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For: Al Alawi AM, Nordenström A, Falhammar H. Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency. Endocrine 2019;63:407-21. [PMID: 30719691 DOI: 10.1007/s12020-018-01835-3] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 8.3] [Reference Citation Analysis]
Number Citing Articles
1 Bouhouche A, Albaroudi N, El Alaoui MA, Askander O, Habbadi Z, El Hassani A, Iraqi H, El Fahime E, Belmekki M. Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome. Exp Eye Res 2021;209:108671. [PMID: 34133966 DOI: 10.1016/j.exer.2021.108671] [Reference Citation Analysis]
2 Aslaksen S, Methlie P, Vigeland MD, Jøssang DE, Wolff AB, Sheng Y, Oftedal BE, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E. Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease. Front Endocrinol (Lausanne) 2019;10:648. [PMID: 31611844 DOI: 10.3389/fendo.2019.00648] [Reference Citation Analysis]
3 Pitsava G, Stratakis CA. Adrenal hyperplasias in childhood: An update. Front Endocrinol 2022;13:937793. [DOI: 10.3389/fendo.2022.937793] [Reference Citation Analysis]
4 He Y, Xie RG, Lou JW, Li YW, Wang CL, Zhang VW, Li DZ. Exome-based preconception carrier testing for consanguineous couples in China. Prenat Diagn 2021;41:1425-9. [PMID: 34486758 DOI: 10.1002/pd.6018] [Reference Citation Analysis]
5 Kocova M, Anastasovska V, Falhammar H. Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocrine 2020;69:262-77. [PMID: 32367336 DOI: 10.1007/s12020-020-02323-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
6 Alkhzouz C, Bucerzan S, Miclaus M, Mirea AM, Miclea D. 46,XX DSD: Developmental, Clinical and Genetic Aspects. Diagnostics (Basel) 2021;11:1379. [PMID: 34441313 DOI: 10.3390/diagnostics11081379] [Reference Citation Analysis]
7 Liu Y, Zheng J, Liu N, Xu X, Zhang X, Zhang Y, Li G, Liu G, Cai C, Shu J. The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l-hydroxylase deficiency in a Chinese cohort. Mol Genet Genomic Med 2020;8:e1501. [PMID: 32959514 DOI: 10.1002/mgg3.1501] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
8 Nermoen I, Falhammar H. Prevalence and Characteristics of Adrenal Tumors and Myelolipomas in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis. Endocr Pract 2020;26:1351-65. [PMID: 33471666 DOI: 10.4158/EP-2020-0058] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 8.0] [Reference Citation Analysis]
9 Chen H, Zhang Q, Chen R, Yuan X, Lin X, Yang X, Zhang Y. Lipoid congenital adrenal hyperplasia due to steroid acute regulatory protein (STAR) variants in Three Chinese patients. J Steroid Biochem Mol Biol 2020;200:105635. [PMID: 32068072 DOI: 10.1016/j.jsbmb.2020.105635] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Finkielstain GP, Vieites A, Bergadá I, Rey RA. Disorders of Sex Development of Adrenal Origin. Front Endocrinol (Lausanne) 2021;12:770782. [PMID: 34987475 DOI: 10.3389/fendo.2021.770782] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Rangaswamaiah S, Gangathimmaiah V, Nordenstrom A, Falhammar H. Bone Mineral Density in Adults With Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis. Front Endocrinol (Lausanne) 2020;11:493. [PMID: 32903805 DOI: 10.3389/fendo.2020.00493] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
12 Török D. Congenital Adrenal Hyperplasia. Exp Suppl 2019;111:245-60. [PMID: 31588535 DOI: 10.1007/978-3-030-25905-1_12] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
13 Baronio F, Ortolano R, Menabò S, Cassio A, Baldazzi L, Di Natale V, Tonti G, Vestrucci B, Balsamo A. 46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features. Int J Mol Sci 2019;20:E4605. [PMID: 31533357 DOI: 10.3390/ijms20184605] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 3.7] [Reference Citation Analysis]
