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1. Saab G, Traboulsi EI: Splenomegaly and iron deficiency
anemia. M E J Anesth 1983; 7: 217-219
2. Traboulsi EI, Dudin GE, To'mey KF, Bashow AO, Solh HMB:
The association of a fragile site on chromosome 10 with the
Sturge-Weber syndrome and congenital glaucoma. Ophthalm Paed
Genet 1983; 3: 135-140, 1983.
3. Mansour AM, Traboulsi EI, To'mey KF: The use of cautery
for trimming exposed nylon sutures. Amer J Ophthalmol 1983;
96: 691.
4. Nasr A, To'mey KF, Ataya KF, Jabbour NM, Traboulsi EI:
Ocular hemodynamics in pre-ecclampsia. J Ocul Therapy
5. Frangieh GT, Traboulsi EI, Faris BM: Occipital cortical
infarction complicating respiratory failure. J Clin Neuro-Ophthalmol
1984; 4: 155-158.6. Traboulsi EI, Nasr AM, Fahd SD, Jabbour
NM, Der Kaloustian VM: Waardenburg's recessive anophthalmia
syndrome. Ophthal Ped Genet 1984; 4: 13-18.
7. Traboulsi EI, Mansour AM, Kaba FW: Congenital ptosis and
cleft lip. Orbit 1984; 3: 149-152.
8. Mansour AM, Traboulsi EI, Frangieh GT, Shehadeh SI: Bilateral
capillary hemangioma of the eyelids. Orbit 1984; 3: 133-134.
9. Mansour AM, Traboulsi EI, Khawam E, Dudin GE, Der Kaloustian
VM: Eye findings in interstitial deletion of band q12 of chromosome
5. Ophthalm Paed Genet 1984; 4: 117-119.
10. Dudin G, Nasr A, Traboulsi EI, Khouri F, Der Kaloustian
VM: Hereditary retinoblastoma and 13q- mosaicism. Cytogenet
Cell Genet 1984; 38: 235-237.
11. Mansour AM, Aswad MI, Traboulsi EI: Spraying topical
ophthalmic preparations. Amer J Ophthalmol 1984; 97: 245.
12. Traboulsi EI, Shammas IV, Massad M, Frangieh GT, Slim
MS: Ophthalmological aspects of metastatic neuroblastoma.
Report of 22 consecutive cases. Orbit 1984; 3: 247-254.
13. Traboulsi EI, Azar DT, Frangieh GT, Salamoun SG, Shehadeh
SI: Benign infantile hemangioendothelioma of the lacrimal
gland. Orbit 1984; 3: 267-273.
14. Traboulsi EI, Shammas IV, Ratl HE, Jarudi NI: Pseudomonas
aeruginosa ophthalmia neonatorum. Amer J Ophthalmol 1984;
98: 801-802.
15. Traboulsi EI, Jalkh AE: RPE tear as a cause of vitreous
hemorrhage. Ann Ophthalmol 1985; 17: 228-230.
16. Frangieh GT, El-Baba F, Traboulsi EI, Green WR: Melanocytoma
of the cilliary body: resentation of four cases and review
of nineteen reports. Surv Ophthalmol 1985; 29: 328-334.
17. Traboulsi EI, Azar DT, Achram M, Faris BM: Brainstem
tuberculoma and isolated third nerve palsy. Neuro-Ophtalmol
1985; 5: 43-45.
18. Traboulsi EI, Mansour AM, Aswad MI, Gharzuddin W, Frayha
RA: Homonymous hemianopia and systemic lupus erythematosus.
J Clin Neuro-Ophthalmol 1985; 5: 63-66.
19. Maumenee IH, Traboulsi EI: The ocular findings in Kniest
dysplasia. Amer J Ophthalmol 1985; 100: 155-160.
20. Traboulsi EI, Azar DT, Jarudi N, Der Kaloustian VM: Ocular
findings in the candidiasis-endocrinopathy syndrome. Am J
Ophthalmol 1985; 99: 486-487.
21. Mansour AM, Traboulsi EI, Frangieh GT: Multiple recurrences
of juvenile xanthogranuloma of the eyelid. J Pediatr Ophthalmol
Strabism 1985; 22: 156-157.
22. Traboulsi EI, El-Baba FZ, Barakat A, Faris BM: The retinopathy
of primary hyperoxaluria. Retina 1985; 5: 151-153.
23. Mansour AM, Traboulsi EI, Jalkh AE: Failure of subretinal
fluid drainage during scleral buckling procedure in high myopia.
Ann Ophthalmol 1985; 17: 636-637.
24. Azar DT, Marouf LM, Achram M, Traboulsi EI, Faris BM:
Computed tomography in posterior orbital foreign bodies. Orbit
1985; 4: 201-205.
25. Traboulsi EI, Jurdi-Nuwayhid F, Frangieh GT, Der Kaloustian
VM: Retinoblastoma in Lebanon. Ophthalm Paed Genet 1986; 7:
29-34.
