Congenital adrenal hyperplasia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Congenital adrenal hyperplasia" in English language version.

refsWebsite

Global rank English rank

40nih.gov

4^th place

23doi.org

2^nd place

13worldcat.org

5^th place

4web.archive.org

1^st place

3semanticscholar.org

11^th place

8^th place

3books.google.com

3^rd place

2nejm.org

2,374^th place

6,027^th place

1bham.ac.uk

6,934^th place

4,192^nd place

1chop.edu

low place

1merckmanuals.com

3,097^th place

2,317^th place

1thelancet.com

2,393^rd place

3,174^th place

1archive.org

6^th place

1medlineplus.gov

1,581^st place

1,299^th place

1evms.edu

low place

1icj.org

low place

1bbc.co.uk

8^th place

10^th place

1yahoo.com

38^th place

40^th place

1chicagotribune.com

95^th place

70^th place

archive.org

Mais, Daniel D. (2008). Quick compendium of clinical pathology (2nd ed.). Chicago: ASCP Press. ISBN 978-0891895671.

bbc.co.uk

"BBC Radio 4 – Changing Sex". Retrieved 6 August 2008.

bham.ac.uk

pure-oai.bham.ac.uk

El-Maouche D, Arlt W, Merke DP (November 2017). "Congenital adrenal hyperplasia" (PDF). Lancet. 390 (10108): 2194–2210. doi:10.1016/S0140-6736(17)31431-9. PMID 28576284. S2CID 13737960.

books.google.com

Aubrey Milunsky; Jeff Milunsky (29 January 2010). Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment. John Wiley and Sons. pp. 600–. ISBN 978-1-4051-9087-9. Retrieved 14 June 2010.
Richard D. McAnulty, M. Michele Burnette (2006) Sex and sexuality, Volume 1, Greenwood Publishing Group, p.165
David A. Warrell (2005). Oxford textbook of medicine: Sections 18-33. Oxford University Press. pp. 261–. ISBN 978-0-19-856978-7. Retrieved 14 June 2010.

chicagotribune.com

Schoenberg, Nara (3 April 2019). "'It's a woman. It's not Pulaski.': New documentary argues Revolutionary War hero was intersex". chicagotribune.com. Archived from the original on 2 November 2019. Retrieved 28 May 2020.

chop.edu

Philadelphia, The Children's Hospital of (19 November 2019). "Classic congenital Adrenal Hyperplasia Diagnosed in the Newborn Period". www.chop.edu. Retrieved 5 September 2020.

