Ophthalmology practice during the COVID-19 pandemic K Safadi, JM Kruger, I Chowers, A Solomon, R Amer, H Aweidah, ... BMJ open ophthalmology 5 (1), e000487, 2020 | 100 | 2020 |
Retinopathy of prematurity: molecular pathology and therapeutic strategies H Mechoulam, EA Pierce American Journal of Pharmacogenomics 3, 261-277, 2003 | 82 | 2003 |
Forty years of changing indications in penetrating keratoplasty in Israel C Yahalom, H Mechoulam, A Solomon, FD Raiskup, J Peer, J Frucht-Pery Cornea 24 (3), 256-258, 2005 | 80 | 2005 |
Iontophoresis–gentamicin delivery into the rabbit cornea, using a hydrogel delivery probe J Frucht-Pery, H Mechoulam, CS Siganos, P Ever-Hadani, M Shapiro, ... Experimental eye research 78 (3), 745-749, 2004 | 61 | 2004 |
Expression and activation of STAT3 in ischemia-induced retinopathy H Mechoulam, EA Pierce Investigative ophthalmology & visual science 46 (12), 4409-4416, 2005 | 54 | 2005 |
Inflamed juvenile conjunctival naevus: clinicopathological characterisation E Zamir, H Mechoulam, A Micera, F Levi-Schaffer, J Pe'er British journal of ophthalmology 86 (1), 28-30, 2002 | 54 | 2002 |
Iontophoretic treatment of experimental pseudomonas keratitis in rabbit eyes using gentamicin-loaded hydrogels J Frucht-Pery, F Raiskup, H Mechoulam, M Shapiro, E Eljarrat-Binstock, ... Cornea 25 (10), 1182-1186, 2006 | 49 | 2006 |
Oral propranolol versus placebo for retinopathy of prematurity: a pilot, randomised, double-blind prospective study IR Makhoul, O Peleg, B Miller, B Bar-Oz, O Kochavi, H Mechoulam, ... Archives of disease in childhood 98 (7), 565-567, 2013 | 47 | 2013 |
Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity J Klammt, L Kobelt, D Aktas, I Durak, A Gokbuget, Q Hughes, M Irkec, ... Thrombosis and haemostasis 105 (03), 454-460, 2011 | 46 | 2011 |
Nerve growth factor and eosinophils in inflamed juvenile conjunctival nevus F Levi-Schaffer, A Micera, E Zamir, H Mechoulam, I Puxeddu, ... Investigative ophthalmology & visual science 43 (6), 1850-1856, 2002 | 36 | 2002 |
Strabismus surgery outcome among children and young adults with Down syndrome C Yahalom, H Mechoulam, E Cohen, I Anteby Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2010 | 34 | 2010 |
The distribution of gentamicin in the rabbit cornea following iontophoresis to the central cornea J FRUCHT-PERY, D GOREN, A SOLOMON, CS SIGANOS, ... Journal of ocular pharmacology and therapeutics 15 (3), 251-256, 1999 | 27 | 1999 |
Expression and activation of toll-like receptor 3 and toll-like receptor 4 on human corneal epithelial and conjunctival fibroblasts N Erdinest, G Aviel, E Moallem, I Anteby, C Yahalom, H Mechoulam, ... Journal of Inflammation 11, 1-10, 2014 | 25 | 2014 |
Strabismus developing after unilateral and bilateral cataract surgery in children R David, J Davelman, H Mechoulam, E Cohen, I Karshai, I Anteby Eye 30 (9), 1210-1214, 2016 | 20 | 2016 |
Nitric oxide secretion in human conjunctival fibroblasts is inhibited by alpha linolenic acid N Erdinest, N Shohat, E Moallem, C Yahalom, H Mechoulam, I Anteby, ... Journal of Inflammation 12, 1-9, 2015 | 16 | 2015 |
Astigmatism after mersilene and nylon suture use for penetrating keratoplasty D Landau, CS Siganos, H Mechoulam, A Solomon, J Frucht-Pery Cornea 25 (6), 691-694, 2006 | 14 | 2006 |
Ophthalmologic findings in H syndrome: a unique diagnostic clue V Molho-Pessach, H Mechoulam, R Siam, S Babay, Y Ramot, ... Ophthalmic Genetics 36 (4), 365-368, 2015 | 10 | 2015 |
Congenital cytomegalovirus infection and Wiskott–Aldrich syndrome successfully treated with unrelated cord blood transplantation Y Almagor, S Revel‐Vilk, D Averbuch, H Mechoulam, D Engelhard, ... Pediatric Blood & Cancer 57 (4), 681-683, 2011 | 10 | 2011 |
An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers A Kimchi, V Meiner, S Silverstein, M Macarov, H Mor-Shaked, ... Ophthalmic Genetics 40 (5), 443-448, 2019 | 8 | 2019 |
Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delay T Harel, E Levy-Lahad, M Daana, H Mechoulam, S Horowitz-Cederboim, ... European Journal of Human Genetics 27 (8), 1315-1319, 2019 | 7 | 2019 |