26. Traboulsi EI, Faris BM, Der Kaloustian VM: Persistent
hyperplastic primary vitreous and recessive oculo-dento-osseous
dysplasia. Amer J Med Genet 1986; 24: 95-100.
27. Itani K, Traboulsi EI, Abdul-Karim FW, Marouf L, Frangieh
GT, Salamoun SG: Conservative surgery in orbital teratoma.
Orbit 1986; 5: 61-65.
28. Traboulsi EI, Maumenee IH: Extraocular muscle aplasia
in Moebius syndrome. J Pediatr Ophthalmol Strabism 1986; 23:
120-122.
29. Traboulsi EI: Genetic eye diseases in Lebanon. Leb Med
J 1986; 36: 89-91.
30. Traboulsi EI, Jurdi-Nuwayhid F, Torbey N, Frangieh GT:
Aniridia, atypical iris defects, optic pit and the morning
glory disc anomaly in a family. Ophthalm Paed Genet 1986;
7: 131-135.
31. Traboulsi EI, Maumenee IH: Periocular pigmentation in
the Peutz-Jeghers syndrome. Amer J Ophthalmol 1986; 102: 126-127.
32. Traboulsi EI, Maumenee IH: Hereditary pigmented paravenous
chorioretinal atrophy. Arch Ophthalmol 1986; 104: 1636-1640.
33. Traboulsi EI, Maumenee IH: Ocular findings in mucolipidosis
III. Amer J Ophthalmol 1986; 102: 592-597.
34. Traboulsi EI, Maumenee IH: Bilateral melanosis of the
iris. Amer J Ophthalmol 1987; 103: 115-116.
35. Traboulsi EI, Maumenee IH: Ophthalmologic manifestations
of X-linked childhood adrenoleukodystrophy. Ophthalmology
1987; 94: 47-52.
36. Traboulsi EI, Jalkh AE, Frangieh GT, Tomb J: Vitreous
histocytology of primary choroidal malignant melanoma. Ann
Ophthalmol 1987; 19: 45-47.
37. Traboulsi EI, Krush AJ, Gardner EJ, Booker SV, Offerhaus
GJA, Yardley JH, Hamilton SR, Luk GD, Giardiello FM, Welsh
SB, Hughes JP, and Maumenee IH: Prevalence and importance
of pigmented ocular fundus lesions in Gardner's syndrome.
N Engl J Med 1987; 316: 661-667.
38. Traboulsi EI, Faris BM: Crystalline retinopathy. Ann
Ophthalmol 1987; 19: 156-158.
39. Traboulsi EI, Aswad MI, Jalkh AE, Malouf J: Ocular findings
in the mitral valve prolapse syndrome. Ann Opthalmol 1987;
19: 354-359.
40. Traboulsi EI, Green WR, de la Cruz ZC, Luckenbach MW,
Moser HW: The neuronal ceroid lipofuscinoses. Ocular histopathologic
studies in the late infantile, juvenile and adult forms. Graefe's
Arch Clin Exp Ophthalmol 1987; 225: 391-402.
41. Traboulsi EI, Azar DT, Khattar J, Salamoun SG: "A','-scan
ultrasonography in the diagnosis of orbital dermoid cysts.
Ann Ophthalmol 1988; 20: 229-232.
42. Krush AJ, Traboulsi EI, Offerhaus GJA, Maumenee IH, Yardley
JH, Levin LS: Hepatoblastoma, pigmented ocular fundus lesions
and jaw lesions in Gardner syndrome. Amer J Med Genet 1988;
29: 323-332.
43. Traboulsi EI, O'Neill JF: The spectrum in the morphology
of the so-called "Morning Glory',' anomaly of the optic
disc. J Pediatr Ophthalmol Strabism 1988; 25: 93-98.
44. Traboulsi EI, Pilkerton AR: Rhegmatogenous retinal detachment
with a pit of the optic nerve. Ophthalm Surg 1988; 19: 257-258.
45. Traboulsi EI, Lenz W, Gonzales-Ramos M, Siegel J, Macrae
WG, Maumenee IH: The Lenz microphthalmia syndrome. Amer J
Ophthalmol 1988; 105: 40-45.
46. Traboulsi EI, Zimmerman LE, Manz H: Cutaneous malignant
melanoma in survivors of heritable retinoblastoma. Arch Ophthalmol
1988; 106: 1059-1061.
47. Traboulsi EI, Maumenee IH, Green WR, Freimer ML, Moser
H: Olivopontocerebellar atrophy with retinal degeneration.
A clinical and ocular histopathologic study. Arch Ophthalmol
1988; 106: 801-806.
48. Traboulsi EI, Levine E, Mets MB, Parelhoff ES, O'Neill
JF, Gaasterland DE: Infantile glaucoma in Down syndrome (trisomy
21). Amer J Ophthalmol 1988; 105: 389-394.