doi.org

El-Maouche D, Arlt W, Merke DP (November 2017). "Congenital adrenal hyperplasia" (PDF). Lancet. 390 (10108): 2194–2210. doi:10.1016/S0140-6736(17)31431-9. PMID 28576284. S2CID 13737960.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC (2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
Speiser PW, White PC (August 2003). "Congenital adrenal hyperplasia". The New England Journal of Medicine. 349 (8): 776–88. doi:10.1056/NEJMra021561. PMID 12930931.
La, Betty; Tung, Celestine; Choi, Eugene A.; Nguyen, Ha (1 November 2021). "A Gigantic Uterine Leiomyoma and Big Bilateral Adrenal Myelolipomas as a Result of Untreated Congenital Adrenal Hyperplasia". AACE Clinical Case Reports. 7 (6): 342–345. doi:10.1016/j.aace.2021.05.002. PMC 8573279. PMID 34765728.
Krone N, Arlt W (April 2009). "Genetics of congenital adrenal hyperplasia". Best Practice & Research. Clinical Endocrinology & Metabolism. 23 (2): 181–92. doi:10.1016/j.beem.2008.10.014. PMC 5576025. PMID 19500762.
Turcu AF, Nanba AT, Chomic R, Upadhyay SK, Giordano TJ, Shields JJ, Merke DP, Rainey WE, Auchus RJ (May 2016). "Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency". European Journal of Endocrinology. 174 (5): 601–9. doi:10.1530/EJE-15-1181. PMC 4874183. PMID 26865584.
Speiser, Phyllis W.; Arlt, Wiebke; Auchus, Richard J.; Baskin, Laurence S.; Conway, Gerard S.; Merke, Deborah P.; Meyer-Bahlburg, Heino F. L.; Miller, Walter L.; Murad, M. Hassan; Oberfield, Sharon E.; White, Perrin C. (1 November 2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. ISSN 1945-7197. PMC 6456929. PMID 30272171.
Nordenström, Anna; Lajic, Svetlana; Falhammar, Henrik (8 July 2022). "Long-Term Outcomes of Congenital Adrenal Hyperplasia". Endocrinology and Metabolism. 37 (4): 587–598. doi:10.3803/EnM.2022.1528. ISSN 2093-596X. PMC 9449109. PMID 35799332.
Dauber A, Kellogg M, Majzoub JA (2010). "Monitoring of therapy in congenital adrenal hyperplasia". Clinical Chemistry. 56 (8): 1245–51. doi:10.1373/clinchem.2010.146035. PMID 20558634.
Merke DP, Auchus RJ (September 2020). "Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency". The New England Journal of Medicine. 383 (13): 1248–1261. doi:10.1056/NEJMra1909786. PMID 32966723. S2CID 221884108.
Adriaansen, Bas P. H.; Schröder, Mariska A. M.; Span, Paul N.; Sweep, Fred C. G. J.; van Herwaarden, Antonius E.; Claahsen-van der Grinten, Hedi L. (12 December 2022). "Challenges in treatment of patients with non-classic congenital adrenal hyperplasia". Frontiers in Endocrinology. 13. doi:10.3389/fendo.2022.1064024. PMC 9791115. PMID 36578966.
Gidlöf, Sebastian; Falhammar, Henrik; Thilén, Astrid; Döbeln, Ulrika von; Ritzén, Martin; Wedell, Anna; Nordenström, Anna (1 September 2013). "One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study". The Lancet Diabetes & Endocrinology. 1 (1): 35–42. doi:10.1016/S2213-8587(13)70007-X. ISSN 2213-8587. PMID 24622265.
Arlt, Wiebke; Willis, Debbie S.; Wild, Sarah H.; Krone, Nils; Doherty, Emma J.; Hahner, Stefanie; Han, Thang S.; Carroll, Paul V.; Conway, Gerry S.; Rees, D. Aled; Stimson, Roland H.; Walker, Brian R.; Connell, John M. C.; Ross, Richard J. (18 August 2010). "Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients". The Journal of Clinical Endocrinology & Metabolism. 95 (11): 5110–5121. doi:10.1210/jc.2010-0917. ISSN 0021-972X. PMC 3066446. PMID 20719839.
Strömer, H.; Cittadini, A.; Douglas, P. S.; Morgan, J. P. (12 January 2022). "Exogenously administered growth hormone and insulin-like growth factor-I alter intracellular Ca2+ handling and enhance cardiac performance. In vitro evaluation in the isolated isovolumic buffer-perfused rat heart". Circulation Research. 79 (2): 227–236. doi:10.1161/01.res.79.2.227. ISSN 0009-7330. PMID 8755999.
Miller WL (January 2012). "The syndrome of 17,20 lyase deficiency". The Journal of Clinical Endocrinology and Metabolism. 97 (1): 59–67. doi:10.1210/jc.2011-2161. PMC 3251937. PMID 22072737.
White, P. C.; Speiser, P. W. (1 June 2000). "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency". Endocrine Reviews. 21 (3): 245–291. doi:10.1210/edrv.21.3.0398. ISSN 0163-769X. PMID 10857554.
Häggström, Mikael; Richfield, David (2014). "Diagram of the pathways of human steroidogenesis". WikiJournal of Medicine. 1 (1). doi:10.15347/wjm/2014.005. ISSN 2002-4436.
AbdAlmageed, Wael; Mirzaalian, Hengameh; Guo, Xiao; Randolph, Linda M.; Tanawattanacharoen, Veeraya K.; Geffner, Mitchell E.; Ross, Heather M.; Kim, Mimi S. (18 November 2020). "Assessment of Facial Morphologic Features in Patients With Congenital Adrenal Hyperplasia Using Deep Learning". JAMA Network Open. 3 (11): e2022199. doi:10.1001/jamanetworkopen.2020.22199. ISSN 2574-3805. PMC 7675110. PMID 33206189.
Adriaansen, Bas P. H.; Kamphuis, Johannes S.; Schröder, Mariska A. M.; Olthaar, André J.; Bock, Carina; Brandt, André; Stikkelbroeck, Nike M. M. L.; Lentjes, Eef G. W. M.; Span, Paul N.; Sweep, Fred C. G. J.; Claahsen-van der Grinten, Hedi L.; van Herwaarden, Antonius E. (2022). "Diurnal salivary androstenedione and 17-hydroxyprogesterone levels in healthy volunteers for monitoring treatment efficacy of patients with congenital adrenal hyperplasia". Clinical Endocrinology. 97 (1): 36–42. doi:10.1111/cen.14690. ISSN 0300-0664. PMC 9542109. PMID 35150157.
Auchus, Richard J.; Hamidi, Oksana; Pivonello, Rosario; Bancos, Irina; Russo, Gianni; Witchel, Selma F.; Isidori, Andrea M.; Rodien, Patrice; Srirangalingam, Umasuthan; Kiefer, Florian W.; Falhammar, Henrik; Merke, Deborah P.; Reisch, Nicole; Sarafoglou, Kyriakie; Cutler, Gordon B. (June 2024). "Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404656. ISSN 0028-4793. PMID 38828955.
Sarafoglou, Kyriakie; Kim, Mimi S.; Lodish, Maya; Felner, Eric I.; Martinerie, Laetitia; Nokoff, Natalie J.; Clemente, María; Fechner, Patricia Y.; Vogiatzi, Maria G.; Speiser, Phyllis W.; Auchus, Richard J.; Rosales, Gelliza B.G.; Roberts, Eiry; Jeha, George S.; Farber, Robert H. (2 June 2024). "Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404655. ISSN 0028-4793. PMID 38828945.
Kruse, B.; Riepe, F. G.; Krone, N.; Bosinski, H. a. G.; Kloehn, S.; Partsch, C. J.; Sippell, W. G.; Mönig, H. (July 2004). "Congenital adrenal hyperplasia — how to improve the transition from adolescence to adult life". Experimental and Clinical Endocrinology & Diabetes. 112 (7): 343–355. doi:10.1055/s-2004-821013. ISSN 0947-7349. PMID 15239019. S2CID 260138410.
Bongiovanni AM, Root AW (1963). "The Adrenogenital Syndrome". The New England Journal of Medicine. 268 (23): 1283–9 contd. doi:10.1056/NEJM196306062682308. PMID 13968788.

