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Sawsan R Nowilaty

Showing results (11-20 of 39) with videos related to

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Middle East African Journal of Ophthalmology|September 17, 2010
Characteristics of optic disc melanocytomas presenting with visual dysfunctionSaba Al-Rashaed, Emad B Abboud, Sawsan R Nowilaty
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|April 11, 2015
Nanophthalmos and hemiretinal vein occlusion: A case reportAhmad A Albar, Sawsan R Nowilaty, Nicola G Ghazi
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|April 4, 2025
Juxtapapillary congenital hypertrophy of the retinal pigment epithelium: A report of two casesHanan A Alshalan, Abrar K Alsalamah, Sawsan R Nowilaty
Ophthalmic Genetics|November 27, 2020
A novel c.980C>G variant in <i>OAT</i> results in identifiable gyrate atrophy phenotype associated with retinal detachment in a young femaleMoustafa Magliyah, Abrar K Alsalamah, Majeedah AlOtaibi, et al.
Middle East African Journal of Ophthalmology|September 17, 2010
Idiopathic juxtafoveolar retinal telangiectasis: a current reviewSawsan R Nowilaty, Hanan N Al-Shamsi, Wajeeha Al-Khars
Ophthalmic Genetics|April 20, 2026
Unusual presentation of cone dysfunction consequent upon a homozygous <i>FAM161A</i> variantJinan Alhamad, Enas Magharbil, Sawsan R Nowilaty, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 21, 2020
Evolution of macular hole in enhanced S-cone syndromeMoustafa S Magliyah, Sulaiman M AlSulaiman, Patrik Schatz, et al.
American Journal of Ophthalmology Case Reports|April 25, 2022
Retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome can be associated with coronary and major systemic arterial diseaseDeema E Jomar, Amani S Albakri, Leen Abu Safieh, et al.
Retinal Cases & Brief Reports|December 5, 2017
DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1Hamad M Alsulaiman, Patrik Schatz, Sawsan R Nowilaty, et al.
Retinal Cases & Brief Reports|May 11, 2021
FAMILIAL EXUDATIVE VITREOTINOPATHY-LIKE FEATURES IN STICKLER TYPE IV ASSOCIATED WITH NOVEL VARIANTS IN COL9A1Hamad F Alsubaie, Moustafa S Magliyah, Osama AlRaddadi, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Middle East African Journal of Ophthalmology|September 17, 2010
Characteristics of optic disc melanocytomas presenting with visual dysfunctionSaba Al-Rashaed, Emad B Abboud, Sawsan R Nowilaty
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|April 11, 2015
Nanophthalmos and hemiretinal vein occlusion: A case reportAhmad A Albar, Sawsan R Nowilaty, Nicola G Ghazi
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|April 4, 2025
Juxtapapillary congenital hypertrophy of the retinal pigment epithelium: A report of two casesHanan A Alshalan, Abrar K Alsalamah, Sawsan R Nowilaty
Ophthalmic Genetics|November 27, 2020
A novel c.980C>G variant in <i>OAT</i> results in identifiable gyrate atrophy phenotype associated with retinal detachment in a young femaleMoustafa Magliyah, Abrar K Alsalamah, Majeedah AlOtaibi, et al.
Middle East African Journal of Ophthalmology|September 17, 2010
Idiopathic juxtafoveolar retinal telangiectasis: a current reviewSawsan R Nowilaty, Hanan N Al-Shamsi, Wajeeha Al-Khars
Ophthalmic Genetics|April 20, 2026
Unusual presentation of cone dysfunction consequent upon a homozygous <i>FAM161A</i> variantJinan Alhamad, Enas Magharbil, Sawsan R Nowilaty, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 21, 2020
Evolution of macular hole in enhanced S-cone syndromeMoustafa S Magliyah, Sulaiman M AlSulaiman, Patrik Schatz, et al.
American Journal of Ophthalmology Case Reports|April 25, 2022
Retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome can be associated with coronary and major systemic arterial diseaseDeema E Jomar, Amani S Albakri, Leen Abu Safieh, et al.
Retinal Cases & Brief Reports|December 5, 2017
DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1Hamad M Alsulaiman, Patrik Schatz, Sawsan R Nowilaty, et al.
Retinal Cases & Brief Reports|May 11, 2021
FAMILIAL EXUDATIVE VITREOTINOPATHY-LIKE FEATURES IN STICKLER TYPE IV ASSOCIATED WITH NOVEL VARIANTS IN COL9A1Hamad F Alsubaie, Moustafa S Magliyah, Osama AlRaddadi, et al.
Pageof 4