Tribune of the Underclass
- 期刊名称Reviews in American History
- 作者Review by: Stephen B. Oates
- 卷第7卷
- 期第2期
- 印刷ISSN0048-7511
- 电子ISSN1080-6628
- 文件大小596.99KB
- 发表时间1979-06
- DOI10.2307/2701107
- 页码286-292
Congenital Adrenal Hyperplasia || Genetics of Congenital Adrenal HyperplasiaHindmarsh, Peter C. · 2017
Congenital Adrenal Hyperplasia || Common Forms of Congenital Adrenal HyperplasiaHindmarsh, Peter C. · 2017
Congenital Adrenal Hyperplasia || Other Blocks in the Pathway Causing Congenital Adrenal HyperplasiaHindmarsh, Peter C. · 2017
Congenital Adrenal Hyperplasia || Other Treatments for Congenital Adrenal Hyperplasia—Prednisolone, Dexamethasone and AdrenalectomyHindmarsh, Peter C. · 2017
Adrenal Glands || Classic Congenital Adrenal HyperplasiaLinos, Dimitrios; van Heerden, Jon A. · 2005
Testicular Adrenal Rests in Congenital Adrenal HyperplasiaYannes, Michael; Tublin, Mitchell · Ultrasound Quarterly · 2015
Adrenal Disorders: II. Congenital Virilizing Adrenal HyperplasiaWilkins, L. · Archives of Disease in Childhood · 1962
Experimental Congenital Adrenal Cortical Hyperplasia: Prevention of Adrenal Hyperplasia and Clitoral Hypertrophy by Corticosterone. ()Goldman, A. S.; Yakovac, W. C. · Experimental Biology and Medicine · 1966
Molecular Genetic Analysis of Nonclassic Steroid 21 -Hydroxylase Deficiency Associated with HLA-B14, DRISPEISER, PHYLLIS W.; NEW, MARIA I.; WHITE, PERRIN C. · Obstetrical & Gynecological Survey · 1988
Molecular Genetic Analysis of Nonclassic Steroid 21-Hydroxylase Deficiency Associated with HLA-B14,DR1Speiser, Phyllis W.; New, Maria I.; White, Perrin C. · New England Journal of Medicine · 1988
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice GuidelineSpeiser, Phyllis W.; Azziz, Ricardo; Baskin, Laurence S.; Ghizzoni, Lucia; Hensle, Terry W.; Merke, Deborah P.; Meyer-Bahlburg, Heino F. L.; Miller, Walter L.; Montori, Victor M.; Oberfield, Sharon E.; Ritzen, Martin; White, Perrin C. · The Journal of Clinical Endocrinology & Metabolism · 2010
A Mutation (Pro-30 to Leu) in <i>CYP</i> 21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency AlleleTusie-Luna, Maria-Teresa; Speiser, Phyllis W.; Dumic, Miro; New, Maria I.; White, Perrin C. · Molecular Endocrinology · 1991
Structure of the Human RD Gene: A Highly Conserved Gene in the Class III Region of the Major Histocompatibility ComplexSPEISER, PHYLLIS W.; WHITE, PERRIN C. · DNA · 1989
A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase DeficiencySpeiser, Phyllis W.; Azziz, Ricardo; Baskin, Laurence S.; Ghizzoni, Lucia; Hensle, Terry W.; Merke, Deborah P.; Meyer-Bahlburg, Heino F. L.; Miller, Walter L.; Montori, Victor M.; Oberfield, Sharon E.; Ritzen, Martin; White, Perrin C. · International Journal of Pediatric Endocrinology · 2010