evms.edu

pediatrics.evms.edu

Kenneth A. Pass; Eurico Carmago Neto (2005). Update: Newborn Screening for Endocrinopathies (PDF). pp. 831–834. Archived from the original (PDF) on 1 January 2014. Retrieved 12 December 2013.

icj.org

International Commission of Jurists (2017). "Republic of the Philippines v. Jennifer Cagandahan, Supreme Court of the Philippines, Second Division (12 September 2008)". International Commission of Jurists. Retrieved 19 March 2021.

medlineplus.gov

"3-beta-hydroxysteroid dehydrogenase deficiency". MedlinePlus. Archived from the original on 28 September 2020. Retrieved 2 June 2021.

merckmanuals.com

"Genital Birth Defects — Children's Health Issues". Merck Manuals Consumer Version. Retrieved 5 September 2020.

nejm.org

Auchus, Richard J.; Hamidi, Oksana; Pivonello, Rosario; Bancos, Irina; Russo, Gianni; Witchel, Selma F.; Isidori, Andrea M.; Rodien, Patrice; Srirangalingam, Umasuthan; Kiefer, Florian W.; Falhammar, Henrik; Merke, Deborah P.; Reisch, Nicole; Sarafoglou, Kyriakie; Cutler, Gordon B. (June 2024). "Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404656. ISSN 0028-4793. PMID 38828955.
Sarafoglou, Kyriakie; Kim, Mimi S.; Lodish, Maya; Felner, Eric I.; Martinerie, Laetitia; Nokoff, Natalie J.; Clemente, María; Fechner, Patricia Y.; Vogiatzi, Maria G.; Speiser, Phyllis W.; Auchus, Richard J.; Rosales, Gelliza B.G.; Roberts, Eiry; Jeha, George S.; Farber, Robert H. (2 June 2024). "Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404655. ISSN 0028-4793. PMID 38828945.