49. Traboulsi EI, Maumenee IH, Krush AJ, Giardiello FM, Levin
LS, Hamilton SR: Pigmented ocular fundus lesions in the inherited
gastrointestinal polyposis syndromes and in hereditary nonpolyposis
colorectal cancer. Ophthalmol 1988; 95: 964-969.
50. Traboulsi EI, O'Neill JF, Maumenee IH: Pericentral pigmentary
retinopathy. A distinct autosomal recessive disease. Amer
J Ophthalmol 1988; 106: 551-556.
51. Chrousos GA, O'Neill JF, Traboulsi EI, Richmond A, Rosenbaum
KN: Ocular findings in partial trisomy 3q. Ophthalm Paediatr
Genet 1988; 9: 127-130.
52. Traboulsi EI, Parver LM: Steering-wheel injuries. Orbit
1988; 4:267-268.
53. Escallon F, Traboulsi EI, Infante R: A family with the
Bardet-Biedl syndrome and diabetes mellitus. Arch Ophthalmol
1989; 107: 855-857.
54. Traboulsi EI, Weinberg RJ: Familial congenital cornea
guttata with anterior polar cataracts. Amer J Ophthalmol 1989;
108: 123-125.
55. Traboulsi EI, Lustbader J, Lemp MA: Keratoconus in Alagille
syndrome. Amer J Ophthalmol 1989; 108: 332-333.
56. Traboulsi EI, Parks MM: Glaucoma in oculo-dento-osseous
dysplasia. Amer J Ophthalmol 1990; 109(3): 310-3.
57. Traboulsi EI, Maumenee IH, Krush AJ, Alcorn D, Giardiello
FM, Burt RW, Hughes JP, Hamilton SR: Congenital hypertrophy
of the retinal pigment epithelium predicts polyposis in familial
adenomatous polyposis with extraintestinal manifestations
(Gardner's syndrome). Arch Ophthalmol 1990; 108: 525-526.
58. Kozma C, Hunt M, Meck J, Traboulsi EI, Scribanu N: Familial
Wolf-Hirshhorn syndrome associated with Rieger anomaly of
the eye. Ophthalm Ped Genet 1990; 11: 23-30.
59. Rubinfeld R, Traboulsi EI, Arentsen R, Eagle R: Recurrence
of keratoconus after penetrating keratoplasty. Ophthalm Surg
1990; 21: 420-422.
60. Traboulsi EI, Murphy SF, Maumenee IH, DeLaCruz ZC, Green
WR: A clinico-pathologic study of the eyes in familial adenomatous
polyposis with extracolonic manifestations (Gardner's syndrome).
Amer J Ophthalmol 1990; 110: 550-561.
61. Holzman AE, Chrousos GA, Kozma C, Traboulsi EI: Duane's
retraction and the fetal alcohol syndrome. Amer J Ophthalmol
1990; 110: 565-566.
62. Collins ML, Traboulsi EI, Maumenee IH: Optic nerve head
swelling and optic atrophy in the mucopolysaccharidoses. Ophthalmol
1990; 97: 1445-1449.
63. Traboulsi EI, Jaafar MS, Wilson EM, Parks MM: Hypoplasia
of the iris: the aniridia spectrum. Two case reports and review
of the literature. J Int Pediatr 1990; 5: 275-278.
64. Hashemi K, Traboulsi EI, Chrousos GA, Scribanu N, Chavis
R: Chorioretinal lacuna in the amniotic band syndrome. J Pediatr
Ophthalmol Strabism 1990; 28: 238-239.
65. Pasquale LR, Smith SG, Traboulsi EI, Jampel H: Spontaneous
filtering blebs in a patient with microspherophakia. Amer
J Ophthalmol 1991; 112: 350-352.
66. Giardiello F, Offerhaus J, Traboulsi EI, et al: The value
of combined phenotypic markers in dentifying inheritance of
familial adenomatous polyposis. GUT 1991; 32: 1170-1174.
67. Heher K, Traboulsi EI, Maumenee IH: The natural history
of Leber's congenital amaurosis. Age-related findings in 35
patients. Ophthalmol 1992; 99: 241-245.
68. Traboulsi EI, Maumenee IH, Geraghty MT, Valle DL, Silva
JC, Green WR: Ocular histopathology in the cobalamin C type
of vitamin B12 defect with methhylmalonic aciduria andhomocystinuria.
Amer J Ophthalmol. 1992; 113: 269-280.
69. Kasner L, Traboulsi EI, DeLaCruz Z, Green WR: A histopathological
study of the pigmented fundus lesions in familial adenomatous
polyposis. Retina 1992; 12: 35-42.
70. Drack AV, Traboulsi EI, Maumenee IH: Progression of fundus
findings in olivopontocerebellar atrophy with retinal degeneration.
Arch Ophthalmol 1992; 110: 712-713.
71. Saal HM, Traboulsi EI, Gavaris P, Samango-Sprouse CA,
Parks M: Dominant syndrome with isolated cryptophthalmos and
ocular anomalies. Amer J Med Genet 1992; 43: 785-788.
