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Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3rd-Nerve Palsy.
Am J Ophthalmol. 2022 Oct;242:165-172. doi: 10.1016/j.ajo.2022.06.010. Epub 2022 Jun 22.
Am J Ophthalmol. 2022.
PMID: 35750218
Free article.
Worldwide outcomes of nasal transposition of the split lateral rectus muscle for strabismus associated with 3rd-nerve palsy.
Shah AS, Dodd MU, Gokyigit B, Lorenz B, Laurent E, Sadiq MAA, Tsai CB, Gravier N, Goberville M, Basiakos S, Zurakowski D, Dagi LR; NTSLR3NP Study Group.
Shah AS, et al.
Br J Ophthalmol. 2023 May;107(5):725-731. doi: 10.1136/bjophthalmol-2021-319667. Epub 2021 Dec 8.
Br J Ophthalmol. 2023.
PMID: 34880051
Free PMC article.
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Aberrant regeneration in an international registry of patients with 3rd-nerve palsy.
Oke I, Lorenz B, Basiakos S, Gokyigit B, Laurent E, Tsai CB, Orge F, Heidary G, Tjeerd de Faber J, Jeddawi L, Sadiq MA, Strominger M, Dodd MU, Shah AS, Dagi LR; NTSLR3NP Study Group.
Oke I, et al. Among authors: jeddawi l.
Eur J Ophthalmol. 2023 Nov;33(6):2154-2161. doi: 10.1177/11206721231161377. Epub 2023 Mar 9.
Eur J Ophthalmol. 2023.
PMID: 37265190
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Accuracy of formulae for secondary intraocular lens power calculations in pediatric aphakia.
Nakhli FR, Emarah K, Jeddawi L.
Nakhli FR, et al. Among authors: jeddawi l.
J Curr Ophthalmol. 2017 Jun 13;29(3):199-203. doi: 10.1016/j.joco.2017.05.007. eCollection 2017 Sep.
J Curr Ophthalmol. 2017.
PMID: 28913511
Free PMC article.
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Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
Mechaussier S, Almoallem B, Zeitz C, Van Schil K, Jeddawi L, Van Dorpe J, Dueñas Rey A, Condroyer C, Pelle O, Polak M, Boddaert N, Bahi-Buisson N, Cavallin M, Bacquet JL, Mouallem-Bézière A, Zambrowski O, Sahel JA, Audo I, Kaplan J, Rozet JM, De Baere E, Perrault I.
Mechaussier S, et al. Among authors: jeddawi l.
Am J Hum Genet. 2020 Jun 4;106(6):859-871. doi: 10.1016/j.ajhg.2020.04.018. Epub 2020 May 28.
Am J Hum Genet. 2020.
PMID: 32470375
Free PMC article.
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Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
Mechaussier S, Almoallem B, Zeitz C, Van Schil K, Jeddawi L, Van Dorpe J, Rey AD, Condroyer C, Pelle O, Polak M, Boddaert N, Bahi-Buisson N, Cavallin M, Bacquet JL, Mouallem-Bézière A, Zambrowski O, Sahel JA, Audo I, Kaplan J, Rozet JM, De Baere E, Perrault I.
Mechaussier S, et al. Among authors: jeddawi l.
Am J Hum Genet. 2020 Sep 3;107(3):580. doi: 10.1016/j.ajhg.2020.08.004.
Am J Hum Genet. 2020.
PMID: 32888510
Free PMC article.
No abstract available.
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Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform.
Del Pozo-Valero M, Almoallem B, Dueñas Rey A, Mahieu Q, Van Heetvelde M, Jeddawi L, Bauwens M, De Baere E.
Del Pozo-Valero M, et al. Among authors: jeddawi l.
Clin Genet. 2024 Mar 11. doi: 10.1111/cge.14517. Online ahead of print.
Clin Genet. 2024.
PMID: 38468396
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Cyclic Esotropia Managed With Botulinum A Toxin Injections: A Report of Four Cases and Literature Review.
Abdelaal AM, Alhemidan A, Alabdulqader RA, Jeddawi LH.
Abdelaal AM, et al. Among authors: jeddawi lh.
Cureus. 2023 Sep 30;15(9):e46266. doi: 10.7759/cureus.46266. eCollection 2023 Sep.
Cureus. 2023.
PMID: 37908945
Free PMC article.
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