Similar articles for PMID: 15652857

Year	Number of Results
1870	1
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2024	0

1

Macular abnormalities and optic disk anomaly associated with a new PAX2 missense mutation.

Higashide T, Wada T, Sakurai M, Yokoyama H, Sugiyama K. Higashide T, et al. Am J Ophthalmol. 2005 Jan;139(1):203-5. doi: 10.1016/j.ajo.2004.07.021. Am J Ophthalmol. 2005. PMID: 15652857

2

De Novo PAX2 Mutation With Associated Papillorenal Syndrome: A Case Report and Literature Review of Penetrance and Expressivity.

Ali M, Chang M, Leys M. Ali M, et al. Cureus. 2022 Sep 11;14(9):e29026. doi: 10.7759/cureus.29026. eCollection 2022 Sep. Cureus. 2022. PMID: 36249605 Free PMC article.

3

Detection of De Novo PAX2 Variants and Phenotypes in Chinese Population: A Single-Center Study.

Xiong HY, Shi YQ, Zhong C, Yang Q, Zhang G, Yang H, Wu D, Chen Y, Li Q, Wang M. Xiong HY, et al. Front Genet. 2022 Mar 31;13:799562. doi: 10.3389/fgene.2022.799562. eCollection 2022. Front Genet. 2022. PMID: 35444690 Free PMC article.

4

PAX2 Mutation-Related Renal Hypodysplasia: Review of the Literature and Three Case Reports.

Chang YM, Chen CC, Lee NC, Sung JM, Chou YY, Chiou YY. Chang YM, et al. Front Pediatr. 2022 Jan 11;9:765929. doi: 10.3389/fped.2021.765929. eCollection 2021. Front Pediatr. 2022. PMID: 35087773 Free PMC article.

5

Cavitary Optic Disc Anomaly.

Alawa KA, Fingert JH, Sears NC. Alawa KA, et al. Ophthalmol Glaucoma. 2022 Jan-Feb;5(1):76. doi: 10.1016/j.ogla.2021.09.008. Ophthalmol Glaucoma. 2022. PMID: 35067279 No abstract available.

6

Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings.

Liu B, Chen M, Yang Y, Huang Y, Qian Y, Dong M. Liu B, et al. Clin Chim Acta. 2022 Jan 15;525:23-28. doi: 10.1016/j.cca.2021.12.007. Epub 2021 Dec 11. Clin Chim Acta. 2022. PMID: 34906559

7

Ocular phenotype in a patient with PAX2 gene mutation-associated papillorenal syndrome.

Benador-Shen CL, Reichel E, Reed D, Milner LS, Pinnell N, Choi CS. Benador-Shen CL, et al. Ophthalmic Genet. 2022 Jun;43(3):385-388. doi: 10.1080/13816810.2021.2015786. Epub 2021 Dec 10. Ophthalmic Genet. 2022. PMID: 34889688

8

Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.

Yang X, Li Y, Fang Y, Shi H, Xiang T, Liu J, Liu J, Tang X, Fang X, Chen J, Zhai Y, Shen Q, Bi Y, Qian Y, Wu B, Wang H, Zhou W, Ma D, Bai H, Mao J, Chen L, Wang X, Gao X, Zhang R, Zhuang J, Zhang A, Jiang X, Xu H, Rao J. Yang X, et al. BMC Med Genomics. 2021 Oct 25;14(1):250. doi: 10.1186/s12920-021-01102-x. BMC Med Genomics. 2021. PMID: 34696790 Free PMC article.

9

[A family of renal coloboma syndrome].

Li CY, Xiao J. Li CY, et al. Zhonghua Yan Ke Za Zhi. 2021 Jun 11;57(6):454-457. doi: 10.3760/cma.j.cn112142-20201016-00807. Zhonghua Yan Ke Za Zhi. 2021. PMID: 34098695 Chinese.

10

A novel PAX2 heterozygous mutation in a family with Papillorenal syndrome: A case report and review of the literature.

Liu S, Zhang P, Wu J, Chang Q. Liu S, et al. Am J Ophthalmol Case Rep. 2021 Apr 22;22:101091. doi: 10.1016/j.ajoc.2021.101091. eCollection 2021 Jun. Am J Ophthalmol Case Rep. 2021. PMID: 33997468 Free PMC article.

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