180 related articles for article (PubMed ID: 37895187)
1. Whole-Exome Sequencing of 24 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Keratoconus.
González-Atienza C; Sánchez-Cazorla E; Villoldo-Fernández N; Del Hierro A; Boto A; Guerrero-Carretero M; Nieves-Moreno M; Arruti N; Rodríguez-Solana P; Mena R; Rodríguez-Jiménez C; Rosa-Pérez I; Acal JC; Blasco J; Naranjo-Castresana M; Ruz-Caracuel B; Montaño VEF; Ortega Patrón C; Rubio-Martín ME; García-Fernández L; Rikeros-Orozco E; Gómez-Cano MLÁ; Delgado-Mora L; Noval S; Vallespín E
Genes (Basel); 2023 Sep; 14(10):. PubMed ID: 37895187
[TBL] [Abstract][Full Text] [Related]
2. Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts.
Rodríguez-Solana P; Arruti N; Nieves-Moreno M; Mena R; Rodríguez-Jiménez C; Guerrero-Carretero M; Acal JC; Blasco J; Peralta JM; Del Pozo Á; Montaño VEF; Dios-Blázquez L; Fernández-Alcalde C; González-Atienza C; Sánchez-Cazorla E; Gómez-Cano MLÁ; Delgado-Mora L; Noval S; Vallespín E
Int J Mol Sci; 2023 Jul; 24(14):. PubMed ID: 37511188
[TBL] [Abstract][Full Text] [Related]
3. Familial case of keratoconus with corneal granular dystrophy.
Mitsui M; Sakimoto T; Sawa M; Katami M
Jpn J Ophthalmol; 1998; 42(5):385-8. PubMed ID: 9822968
[TBL] [Abstract][Full Text] [Related]
4. Whole-exome sequencing in familial keratoconus: the challenges of a genetically complex disorder.
Magalhães OA; Kowalski TW; Wachholz GE; Schuler-Faccini L
Arq Bras Oftalmol; 2019; 82(6):453-459. PubMed ID: 31482965
[TBL] [Abstract][Full Text] [Related]
5. A case of concomitant keratoconus and granular corneal dystrophy type II.
Rho CR; Park JH; Jung YH; Kim MS
Cont Lens Anterior Eye; 2014 Aug; 37(4):314-6. PubMed ID: 24582869
[TBL] [Abstract][Full Text] [Related]
6. Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families.
Froukh T; Hawwari A; Al Zubi K
BMC Med Genet; 2020 Sep; 21(1):177. PubMed ID: 32887565
[TBL] [Abstract][Full Text] [Related]
7. Concomitant keratoconus and macular corneal dystrophy.
Javadi MA; Rafee'i AB; Kamalian N; Karimian F; Ja'farinasab MR; Yazdani S
Cornea; 2004 Jul; 23(5):508-12. PubMed ID: 15220737
[TBL] [Abstract][Full Text] [Related]
8. Autosomal Recessive Non-syndromic Keratoconus: Homozygous Frameshift Variant in the Candidate Novel Gene GALNT14.
Froukh T; Hawwari A
Curr Mol Med; 2019; 19(9):683-687. PubMed ID: 31362688
[TBL] [Abstract][Full Text] [Related]
9. Keratoconus and Fuchs' corneal endothelial dystrophy in a patient and her family.
Lipman RM; Rubenstein JB; Torczynski E
Arch Ophthalmol; 1990 Jul; 108(7):993-4. PubMed ID: 2369360
[TBL] [Abstract][Full Text] [Related]
10. [A familial case of keratoconus with corneal granular dystrophy].
Mitsui M; Sakimoto T; Sawa M; Katami M
Nippon Ganka Gakkai Zasshi; 1996 Nov; 100(11):916-9. PubMed ID: 8953898
[TBL] [Abstract][Full Text] [Related]
11. Concurrent macular corneal dystrophy and keratoconus.
Mohammad-Rabei H; Shojaei A; Aslani M
Middle East Afr J Ophthalmol; 2012; 19(2):251-3. PubMed ID: 22623870
[TBL] [Abstract][Full Text] [Related]
12. [Incidence of primary band-shaped corneal dystrophy, other degenerative corneal lesions, and keratoconus in a family (author's transl)].
Lisch W
Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1974; 191(1):37-43. PubMed ID: 4547047
[No Abstract] [Full Text] [Related]
13. Trio-based exome sequencing broaden the genetic spectrum in keratoconus.
Xu L; Yang K; Zhu M; Yin S; Gu Y; Fan Q; Wang Y; Pang C; Ren S
Exp Eye Res; 2023 Jan; 226():109342. PubMed ID: 36502923
[TBL] [Abstract][Full Text] [Related]
14. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
[TBL] [Abstract][Full Text] [Related]
15. Association of keratoconus with granular corneal dystrophy.
Vajpayee RB; Snibson GR; Taylor HR
Aust N Z J Ophthalmol; 1996 Nov; 24(4):369-71. PubMed ID: 8985551
[TBL] [Abstract][Full Text] [Related]
16. Keratoconus associated with other corneal dystrophies.
Cremona FA; Ghosheh FR; Rapuano CJ; Eagle RC; Hammersmith KM; Laibson PR; Ayres BD; Cohen EJ
Cornea; 2009 Feb; 28(2):127-35. PubMed ID: 19158551
[TBL] [Abstract][Full Text] [Related]
17. Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus.
Shinde V; Sobreira N; Wohler ES; Maiti G; Hu N; Silvestri G; George S; Jackson J; Chakravarti A; Willoughby CE; Chakravarti S
Hum Mol Genet; 2021 May; 30(8):658-671. PubMed ID: 33729517
[TBL] [Abstract][Full Text] [Related]
18. [The pathogenesis and treatment of corneal disorders].
Kanai A
Nippon Ganka Gakkai Zasshi; 2002 Dec; 106(12):757-76; discussion 777. PubMed ID: 12610836
[TBL] [Abstract][Full Text] [Related]
19. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
[TBL] [Abstract][Full Text] [Related]
20. Exome sequencing identification of susceptibility genes in Chinese patients with keratoconus.
Xu L; Yang K; Fan Q; Gu Y; Zhang B; Pang C; Ren S
Ophthalmic Genet; 2020 Dec; 41(6):518-525. PubMed ID: 32744102
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
