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2. Delle Piane L, Rinaudo P.F, Miller W.L (2015). 150 years of congenital adrenal hyperplasia: translation and commentary of De Crecchio‟s classic paper from 1865. Endocrinology, 156(4), 1210-1217 |
Sách, tạp chí |
Tiêu đề: |
Endocrinology, 156 |
Tác giả: |
Delle Piane L, Rinaudo P.F, Miller W.L |
Năm: |
2015 |
|
3. Turcu A.F, Auchus R.J (2015). The next 150 years of congenital adrenal hyperplasia. The Journal of Steroid Biochemistry and Molecular Biology, 153, 63-71 |
Sách, tạp chí |
Tiêu đề: |
The Journal of Steroid Biochemistry and Molecular Biology, 153 |
Tác giả: |
Turcu A.F, Auchus R.J |
Năm: |
2015 |
|
4. Grumbach M.M, Shaw E.B (1998). Further studies on the treatment of congenital adrenal hyperplasia with cortisone: IV. Effect of cortisone and compound B in infants with disturbed electrolyte metabolism, by John F. Crigler Jr, MD, Samuel H. Silverman, MD, and Lawson Wilkins, MD, Pediatrics, 1952;10:397-413. Pediatrics, 102(1 Pt 2), 215-221 |
Sách, tạp chí |
Tiêu đề: |
Further studies on the treatment of congenital adrenal hyperplasia with cortisone: IV. Effect of cortisone and compound B in infants with disturbed electrolyte metabolism |
Tác giả: |
Grumbach M.M, Shaw E.B, John F. Crigler Jr, MD, Samuel H. Silverman, MD, Lawson Wilkins, MD |
Nhà XB: |
Pediatrics |
Năm: |
1998 |
|
5. Engel F.L, Owen J.A, Wester T.B (1957). 9-alpha- Fluorohydrocortisone-induced hypertension in a male infant with adrenogenitalism, and in 6 adults with Addison‟s disease. The Journal of Clinical Endocrinology and Metabolism, 17(2), 272-279 |
Sách, tạp chí |
Tiêu đề: |
9-alpha- Fluorohydrocortisone-induced hypertension in a male infant with adrenogenitalism, and in 6 adults with Addison‟s disease |
Tác giả: |
Engel F.L, Owen J.A, Wester T.B |
Nhà XB: |
The Journal of Clinical Endocrinology and Metabolism |
Năm: |
1957 |
|
6. Dupont B, Oberfield S.E, Smithwick E.M et al (1977). Close genetic linkage between HLA and congenital adrenal hyperplasia (21- hydroxylase deficiency). Lancet (London, England), 2(8052-8053), 1309-1312 |
Sách, tạp chí |
Tiêu đề: |
Close genetic linkage between HLA and congenital adrenal hyperplasia (21- hydroxylase deficiency) |
Tác giả: |
Dupont B, Oberfield S.E, Smithwick E.M, et al |
Nhà XB: |
Lancet (London, England) |
Năm: |
1977 |
|
7. Wedell A, Thilén A, Ritzén E.M et al (1994). Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation. The Journal of Clinical Endocrinology and Metabolism, 78(5), 1145-1152 |
Sách, tạp chí |
Tiêu đề: |
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation |
Tác giả: |
Wedell A, Thilén A, Ritzén E.M |
Nhà XB: |
The Journal of Clinical Endocrinology and Metabolism |
Năm: |
1994 |
|
8. Wedell A, Ritzén E.M, Haglund-Stengler B et al (1992). Steroid 21- hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations. Proceedings of the National Academy of Sciences of the United States of America, 89(15), 7232-7236 |
Sách, tạp chí |
Tiêu đề: |
Steroid 21- hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations |
Tác giả: |
Wedell A, Ritzén E.M, Haglund-Stengler B |
Nhà XB: |
Proceedings of the National Academy of Sciences of the United States of America |
Năm: |
1992 |
|
9. Krone N, Arlt W (2009). Genetics of congenital adrenal hyperplasia. Best Practice & Research. Clinical Endocrinology & Metabolism, 23(2), 181-192 |
Sách, tạp chí |
Tiêu đề: |
Best Practice & Research. Clinical Endocrinology & Metabolism, 23 |
Tác giả: |
Krone N, Arlt W |
Năm: |
2009 |
|
10. Miller W.L, Auchus R.J (2011). The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocrine Reviews, 32(1), 81-151 |
Sách, tạp chí |
Tiêu đề: |
The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders |
Tác giả: |
Miller W.L, Auchus R.J |
Nhà XB: |
Endocrine Reviews |
Năm: |
2011 |
|
11. Speiser P.W, Azziz R, Baskin L.S et al (2010). Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. The Journal of Clinical Endocrinology and Metabolism, 95(9), 4133-4160 |
