Sean P Donahue
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Explore the profile of Sean P Donahue including associated specialties, affiliations and a list of published articles.
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121
Citations
1419
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Recent Articles
1.
Pruett J, Linton E, Donahue S, Groth S
J Pediatr Ophthalmol Strabismus
. 2024 Feb;
61(4):262-266.
PMID: 38380937
Purpose: To determine normal threshold values for the 24-2 program of the VisuALL-K (Olleyes, Inc), a portable static automated virtual reality perimeter that uses a video game-based testing modality on...
2.
Hilliard G, Pruett J, Donahue S, Velez F, Peragallo J, Ditta L, et al.
Am J Ophthalmol
. 2024 Jan;
262:186-191.
PMID: 38191066
Purpose: To investigate the results of patients undergoing surgical treatment for strabismic diplopia in thyroid eye disease (TED) following teprotumumab. Design: Multicenter, retrospective, case series. Methods: We report 28 patients...
3.
Groth S, Donahue S
JAMA Ophthalmol
. 2023 Oct;
141(11):1089-1090.
PMID: 37856134
No abstract available.
4.
Pruett J, Umfress A, Donahue S
J AAPOS
. 2023 Sep;
27(5):283.e1-283.e4.
PMID: 37716432
Purpose: To analyze the surgical results of patients treated for superior oblique palsy with coexisting exotropia. Methods: The medical records of patients with superior oblique palsy and exotropia who underwent...
5.
Donahue S, Chandler D, Wu R, Marsh J, Law C, Areaux Jr R, et al.
Ophthalmology
. 2023 Sep;
131(1):98-106.
PMID: 37696452
Purpose: To report 8-year outcomes from a randomized controlled trial (RCT) comparing bilateral lateral rectus muscle recession (BLRc) with unilateral recession-resection (R&R) for childhood intermittent exotropia (IXT). Design: Eight-year follow-up...
6.
Freedman S, Del Monte M, Diva U, Donahue S, Drack A, Dutta R, et al.
J AAPOS
. 2023 Jun;
27(4):208-211.
PMID: 37321343
Cerebrotendinous xanthomatosis (CTX) is a rare, autosomal recessive bile acid synthesis disorder caused by pathologic variants in CYP27A1, a gene involved in bile acid synthesis. Impaired function in this gene...
7.
Groth S, Linton E, Brown E, Makadia F, Donahue S
Transl Vis Sci Technol
. 2023 Jan;
12(1):6.
PMID: 36598458
Purpose: The Olleyes VisuALL-K is a pediatric videogame-based static threshold perimeter using a virtual reality headset. We determined normal threshold sensitivities for the 24-2 test locations using the virtual reality...
8.
Vignal-Clermont C, Yu-Wai-Man P, Newman N, Carelli V, Moster M, Biousse V, et al.
Am J Ophthalmol
. 2022 Dec;
249:108-125.
PMID: 36496192
Purpose: To evaluate the safety profile of lenadogene nolparvovec (Lumevoq) in patients with Leber hereditary optic neuropathy. Design: Pooled analysis of safety data from 5 clinical studies. Methods: A total...
9.
Carelli V, Newman N, Yu-Wai-Man P, Biousse V, Moster M, Subramanian P, et al.
Ophthalmol Ther
. 2022 Nov;
12(1):401-429.
PMID: 36449262
Introduction: Lenadogene nolparvovec is a promising novel gene therapy for patients with Leber hereditary optic neuropathy (LHON) carrying the m.11778G>A ND4 mutation (MT-ND4). A previous pooled analysis of phase 3...
10.
Newman N, Yu-Wai-Man P, Subramanian P, Moster M, Wang A, Donahue S, et al.
Brain
. 2022 Nov;
146(4):1328-1341.
PMID: 36350566
Leber hereditary optic neuropathy (LHON) is an important example of mitochondrial blindness with the m.11778G>A mutation in the MT-ND4 gene being the most common disease-causing mtDNA variant worldwide. The REFLECT...