Meallet MA - Search Results

1

Subpalpebral lavage antibiotic treatment for severe infectious scleritis and keratitis.

Meallet MA. Meallet MA. Cornea. 2006 Feb;25(2):159-63. doi: 10.1097/01.ico.0000177837.31249.19. Cornea. 2006. PMID: 16371774

2

No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.

Aldave AJ, Rayner SA, King JA, Salem AK, Prechanond A, Hashida S, Affeldt JC, Meallet MA, Glasgow BJ, Small KW, Yellore VS. Aldave AJ, et al. Among authors: meallet ma. Cornea. 2006 May;25(4):413-5. doi: 10.1097/01.ico.0000225260.41594.4a. Cornea. 2006. PMID: 16670477

3

Thomas A. Swift's Electric Rifle Injuries to the Eye and Ocular Adnexa: The Management of Complex Trauma.

Moysidis SN, Koulisis N, Rodger DC, Chao JR, Leng T, de Carlo T, Burkemper B, Ediriwickrema LS, George MS, Jiang Y, Bohm KJ, Gulati S, Torres RJ, Meallet MA, Moshfeghi AA, Flynn HW Jr, Mieler WF, Williams GA, Humayun MS, Eliott D. Moysidis SN, et al. Among authors: meallet ma. Ophthalmol Retina. 2019 Mar;3(3):258-269. doi: 10.1016/j.oret.2018.10.005. Epub 2018 Oct 10. Ophthalmol Retina. 2019. PMID: 31014704

4

An extreme case of retinal avascularity in a female neonate with incontinentia pigmenti.

Meallet MA, Song J, Stout JT. Meallet MA, et al. Retina. 2004 Aug;24(4):613-5. doi: 10.1097/00006982-200408000-00017. Retina. 2004. PMID: 15300085 No abstract available.

5

Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.

Aldave AJ, Gutmark JG, Yellore VS, Affeldt JA, Meallet MA, Udar N, Rao NA, Small KW, Klintworth GK. Aldave AJ, et al. Among authors: meallet ma. Am J Ophthalmol. 2004 Nov;138(5):772-81. doi: 10.1016/j.ajo.2004.06.021. Am J Ophthalmol. 2004. PMID: 15531312

6

An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His beta iG-H3 mutation in an African-American woman.

Meallet MA, Affeldt JA, McFarland TJ, Appukuttan B, Read R, Stout JT, Rao NA. Meallet MA, et al. Am J Ophthalmol. 2004 Apr;137(4):765-7. doi: 10.1016/j.ajo.2003.09.062. Am J Ophthalmol. 2004. PMID: 15059726

7

Amniotic membrane transplantation with conjunctival limbal autograft for total limbal stem cell deficiency.

Meallet MA, Espana EM, Grueterich M, Ti SE, Goto E, Tseng SC. Meallet MA, et al. Ophthalmology. 2003 Aug;110(8):1585-92. doi: 10.1016/S0161-6420(03)00503-7. Ophthalmology. 2003. PMID: 12917178

8

A 26-year-old man with renal failure and vision loss.

Alasil T, Meallet M. Alasil T, et al. Digit J Ophthalmol. 2008 Jul 12;14:30-34. doi: 10.5693/djo.03.2008.010. eCollection 2008. Digit J Ophthalmol. 2008. PMID: 29440977 Free PMC article. No abstract available.

9

Mutations in PIP5K3 are associated with François-Neetens mouchetée fleck corneal dystrophy.

Li S, Tiab L, Jiao X, Munier FL, Zografos L, Frueh BE, Sergeev Y, Smith J, Rubin B, Meallet MA, Forster RK, Hejtmancik JF, Schorderet DF. Li S, et al. Among authors: meallet ma. Am J Hum Genet. 2005 Jul;77(1):54-63. doi: 10.1086/431346. Epub 2005 May 18. Am J Hum Genet. 2005. PMID: 15902656 Free PMC article.

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