Alabek M - Search Results

1

Developing a pediatric ophthalmology telemedicine program in the COVID-19 crisis.

Kapoor S, Eldib A, Hiasat J, Scanga H, Tomasello J, Alabek M, Ament K, Arner D, Benson A, Berret K, Blaha B, Brinza M, Caterino R, Chauhan B, Churchfield W, Fulwylie C, Gruszewski J, Hrinak D, Johnston L, Meyer C, Nanda K, Newton T, Pomycala B, Runkel L, Sanchez K, Skellett S, Steigerwald J, Mitchell E, Pihlblad M, Luchansky C, Keim E, Yu J, Quinn P, Mittal A, Pitetti R, Patil-Chhablani P, Liasis A, Nischal KK. Kapoor S, et al. Among authors: alabek m. J AAPOS. 2020 Aug;24(4):204-208.e2. doi: 10.1016/j.jaapos.2020.05.008. Epub 2020 Sep 2. J AAPOS. 2020. PMID: 32890736 Free PMC article.

2

Ocular findings of albinism in DYRK1A-related intellectual disability syndrome.

Ernst J, Alabek ML, Eldib A, Madan-Khetarpal S, Sebastian J, Bhatia A, Liasis A, Nischal KK. Ernst J, et al. Among authors: alabek ml. Ophthalmic Genet. 2020 Dec;41(6):650-655. doi: 10.1080/13816810.2020.1814349. Epub 2020 Aug 24. Ophthalmic Genet. 2020. PMID: 32838606

3

Expansion of the ophthalmic phenotype of SPINT2-related syndromic congenital sodium diarrhea.

Ernst J, Hiasat J, Alabek ML, Scanga HL, Motley W, Nischal KK. Ernst J, et al. Among authors: alabek ml. Am J Med Genet A. 2021 Apr;185(4):1270-1274. doi: 10.1002/ajmg.a.62094. Epub 2021 Feb 5. Am J Med Genet A. 2021. PMID: 33547739

4

Congenital Corneal Opacity in 22q11.2 Deletion Syndrome: A Case Series.

Franco E, Iqbal N, Shah PR, Alabek M, Tripi KS, Prescott C, Scanga HL, Chu CT, Nischal KK. Franco E, et al. Among authors: alabek m. Cornea. 2023 Mar 1;42(3):344-350. doi: 10.1097/ICO.0000000000003155. Epub 2022 Nov 30. Cornea. 2023. PMID: 36455075

5

Inhibitor development in two cousins receiving full-length factor VIII (FVIII) and FVIII-Fc fusion protein.

Ragni MV, Alabek M, Malec LM. Ragni MV, et al. Among authors: alabek m. Haemophilia. 2016 Sep;22(5):e462-4. doi: 10.1111/hae.13032. Epub 2016 Aug 8. Haemophilia. 2016. PMID: 27501368 No abstract available.

6

The genetic counselor workforce in inherited retinal disease clinics: a descriptive assessment.

Alabek M, Andersen K, Everett L, Marra M. Alabek M, et al. Ophthalmic Genet. 2023 Dec;44(6):553-558. doi: 10.1080/13816810.2023.2239910. Epub 2023 Aug 2. Ophthalmic Genet. 2023. PMID: 37530443

7

Recurrent retinal detachment in Stickler Syndrome.

Chen TH, Fooladi MI, Alabek M, Scanga HL, Tripi KS, Nischal KK, Martel JN. Chen TH, et al. Among authors: alabek m. Eye (Lond). 2024 Oct 18. doi: 10.1038/s41433-024-03402-9. Online ahead of print. Eye (Lond). 2024. PMID: 39424914

8

Genetic counselors' awareness and attitudes regarding gene therapies.

Walsh C, Durst AL, Ortiz D, Miller RG, Alabek M. Walsh C, et al. Among authors: alabek m. J Genet Couns. 2024 Jul 23. doi: 10.1002/jgc4.1953. Online ahead of print. J Genet Couns. 2024. PMID: 39039945

9

Recurrent Retinal Detachment in Stickler Syndrome.

Chen T, Fooladi M, Alabek M, Scanga H, Tripi K, Nischal K, Martel J. Chen T, et al. Among authors: alabek m. Res Sq [Preprint]. 2024 Apr 5:rs.3.rs-3941698. doi: 10.21203/rs.3.rs-3941698/v1. Res Sq. 2024. Update in: Eye (Lond). 2024 Oct 18. doi: 10.1038/s41433-024-03402-9 PMID: 38645110 Free PMC article. Updated. Preprint.

10

An Optical Coherence Tomography-Based Measure as an Independent Estimate of Retinal Function in Retinitis Pigmentosa.

Paez-Escamilla M, Alabek ML, Beale O, Prensky CJ, Lejoyeux R, Friberg TR, Sahel JA, Rosin B. Paez-Escamilla M, et al. Among authors: alabek ml. Diagnostics (Basel). 2023 Nov 24;13(23):3521. doi: 10.3390/diagnostics13233521. Diagnostics (Basel). 2023. PMID: 38066762 Free PMC article.

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