Items where Author is "Kianersi, H."
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(2024) Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia. Bmc Medical Genomics. p. 10.
(2024) Comparative analysis of optical coherence tomography angiography (OCTA) results between Behçet's disease patients and a healthy control group. Clinical Rheumatology. pp. 1127-1133. ISSN 0770-3198
(2024) Fuchs' uveitis syndrome: a 20-year experience in 466 patients. Scientific Reports. p. 6. ISSN 2045-2322
(2024) Retinal and choroidal thickness in fuchs uveitis syndrome: a contralateral eye study. Bmc Ophthalmology. p. 6.