先天性腎上腺增生症 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "先天性腎上腺增生症" in Chinese language version.

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7nih.gov

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archive.org

Dauber A, Kellogg M, Majzoub JA. Monitoring of therapy in congenital adrenal hyperplasia. Clinical Chemistry. 2010, 56 (8): 1245–51. PMID 20558634. doi:10.1373/clinchem.2010.146035 .
Mais, Daniel D. Quick compendium of clinical pathology 2nd. Chicago: ASCP Press. 2008. ISBN 978-0891895671.

books.google.com

David A. Warrell. Oxford textbook of medicine: Sections 18-33. Oxford University Press. 2005: 261– [2010-06-14]. ISBN 978-0-19-856978-7. （原始内容存档于2013-06-10）.

doi.org

Dauber A, Kellogg M, Majzoub JA. Monitoring of therapy in congenital adrenal hyperplasia. Clinical Chemistry. 2010, 56 (8): 1245–51. PMID 20558634. doi:10.1373/clinchem.2010.146035 .
Merke DP, Auchus RJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. The New England Journal of Medicine. September 2020, 383 (13): 1248–1261. PMID 32966723. S2CID 221884108. doi:10.1056/NEJMra1909786.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology and Metabolism. 2018, 103 (11): 4043–4088. PMC 6456929 . PMID 30272171. doi:10.1210/jc.2018-01865.
Miller WL. The syndrome of 17,20 lyase deficiency. The Journal of Clinical Endocrinology and Metabolism. January 2012, 97 (1): 59–67. PMC 3251937 . PMID 22072737. doi:10.1210/jc.2011-2161.
Häggström, Mikael; Richfield, David. Diagram of the pathways of human steroidogenesis. WikiJournal of Medicine. 2014, 1 (1). ISSN 2002-4436. doi:10.15347/wjm/2014.005 .
Kruse, B.; Riepe, F. G.; Krone, N.; Bosinski, H. a. G.; Kloehn, S.; Partsch, C. J.; Sippell, W. G.; Mönig, H. Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life. Experimental and Clinical Endocrinology & Diabetes. July 2004, 112 (7): 343–355. ISSN 0947-7349. PMID 15239019. doi:10.1055/s-2004-821013.

medlineplus.gov

3-beta-hydroxysteroid dehydrogenase deficiency. MedlinePlus. [2021-06-02]. （原始内容存档于2020-09-28）.

nih.gov

ncbi.nlm.nih.gov

Feingold KR, Anawalt B, Boyce A, Chrousos G, de Herder WW, Dungan K, Grossman A, Hershman JM, Hofland HJ, Kaltsas G, Koch C, Kopp P, Korbonits M, McLachlan R, Morley JE, New M, Purnell J, Singer F, Stratakis CA, Trence DL, Wilson DP, New M, Yau M, Lekarev O, Lin-Su K, Parsa A, Pina C, Yuen T, Khattab A. Congenital Adrenal Hyperplasia. MDText.com, Inc. 2017-03-15 [2022-02-28]. PMID 25905188. （原始内容存档于2020-11-12）.
Dauber A, Kellogg M, Majzoub JA. Monitoring of therapy in congenital adrenal hyperplasia. Clinical Chemistry. 2010, 56 (8): 1245–51. PMID 20558634. doi:10.1373/clinchem.2010.146035 .
Merke DP, Auchus RJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. The New England Journal of Medicine. September 2020, 383 (13): 1248–1261. PMID 32966723. S2CID 221884108. doi:10.1056/NEJMra1909786.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology and Metabolism. 2018, 103 (11): 4043–4088. PMC 6456929 . PMID 30272171. doi:10.1210/jc.2018-01865.
Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment. MDText.com. 2000 [2022-02-28]. （原始内容存档于2020-11-14）.
Miller WL. The syndrome of 17,20 lyase deficiency. The Journal of Clinical Endocrinology and Metabolism. January 2012, 97 (1): 59–67. PMC 3251937 . PMID 22072737. doi:10.1210/jc.2011-2161.
Kruse, B.; Riepe, F. G.; Krone, N.; Bosinski, H. a. G.; Kloehn, S.; Partsch, C. J.; Sippell, W. G.; Mönig, H. Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life. Experimental and Clinical Endocrinology & Diabetes. July 2004, 112 (7): 343–355. ISSN 0947-7349. PMID 15239019. doi:10.1055/s-2004-821013.

semanticscholar.org

api.semanticscholar.org

Merke DP, Auchus RJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. The New England Journal of Medicine. September 2020, 383 (13): 1248–1261. PMID 32966723. S2CID 221884108. doi:10.1056/NEJMra1909786.

web.archive.org

用于死因与疾病统计的ICD-11. 世界卫生组织. [2022-02-28]. （原始内容存档于2021-09-15）（中文）.
Feingold KR, Anawalt B, Boyce A, Chrousos G, de Herder WW, Dungan K, Grossman A, Hershman JM, Hofland HJ, Kaltsas G, Koch C, Kopp P, Korbonits M, McLachlan R, Morley JE, New M, Purnell J, Singer F, Stratakis CA, Trence DL, Wilson DP, New M, Yau M, Lekarev O, Lin-Su K, Parsa A, Pina C, Yuen T, Khattab A. Congenital Adrenal Hyperplasia. MDText.com, Inc. 2017-03-15 [2022-02-28]. PMID 25905188. （原始内容存档于2020-11-12）.
Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment. MDText.com. 2000 [2022-02-28]. （原始内容存档于2020-11-14）.
David A. Warrell. Oxford textbook of medicine: Sections 18-33. Oxford University Press. 2005: 261– [2010-06-14]. ISBN 978-0-19-856978-7. （原始内容存档于2013-06-10）.
3-beta-hydroxysteroid dehydrogenase deficiency. MedlinePlus. [2021-06-02]. （原始内容存档于2020-09-28）.

who.int

icd.who.int

用于死因与疾病统计的ICD-11. 世界卫生组织. [2022-02-28]. （原始内容存档于2021-09-15）（中文）.

worldcat.org

Kumar, Vinay; Abbas, Abul K.; Aster, Jon C. Robbins and Cotran pathologic basis of disease. Kumar, Vinay, 1944-, Abbas, Abul K.,, Aster, Jon C.,, Perkins, James A. Ninth. Philadelphia, PA. 2014: 1128. ISBN 9781455726134. OCLC 879416939.
Häggström, Mikael; Richfield, David. Diagram of the pathways of human steroidogenesis. WikiJournal of Medicine. 2014, 1 (1). ISSN 2002-4436. doi:10.15347/wjm/2014.005 .
Kruse, B.; Riepe, F. G.; Krone, N.; Bosinski, H. a. G.; Kloehn, S.; Partsch, C. J.; Sippell, W. G.; Mönig, H. Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life. Experimental and Clinical Endocrinology & Diabetes. July 2004, 112 (7): 343–355. ISSN 0947-7349. PMID 15239019. doi:10.1055/s-2004-821013.