nih.gov

pubmed.ncbi.nlm.nih.gov

El-Maouche D, Arlt W, Merke DP (November 2017). "Congenital adrenal hyperplasia" (PDF). Lancet. 390 (10108): 2194–2210. doi:10.1016/S0140-6736(17)31431-9. PMID 28576284. S2CID 13737960.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC (2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
Speiser PW, White PC (August 2003). "Congenital adrenal hyperplasia". The New England Journal of Medicine. 349 (8): 776–88. doi:10.1056/NEJMra021561. PMID 12930931.
La, Betty; Tung, Celestine; Choi, Eugene A.; Nguyen, Ha (1 November 2021). "A Gigantic Uterine Leiomyoma and Big Bilateral Adrenal Myelolipomas as a Result of Untreated Congenital Adrenal Hyperplasia". AACE Clinical Case Reports. 7 (6): 342–345. doi:10.1016/j.aace.2021.05.002. PMC 8573279. PMID 34765728.
Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, New MI (July 1985). "High frequency of nonclassical steroid 21-hydroxylase deficiency". American Journal of Human Genetics. 37 (4): 650–67. PMC 1684620. PMID 9556656.
Krone N, Arlt W (April 2009). "Genetics of congenital adrenal hyperplasia". Best Practice & Research. Clinical Endocrinology & Metabolism. 23 (2): 181–92. doi:10.1016/j.beem.2008.10.014. PMC 5576025. PMID 19500762.
Turcu AF, Nanba AT, Chomic R, Upadhyay SK, Giordano TJ, Shields JJ, Merke DP, Rainey WE, Auchus RJ (May 2016). "Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency". European Journal of Endocrinology. 174 (5): 601–9. doi:10.1530/EJE-15-1181. PMC 4874183. PMID 26865584.
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 (15 March 2017). Congenital Adrenal Hyperplasia. MDText.com, Inc. PMID 25905188.
Speiser, Phyllis W.; Arlt, Wiebke; Auchus, Richard J.; Baskin, Laurence S.; Conway, Gerard S.; Merke, Deborah P.; Meyer-Bahlburg, Heino F. L.; Miller, Walter L.; Murad, M. Hassan; Oberfield, Sharon E.; White, Perrin C. (1 November 2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. ISSN 1945-7197. PMC 6456929. PMID 30272171.
Nordenström, Anna; Lajic, Svetlana; Falhammar, Henrik (8 July 2022). "Long-Term Outcomes of Congenital Adrenal Hyperplasia". Endocrinology and Metabolism. 37 (4): 587–598. doi:10.3803/EnM.2022.1528. ISSN 2093-596X. PMC 9449109. PMID 35799332.
Dauber A, Kellogg M, Majzoub JA (2010). "Monitoring of therapy in congenital adrenal hyperplasia". Clinical Chemistry. 56 (8): 1245–51. doi:10.1373/clinchem.2010.146035. PMID 20558634.
Merke DP, Auchus RJ (September 2020). "Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency". The New England Journal of Medicine. 383 (13): 1248–1261. doi:10.1056/NEJMra1909786. PMID 32966723. S2CID 221884108.
Adriaansen, Bas P. H.; Schröder, Mariska A. M.; Span, Paul N.; Sweep, Fred C. G. J.; van Herwaarden, Antonius E.; Claahsen-van der Grinten, Hedi L. (12 December 2022). "Challenges in treatment of patients with non-classic congenital adrenal hyperplasia". Frontiers in Endocrinology. 13. doi:10.3389/fendo.2022.1064024. PMC 9791115. PMID 36578966.
Yau, M.; et al. (2000). Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment. MDText.com. PMID 25905311.
Gidlöf, Sebastian; Falhammar, Henrik; Thilén, Astrid; Döbeln, Ulrika von; Ritzén, Martin; Wedell, Anna; Nordenström, Anna (1 September 2013). "One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study". The Lancet Diabetes & Endocrinology. 1 (1): 35–42. doi:10.1016/S2213-8587(13)70007-X. ISSN 2213-8587. PMID 24622265.
