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プロフィール詳細
プロジェクトを作成
★★★★★
☆☆☆☆☆
Dr. Reham M.に依頼
United Arab Emirates

Medical Communications Consultant & Writer

プロフィール概要
専門分野
サービス
Writing Clinical Trial Documentation, Medical Writing, General Proofreading & Editing
Research Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection
Consulting Healthcare Consulting
職務経験

Medical Communications Consultant & Writer

Freelance

4月 2016 - 現在

Assistant Professor of Natural and Applied Sciences

University of Dubai

8月 2017 - 1月 2020

Postdoctoral Fellow | Postgraduate researcher

United Arab Emirates University

3月 2011 - 4月 2016

Science Advisor | Curriculum Support Specialist

Nord Anglia Education

8月 2007 - 3月 2011

学歴

PhD in Molecular Cellular Pathology

United Arab Emirates University

3月 2011 - 2月 2015

MSc Clinical Biochemistry

University of Newcastle-upon-Tyne, UK

9月 1996 - 9月 1997

認定資格
  • 認定資格の詳細は未入力です。
出版物
JOURNAL ARTICLE
Milhem, R.M., Ali, B.R.(2019). Disorders of FZ-CRD; Insights towards FZ-CRD folding and therapeutic landscape . Molecular Medicine. 26. (1).
Ahmad, M.A., Milhem, R.M., Panicker, N.G., Rizvi, T.A., Mustafa, F.(2016). Electrical characterization of DNA supported on nitrocellulose membranes . Scientific Reports. 6.
Milhem, R.M., Al-Gazali, L., Ali, B.R.(2015). Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome . International Journal of Biochemistry and Cell Biology. 60. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 119-129.
Matlik, H.N., Milhem, R.M., Saadeldin, I.Y., Al-Jaibeji, H.S., Al-Gazali, L., Ali, B.R.(2014). Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian family . Pediatric Neurology. 51. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 165-169.
Milhem, R.M., Ben-Salem, S., Al-Gazali, L., Ali, B.R.(2014). Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy . Investigative Ophthalmology and Visual Science. 55. (6). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 3423-3431.
Saadeldin, I.Y., Milhem, R.M., Al-Gazali, L., Ali, B.R.(2013). Novel KCNQ2 mutation in a large emirati family with benign familial neonatal seizures . Pediatric Neurology. 48. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 63-66.
Ali, B.R., Ben-Rebeh, I., John, A., Akawi, N.A., Milhem, R.M., Al-Shehhi, N.A., Al-Ameri, M.M., Al-Shamisi, S.A., Al-Gazali, L.(2011). Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia . PLoS ONE. 6. (10).