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KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1.
Georgiou M, Robson AG, Fujinami K, Leo SM, Vincent A, Nasser F, Cabral De Guimarães TA, Khateb S, Pontikos N, Fujinami-Yokokawa Y, Liu X, Tsunoda K, Hayashi T, Vargas ME, Thiadens AAHJ, de Carvalho ER, Nguyen XT, Arno G, Mahroo OA, Martin-Merida MI, Jimenez-Rolando B, Gordo G, Carreño E, Ayuso C, Sharon D, Kohl S, Huckfeldt RM, Wissinger B, Boon CJF, Banin E, Pennesi ME, Khan AO, Webster AR, Zrenner E, Héon E, Michaelides M. Georgiou M, et al. Among authors: khan ao. Am J Ophthalmol. 2021 May;225:95-107. doi: 10.1016/j.ajo.2020.11.022. Epub 2020 Dec 11. Am J Ophthalmol. 2021. PMID: 33309813 Free PMC article.
Recognizing posterior microphthalmos.
Khan AO. Khan AO. Ophthalmology. 2006 Apr;113(4):718. doi: 10.1016/j.ophtha.2006.01.013. Ophthalmology. 2006. PMID: 16581441 No abstract available.
Newborn glaucoma on the Arabian Peninsula.
Khan AO. Khan AO. Surv Ophthalmol. 2013 Sep-Oct;58(5):502. doi: 10.1016/j.survophthal.2013.05.002. Surv Ophthalmol. 2013. PMID: 23969023 No abstract available.
Rate of penetrating keratoplasty.
Khan AO. Khan AO. Ophthalmology. 2007 Jul;114(7):1414. doi: 10.1016/j.ophtha.2007.03.024. Ophthalmology. 2007. PMID: 17613332 No abstract available.
Nodal point of the eye.
Khan AO. Khan AO. Ophthalmology. 2007 Sep;114(9):1791. doi: 10.1016/j.ophtha.2007.04.025. Ophthalmology. 2007. PMID: 17822987 No abstract available.
A founder variant expands the phenotype of WNT7B-related PDAC syndrome.
AlAbdi L, Rahbeeni Z, Maddirevula S, Helaby R, Abdulwahab F, Khan AO, Riley LG, Alhashem A, Chassaing N, Jamieson RV, Alkuraya FS. AlAbdi L, et al. Among authors: khan ao. Clin Genet. 2024 Feb 28. doi: 10.1111/cge.14512. Online ahead of print. Clin Genet. 2024. PMID: 38417950
364 results