PubMed for id: 56349

Year	Number of Results
1976	1
1977	1
1978	1
1979	1
1980	2
1981	1
1982	3
1983	3
1984	1
1985	1
1986	5
1987	2
1988	1
1989	5
1990	3
1991	1
1992	2
1993	5
1994	1
1995	3
1996	2
1997	2
1998	1
1999	2
2000	1
2001	2
2002	5
2003	3
2004	1
2005	2
2006	2
2007	2
2008	3
2009	7
2010	4
2012	5
2013	4
2014	3
2015	2
2016	4
2017	3
2018	3
2019	5
2020	4
2021	4
2022	2
2023	5
2024	2

1

A novel missense mutation in the CRYBA2 caused autosomal dominant presenile cataract in a Chinese family.

Kong Y, Yi H, Li F, Duan X, Yang L, Fan X, Wu G, Ma M, Zha X, He Y. Kong Y, et al. Mol Genet Genomics. 2023 Sep;298(5):1237-1244. doi: 10.1007/s00438-023-02052-y. Epub 2023 Jul 12. Mol Genet Genomics. 2023. PMID: 37438446

2

Structural Characteristics of the Lens in Presenile Cataract.

Andjelic S, Drašlar K, Hvala A, Hawlina M. Andjelic S, et al. Front Med (Lausanne). 2021 Dec 22;8:802275. doi: 10.3389/fmed.2021.802275. eCollection 2021. Front Med (Lausanne). 2021. PMID: 35004779 Free PMC article.

3

Clinical Characteristics of Presenile Cataract: Change over 10 Years in Southern Taiwan.

Yu HJ, Kuo MT, Wu PC. Yu HJ, et al. Biomed Res Int. 2021 Mar 20;2021:9385293. doi: 10.1155/2021/9385293. eCollection 2021. Biomed Res Int. 2021. PMID: 33834076 Free PMC article.

4

Scanning and transmission electron microscopy study of anterior lens epithelium in presenile cataract.

Wu J, Zhou J, Ping X, Xu X, Cui Y, Yang H, Yin Q, Shentu X. Wu J, et al. Int Ophthalmol. 2020 Jun;40(6):1411-1418. doi: 10.1007/s10792-020-01307-6. Epub 2020 Mar 6. Int Ophthalmol. 2020. PMID: 32144529

5

Presenile cataract and its risk factors: A case control study.

Das GK, Boriwal K, Chhabra P, Sahu PK, Kumar S, Kumar N. Das GK, et al. J Family Med Prim Care. 2019 Jun;8(6):2120-2123. doi: 10.4103/jfmpc.jfmpc_267_19. J Family Med Prim Care. 2019. PMID: 31334190 Free PMC article.

6

Premature Expression of Pseudoexfoliation Syndrome With Presenile Cataract in a 28-Year-Old Lady.

Kumar PS, Rao A, Senthil S. Kumar PS, et al. J Glaucoma. 2019 Jul;28(7):e115-e117. doi: 10.1097/IJG.0000000000001219. J Glaucoma. 2019. PMID: 30807439

7

Association of presenile cataract with galactose-1-phosphate uridyl transferase gene mutations.

Nema N, Kumar R, Verma A, Verma S, Chaturvedi K. Nema N, et al. Natl Med J India. 2017 Mar-Apr;30(2):73-75. Natl Med J India. 2017. PMID: 28816213 Free article.

8

Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation.

Thomas S, Thomas MG, Andrews C, Chan WM, Proudlock FA, McLean RJ, Pradeep A, Engle EC, Gottlob I. Thomas S, et al. Eur J Hum Genet. 2014 Mar;22(3):344-9. doi: 10.1038/ejhg.2013.162. Epub 2013 Aug 14. Eur J Hum Genet. 2014. PMID: 23942204 Free PMC article.

9

Economou M, Batzios SP, Pecci A, Printza N, Savoia A, Barozzi S, Theodoridou S, Teli A, Psillas G, Zafeiriou DI. Economou M, et al. J Pediatr Hematol Oncol. 2012 Aug;34(6):412-5. doi: 10.1097/MPH.0b013e318257a64b. J Pediatr Hematol Oncol. 2012. PMID: 22627578

10

Synergistic effect of high lactase activity genotype and galactose-1-phosphate uridyl transferase (GALT) mutations on idiopathic presenile cataract formation.

Karas-Kuzelicki N, Pfeifer V, Lukac-Bajalo J. Karas-Kuzelicki N, et al. Clin Biochem. 2008 Jul;41(10-11):869-74. doi: 10.1016/j.clinbiochem.2008.04.002. Epub 2008 Apr 18. Clin Biochem. 2008. PMID: 18454942

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