72. Bleik J, Traboulsi EI, Maumenee IH: Familial posterior
lenticonus. Arch Ophthalmol 1992; 110: 1208.
73. Traboulsi EI, Maumenee IH: Peters' anomaly and associated
congenital malformations. Arch Ophthalmol 1992; 110: 1739-1742.
74. Traboulsi EI, DeBecker I, Maumenee IH: Ocular findings
in Cockayne syndrome. Am J Ophthalmol 1992; 114: 579-583.
75. Izquierdo NJ, Traboulsi EI, Enger C, Maumenee IH: Glaucoma
in the Marfan syndrome. Tr Am Ophthalmol Soc 1992; 90: 111-122.
76. Traboulsi EI: Editorial. Developmental genes and ocular
malformation syndromes. Am J Ophthalmol 1993; 115: 105-107.
77. Traboulsi EI, Payne J: Autosomal dominant vitreoretinochoroidopathy
and presenile cataracts. Report of the third family. Arch
Ophthalmol 1993; 111: 194-196.
78. Aiello LP, Traboulsi EI: Pigmented fundus lesions in
a pre-term infant with familial adenomatous polyposis. Arch
Ophthalmol 1993; 111: 302-303.
79. Eliott D, Traboulsi EI, Maumenee IH: Visual prognosis
in Kjer type autosomal dominant optic atrophy. Am J Ophthalmol.
1993; 115: 360-367.
80. Traboulsi EI, Jaafar MS, Kattan H, Parks MM: Congenital
fibrosis of the extraocular muscles: Report of 24 cases illustrating
the clinical spectrum and surgical management. Am Orthop J
1993; 43: 45-53.
81. Dunya I, Hoon A, Traboulsi EI: Retinal dystrophy in the
cardio-facio-cutaneous syndrome. J Pediatr Ophthalmol Strabism
1993; 30: 264-265.
82. Izquierdo N, Traboulsi EI, Maumenee IH: Ocular findings
in 18q- syndrome. Ophthalm Paediatr Genet 1993; 14: 91-94.
83. Traboulsi EI: Editorial. Ophthalm Paediatr Genet 1993;
14:57-59.
84. Nathans J, Maumenee IH,..., Traboulsi EI, et al: Genetic
heterogeneity among blue cone monochromats. Am J Hum Genet
1993; 53: 987-1000.
85. Traboulsi EI, Lim JI, Pyeritz R, Goldberg HK, Haller
JA: A new syndrome of myelinated nerve fibers, vitreoretinopathy
and skeletal malformations. Arch Ophthalmol 1993; 111: 1543-1545.
86. Al Hazzaa SAF, Traboulsi EI, Maumenee IH: Ocular findings
in adults with mucopolysaccharidosis II-B (Hunter syndrome
- mild). Mid East J Ophthalmol 1993; 1: 15-17.
87. Hamush N, Traboulsi EI: Visual loss in the Miller-Dieker
syndrome. Mid East J Ophthalmol 1993; 1: 48-50.
88. Izquierdo N, Traboulsi EI, Enger C, Maumenee IH: Strabismus
in the Marfan syndrome. Am J Ophthalmol 1994; 117: 632-635.
89. Gollamudi SR, Traboulsi EI, Chamon W, Stark WJ, Maumenee
IH: Visual outcome after surgery for Peters' anomaly. Ophthalm
Genet 1994; 15: 31-35.
90. Traboulsi EI: Intraocular lenses in children. Editorial.
Mid E J Ophthalmol 1994: 2(3); 152.
91. Traboulsi EI, Maumenee IH: Photoaversion in Leber's congenital
amaurosis. Ophthalm Genet 1995; 16: 27-30.
92. Traboulsi EI: The Genetics of Glaucoma. Mid E J Ophthalmol
1995: 3: 72-73.
93. Koenekoop RK, Rosenbaum KN, Traboulsi, EI: Ocular findings
in a family with Sotos syndrome (cerebral gigantism). Am J
Ophthalmol 1995; 119(5): 657-658.
94. Shawaf S, Noureddin B, Khouri A, Traboulsi EI: A family
with a syndrome of ectopia lentis, spontaneous filtering blebs,
and craniofacial dysmorphism. Ophthalm Genet 1995; 16(4):
163-169.
95. Traboulsi EI: Practice guidelines for the patient with
suspected ocular nonretinal genetic disorder. Semin Ophthalmol
1995; 10(4): 318-322.
96. Wheatley HM, Traboulsi EI, Flowers BE, Maumenee IH, Whittum-Hudson
J. Immunohistochemical localization of fibrillin in human
ocular tissues. Arch Ophthalmol 1995; 113:103-109.
97. Traboulsi EI, Lorenz B. A tribute to Mette Warburg. Editorial.
Ophthalm Genet 1996; 17: 123-125.
