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Open Access Macedonian Journal of Medical Sciences
|
May 22, 2019
Refractive Status in Children with Laser-Treated Retinopathy of Prematurity: Our Experience in Bulgaria
Nevyana Veleva, Violeta Chernodrinska
Nepalese Journal of Ophthalmology : a Biannual Peer-Reviewed Academic Journal of the Nepal Ophthalmic Society : NEPJOPH
|
July 27, 2025
TIMP3 c.319C>T, p.(Arg107Cys): Novel Sequence Variant In Sorsby Fundus Dystrophy
Rozaliya Hristova, Nevyana Veleva, Alexander Oscar, et al.
Genes
|
May 4, 2026
A Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the <i>CPAMD8</i> Gene
Nevyana Veleva-Krasteva, Kiril Genov, Kunka Kamenarova, et al.
Molecular Genetics & Genomic Medicine
|
June 3, 2022
Panel-based next-generation sequencing identifies novel mutations in Bulgarian patients with inherited retinal dystrophies
Kunka Kamenarova, Kalina Mihova, Nevyana Veleva, et al.
Molecular Genetics & Genomic Medicine
|
June 26, 2026
Gene Panel Analysis Reveals Overlapping Genetic Causes of Inherited Cataracts and Other Ocular Phenotypes in Bulgarian Patients
Kristiyana Vitanova, Kunka Kamenarova, Nevyana Veleva-Krasteva, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
June 28, 2014
Amblyopia screening in Bulgaria
Alexander Oscar, Sylvia Cherninkova, Vasil Haykin, et al.
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Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Open Access Macedonian Journal of Medical Sciences
|
May 22, 2019
Refractive Status in Children with Laser-Treated Retinopathy of Prematurity: Our Experience in Bulgaria
Nevyana Veleva, Violeta Chernodrinska
Nepalese Journal of Ophthalmology : a Biannual Peer-Reviewed Academic Journal of the Nepal Ophthalmic Society : NEPJOPH
|
July 27, 2025
TIMP3 c.319C>T, p.(Arg107Cys): Novel Sequence Variant In Sorsby Fundus Dystrophy
Rozaliya Hristova, Nevyana Veleva, Alexander Oscar, et al.
Genes
|
May 4, 2026
A Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the <i>CPAMD8</i> Gene
Nevyana Veleva-Krasteva, Kiril Genov, Kunka Kamenarova, et al.
Molecular Genetics & Genomic Medicine
|
June 3, 2022
Panel-based next-generation sequencing identifies novel mutations in Bulgarian patients with inherited retinal dystrophies
Kunka Kamenarova, Kalina Mihova, Nevyana Veleva, et al.
Molecular Genetics & Genomic Medicine
|
June 26, 2026
Gene Panel Analysis Reveals Overlapping Genetic Causes of Inherited Cataracts and Other Ocular Phenotypes in Bulgarian Patients
Kristiyana Vitanova, Kunka Kamenarova, Nevyana Veleva-Krasteva, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
June 28, 2014
Amblyopia screening in Bulgaria
Alexander Oscar, Sylvia Cherninkova, Vasil Haykin, et al.
Page
of 1