Arlt, Wiebke; Willis, Debbie S.; Wild, Sarah H.; Krone, Nils; Doherty, Emma J.; Hahner, Stefanie; Han, Thang S.; Carroll, Paul V.; Conway, Gerry S.; Rees, D. Aled; Stimson, Roland H.; Walker, Brian R.; Connell, John M. C.; Ross, Richard J. (18 August 2010). "Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients". The Journal of Clinical Endocrinology & Metabolism. 95 (11): 5110–5121. doi:10.1210/jc.2010-0917. ISSN 0021-972X. PMC 3066446. PMID 20719839.
Strömer, H.; Cittadini, A.; Douglas, P. S.; Morgan, J. P. (12 January 2022). "Exogenously administered growth hormone and insulin-like growth factor-I alter intracellular Ca2+ handling and enhance cardiac performance. In vitro evaluation in the isolated isovolumic buffer-perfused rat heart". Circulation Research. 79 (2): 227–236. doi:10.1161/01.res.79.2.227. ISSN 0009-7330. PMID 8755999.
Miller WL (January 2012). "The syndrome of 17,20 lyase deficiency". The Journal of Clinical Endocrinology and Metabolism. 97 (1): 59–67. doi:10.1210/jc.2011-2161. PMC 3251937. PMID 22072737.
White, P. C.; Speiser, P. W. (1 June 2000). "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency". Endocrine Reviews. 21 (3): 245–291. doi:10.1210/edrv.21.3.0398. ISSN 0163-769X. PMID 10857554.
AbdAlmageed, Wael; Mirzaalian, Hengameh; Guo, Xiao; Randolph, Linda M.; Tanawattanacharoen, Veeraya K.; Geffner, Mitchell E.; Ross, Heather M.; Kim, Mimi S. (18 November 2020). "Assessment of Facial Morphologic Features in Patients With Congenital Adrenal Hyperplasia Using Deep Learning". JAMA Network Open. 3 (11): e2022199. doi:10.1001/jamanetworkopen.2020.22199. ISSN 2574-3805. PMC 7675110. PMID 33206189.
Adriaansen, Bas P. H.; Kamphuis, Johannes S.; Schröder, Mariska A. M.; Olthaar, André J.; Bock, Carina; Brandt, André; Stikkelbroeck, Nike M. M. L.; Lentjes, Eef G. W. M.; Span, Paul N.; Sweep, Fred C. G. J.; Claahsen-van der Grinten, Hedi L.; van Herwaarden, Antonius E. (2022). "Diurnal salivary androstenedione and 17-hydroxyprogesterone levels in healthy volunteers for monitoring treatment efficacy of patients with congenital adrenal hyperplasia". Clinical Endocrinology. 97 (1): 36–42. doi:10.1111/cen.14690. ISSN 0300-0664. PMC 9542109. PMID 35150157.
Auchus, Richard J.; Hamidi, Oksana; Pivonello, Rosario; Bancos, Irina; Russo, Gianni; Witchel, Selma F.; Isidori, Andrea M.; Rodien, Patrice; Srirangalingam, Umasuthan; Kiefer, Florian W.; Falhammar, Henrik; Merke, Deborah P.; Reisch, Nicole; Sarafoglou, Kyriakie; Cutler, Gordon B. (June 2024). "Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404656. ISSN 0028-4793. PMID 38828955.
Sarafoglou, Kyriakie; Kim, Mimi S.; Lodish, Maya; Felner, Eric I.; Martinerie, Laetitia; Nokoff, Natalie J.; Clemente, María; Fechner, Patricia Y.; Vogiatzi, Maria G.; Speiser, Phyllis W.; Auchus, Richard J.; Rosales, Gelliza B.G.; Roberts, Eiry; Jeha, George S.; Farber, Robert H. (2 June 2024). "Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia". New England Journal of Medicine. doi:10.1056/NEJMoa2404655. ISSN 0028-4793. PMID 38828945.
Kruse, B.; Riepe, F. G.; Krone, N.; Bosinski, H. a. G.; Kloehn, S.; Partsch, C. J.; Sippell, W. G.; Mönig, H. (July 2004). "Congenital adrenal hyperplasia — how to improve the transition from adolescence to adult life". Experimental and Clinical Endocrinology & Diabetes. 112 (7): 343–355. doi:10.1055/s-2004-821013. ISSN 0947-7349. PMID 15239019. S2CID 260138410.
Bongiovanni AM, Root AW (1963). "The Adrenogenital Syndrome". The New England Journal of Medicine. 268 (23): 1283–9 contd. doi:10.1056/NEJM196306062682308. PMID 13968788.