98. Traboulsi EI, Apostolides J, Giardiello F, Krush A, Hamilton
S, Maumenee IH: APC mutations and pigmented ocular fundus
lesions in familial adenomatous polyposis. Ophthalm Genet
1996; 17: 167-174.
99. Robitaille J, Traboulsi EI. Coats' disease and central
nervous system malformation. Ophth Genet 1996; 17: 215-218.
100. Traboulsi, EI. Scientific communications and the peer
review process. M E J Ophthalmol 4: 3-4, 1996.
101. Giardiello FM, Petersen M, Piantadosi S, Gruber SB,
Traboulsi EI, Offerhaus GJ, Muro K, Krush AJ, Booker SV, Luce
MC, Laken SJ, Kinzler KW, Vogelstein B, Hamilton SR. APC gene
mutations and extrainstestinal phenotype of familial adenomatous
polyposis. Gut 1997; 40: 521-525.
102. Stefko T, Campochiario P, Zhu DP, Pei W, Li Y, Traboulsi
EI. Autosomal dominant inheritance of optic pits Am J Ophthalmol
1997; 124: 112-113.
103. Mir S, Wheatley HM, Maumenee Hussels IE, Whittum-Hudson
J, Traboulsi EI. A comparative study of the fibrillin microfibrillar
system in the lens capsule of normal and Marfan syndrome patients.
Invest Ophthalmol Vis Sci 1998; 39: 84-93
104. Samaha, A, Traboulsi EI, Green WR, Ma'luf R. Tick infestation
of the eyelid. Am J Ophthalmol 1998; 125: 263-264.
105. Trifan OC, Traboulsi EI, Stoilova D, Alozie I, Nguyen
RL, Raja S, Sarfarazi M. A third locus (GLC1D) for adult onset
glaucoma maps to the 8q23 region. 1998; 126: 17-28.
106. Fard A, Green WR, Traboulsi EI. Histologic study study
of a torn inferior oblique muscle. JAAPOS 1998; 2: 124-126.
107. Guemes A, Kosmorsky GS, Moodie DS, Meisler D, Clark
B, Traboulsi EI. Corneal Opacities in Gaucher Disease. Am
J Ophthalmol 1998; 126: 833-835
108. Traboulsi EI. Ocular malformations and developmental
genes. J AAPOS 2: 317-323, 1998
109. Fard A, Traboulsi, EI. Coloboma of the lens, optic nerve
hypoplasia, and orbital hemangioma - A possible developmental
field defect. Ophthalmic Genetics 1998; 19: 209-212.
110. Bakri S, Siker D, Masaryk T, Luciano MG, Traboulsi EI.
Moyamoya disease, ocular malformations and midline cranial
defects - A distinct syndrome. Am J Ophthalmol 1999; 127:
356-357.
111. Megarbane A, Haddad-Zebouni S, Nabbout R, Khoury A,
Traboulsi EI. Microcephaly, colobomatous microphthalmia, short
stature and severe psychomotor retardation in two male cousins:
A new MCA/MR syndrome? Am J Med Genet 1999; 83: 82-87.
112. Griebel SR, Burnstine R, Traboulsi EI. Juvenile xanthogranuloma
of the iris: Case report and review of the literature. Mid
E J Ophthalmol 1999; 7: 95-97.
113. Traboulsi EI, Zin A, Massicotte SJ, Kosmorsky G, Kotagal
P, Ellis D. Posterior scleral choristoma in the organoid nevus
syndrome (linear nevus sebaceous of Jadassohn) Ophthalmology
1999; 106: 2126-2130.
114. Ruttum M, Connor TB Jr, Traboulsi EI A 14-year old boy
with presumed autosomal dominant macular dystrophy causing
moderate visual impairment with no discernible progression
over several years. J Pediatr Ophthalmol Strabism 36:287-91,
1999
115. Krishnan K, Roy A, Traboulsi EI. Morning glory disc
anomaly and moyamoya disease. Ophthalm Genet 21: 21-24, March
2000.
116. Traboulsi EI, Whittum-Hudson J, Mir S, Maumenee IH.
Microfibril Abnormalities of the Lens Capsule in Patients
with Marfan Syndrome and Ectopia Lentis. Ophthalm Genet 21:
9-15, 2000.
117. Percin EF, Ploder L, Yu JJ, Arici K, Horsford J, Bapat
B, Rutherford A, Cox D, Duncan AMV, Kalnins VI, Kocak-Altintas
A, Akarsu AN, Sowden JC, Traboulsi EI, Sarfarazi M, McInnes
RR. Human microphthalmia associated with mutations in the
retinal homeobox gene CHX10. Nat Genet 25: 397-401, 2000
118. Traboulsi EI, Lee BA, Mousawi A, Khamis AR, Engle EC.
Evidence of genetic heterogeneity in autosomal recessive congenital
fibrosis of the extraocular muscles. Am J Ophthalmol 129:
658-662, 2000.
