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Hadas Mechoulam
Hadas Mechoulam
Hadassah University Hospital
Verified email at hadassah.org.il - Homepage
Title
Cited by
Cited by
Year
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
1002020
Retinopathy of prematurity: molecular pathology and therapeutic strategies
H Mechoulam, EA Pierce
American Journal of Pharmacogenomics 3, 261-277, 2003
822003
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
802005
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
612004
Expression and activation of STAT3 in ischemia-induced retinopathy
H Mechoulam, EA Pierce
Investigative ophthalmology & visual science 46 (12), 4409-4416, 2005
542005
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
542002
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
492006
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
472013
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
462011
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
362002
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
342010
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
271999
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
252014
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
202016
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
162015
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
142006
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
102015
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
102011
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
82019
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
72019
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Articles 1–20