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Comparison of Glaucoma Therapy Escalation After Penetrating Keratoplasty to Descemet Stripping Automated Endothelial Keratoplasty for the Treatment of Pseudophakic Bullous Keratopathy: A Cohort Study.

Autor: Aldarrab A; Department of Surgery, College of Medicine, Prince Sattam Bin Abdulaziz University, AlKharj, Saudi Arabia.; Glaucoma Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Alsakran W; Retina Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Al-Swailem SA; Anterior Segment Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Al-Shahwan SA; Glaucoma Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

Publikováno v: Middle East African journal of ophthalmology [Middle East Afr J Ophthalmol] 2023 Feb 24; Vol. 29 (2), pp. 72-79. Date of Electronic Publication: 2023 Feb 24 (Print Publication: 2022).

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Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome.

Autor: McRae, Helen M.^1,2 (AUTHOR), Leong, Melody P. Y.^1,2 (AUTHOR), Bergamasco, Maria I.^1,2 (AUTHOR), Garnham, Alexandra L.^1,2 (AUTHOR), Hu, Yifang¹ (AUTHOR), Corbett, Mark A.³ (AUTHOR), Whitehead, Lachlan^1,2 (AUTHOR), El-Saafin, Farrah^1,2 (AUTHOR), Sheikh, Bilal N.^1,2 (AUTHOR), Wilcox, Stephen^1,2 (AUTHOR), Hannan, Anthony J.^4,5 (AUTHOR), Gécz, Jozef^3,6 (AUTHOR), Smyth, Gordon K.^1,7 (AUTHOR), Thomas, Tim^1,2 (AUTHOR) tthomas@wehi.edu.au, Voss, Anne K.^1,2 (AUTHOR) tthomas@wehi.edu.au

Publikováno v: PLoS Genetics. 10/15/2024, Vol. 20 Issue 10, p1-35. 35p.

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Akademický článek

Descemet membrane endothelial keratoplasty and penetrating keratoplasty in pseudophakic bullous keratopathy: comparison of visual outcomes, graft survival rates, and complications.

Autor: Balıkçı, Ayşe Tüfekçi¹ drtufekciayşe@yahoo.com, Demir, Nurşah¹, Burcu, Ayşe¹, Akkaya, Züleyha Yalnız¹, Şingar, Evin¹, Uzman, Selma¹

Publikováno v: European Research Journal. Jul2024, Vol. 10 Issue 4, p380-387. 8p.

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Akademický článek

Primary congenital glaucoma: An updated review.

Autor: Badawi AH; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Al-Muhaylib AA; Department of Ophthalmology, College of Medicine, Qassim University, AlQassim, Saudi Arabia., Al Owaifeer AM; Faculty of Ophthalmology, College of Medicine, King Faisal University, Al-Hasa, Saudi Arabia., Al-Essa RS; Department of Ophthalmology, King Saud University, Riyadh, Saudi Arabia., Al-Shahwan SA; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

Publikováno v: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society [Saudi J Ophthalmol] 2019 Oct-Dec; Vol. 33 (4), pp. 382-388. Date of Electronic Publication: 2019 Nov 07.

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Akademický článek

Mutation Screening of the CYP1B1 Gene Reveals Novel and Recurrent Pathogenic Variants in Pakistani Primary Congenital Glaucoma Patients.

Autor: Surhio, Waqas Ali¹, Khidri, Feriha Fatima², Haroon, Mohsin Iqbal³, Mehmood, Samia⁴, Waryah, Yar Muhammad⁵ yarmwaryah@hotmail.com

Publikováno v: Journal of Liaquat University of Medical & Health Sciences. Apr-Jun2024, Vol. 23 Issue 2, p140-145. 6p.

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Akademický článek

Effect of Trabeculodescemetic Window Perforation in Deep Sclerectomy on Intraocular Pressure in Primary Congenital Glaucoma.

Autor: AlQattan, Abdulaziz¹ (AUTHOR), Schargel, Konrad² (AUTHOR), AlJadaan, Ibrahim² (AUTHOR), AlZendi, Nouf² (AUTHOR), Sesma, Gorka¹ (AUTHOR) gsesma@kkesh.med.sa

Publikováno v: Ophthalmology & Therapy. Feb2024, Vol. 13 Issue 2, p581-596. 16p.

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Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Autor: Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, Nilgün Y, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, Paoli D, Schlottmann PG, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M, Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Shahwan SA, Fogarty RA, Leo P, Yetkin Y, Oğuz Ç, Kanavi MR, Beni AN, Yazdani S, Akopov EL, Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U, Krumbiegel M, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM, Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T, Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Guadarrama-Vallejo D, Cheng CY, Perera SA, Husain R, Ho SL, Welge-Luessen UC, Mardin C, Schloetzer-Schrehardt U, Hillmer AM, Herms S, Moebus S, Nöthen MM, Weisschuh N, Shetty R, Ghosh A, Teo YY, Brown MA, Lischinsky I, Crowston JG, Coote M, Zhao B, Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Reis A, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Pasutto F, Topouzis F, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC

Publikováno v: Nature genetics [Nat Genet] 2015 Jun; Vol. 47 (6), pp. 689.

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