Research output per year
Research output per year
Search results
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2021
Poretti-Boltshauser syndrome: a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration
Alahmadi, A. S., Badawi, A. H., Magliyah, M. S., Albakri, A. & Schatz, P., 2021, In: Ophthalmic Genetics. 42, 1, p. 96-98Research output: Contribution to journal › Letter › peer-review
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2020
Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy
Magliyah, M., Al Dhibi, H. & Schatz, P., 2020 Nov, In: Eye (Basingstoke). 34, 11, p. 2135-2137 3 p.Research output: Contribution to journal › Letter › peer-review
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Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm
AlZaid, A., Magliyah, M., Schatz, P. & Al-Dhibi, H., 2020, In: Ophthalmic Genetics. 41, 4, p. 394-396 3 p.Research output: Contribution to journal › Letter › peer-review
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2019
Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis
Magliyah, M., AlRaddadi, O., Balbaid, A. & Schatz, P., 2019, In: Ophthalmic Genetics. 40, 6, p. 588-590 3 p.Research output: Contribution to journal › Letter › peer-review
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Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
Aldrees, A., Abdelkader, E., Al-Habboubi, H., Alrwebah, H., Rahbeeni, Z. & Schatz, P., 2019, In: Ophthalmic Genetics. 40, 1, p. 77-79Research output: Contribution to journal › Letter › peer-review
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2018
Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F
Abdelkader, E., AlHilali, S., Neuhaus, C., Bergmann, C., AlMurshed, T. & Schatz, P., 2018, In: Ophthalmic Genetics. 39, 5, p. 659-661 3 p.Research output: Contribution to journal › Letter › peer-review