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Results: 1-25 | 26-29
Results: 1-25/29
Comparison of clinical characteristics of familial and sporadic acquired accommodative esotropia
Authors: Seeley, MZ Paul, TO Crowe, S Dahms, G Lichterman, S Traboulsi, EI
Citation: Mz. Seeley et al., Comparison of clinical characteristics of familial and sporadic acquired accommodative esotropia, J AAPOS, 5(1), 2001, pp. 18-20
Anterior transposition of the inferior oblique muscle as the initial treatment of a snapped inferior rectus muscle
Authors: Aguirre-Aquino, BI Riemann, CD Lewis, H Traboulsi, EI
Citation: Bi. Aguirre-aquino et al., Anterior transposition of the inferior oblique muscle as the initial treatment of a snapped inferior rectus muscle, J AAPOS, 5(1), 2001, pp. 52-54
Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance
Authors: Haddad, R Uwaydat, S Dakroub, R Traboulsi, EI
Citation: R. Haddad et al., Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance, AM J MED G, 99(3), 2001, pp. 185-189
Dominant radial drusen and Arg345Trp EFEMP1 mutation
Authors: Matsumoto, M Traboulsi, EI
Citation: M. Matsumoto et Ei. Traboulsi, Dominant radial drusen and Arg345Trp EFEMP1 mutation, AM J OPHTH, 131(6), 2001, pp. 810-812
Oral erythromycin treatment for childhood blepharokeratitis
Authors: Meisler, DM Raizman, MB Traboulsi, EI
Citation: Dm. Meisler et al., Oral erythromycin treatment for childhood blepharokeratitis, J AAPOS, 4(6), 2000, pp. 379-380
A patient with de Morsier and Duane syndromes
Authors: Aguirre-Aquino, BI Rogers, DG Traboulsi, EI
Citation: Bi. Aguirre-aquino et al., A patient with de Morsier and Duane syndromes, J AAPOS, 4(4), 2000, pp. 243-245
Screening relatives of patients with familial chronic open angle glaucoma
Authors: Nguyen, RL Raja, SC Traboulsi, EI
Citation: Rl. Nguyen et al., Screening relatives of patients with familial chronic open angle glaucoma, OPHTHALMOL, 107(7), 2000, pp. 1294-1297
A new locus for dominant drusen and macular degeneration maps to chromosome 6q14
Authors: Kniazeva, M Traboulsi, EI Yu, ZY Stefko, ST Gorin, MB Shugart, YY O'Connell, JR Blaschak, CJ Cutting, G Han, M Zhang, K
Citation: M. Kniazeva et al., A new locus for dominant drusen and macular degeneration maps to chromosome 6q14, AM J OPHTH, 130(2), 2000, pp. 197-202
Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration
Authors: Stefko, ST Zhang, K Gorin, MB Traboulsi, EI
Citation: St. Stefko et al., Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration, AM J OPHTH, 130(2), 2000, pp. 203-208
Choroidal rupture associated with forceps delivery
Authors: Estafanous, MFG Seeley, M Traboulsi, EI
Citation: Mfg. Estafanous et al., Choroidal rupture associated with forceps delivery, AM J OPHTH, 129(6), 2000, pp. 819-820
Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles
Authors: Traboulsi, EI Lee, BA Mousawi, A Khamis, AR Engle, EC
Citation: Ei. Traboulsi et al., Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles, AM J OPHTH, 129(5), 2000, pp. 658-662
Posterior scleral choristoma in the organoid nevus syndrome (Linear nevus sebaceus of Jadassohn)
Authors: Traboulsi, EI Zin, A Massicotte, SJ Kosmorsky, G Kotagal, P Ellis, FD
Citation: Ei. Traboulsi et al., Posterior scleral choristoma in the organoid nevus syndrome (Linear nevus sebaceus of Jadassohn), OPHTHALMOL, 106(11), 1999, pp. 2126-2130
Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: A new MCA/MR syndrome?
Authors: Megarbane, A Haddad-Zebouni, S Nabbout, R Khoury, AH Traboulsi, EI
Citation: A. Megarbane et al., Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: A new MCA/MR syndrome?, AM J MED G, 83(2), 1999, pp. 82-87
Ocular malformations, moyamoya disease, and midline cranial defects: A distinct syndrome
Authors: Bakri, SJ Siker, D Masaryk, T Luciano, MG Traboulsi, EI
Citation: Sj. Bakri et al., Ocular malformations, moyamoya disease, and midline cranial defects: A distinct syndrome, AM J OPHTH, 127(3), 1999, pp. 356-357
Corneal opacities in Gaucher disease
Authors: Guemes, A Kosmorsky, GS Moodie, DS Clark, B Meisler, D Traboulsi, EI
Citation: A. Guemes et al., Corneal opacities in Gaucher disease, AM J OPHTH, 126(6), 1998, pp. 833-835
Malformations of the ocular adnexae
Authors: Traboulsi, EI
Citation: Ei. Traboulsi, Malformations of the ocular adnexae, OX MG MED G, (36), 1998, pp. 31-43
Colobomatous microphthalmia, anophthalmia, and associated malformation syndromes
Authors: Traboulsi, EI
Citation: Ei. Traboulsi, Colobomatous microphthalmia, anophthalmia, and associated malformation syndromes, OX MG MED G, (36), 1998, pp. 51-80
Malformations of the anterior segment of the eye
Authors: Traboulsi, EI
Citation: Ei. Traboulsi, Malformations of the anterior segment of the eye, OX MG MED G, (36), 1998, pp. 81-98
Aniridia
Authors: Traboulsi, EI Zhu, ZP Maumenee, IH
Citation: Ei. Traboulsi et al., Aniridia, OX MG MED G, (36), 1998, pp. 99-114
Congenital anomalies of the optic nerve head
Authors: Aroichane, M Traboulsi, EI
Citation: M. Aroichane et Ei. Traboulsi, Congenital anomalies of the optic nerve head, OX MG MED G, (36), 1998, pp. 115-141
Congenital abnormalities of the retinal pigment epithelium
Authors: Santos, A Humayun, M Traboulsi, EI
Citation: A. Santos et al., Congenital abnormalities of the retinal pigment epithelium, OX MG MED G, (36), 1998, pp. 143-162
Cone dystrophies
Authors: Traboulsi, EI
Citation: Ei. Traboulsi, Cone dystrophies, OX MG MED G, (36), 1998, pp. 357-365
Leber's congenital amaurosis, Stargardt disease, and pattern dystrophies
Authors: Koenekoop, RK Traboulsi, EI
Citation: Rk. Koenekoop et Ei. Traboulsi, Leber's congenital amaurosis, Stargardt disease, and pattern dystrophies, OX MG MED G, (36), 1998, pp. 373-387
Subluxation of the crystalline lens and associated systemic disease
Authors: Traboulsi, EI Maumenee, IH
Citation: Ei. Traboulsi et Ih. Maumenee, Subluxation of the crystalline lens and associated systemic disease, OX MG MED G, (36), 1998, pp. 605-627
Pigmentary retinopathy and systemic disease
Authors: Traboulsi, EI Drack, AV Salama, H
Citation: Ei. Traboulsi et al., Pigmentary retinopathy and systemic disease, OX MG MED G, (36), 1998, pp. 629-662
Risultati: 1-25 | 26-29