119. Nguyen RL, Raja SC, Traboulsi EI. Screening relatives
of patients with familial chronic open angle glaucoma. Ophthalmology107:
1294-1297, 2000
120. Aguirre-Aquino B, Traboulsi EI. A patient with DeMorsier
and Duane syndromes. J AAPOS 4: 243-245, 2000.
121. Krishnan C, Roy A, Traboulsi EI. Optic nerve malformation
and Moyamoya syndrome. Ophthalm Genet 21: 21-24, 2000.
122. Estafanous M, Seeley M, Traboulsi EI. Choroidal rupture
with forceps delivery. Am J Ophthalmol 129: 819-820, 2000.
123. Kniazeva M, Traboulsi EI, Stefko ST, Gorin MB, Blaschak
CJ, Cutting G, Han M, Zhang K. A New Locus for Dominant Drusen
with Macular Degeneration Maps to Chromosome 6q14. Am J Ophthalmol
130: 197-202, 2000.
124. Stefko ST, Gorin M, Zhang K, Traboulsi EI. Clinical
spectrum of Chromosome 6 - linked Autosomal Dominant Drusen
and Macular Degeneration. Am J Ophthalmol 130: 203-208, 2000.
125. Haddad R, Uwaydat S, Dakroub R, Traboulsi EI. Confirmation
of the Autosomal Recessive Syndrome of Ectopia Lentis and
Distinctive Craniofacial Appearance. Am J Med Genet 99: 185-189,
2001.126. Meisler DM, Raizman MB, Traboulsi EI. Oral erythromycin
treatment for childhood blepharokeratitis. JAAPOS 4(6) December
2000: 379-380.
127. Dhamaraj S, Silva E, Pina AL, Li Y, Yang J-M, Carter
RC, Loyer M, El-Hilali H, Traboulsi EI, Sundin O, Zhu D, Maumenee
IH, Koenekoop R. Mutational analysis and clinical correlation
in Leber congenital amaurosis. Ophthalmic Genetics 21(3):
135-150, September 2000.
128. Aguirre-Aquino B, Riemann C, Lewis H, Traboulsi EI.
Transposition of the inferior oblique muscle for the treatment
of a torn inferior rectus muscle. J AAPOS 5:52-54, 2001.
129. Matsumoto M, Traboulsi EI. Dominant radial drusen and
EFEMP-1 mutation. Am J Ophthalmol 131: 810-812, 2001.
130. Seeley MZ, Paul O, Crowe S, Dahms G, Lichterman S, Traboulsi
EI. Comparison of Clinical Characteristics of Familial and
Sporadic Acquired Accommodative Esotropia. J AAPOS 5:18-20,
2001
131. Traboulsi EI. The genetics of strabismus - The John
Pratt-Johnson Lectureship. (In Press, Am Orthoptic J)
132. Plotkin ES, Traboulsi EI. From the Middle East to The
Midwest. Eyenet August 2001; Vol 5 No. 8: 49-50
133. Gupta PC, Peralta D, parker M, Crowe C, Clark B, Traboulsi
EI. A patient with bilateral microphthalmos with cyst, facial
clefts and limb anomalies: A new syndrome with features of
Waardenburg syndrome, cerebro-oculo-nasal syndrome, and craniotelencephalic
dysplasia. (Submitted, Am J Med Genet)
134. Garcia ML, Huang D, Crowe S, Traboulsi EI. Relationship
between the axis and degree of high astigmatism and obliquity
of palpebral fissure. (Submitted, Arch Ophthalmol)
135. Zervos A, Hunt KE, Tong H-Q, Avallone J, Morales J,
Friedman N, Cohen BH, Clark B, Guo S, Gazda H, Beggs AH, Traboulsi
EI. Clinical, Genetic and Histopathologic Findings in Two
Siblings with Muscle-Eye-Brain Disease. (Submitted, Ophthalmology)
136. Kim JI, Dell'Osso LF, Traboulsi EI. Latent/manifest
latent and "uniocular" acquired pendular nystagmus.
(Submitted, Neuro-Ophthalmology)
137. Yang Z, Lin W, Moshfeghi DM, Thirumalaichary S, Zhang
H, Kaiser P, Traboulsi EI, Zhang K. A Novel Mutation in the
Peripherin/RDS Gene Causes Adult-Onset Foveomacular Dystrophy.
(Submitted J Med Genet)
138. Wang Q, Chen Q, Zhao K, Wang L, Wang L, Traboulsi EI.
Update on the molecular genetics of retinitis pigmentosa.
Ophthalmic Genetics 2001; Vol 22 No. 3: 133-154.
Correspondence, Book Chapters, CD-ROM
Presentations
1. Traboulsi EI: Waardenburg's recessive anophthalmia. (Letter)
Ophthalm Ped Genet 1984; 4: 203.
2. Traboulsi EI: Kjellin's syndrome. (Correspondence) Amer
J Ophthalmol 1985; 99: 737-738.
3. Maumenee IH, Traboulsi EI: The ocular findings in Kniest
dysplasia. (Correspondence). AmerJ Ophthalmol 1985; 100: 861.