14 Niang B, Ly F, Ba A, Mbaye A, Boiro D, Faye PM, Dieng YJ, Sow A, Thiongane A, Ba ID, Thiam L, Fall AL, Ndiaye O. Congenital Adrenal Hyperplasia: Diagnostic Features in a Limited Resource Country, Senegal. OJPed 2020;10:137-46. [DOI: 10.4236/ojped.2020.101013] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Fanis P, Neocleous V, Kosta K, Karipiadou A, Hartmann MF, Wudy SA, Karantaglis N, Papadimitriou DT, Skordis N, Tsikopoulos G, Phylactou LA, Roilides E, Papagianni M. Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene. J Pediatr Endocrinol Metab 2021;34:131-6. [PMID: 33180036 DOI: 10.1515/jpem-2020-0245] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Balsamo A, Baronio F, Ortolano R, Menabo S, Baldazzi L, Di Natale V, Vissani S, Cassio A. Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant. Front Pediatr 2020;8:593315. [PMID: 33415088 DOI: 10.3389/fped.2020.593315] [Reference Citation Analysis]
17 Pineles SL, Nillni YI, Pinna G, Webb A, Arditte Hall KA, Fonda JR, Irvine J, King MW, Hauger RL, Resick PA, Orr SP, Rasmusson AM. Associations between PTSD-Related extinction retention deficits in women and plasma steroids that modulate brain GABAA and NMDA receptor activity. Neurobiol Stress 2020;13:100225. [PMID: 32490055 DOI: 10.1016/j.ynstr.2020.100225] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
18 Daae E, Feragen KB, Waehre A, Nermoen I, Falhammar H. Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review. Front Behav Neurosci 2020;14:38. [PMID: 32231525 DOI: 10.3389/fnbeh.2020.00038] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
19 Falhammar H, Frisén L, Hirschberg AL, Nordenskjöld A, Almqvist C, Nordenström A. Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study. J Endocr Soc 2019;3:1039-52. [PMID: 31065621 DOI: 10.1210/js.2019-00122] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
20 Hathi D, Goswami S, Sengupta N, Acharya S, Kumar S, Talwar D. Myriad Manifestations of 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency—A Tale of Two Infants. Cureus. [DOI: 10.7759/cureus.21779] [Reference Citation Analysis]
21 Jha S, Turcu AF. Nonclassic Congenital Adrenal Hyperplasia: What Do Endocrinologists Need to Know? Endocrinol Metab Clin North Am 2021;50:151-65. [PMID: 33518183 DOI: 10.1016/j.ecl.2020.10.008] [Reference Citation Analysis]
22 Naelitz BD, Sharifi N. Through the Looking-Glass: Reevaluating DHEA Metabolism Through HSD3B1 Genetics. Trends Endocrinol Metab 2020;31:680-90. [PMID: 32565196 DOI: 10.1016/j.tem.2020.05.006] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
23 Guran T, Kara C, Yildiz M, Bitkin EC, Haklar G, Lin J, Keskin M, Barnard L, Anik A, Catli G, Guven A, Kirel B, Tutunculer F, Onal H, Turan S, Akcay T, Atay Z, Yilmaz GC, Mamadova J, Akbarzade A, Sirikci O, Storbeck K, Baris T, Chung B, Bereket A. Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases. The Journal of Clinical Endocrinology & Metabolism 2020;105:e1718-28. [DOI: 10.1210/clinem/dgaa022] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
24 Conlon TA, Hawkes CP, Brady JJ, Murphy NP. The presentation of congenital adrenal hyperplasia in an unscreened population. J Pediatr Endocrinol Metab 2021;34:1123-9. [PMID: 34167176 DOI: 10.1515/jpem-2021-0123] [Reference Citation Analysis]
25 Alkhatib EH, Adams SD, Miller ER. Case of an unreported genetic variant of salt losing 3-β-hydroxysteroid dehydrogenase deficiency. Oxf Med Case Reports 2021;2021:omab021. [PMID: 34055358 DOI: 10.1093/omcr/omab021] [Reference Citation Analysis]