Randa Haddad

Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

Nisha Patel, Arif O. Khan, Ahmad M. Mansour et al. · The American Journal of Human Genetics · 2014 · 69 citations · Full text

Developmental Anomaly, Ophthalmology, Genetic Disorder +6

Intravitreal Tissue Plasminogen Activator in the Management of Central Retinal Vein Occlusion

Nicola G. Ghazi, Baha’ N. Noureddine, Randa Haddad et al. · Retina · 2003 · 68 citations

Recalcitrant Post-LASIK Mycobacterium chelonae Keratitis Eradicated after the Use of Fourth-Generation Fluoroquinolone

Rola N. Hamam, Baha’ N. Noureddin, Haytham I. Salti et al. · Ophthalmology · 2006 · 40 citations

Ophthalmology, Fourth-generation Fluoroquinolone, Ocular Pathology +3

Corneal Topography After Ocular Rubbing

Ahmad M. Mansour, Randa Haddad · Cornea · 2002 · 39 citations

Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance

Randa Haddad, Sami H. Uwaydat, Rola Dakroub et al. · American Journal of Medical Genetics · 2001 · 34 citations

Developmental Anomaly, Mendelian Disorder, Ophthalmology +11