Item request has been placed!

Item request cannot be made.

Processing Request

نتائج البحث

Display Settings

النتائج لكل صفحة: 10

Sort By: Relevance

Filter

فلترة النتائج

إعادة تعيين خيارات الفبترة

Item request has been placed!

Item request cannot be made.

Processing Request

Academic Journal

Foveal hypoplasia in oculocutaneous albinism: An optical coherence tomography study.

Authors : Pillay, Ethan¹ (AUTHOR); Rampersad, Nishanee¹ (AUTHOR)

Source: African Vision & Eye Health. 2023, Vol. 82 Issue 1, p1-7. 7p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Foveal Hypoplasia in CRB1 -Related Retinopathies.

Authors : Rodriguez-Martinez, Ana Catalina^1,2,3 (AUTHOR) ; Higgins, Bethany Elora^1,2 (AUTHOR) ; Tailor-Hamblin, Vijay^1,2,4 (AUTHOR)

Source: International Journal of Molecular Sciences. Sep2023, Vol. 24 Issue 18, p13932. 13p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Characterizing Foveal Hypoplasia Using Optical Coherence Tomography Angiography: Evaluation of Microvascular Abnormalities and Clinical Significance.

Authors : Storp, Jens Julian¹ (AUTHOR) ; Zimmermann, Julian Alexander¹ (AUTHOR) ; Danzer, Moritz Fabian² (AUTHOR)

Source: Journal of Clinical Medicine. Aug2023, Vol. 12 Issue 15, p4992. 15p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity.

Authors : Hallali, Gabriel^1,2 (AUTHOR) ; Loudon, Sjoukje E.³ (AUTHOR); Robson, Anthony G.^4,5 (AUTHOR)

Source: Acta Ophthalmologica (1755375X). Mar2023, Vol. 101 Issue 2, pe261-e263. 3p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Expanding the mutational spectrum of FHONDA syndrome.

Authors : Shoji, Marissa K.¹ (AUTHOR) ; Khodeiry, Mohamed M.¹ (AUTHOR); Sengillo, Jesse D.¹ (AUTHOR)

Source: Ophthalmic Genetics. Dec2023, Vol. 44 Issue 6, p602-605. 4p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Ocular findings and a comparative study of hair, skin and iris color in Chinese patients with albinism.

Authors : Arcot Sadagopan, Karthikeyan^1,2,3 (AUTHOR) ; Teng, Chih-Hao⁴ (AUTHOR); Hui, Gong^5,6 (AUTHOR)

Source: Ophthalmic Genetics. Feb2023, Vol. 44 Issue 1, p54-69. 16p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Familial Congenital Aniridia with Subluxated Lens and Glaucoma.

Authors : Perwitasari, Birgitta Henny¹ ; Hermawan, Dicky¹

Source: Vision Science & Eye Health Journal. Nov2023, Vol. 3 Issue 1, p17-22. 6p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Genetic variants in melanogenesis proteins TYRP1 and TYR are associated with the golden rhesus macaque phenotype.

Authors : Peterson, Samuel M.¹ ; Watowich, Marina M.^2,3,4; Renner, Lauren M.⁵

Source: G3: Genes | Genomes | Genetics. Oct2023, Vol. 13 Issue 10, p1-11. 11p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Vision-Related Quality of Life in Danish Patients with Albinism and the Impact of an Updated Optical Rehabilitation.

Authors : Lisbjerg, Kristian¹ (AUTHOR) ; Jordana, Joaquim Torner¹ (AUTHOR) ; Brandt, Vibeke N.¹ (AUTHOR)

Source: Journal of Clinical Medicine. Sep2023, Vol. 12 Issue 17, p5451. 9p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

A novel PAX6 variant as the cause of aniridia in a Chinese patient with SRRRD.

Authors : Wang, Qian¹ (AUTHOR); Wei, Wen Bin¹ (AUTHOR); Shi, Xiang Yu¹ (AUTHOR)

Source: BMC Medical Genomics. 8/4/2023, Vol. 16 Issue 1, p1-11. 11p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

نتائج البحث

فلترة النتائج

Foveal hypoplasia in oculocutaneous albinism: An optical coherence tomography study.

Foveal Hypoplasia in CRB1 -Related Retinopathies.

Characterizing Foveal Hypoplasia Using Optical Coherence Tomography Angiography: Evaluation of Microvascular Abnormalities and Clinical Significance.

Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity.

Expanding the mutational spectrum of FHONDA syndrome.

Ocular findings and a comparative study of hair, skin and iris color in Chinese patients with albinism.

Familial Congenital Aniridia with Subluxated Lens and Glaucoma.

Genetic variants in melanogenesis proteins TYRP1 and TYR are associated with the golden rhesus macaque phenotype.

Vision-Related Quality of Life in Danish Patients with Albinism and the Impact of an Updated Optical Rehabilitation.

A novel PAX6 variant as the cause of aniridia in a Chinese patient with SRRRD.

اتصل بنا

اتبع