These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
92 related articles for article (PubMed ID: 34644435)
41. Ocular abnormalities and complications in anterior megalophthalmos: a case series. Kumawat D; Alam T; Sahay P; Chawla R Eye (Lond); 2019 May; 33(5):826-832. PubMed ID: 30617289 [TBL] [Abstract][Full Text] [Related]
42. Alveolar capillary dysplasia without misalignment of pulmonary veins, hyperinflammation, megalocornea and overgrowth - Association with a homozygous 2bp-insertion in LTBP2? Vollbach K; Trepels-Kottek S; Elbracht M; Kurth I; Wagner N; Orlikowsky T; Braunschweig T; Tenbrock K Eur J Med Genet; 2021 Jun; 64(6):104209. PubMed ID: 33766794 [TBL] [Abstract][Full Text] [Related]
43. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
44. Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India. Shetty R; Nuijts RM; Nanaiah SG; Anandula VR; Ghosh A; Jayadev C; Pahuja N; Kumaramanickavel G; Nallathambi J BMC Med Genet; 2015 May; 16():33. PubMed ID: 25963163 [TBL] [Abstract][Full Text] [Related]
45. [Cysts of septum pellucidum, cavum vergae and cavum veli interpositi. Meta-analysis of 368 cases]. Kryukov EV; Stanishevsky AV; Gavrilov GV; Gizatullin SK Zh Vopr Neirokhir Im N N Burdenko; 2020; 84(4):111-118. PubMed ID: 32759934 [TBL] [Abstract][Full Text] [Related]
46. Potential complications of ocular surgery in patients with coexistent keratoconus and Fuchs' endothelial dystrophy. Jurkunas U; Azar DT Ophthalmology; 2006 Dec; 113(12):2187-97. PubMed ID: 16996603 [TBL] [Abstract][Full Text] [Related]
47. MEGALOCORNEA AND MOSAIC DYSTROPHY OF THE CORNEA. MALBRAN E; D ALESSANDRO C; VALENZUELA J Ophthalmologica; 1965; 149():161-76. PubMed ID: 14315342 [No Abstract] [Full Text] [Related]
49. Effect of heterozygous pathogenic COL4A3 or COL4A4 variants on patients with X-linked Alport syndrome. Zhang Y; Ding J; Zhang H; Yao Y; Xiao H; Wang S; Wang F Mol Genet Genomic Med; 2019 May; 7(5):e647. PubMed ID: 30883042 [TBL] [Abstract][Full Text] [Related]
50. Comparative evaluation of Scheimpflug tomography parameters between thin non-keratoconic, subclinical keratoconic, and mild keratoconic corneas. Huseynli S; Salgado-Borges J; Alio JL Eur J Ophthalmol; 2018 Sep; 28(5):521-534. PubMed ID: 29566542 [TBL] [Abstract][Full Text] [Related]
51. Genetic and clinical findings of panel-based targeted exome sequencing in a northeast Chinese cohort with retinitis pigmentosa. Sun Y; Li W; Li JK; Wang ZS; Bai JY; Xu L; Xing B; Yang W; Wang ZW; Wang LS; He W; Chen F Mol Genet Genomic Med; 2020 Apr; 8(4):e1184. PubMed ID: 32100970 [TBL] [Abstract][Full Text] [Related]
52. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome]. Kamińska A; Sokołowska-Oracz A; Pawluczyk-Dyjecińska M; Szaflik JP Klin Oczna; 2007; 109(7-9):321-6. PubMed ID: 18260289 [TBL] [Abstract][Full Text] [Related]
53. Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus. Lam HY; Wiggs JL; Jurkunas UV Cornea; 2010 Oct; 29(10):1180-5. PubMed ID: 20567203 [TBL] [Abstract][Full Text] [Related]
54. Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. Wesdorp M; Schreur V; Beynon AJ; Oostrik J; van de Kamp JM; Elting MW; van den Boogaard MH; Feenstra I; Admiraal RJC; Kunst HPM; Hoyng CB; Kremer H; Yntema HG; Pennings RJE; Schraders M Clin Genet; 2018 Aug; 94(2):221-231. PubMed ID: 29676012 [TBL] [Abstract][Full Text] [Related]
55. Corneal Cross-linking in Thin Corneas: 1-Year Results of Accelerated Contact Lens-Assisted Treatment of Keratoconus. Knyazer B; Kormas RM; Chorny A; Lifshitz T; Achiron A; Mimouni M J Refract Surg; 2019 Oct; 35(10):642-648. PubMed ID: 31610005 [TBL] [Abstract][Full Text] [Related]
56. Genetic eye research in Tasmania: a historical overview. Mackey DA Clin Exp Ophthalmol; 2012 Mar; 40(2):205-10. PubMed ID: 22044574 [TBL] [Abstract][Full Text] [Related]
57. Congenital keratoglobus with blue sclera in two siblings with overlapping Marshall/Stickler phenotype. Imamoglu S; Kaya V; Imamoglu EY; Gok K Indian J Ophthalmol; 2016 Nov; 64(11):856-859. PubMed ID: 27958215 [TBL] [Abstract][Full Text] [Related]