multicenter study

Moran, C., Azziz, R., Carmina, E., Dewailly, D., Fruzzetti, F., Ibañez, L., Knochenhauer, E. S., Marcondes, J. A. M., Mendonca, B. B., Pignatelli, D., et al. (2000) · American Journal of Obstetrics and Gynecology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 185

A Mutation (Pro-30 to Leu) in CYP 21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

Tusie-Luna, M.-T., Speiser, P. W., Dumic, M., New, M. I., & White, P. C. (1991) · Molecular Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 183

Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia

Moran, C., Azziz, R., Weintrob, N., Witchel, S. F., Rohmer, V., Dewailly, D., Marcondes, J. A. M., Pugeat, M., Speiser, P. W., Pignatelli, D., et al. (2006) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 174

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency.

Speiser, P. W., Serrat, J., New, M. I., & Gertner, J. M. (1992) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 143

Mutations in steroid 21-hydroxylase (CYP21)

White, P. C., Tusie-Luna, M.-T., New, M. I., & Speiser, P. W. (1994) · Human Mutation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 129

Genital Reconstructive Surgery in Females With Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

Almasri, J., Zaiem, F., Rodriguez-Gutierrez, R., Tamhane, S. U., Iqbal, A. M., Prokop, L. J., Speiser, P. W., Baskin, L. S., Bancos, I., & Murad, M. H. (2018) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersUrological Disorders and Treatments

Cited by 127

Cardiovascular and Metabolic Outcomes in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

Tamhane, S., Rodriguez-Gutierrez, R., Iqbal, A. M., Prokop, L. J., Bancos, I., Speiser, P. W., & Murad, M. H. (2018) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 123

A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotype

Speiser, P. W., Knochenhauer, E. S., Dewailly, D., Fruzzetti, F., Marcondes, J. A. M., & Azziz, R. (2000) · Molecular Genetics and Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 89

Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophy

Nass, R., Heier, L., Moshang, T., Oberfield, S., George, A., New, M. I., & Speiser, P. W. (1997) · Journal of Child Neurology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 67

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Speiser, P. W., & White, P. C. (1998) · Clinical Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 39

Newborn screening protocols and positive predictive value for congenital adrenal hyperplasia vary across the United States

Speiser, P., Chawla, R., Chen, M., Diaz-Thomas, A., Finlayson, C., Rutter, M., Sandberg, D., Shimy, K., Talib, R., Cerise, J., et al. (2020) · International Journal of Neonatal Screening

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 36

Iatrogenic Cushing syndrome in a child with congenital adrenal hyperplasia: erroneous compounding of hydrocortisone

Barillas, J. E., Eichner, D., Van Wagoner, R., & Speiser, P. W. (2018) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 35

An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population

Dumić, M., Brkljačić, L., Speiser, P. W., Wood, E., Crawford, C., Plavšić, V., Baničeviác, M., Radmanović, S., Radica, A., Kaštelan, A., et al. (1990) · Acta Endocrinologica

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 33

Steroid 21-hydroxylase expression and activity in human lymphocytes

Zhou, Z., Agarwal, V. R., Dixit, N., White, P., & Speiser, P. W. (1997) · Molecular and Cellular Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 28