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Cited by in F6Publishing
For: de Bruin C, Orbak Z, Andrew M, Hwa V, Dauber A. Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 Deficiency. Horm Res Paediatr. 2016;85:358-362. [PMID: 26789720 DOI: 10.1159/000443684] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Bağlan E, Özdel S, Güngör T, Karakuş R, Bağrıaçık EÜ, Yücel AA, Bülbül M. Spondylenchondrodysplasia mimicking a systemic lupus erythematosus: A diagnostic challenge in a pediatric patient. Eur J Med Genet 2021;64:104286. [PMID: 34245909 DOI: 10.1016/j.ejmg.2021.104286] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Ramesh J, Parthasarathy LK, Janckila AJ, Begum F, Murugan R, Murthy BPSS, El-Mallakh RS, Parthasarathy RN, Venugopal B. Characterisation of ACP5 missense mutations encoding tartrate-resistant acid phosphatase associated with spondyloenchondrodysplasia. PLoS One 2020;15:e0230052. [PMID: 32214327 DOI: 10.1371/journal.pone.0230052] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
3 虞佳音, 汪静宇. 抗酒石酸酸性磷酸酶在恶性肿瘤中的研究进展. 世界华人消化杂志 2017; 25(23): 2133-2138 [DOI: 10.11569/wcjd.v25.i23.2133] [Reference Citation Analysis]
4 Utsumi T, Okada S, Izawa K, Honda Y, Nishimura G, Nishikomori R, Okano R, Kobayashi M. A Case with Spondyloenchondrodysplasia Treated with Growth Hormone. Front Endocrinol (Lausanne) 2017;8:157. [PMID: 28740483 DOI: 10.3389/fendo.2017.00157] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]