Sách, tạp chí |
Tiêu đề: |
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline |
Tác giả: |
Speiser P.W, Azziz R, Baskin L.S, et al |
Nhà XB: |
The Journal of Clinical Endocrinology and Metabolism |
Năm: |
2010 |
|
12. Higashijima M, Nawata H, Kato K et al (1987). Studies on lipoprotein and adrenal steroidogenesis: I. Roles of low density lipoprotein- and high density lipoprotein-cholesterol in steroid production in cultured human adrenocortical cells. Endocrinologia Japonica, 34(5), 635-645 |
Sách, tạp chí |
Tiêu đề: |
Studies on lipoprotein and adrenal steroidogenesis: I. Roles of low density lipoprotein- and high density lipoprotein-cholesterol in steroid production in cultured human adrenocortical cells |
Tác giả: |
Higashijima M, Nawata H, Kato K |
Nhà XB: |
Endocrinologia Japonica |
Năm: |
1987 |
|
13. Miller W.L (2007). Steroidogenic acute regulatory protein (StAR), a novel mitochondrial cholesterol transporter. Biochimica Et Biophysica Acta, 1771(6), 663-676 |
Sách, tạp chí |
Tiêu đề: |
Biochimica Et Biophysica Acta, 1771 |
Tác giả: |
Miller W.L |
Năm: |
2007 |
|
14. Parker K.L, Schimmer B.P (1995). Transcriptional regulation of the genes encoding the cytochrome P-450 steroid hydroxylases. Vitamins and Hormones, 51, 339-370 |
Sách, tạp chí |
Tiêu đề: |
Transcriptional regulation of the genes encoding the cytochrome P-450 steroid hydroxylases |
Tác giả: |
Parker K.L, Schimmer B.P |
Nhà XB: |
Vitamins and Hormones |
Năm: |
1995 |
|
15. Yau M, Khattab A, New M.I (2016). Prenatal Diagnosis of Congenital Adrenal Hyperplasia. Endocrinology and Metabolism Clinics of North America, 45(2), 267-281 |
Sách, tạp chí |
Tiêu đề: |
Prenatal Diagnosis of Congenital Adrenal Hyperplasia |
Tác giả: |
Yau M, Khattab A, New M.I |
Nhà XB: |
Endocrinology and Metabolism Clinics of North America |
Năm: |
2016 |
|
16. Speiser P.W, White P.C (2003). Congenital adrenal hyperplasia. The New England Journal of Medicine, 349(8), 776-788 |
Sách, tạp chí |
Tiêu đề: |
Congenital adrenal hyperplasia |
Tác giả: |
Speiser P.W, White P.C |
Nhà XB: |
The New England Journal of Medicine |
Năm: |
2003 |
|
17. White P.C, Speiser P.W (2000). Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocrine Reviews, 21(3), 245-291 |
Sách, tạp chí |
Tiêu đề: |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
Tác giả: |
White P.C, Speiser P.W |
Nhà XB: |
Endocrine Reviews |
Năm: |
2000 |
|
18. Merke D.P, Bornstein S.R (2005). Congenital adrenal hyperplasia. Lancet (London, England), 365(9477), 2125-2136 |
Sách, tạp chí |
Tiêu đề: |
Lancet (London, England), 365 |
Tác giả: |
Merke D.P, Bornstein S.R |
Năm: |
2005 |
|
19. Pallan P.S, Wang C, Lei L et al (2015). Human Cytochrome P450 21A2, the Major Steroid 21-Hydroxylase: structure of the enzyme progesterone substrate complex and rate-limiting C-H bond cleavage.The Journal of Biological Chemistry, 290(21), 13128-13143 |
Sách, tạp chí |
Tiêu đề: |
Human Cytochrome P450 21A2, the Major Steroid 21-Hydroxylase: structure of the enzyme progesterone substrate complex and rate-limiting C-H bond cleavage |
Tác giả: |
P.S. Pallan, C. Wang, L. Lei |
Nhà XB: |
The Journal of Biological Chemistry |
Năm: |
2015 |
|
20. Dacou-Voutetakis C, Dracopoulou M (1999). High incidence of molecular defects of the CYP21 gene in patients with premature adrenarche. The Journal of Clinical Endocrinology and Metabolism, 84(5), 1570-1574 |
Sách, tạp chí |
Tiêu đề: |
High incidence of molecular defects of the CYP21 gene in patients with premature adrenarche |
Tác giả: |
Dacou-Voutetakis C, Dracopoulou M |
Nhà XB: |
The Journal of Clinical Endocrinology and Metabolism |
Năm: |
1999 |
|
21. Parsa, A. A., & New, M. I. (2017). Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. The Journal of Steroid Biochemistry and Molecular Biology, 165(Pt A):2-11 |
Sách, tạp chí |
Tiêu đề: |
The Journal of Steroid Biochemistry and Molecular Biology |
Tác giả: |
Parsa, A. A., & New, M. I |
Năm: |
2017 |
|