4. Maumenee IH, Traboulsi EI: Hereditary retinal dystrophy.
Olivopontocerebellar atrophy with retinal degeneration. Clin
Decisions in Ophthalmol 1986; 10 (3): 1-9.
5. Traboulsi EI: Neovascular glaucoma and Ischemia in Wyburn-Mason
syndrome. (Letter) J Clin Neuro-Ophthalmol 1986; 6: 126-127.
6. Traboulsi EI: Corneal changes in familial iris coloboma.
(Correspondence) Ophthalmol 1986; 93: 1369.
7. Traboulsi EI, Levine E, Mets MB, Parelhoff ES, O'Neill
JF, Gaasterland DE: Infantile glaucoma in Down's syndrome
(trisomy 21). Reply to Tord Jerndal, M.D. (Correspondence)
Amer J Ophthalmol 1988; 106: 638-639.
8. Traboulsi EI: CHRPE in Non-Gardner's familial polyposis
patients. (Correspondence) Ophthalmol 1989; 96: 399-400.
9. Traboulsi EI, O'Neill JF, Maumenee IH: Autosomal recessive
pericentral pigmentary retinopathy (Correspondence). Amer
J Ophthalmol 1989; 107: 438-439.
10. Traboulsi EI: Familial adenomatous polyposis. (Correspondence)
Dis Col Rectum 1989; 32: 633-634.
11. Traboulsi EI: Report on "Symposium on Coping with
Advances in Ophthalmology in a Cost-Containment Environment',',
Washington, D.C. November 3, 1988. Published by The Institute
of Health Policy Analysis, Georgetown University Medical Center,
1989.
12. Traboulsi EI, Weinberg RG: Familial congenital cornea
guttata with anterior polar cataracts. (Correspondence) Amer
J Ophthalmol 1990; 109: 245.
13. Traboulsi EI: Genetic and metabolic diseases and congenital
defects. Current Opinion in Ophthalmol 1990; 1: 149-157.
14. Traboulsi EI: X-linked microphthalmia syndrome. Amer
J Med Genet (Letter to the Editor) 1990; 37: 291.
15. Traboulsi EI, Maumenee IH: Eye Problems. In Textbook
of Pediatrics, Oski F (ed), WB Lippincott Co, 1990, pp. 805-825.
16. Traboulsi EI, Maumenee IH: Ophthalmologic abnormalities
in patients with familial adenomatous polyposis. In Familial
Adenomatous Polyposis. Herrera L (ed), Alan R. Liss, Inc.,
New York, 1990, pp. 125-131.
17. Traboulsi EI, Chrousos GA: Ocular findings in Turner
syndrome. In The Eye in Systemic Disease. Gold DH, Weingeist
TA (eds), WB Lippincott Co., 1990, pp. 26-27.
18. Frangieh GT, Traboulsi EI, Kenyon KR: The eye in the
mucopolysaccharidoses. In The Eye in Systemic Disease. Gold
DH, Weingeist TA (eds), WB Lippincott Co., 1990, pp. 372-376.
19. Traboulsi EI: Section Editor, Ophthalmology. In the Birth
Defects Encyclopedia. Buyse ML (ed), Blackwell Scientific
Publ, 1990. Wrote chapters on: The morning glory disc anomaly,
Congenital orbital, teratoma, Blepharophimosis syndrome, Familial
exudative vitreoretinopathy, Congenital hypertrophy of the
retinal pigment epithelium, Retinal dysplasia, Coats' disease,
The neuronal ceroid lipofuscinoses, Choroideremia, Kjer optic
atrophy, Goldman-Favre disease, Forsius-Eriksson syndrome
20. Drack AV, Traboulsi EI: Systemic associations of pigmentary
retinopathy. Int Ophthalm Clin 35-59, 1991.
21. Connor T, Traboulsi EI: Retinopathies and nyctalopia.
In Clinical Decisions in Pediatric Ophthalmology, Cibis G,
Cibis-Tongue A, Stass-Isern ML (Eds), Mosby-year Book, Inc.
Publ, 1993, pp. 216-219.
22. Traboulsi EI: Congenital Malformations of the Eye and
Ocular Adnexae. In: Human Malformations. Oxford University
Press, Oxford Monographs on Medical Genetics, #27, vol 2,
1993, pp. 163-192.
23. Traboulsi EI: Antenatal diagnosis of ophthalmic disease.
In The Eye in Infancy. Isenberg S, Ed., C.V. Mosby Co., 2nd
Ed, 1994, pp. 29-35.
24. Traboulsi EI, Maumenee IH. Eye Problems. In Principles
and Practice of Pediatrics, 2nd edition, Oski F, ed, JB Lippincott,
1993, pp. 878-898.
25. Traboulsi EI: Bread-crumb retinopathy. (Letter to the
Editor) Retina 1993; 13(3):269.
26. Traboulsi EI: Morning glory disc anomaly or optic disc
coloboma. (Letter to the Editor) Arch Ophthalmol 1994; 112:
153.
