M. Barsoum-Homsy

发表

On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness

M. Roy, J. Jacob, M. Quigley, 1996, Documenta Ophthalmologica.

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, Human molecular genetics.

Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.

M. Sarfarazi, N. Akarsu, M. Barsoum-Homsy, 1995, Genomics.

Pattern electroretinogram and spatial contrast sensitivity in primary congenital glaucoma.

M. Roy, G. Trick, M. Barsoum-Homsy, 1997, Ophthalmology.

Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.

A. Child, G. Brice, M. Sarfarazi, 1998, American journal of human genetics.

Incidence and prognosis of childhood glaucoma. A study of 63 cases.

M. Barsoum-Homsy, L. Chevrette, 1986, Ophthalmology.

Incidence and prognosis of childhood glaucoma

M. Barsoum-Homsy, L. Chevrette, 1986 .

Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, American journal of medical genetics.

Peters' anomaly. The spectrum of associated ocular and systemic malformations.

E. Héon, J. Jacob, M. Musarella, 1992, Ophthalmic paediatrics and genetics.

Clinical evaluation of aminocaproic acid for managing traumatic hyphema in children.

J. Jacob, M. Barsoum-Homsy, L. Chevrette, 1995, Ophthalmology (Rochester, Minn.).

First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13.

J. Michaud, M. Barsoum-Homsy, J. Milot, 1989, Cancer genetics and cytogenetics.

Nonteratoicl Medulloepiothelioma of the Ciliary Body

M. Barsoum-Homsy, S. Brownstein, G. Condon, 1984 .

Inferior oblique myositis presenting as superior oblique muscle palsy.

M. Barsoum-Homsy, S. Brownstein, S. Lahoud, 1988, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Medial rectus insertion site in congenital esotropia.

M. Barsoum-Homsy, 1981, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Novel TIGR/MYOC mutations in families with juvenile onset primary open angle glaucoma.

A. Child, H. Garchon, M. Adam, 1998, Journal of medical genetics.

Recombinant interferon alfa-2b in the treatment of vision-threatening capillary hemangiomas in childhood.

M. Barsoum-Homsy, J. Milot, J. Leclerc, 1997, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Congenital double elevator palsy.

M. Barsoum-Homsy, 1983, Journal of pediatric ophthalmology and strabismus.

Maturation of Binocular Pattern Visual Evoked Potentials in Normal Full-Term and Preterm Infants from 1 to 6 Months of Age

M. Roy, M. Barsoum-Homsy, Marie-Sylvie Roy, 1995, Pediatric Research.

Congenital microcephaly, juvenile retinal dystrophy and normal mentation in a mildly dysmorphic child.

V. D. Der Kaloustian, R. Koenekoop, M. Barsoum-Homsy, 2005, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Linkage study between congenital cataracts and five crystallin loci

C. Barr, C. Tsilfidis, A. Levin, 2003, American journal of medical genetics. Part A.

Visual Acuity in Mentally Retarded Children Measured with the Forced-Preferential Looking Procedure and the Scolatest

J. Jacob, M. Barsoum-Homsy, L. Chevrette, 1988 .