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For: Gao Y, Lu L, Yu B, Mao J, Wang X, Nie M, Wu X. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. J Clin Endocrinol Metab 2020;105:dgaa199. [PMID: 32291442 DOI: 10.1210/clinem/dgaa199] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Marino R, Moresco A, Perez Garrido N, Ramirez P, Belgorosky A. Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome. Front Endocrinol 2022;13:803226. [DOI: 10.3389/fendo.2022.803226] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Marino R, Perez Garrido N, Ramirez P, Belgorosky A. Response to Letter to the Editor from Lao and Merke: "Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia". J Clin Endocrinol Metab 2021;106:e2837-8. [PMID: 33901286 DOI: 10.1210/clinem/dgab281] [Reference Citation Analysis]
3 Tsuji-Hosokawa A, Kashimada K. Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan. Int J Neonatal Screen 2021;7:36. [PMID: 34209888 DOI: 10.3390/ijns7030036] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Lao Q, Merke DP. Letter to the Editor from Lao and Merke: "Ehlers-Danlos Syndrome: Molecular and Clirnical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia". J Clin Endocrinol Metab 2021;106:e2835-6. [PMID: 33901292 DOI: 10.1210/clinem/dgab280] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Tantirukdham N, Sahakitrungruang T, Chaisiwamongkol R, Pongpanich M, Srichomthong C, Assawapitaksakul A, Buasong A, Tongkobpetch S, Yeetong P, Shotelersuk V. Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency. J Clin Endocrinol Metab 2022;107:1939-47. [PMID: 35363313 DOI: 10.1210/clinem/dgac187] [Reference Citation Analysis]
6 Marino R, Garrido NP, Ramirez P, Notaristéfano G, Moresco A, Touzon MS, Vaiani E, Finkielstain G, Obregón MG, Balbi V, Soria I, Belgorosky A. Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia. J Clin Endocrinol Metab 2021;106:e2789-802. [PMID: 33482002 DOI: 10.1210/clinem/dgab033] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Lao Q, Merke DP. Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras. Eur J Hum Genet 2021;29:1047-8. [PMID: 33824469 DOI: 10.1038/s41431-021-00870-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Concolino P, Falhammar H. CAH-X Syndrome: Genetic and Clinical Profile. Mol Diagn Ther 2022;26:293-300. [PMID: 35476220 DOI: 10.1007/s40291-022-00588-0] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Miller WL. Tenascin-X-Discovery and Early Research. Front Immunol 2020;11:612497. [PMID: 33505400 DOI: 10.3389/fimmu.2020.612497] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Paragliola RM, Perrucci A, Foca L, Urbani A, Concolino P. Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency. JCM 2022;11:3818. [DOI: 10.3390/jcm11133818] [Reference Citation Analysis]
11 Carrozza C, Foca L, De Paolis E, Concolino P. Genes and Pseudogenes: Complexity of the RCCX Locus and Disease. Front Endocrinol (Lausanne) 2021;12:709758. [PMID: 34394006 DOI: 10.3389/fendo.2021.709758] [Reference Citation Analysis]