27. Traboulsi EI: Mucopolysaccharidosis II. In Current Ocular
Therapy, 4th Ed, Fraunfelder FT, Roy FH, Eds, WB Saunders
Publ, 1995, pp 171-172.
28. Traboulsi EI: Mucopolysaccharidosis III. In Current Ocular
Therapy, 4th Ed, Fraunfelder FT, Roy FH, Eds, WB Saunders
Publ, 1995, pp 172-173.
29. Traboulsi EI: Ectopia lentis and associated systemic
disease. In Wiggs J, Ed, Molecular Genetics of Ocular Disease,
Wiley-Liss, Inc., New York, 1995, pp. 219-233.
30. Traboulsi EI, Murphree AL: Connective Tissue, Skin and
Bone Disorders. In Wright KR, Ed, Pediatric Ophthalmology
and Strabismus, CV Mosby, St. Louis, 1995, pp. 649-672 .
31. Traboulsi EI, Green WR, O'Donnell F: The Eye in Albinism.
In Duane's Clinical Ophthalmology, Lippincott - Raven, 1995,
Vol. 4, Chap 38, pp. 1-20.
32. Traboulsi EI, Kattan H: Skeletal and Connective Tissue
Disorders with Corneal Manifestations. In Cornea, Krachmer
JH, Mannis MJ, Holland EJ (Eds), CV Mosby, St. Louis, 1997,
pp. 925-942.
33. Traboulsi EI. Dominant inheritance of optic pits. (Correspondence)
Am J Ophthalmol 1998; 125: 124-125.
34. Santos A, Traboulsi EI: Congenital pigmentary disorders
of the RPE. In RPE - Current Aspects of Function and Disease,
Marmor MF, Wolfensberger TJ, Eds., Oxford University Press,
New York, 1998, pp. 307-325.
35. Al-Hazzaa S, Ozand P, Traboulsi EI. Metabolic diseases
and the eye. In Duane's Clinical Ophthalmology, Lippincott
- Raven, 1998, Vol 5, Chapter 25, pp.1-47.
36. Traboulsi, EI. 21st Annual Midwest Glaucoma Symposium.
Update on Genetics of Glaucoma and Associated Conditions.
Boston: Ophthalmology Interactive; 1999. (CD-ROM)
37. Traboulsi EI. Surgery for childhood cataracts. In Ophthalmic
Surgery, (Rob & Smith Operative Surgery), Gottsch JD,
Stark WJ, Goldberg MF, Eds., , 5th Edition, London: Arnold,
1998, pp.224-229.
38. Humayun M, Traboulsi EI: Congenital hypertrophy of the
retinal pigment epithelium. In Vitreous, Retina, Macula: A
Comprehensive Textbook, Yannuzzi LA, Guyer DR, Chang S, Shields
J, Green WR, Ed, CV Mosby, St. Louis, 1999, Chapter 88, 1058-1066.
39. Jaafar MS, Traboulsi EI: Management of strabismus associated
with congenital fibrosis of the extraocular muscles. In Clinical
Strabismus Management: Principles and Surgical techniques,
(Rob & Smith's Operative Sugery), Rosenbaum AL, Santiago
AP, Eds., C.V. Mosby, Co. 1999, Chapter 27, pp.363-370.
40. Traboulsi EI, Maumenee IH. Eye Problems. In Principles
and Practice of Pediatrics, 3rd. Edition, McMillan JA, ed,
Lippincott Williams & Wilkins, 1999, Chapter 115, pp.
660-681.
41. Guemes A, Traboulsi EI. Lenticonus and lentiglobus. In
Current Ocular Therapy, 5th Ed, Fraunfelder FT, Roy FH, Eds,
WB Saunders Publ., 2000, pp. 542-543.
42. Traboulsi EI, Guemes A. Microspherophakia. In Current
Ocular Therapy, 5th Ed, Fraunfelder FT, Roy FH, Eds, WB Saunders
Publ., 2000, 543-545.
43. Traboulsi EI: Mucopolysaccharidosis II. In Current Ocular
Therapy, 5th Ed, Fraunfelder FT, Roy FH, Eds, WB Saunders
Publ., 2000, 123-124.
44. Traboulsi EI: Mucopolysaccharidosis III. In Current Ocular
Therapy, 5th Ed, Fraunfelder FT, Roy FH, Eds, WB Saunders
Publ., 2000, 124-125.
45. Traboulsi EI: Genetics and Eye Disease. Review of Ophthalmology.
October 2000. Pp.67-77.
46. Traboulsi EI. Connective tissue, skin and bone disorders.
In Pediatric Ophthalmology and Strabismus, Wright KW and Spiegel
P, Eds., Springer Publ., (In Press)
47. Traboulsi EI. Oculocerebral syndrome with hypopigmentation.
In NORD Guide to Rare Disorders, Lippincott, Williams and
Wilkins, Publ., (In Press).
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