Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy RM Milhem, S Ben-Salem, L Al-Gazali, BR Ali Investigative Ophthalmology & Visual Science 55 (6), 3423-3431, 2014 | 41 | 2014 |
Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia BR Ali, I Ben-Rebeh, A John, NA Akawi, RM Milhem, NA Al-Shehhi, ... PLoS One 6 (10), e26206, 2011 | 40 | 2011 |
Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian family HN Matlik, RM Milhem, IY Saadeldin, HS Al-Jaibeji, L Al-Gazali, BR Ali Pediatric Neurology 51 (1), 165-169, 2014 | 19 | 2014 |
Novel KCNQ2 mutation in a large Emirati family with benign familial neonatal seizures IY Saadeldin, RM Milhem, L Al-Gazali, BR Ali Pediatric Neurology 48 (1), 63-66, 2013 | 13 | 2013 |
Electrical characterization of DNA supported on nitrocellulose membranes MA Ahmad, RM Milhem, NG Panicker, TA Rizvi, F Mustafa Scientific reports 6 (1), 29089, 2016 | 8 | 2016 |
Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome RM Milhem, L Al-Gazali, BR Ali The international journal of biochemistry & cell biology 60, 119-129, 2015 | 6 | 2015 |
Disorders of FZ-CRD; insights towards FZ-CRD folding and therapeutic landscape RM Milhem Molecular Medicine 26, 2019 | 3 | 2019 |
ELUCIDATION OF THE CELLULAR AND MOLECULAR MECHANISMS OF MISSENSE MUTATIONS ASSOCIATED WITH FAMILIAL EXUDATIVE VITREORETINOPATHY AND CONGENITAL MYASTHENIC SYNDROME RMM Milhem United Arab Emirates University, 2015 | 1 | 2015 |
Cover Image RMM Salma Ben-Salem, Lihadh Al-Gazali, Bassam R Ali Investigative ophthalmology & visual science 55 (6), 2014 | | 2014 |