114 related articles for article (PubMed ID: 24547927)
1. Analysis of the SOD1 Gene in Keratoconus Patients from Saudi Arabia.
Al-Muammar AM; Kalantan H; Azad TA; Sultan T; Abu-Amero KK
Ophthalmic Genet; 2015; 36(4):373-5. PubMed ID: 24547927
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia.
Abu-Amero KK; Kalantan H; Al-Muammar AM
Mol Vis; 2011 Mar; 17():667-72. PubMed ID: 21403853
[TBL] [Abstract][Full Text] [Related]
3. SOD1: a candidate gene for keratoconus.
Udar N; Atilano SR; Brown DJ; Holguin B; Small K; Nesburn AB; Kenney MC
Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3345-51. PubMed ID: 16877401
[TBL] [Abstract][Full Text] [Related]
4. Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus.
Moschos MM; Kokolakis N; Gazouli M; Chatziralli IP; Droutsas D; Anagnou NP; Ladas ID
Ophthalmic Genet; 2015; 36(3):213-7. PubMed ID: 24099280
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.
Saee-Rad S; Hashemi H; Miraftab M; Noori-Daloii MR; Chaleshtori MH; Raoofian R; Jafari F; Greene W; Fakhraie G; Rezvan F; Heidari M
Mol Vis; 2011; 17():3128-36. PubMed ID: 22171159
[TBL] [Abstract][Full Text] [Related]
6. Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.
Stabuc-Silih M; Strazisar M; Hawlina M; Glavac D
Cornea; 2010 Feb; 29(2):172-6. PubMed ID: 20023586
[TBL] [Abstract][Full Text] [Related]
7. Genetics and clinical characteristics of keratoconus.
Stabuc-Silih M; Strazisar M; Ravnik-Glavac M; Hawlina M; Glavac D
Acta Dermatovenerol Alp Pannonica Adriat; 2010; 19(2):3-10. PubMed ID: 20664914
[TBL] [Abstract][Full Text] [Related]
8. Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.
De Bonis P; Laborante A; Pizzicoli C; Stallone R; Barbano R; Longo C; Mazzilli E; Zelante L; Bisceglia L
Mol Vis; 2011; 17():2482-94. PubMed ID: 21976959
[TBL] [Abstract][Full Text] [Related]
9. SOD1 haplotypes in familial keratoconus.
Udar N; Atilano SR; Small K; Nesburn AB; Kenney MC
Cornea; 2009 Sep; 28(8):902-7. PubMed ID: 19654524
[TBL] [Abstract][Full Text] [Related]
10. Absence of the c.169+50delTAAACAG mutation of SOD1 gene in a sample of keratoconus patients in Brazilian population.
Lopes AG; de Almeida Júnior GC; Teixeira RM; de Mattos LC; Brandão de Mattos CC; Castiglioni L
BMC Res Notes; 2020 Jul; 13(1):328. PubMed ID: 32646478
[TBL] [Abstract][Full Text] [Related]
11. High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus.
Abu-Amero KK; Hellani AM; Al Mansouri SM; Kalantan H; Al-Muammar AM
Mol Vis; 2011 Mar; 17():822-6. PubMed ID: 21528002
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial sequence changes in keratoconus patients.
Abu-Amero KK; Azad TA; Kalantan H; Sultan T; Al-Muammar AM
Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1706-10. PubMed ID: 24569587
[TBL] [Abstract][Full Text] [Related]
13. The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.
Syriani E; Morales M; Gamez J
J Neurol Sci; 2009 Oct; 285(1-2):46-53. PubMed ID: 19524271
[TBL] [Abstract][Full Text] [Related]
14.
Nejabat M; Naghash P; Dastsooz H; Mohammadi S; Alipour M; Fardaei M
J Ophthalmic Vis Res; 2017; 12(2):135-140. PubMed ID: 28540003
[TBL] [Abstract][Full Text] [Related]
15. Association of mitochondrial haplogroups H and R with keratoconus in Saudi Arabian patients.
Abu-Amero KK; Azad TA; Sultan T; Kalantan H; Kondkar AA; Al-Muammar AM
Invest Ophthalmol Vis Sci; 2014 May; 55(5):2827-31. PubMed ID: 24722698
[TBL] [Abstract][Full Text] [Related]
16. An analysis of the entire SOD1 gene in sporadic ALS.
Luquin N; Yu B; Trent RJ; Morahan JM; Pamphlett R
Neuromuscul Disord; 2008 Jul; 18(7):545-52. PubMed ID: 18504130
[TBL] [Abstract][Full Text] [Related]
17. Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort.
Kalantan H; Kondkar AA; Sultan T; Azad TA; Alsabaani NA; AlQahtani MA; Almummar A; Liu Y; Abu-Amero KK
BMC Res Notes; 2017 Nov; 10(1):652. PubMed ID: 29187250
[TBL] [Abstract][Full Text] [Related]
18. Absence of significant genetic alterations in the
Lopes AG; de Almeida GC; Miola MP; Teixeira RM; Pires FCBL; Miani RA; de Mattos LC; Brandão CC; Castiglioni L
Ophthalmic Genet; 2022 Feb; 43(1):73-79. PubMed ID: 34802378
[TBL] [Abstract][Full Text] [Related]
19. Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
Verma A; Das M; Srinivasan M; Prajna NV; Sundaresan P
BMC Res Notes; 2013 Mar; 6():103. PubMed ID: 23506487
[TBL] [Abstract][Full Text] [Related]
20. DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
Broom WJ; Johnson DV; Garber M; Andersen PM; Lennon N; Landers J; Nusbaum C; Russ C; Brown RH
Neurosci Lett; 2009 Sep; 463(1):64-9. PubMed ID: 19596401
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]