Mustafi D - Search Results

1

Re: Yahya et al.: Late-onset autosomal dominant macular degeneration caused by deletion of the CRX gene (Ophthalmology. 2023;130:68-76).

Mustafi D, Chao JR. Mustafi D, et al. Ophthalmology. 2023 Mar;130(3):e9. doi: 10.1016/j.ophtha.2022.10.014. Epub 2022 Nov 15. Ophthalmology. 2023. PMID: 36400609 No abstract available.

2

Targeted adaptive long-read sequencing for discovery of complex phased variants in inherited retinal disease patients.

Nakamichi K, Van Gelder RN, Chao JR, Mustafi D. Nakamichi K, et al. Among authors: mustafi d. Sci Rep. 2023 May 26;13(1):8535. doi: 10.1038/s41598-023-35791-4. Sci Rep. 2023. PMID: 37237007 Free PMC article.

3

[No title available]

[No authors listed] [No authors listed] PMID: 38109579

4

Diagnostic Role of Oral Fluorescein Angiography in Pediatric Ambulatory Clinics.

Sawyer C, Huang LC, Vincent J, Cabrera MT, Herlihy E, Mustafi D. Sawyer C, et al. Among authors: mustafi d. Ophthalmol Retina. 2024 Feb;8(2):204-206. doi: 10.1016/j.oret.2023.10.014. Epub 2023 Oct 29. Ophthalmol Retina. 2024. PMID: 38707762

5

Reply.

Mustafi D, Sawyer C, Huang LC. Mustafi D, et al. Ophthalmol Retina. 2024 Mar;8(3):e7-e8. doi: 10.1016/j.oret.2023.11.020. Epub 2024 Jan 8. Ophthalmol Retina. 2024. PMID: 38189691 No abstract available.

6

Immunology of Retinitis Pigmentosa and Gene Therapy-Associated Uveitis.

Yang P, Mustafi D, Pepple KL. Yang P, et al. Among authors: mustafi d. Cold Spring Harb Perspect Med. 2024 Jan 2;14(1):a041305. doi: 10.1101/cshperspect.a041305. Cold Spring Harb Perspect Med. 2024. PMID: 37037600 Free PMC article. Review.

7

Successful Treatment Response of a Juxtapapillary Retinal Capillary Hemangioblastoma Due to von Hippel-Lindau Syndrome with Belzutifan in a Pediatric Patient.

Mustafi D, Huang J, Ting MA, Waligorski N, Stacey AW, Huang LC. Mustafi D, et al. Retina. 2024 May 1;44(5):e31-e33. doi: 10.1097/IAE.0000000000003973. Retina. 2024. PMID: 38100768 No abstract available.

8

Familial co-segregation and the emerging role of long-read sequencing to re-classify variants of uncertain significance in inherited retinal diseases.

Gupta P, Nakamichi K, Bonnell AC, Yanagihara R, Radulovich N, Hisama FM, Chao JR, Mustafi D. Gupta P, et al. Among authors: mustafi d. NPJ Genom Med. 2023 Aug 10;8(1):20. doi: 10.1038/s41525-023-00366-9. NPJ Genom Med. 2023. PMID: 37558662 Free PMC article.

9

Targeted long-read sequencing allows for rapid identification of pathogenic disease-causing variants in retinoblastoma.

Nakamichi K, Stacey A, Mustafi D. Nakamichi K, et al. Among authors: mustafi d. Ophthalmic Genet. 2022 Dec;43(6):762-770. doi: 10.1080/13816810.2022.2141797. Epub 2022 Nov 3. Ophthalmic Genet. 2022. PMID: 36325802

10

HUMAN CELLULAR MODELS FOR RETINAL DISEASE: From Induced Pluripotent Stem Cells to Organoids.

Mustafi D, Bharathan SP, Calderon R, Nagiel A. Mustafi D, et al. Retina. 2022 Oct 1;42(10):1829-1835. doi: 10.1097/IAE.0000000000003571. Retina. 2022. PMID: 35858274 Free PMC article. Review.

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