Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma von Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Iqbal, Aftab, Khan, Muhammad Imran, den Hollander, Anneke I

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A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma von Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Villanueva-Mendoza, Cristina, Cortés-González, Vianney, Khan, Muhammad Imran, den Hollander, Anneke I

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Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site... von Afzal, Rabia, Firasat, Sabika, Kaul, Haiba, Ahmed, Bashir, Siddiqui, Sorath N., Zafar, Saemah N., Shahzadi, Misbah, Afshan, Kiran

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Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families von Micheal, Shazia, Niewold, Ilse Therésia Gabriëla, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Khan, Muhammad Imran, Bergen, Arthur A B

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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice von Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, Fitzpatrick, David R

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Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucoma von Micheal, Shazia, Ayub, Humaira, Zafar, Saemah N, Bakker, Bjorn, Ali, Mahmood, Akhtar, Farah, Islam, Farrah, Khan, Muhammad I, Qamar, Raheel, den Hollander, Anneke I

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Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice von Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, FitzPatrick, David R

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Duane's syndrome: surgical outcome and non ophthalmologic associations von Sarfraz, Sarah, Zafar, Saemah Nuzhat, Khan, Ayesha

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Retinoblastoma in an adult von Zafar, Saemah Nuzhat, Ahmad, Saqib Qayyum, Zafar, Nadeem

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Variants in the PRPF8 Gene are Associated with Glaucoma von Micheal, Shazia, Hogewind, Barend F., Khan, Muhammad Imran, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Akhtar, Farah, Qamar, Raheel, Hoyng, Carel B., den Hollander, Anneke I.

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Effects of Artisan aphakic intraocular lens on central corneal thickness and intra ocular pressure in pediatric eyes with crystalline subluxated lenses von Zafar, Saemah, Siddiqui, Sorath, Khan, Ayesha

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Successful treatment of ligneous conjunctivitis with topical cyclosporine and heparin von Azad, Nadia, FCPS, FRCS, Zafar, Saemah, FCPS, FRCS, Khan, Ayesha, FCPS, FRCS

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Vein of Galen aneurysmal malformation masquerading as carotid cavernous fistula in a child with proptosis von Zafar, Sarah, Zafar, Saemah N, Khan, Ayesha, Zafar, Saerah Iffat

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Variable retinal presentations in nanophthalmos von KHAN, Ayesha, SAEMAH NUZHAT ZAFAR

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A case of systemic lupus erythematosus with aplastic anaemia von SAQIB QAYYUM AHMAD, KHAN, Obaidullah, SAERAH IFFAT ZAFAR, SAEMAH NUZHAT ZAFAR

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Ptosis associated with Monocular Elevation Deficiency von SAEMAH NUZHAT ZAFAR, KHAN, Ayesha, AZAD, Nadia, ALI, Mahmood, NASEER, Samina, IQBAL, Sarah

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Retinal Thickness and Visual Acuity in Diabetic Macular Edema: An Optical Coherence Tomography-Based Study von Islam, Farrah

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Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome von Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Venselaar, Hanka, Qamar, Raheel, Khan, Muhammad Imran, den Hollander, Anneke I.

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Tumor Regression Patterns in Retinoblastoma von Zafar, Saemah Nuzhat, Siddiqui, Sorath Noorani, Zaheer, Naima

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Retinoblastoma presenting as total hyphema: Three year follow-up von Zafar, Saemah Nuzhat, Zaheer, Naima, Khan, Mumtaz Ahmad

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