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For: Breil T, Yakovenko V, Inta I, Choukair D, Klose D, Mittnacht J, Schulze E, Alrajab A, Grulich-henn J, Bettendorf M. Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature. Journal of Pediatric Endocrinology and Metabolism 2019;32:259-67. [DOI: 10.1515/jpem-2018-0298] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
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2 Ceccato F, Mantero F. Monogenic Forms of Hypertension. Endocrinol Metab Clin North Am 2019;48:795-810. [PMID: 31655777 DOI: 10.1016/j.ecl.2019.08.009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
3 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]
4 Yildiz M, Isik E, Abali ZY, Keskin M, Ozbek MN, Bas F, Ucakturk SA, Buyukinan M, Onal H, Kara C, Storbeck KH, Darendeliler F, Cayir A, Unal E, Anik A, Demirbilek H, Cetin T, Dursun F, Catli G, Turan S, Falhammar H, Baris T, Yaman A, Haklar G, Bereket A, Guran T. Clinical and hormonal profiles correlate with molecular characteristics in patients with 11β-hydroxylase deficiency. J Clin Endocrinol Metab 2021:dgab225. [PMID: 33830237 DOI: 10.1210/clinem/dgab225] [Reference Citation Analysis]
5 Khandelwal P, Deinum J. Monogenic forms of low-renin hypertension: clinical and molecular insights. Pediatr Nephrol 2021. [PMID: 34414500 DOI: 10.1007/s00467-021-05246-x] [Reference Citation Analysis]