BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Kim CJ. Congenital lipoid adrenal hyperplasia. Ann Pediatr Endocrinol Metab 2014;19:179-83. [PMID: 25654062 DOI: 10.6065/apem.2014.19.4.179] [Cited by in Crossref: 29] [Cited by in F6Publishing: 15] [Article Influence: 3.6] [Reference Citation Analysis]
Number Citing Articles
1 Lee JS, Lee KB, Song H, Sun C, Kim MJ, Cho SI, Lee YK, Park SS, Seong MW. Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases. Eur J Hum Genet 2021;29:463-70. [PMID: 33235377 DOI: 10.1038/s41431-020-00759-9] [Reference Citation Analysis]
2 Holland O, Dekker Nitert M, Gallo LA, Vejzovic M, Fisher JJ, Perkins AV. Review: Placental mitochondrial function and structure in gestational disorders. Placenta 2017;54:2-9. [PMID: 28024805 DOI: 10.1016/j.placenta.2016.12.012] [Cited by in Crossref: 93] [Cited by in F6Publishing: 85] [Article Influence: 15.5] [Reference Citation Analysis]
3 Sahakitrungruang T. Clinical and molecular review of atypical congenital adrenal hyperplasia. Ann Pediatr Endocrinol Metab 2015;20:1-7. [PMID: 25883920 DOI: 10.6065/apem.2015.20.1.1] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 2.1] [Reference Citation Analysis]
4 Gomes LG, Bachega TA, Mendonca BB. Classic congenital adrenal hyperplasia and its impact on reproduction. Fertility and Sterility 2019;111:7-12. [DOI: 10.1016/j.fertnstert.2018.11.037] [Cited by in Crossref: 17] [Cited by in F6Publishing: 12] [Article Influence: 5.7] [Reference Citation Analysis]
5 Miller WL. Steroidogenic electron-transfer factors and their diseases. Ann Pediatr Endocrinol Metab 2021;26:138-48. [PMID: 34610701 DOI: 10.6065/apem.2142154.077] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Ullah A, Bibi F, Haider N, Shahid G, Abdullah, Mustajab T, Khaliq T, Ahmad W. Clinical and genetic characterization of congenital lipoid adrenal hyperplasia. Clin Dysmorphol 2020;29:173-6. [PMID: 32858544 DOI: 10.1097/MCD.0000000000000340] [Reference Citation Analysis]
7 Soffientini U, Graham A. Intracellular cholesterol transport proteins: roles in health and disease. Clinical Science 2016;130:1843-59. [DOI: 10.1042/cs20160339] [Cited by in Crossref: 19] [Cited by in F6Publishing: 7] [Article Influence: 3.2] [Reference Citation Analysis]
8 Albarel F, Perrin J, Jegaden M, Roucher-boulez F, Reynaud R, Brue T, Courbiere B. Successful IVF pregnancy despite inadequate ovarian steroidogenesis due to congenital lipoid adrenal hyperplasia (CLAH): a case report. Hum Reprod 2016;31:2609-12. [DOI: 10.1093/humrep/dew239] [Cited by in Crossref: 14] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
9 Chauhan V, Dada R, Jain V. Retracted: Aetiology and clinical profile of children with 46, XY differences of sex development at an Indian referral centre. Andrologia 2017;49. [PMID: 27501740 DOI: 10.1111/and.12663] [Reference Citation Analysis]
10 Alimussina M, Diver LA, McGowan R, Ahmed SF. Genetic testing of XY newborns with a suspected disorder of sex development. Curr Opin Pediatr 2018;30:548-57. [PMID: 29782383 DOI: 10.1097/MOP.0000000000000644] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
11 Avni FE, Lerisson H, Lobo ML, Cartigny M, Napolitano M, Mentzel HJ, Riccabona M, Wozniak M, Kljucevsek D, Augdal TA, Constanza B, Ibe D, Darge K, Stafrace S, Petit P, Ording Muller LS. Plea for a standardized imaging approach to disorders of sex development in neonates: consensus proposal from European Society of Paediatric Radiology task force. Pediatr Radiol 2019;49:1240-7. [PMID: 31123767 DOI: 10.1007/s00247-019-04414-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Nistal M, Paniagua R, González-peramato P. Nonneoplastic Diseases of the Testis. Urologic Surgical Pathology. Elsevier; 2020. pp. 549-730.e81. [DOI: 10.1016/b978-0-323-54941-7.00012-8] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Pomahačová R, Sýkora J, Zamboryová J, Paterová P, Varvařovská J, Šubrt I, Dort J, Dortová E. First case report of rare congenital adrenal insufficiency caused by mutations in the CYP11A1 gene in the Czech Republic. Journal of Pediatric Endocrinology and Metabolism 2016;29. [DOI: 10.1515/jpem-2015-0255] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
14 Kalra S, Priya G. Lipocrinology - the relationship between lipids and endocrine function. Drugs Context 2018;7:212514. [PMID: 29410685 DOI: 10.7573/dic.212514] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
15 Sluchanko NN, Tugaeva KV, Maksimov EG. Solution structure of human steroidogenic acute regulatory protein STARD1 studied by small-angle X-ray scattering. Biochemical and Biophysical Research Communications 2017;489:445-50. [DOI: 10.1016/j.bbrc.2017.05.167] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
16 Lekarev O, Lin-su K, Vogiatzi MG. Infertility and Reproductive Function in Patients with Congenital Adrenal Hyperplasia. Endocrinology and Metabolism Clinics of North America 2015;44:705-22. [DOI: 10.1016/j.ecl.2015.07.009] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 2.6] [Reference Citation Analysis]
17 Tiboni GM, Ponzano A. Fetal safety profile of aromatase inhibitors: Animal data. Reprod Toxicol 2016;66:84-92. [PMID: 27697604 DOI: 10.1016/j.reprotox.2016.09.016] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
18 Martinez F, Olvera-Sanchez S, Esparza-Perusquia M, Gomez-Chang E, Flores-Herrera O. Multiple functions of syncytiotrophoblast mitochondria. Steroids 2015;103:11-22. [PMID: 26435077 DOI: 10.1016/j.steroids.2015.09.006] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 3.6] [Reference Citation Analysis]
19 Kocova M, Anastasovska V, Bitovska I. The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family. Eur J Med Res 2019;24:21. [PMID: 31217034 DOI: 10.1186/s40001-019-0379-4] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]