ncbi.nlm.nih.gov

Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC (2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
La, Betty; Tung, Celestine; Choi, Eugene A.; Nguyen, Ha (1 November 2021). "A Gigantic Uterine Leiomyoma and Big Bilateral Adrenal Myelolipomas as a Result of Untreated Congenital Adrenal Hyperplasia". AACE Clinical Case Reports. 7 (6): 342–345. doi:10.1016/j.aace.2021.05.002. PMC 8573279. PMID 34765728.
Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, New MI (July 1985). "High frequency of nonclassical steroid 21-hydroxylase deficiency". American Journal of Human Genetics. 37 (4): 650–67. PMC 1684620. PMID 9556656.
Krone N, Arlt W (April 2009). "Genetics of congenital adrenal hyperplasia". Best Practice & Research. Clinical Endocrinology & Metabolism. 23 (2): 181–92. doi:10.1016/j.beem.2008.10.014. PMC 5576025. PMID 19500762.
Turcu AF, Nanba AT, Chomic R, Upadhyay SK, Giordano TJ, Shields JJ, Merke DP, Rainey WE, Auchus RJ (May 2016). "Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency". European Journal of Endocrinology. 174 (5): 601–9. doi:10.1530/EJE-15-1181. PMC 4874183. PMID 26865584.
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 (15 March 2017). Congenital Adrenal Hyperplasia. MDText.com, Inc. PMID 25905188.
Speiser, Phyllis W.; Arlt, Wiebke; Auchus, Richard J.; Baskin, Laurence S.; Conway, Gerard S.; Merke, Deborah P.; Meyer-Bahlburg, Heino F. L.; Miller, Walter L.; Murad, M. Hassan; Oberfield, Sharon E.; White, Perrin C. (1 November 2018). "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. ISSN 1945-7197. PMC 6456929. PMID 30272171.
Nordenström, Anna; Lajic, Svetlana; Falhammar, Henrik (8 July 2022). "Long-Term Outcomes of Congenital Adrenal Hyperplasia". Endocrinology and Metabolism. 37 (4): 587–598. doi:10.3803/EnM.2022.1528. ISSN 2093-596X. PMC 9449109. PMID 35799332.
Adriaansen, Bas P. H.; Schröder, Mariska A. M.; Span, Paul N.; Sweep, Fred C. G. J.; van Herwaarden, Antonius E.; Claahsen-van der Grinten, Hedi L. (12 December 2022). "Challenges in treatment of patients with non-classic congenital adrenal hyperplasia". Frontiers in Endocrinology. 13. doi:10.3389/fendo.2022.1064024. PMC 9791115. PMID 36578966.
Yau, M.; et al. (2000). Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment. MDText.com. PMID 25905311.
New, Maria; Yau, Mabel; Lekarev, Oksana; Lin-Su, Karen; Parsa, Alan; Pina, Christian; Yuen, Tony; Khattab, Ahmed (15 March 2017). "Figure 2, [Different degrees of virilization according...]". www.ncbi.nlm.nih.gov. Retrieved 5 September 2020.
Arlt, Wiebke; Willis, Debbie S.; Wild, Sarah H.; Krone, Nils; Doherty, Emma J.; Hahner, Stefanie; Han, Thang S.; Carroll, Paul V.; Conway, Gerry S.; Rees, D. Aled; Stimson, Roland H.; Walker, Brian R.; Connell, John M. C.; Ross, Richard J. (18 August 2010). "Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients". The Journal of Clinical Endocrinology & Metabolism. 95 (11): 5110–5121. doi:10.1210/jc.2010-0917. ISSN 0021-972X. PMC 3066446. PMID 20719839.
Miller WL (January 2012). "The syndrome of 17,20 lyase deficiency". The Journal of Clinical Endocrinology and Metabolism. 97 (1): 59–67. doi:10.1210/jc.2011-2161. PMC 3251937. PMID 22072737.
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