نتائج البحث

Association of GNB3, ACE polymorphisms with POAG and NTG.

• Authors : Samoylov, Alexander N.^1,2 (AUTHOR); Tumanova, Polina² (AUTHOR); Pankratova, Sofya A.¹ (AUTHOR)

• Source: Ophthalmic Genetics. Feb2024, Vol. 45 Issue 1, p23-27. 5p.

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Microcephaly and chorioretinopathy associated with TUBGCP4: a case report and a review of the literature.

• Authors : Yahalom, Claudia¹ (AUTHOR); Woods, Russell L² (AUTHOR); Akula, James D² (AUTHOR)

• Source: Ophthalmic Genetics. Dec2023, Vol. 44 Issue 6, p585-590. 6p.

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Positive feedback loop between vision-related anxiety and self-reported visual difficulty.

• Authors : Popova, Lilia T.¹ (AUTHOR); Abuzaitoun, Rebhi O.² (AUTHOR); Fresco, David M.³ (AUTHOR)

• Source: Ophthalmic Genetics. Aug2023, Vol. 44 Issue 4, p327-333. 7p.

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MERTK retinopathy: biomarkers assessing vision loss.

• Authors : Sakti, Dhimas H.^1,2 (AUTHOR) ; Cornish, Elisa E.^1,3 (AUTHOR); Mustafic, Nina¹ (AUTHOR)

• Source: Ophthalmic Genetics. Dec 2021, Vol. 42 Issue 6, p706-716. 11p.

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Novel biallelic AHR splice site mutation cause isolated foveal hypoplasia in Saudi patient: a case report.

• Authors : AlMoallem B; Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.; King Saud University Medical City (KSUMC), Riyadh, Saudi Arabia.

Subjects: Receptors, Aryl Hydrocarbon* ; Vision Disorders*; Child Foveal Hypoplasia, Isolated

• Source: Ophthalmic genetics [Ophthalmic Genet] 2022 Jun; Vol. 43 (3), pp. 425-429. Date of Electronic Publication: 2022 Feb 21.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review.

• Authors : Boysen, Kirstine B.¹ (AUTHOR); La Cour, Morten^1,2 (AUTHOR); Kessel, Line^1,2 (AUTHOR)

• Source: Ophthalmic Genetics. Jun2020, Vol. 41 Issue 3, p223-234. 12p.

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Management of a case of Enhanced S-cone syndrome with massive foveoschisis treated with pars plana vitrectomy with silicone oil tamponade.

• Authors : Bechet L; CHNO des Quinze-Vingts, INSERM-DGOS CIC Paris, France.; Atia R

Subjects: Vitrectomy*; Endotamponade/Endotamponade/Endotamponade/*methods ; Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*surgery Enhanced S-Cone Syndrome

• Source: Ophthalmic genetics [Ophthalmic Genet] 2021 Oct; Vol. 42 (5), pp. 615-618. Date of Electronic Publication: 2021 May 10.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity.

• Authors : Meng W; a Division of Population Health and Genomics , Medical Research Institute, Ninewells Hospital and School of Medicine, University of Dundee , Dundee , UK.; Chan BW

Subjects: Genome-Wide Association Study* ; Polymorphism, Single Nucleotide* ; Visual Acuity*

• Source: Ophthalmic genetics [Ophthalmic Genet] 2019 Jun; Vol. 40 (3), pp. 252-258. Date of Electronic Publication: 2019 Jul 02.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Multimodal imaging in CABP4- related retinopathy.

• Authors : Schatz, Patrik^1,2 (AUTHOR) ; Abdalla Elsayed, Maram E. A.³ (AUTHOR); Khan, Arif O.⁴ (AUTHOR)

• Source: Ophthalmic Genetics. Sep/Oct2017, Vol. 38 Issue 5, p459-464. 6p.

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Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.

• Authors : Tourville, Aurore¹ (AUTHOR); Michiels, Christelle¹ (AUTHOR); Condroyer, Christel¹ (AUTHOR)

• Source: Ophthalmic Genetics. Apr2019, Vol. 40 Issue 2, p182-184. 3p.

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