Clinical and Molecular Analysis of a Novel COLQ Missense Mutation Causing Congenital Myasthenic Syndrome in a Syrian Family
Matlik, Hussein N., MD, Milhem, Reham M., MSc, Saadeldin, Imad Y., MD, Al-Jaibeji, Hayat S., BSc, Al-Gazali, Lihadh, MD, Ali, Bassam R., PhD
Published in Pediatric neurology (01.07.2014)
Published in Pediatric neurology (01.07.2014)
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Journal Article
Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia
Ali, Bassam R, Ben-Rebeh, Imen, John, Anne, Akawi, Nadia A, Milhem, Reham M, Al-Shehhi, Nouf A, Al-Ameri, Mouza M, Al-Shamisi, Shamma A, Al-Gazali, Lihadh
Published in PloS one (14.10.2011)
Published in PloS one (14.10.2011)
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Journal Article
Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy
Milhem, Reham M, Ben-Salem, Salma, Al-Gazali, Lihadh, Ali, Bassam R
Published in Investigative ophthalmology & visual science (17.04.2014)
Published in Investigative ophthalmology & visual science (17.04.2014)
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Journal Article
Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome
Milhem, Reham M., Al-Gazali, Lihadh, Ali, Bassam R.
Published in The international journal of biochemistry & cell biology (01.03.2015)
Published in The international journal of biochemistry & cell biology (01.03.2015)
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Journal Article
Electrical characterization of DNA supported on nitrocellulose membranes
Ahmad, Mahmoud Al, Milhem, Reham M, Panicker, Neena G, Rizvi, Tahir A, Mustafa, Farah
Published in Scientific reports (12.07.2016)
Published in Scientific reports (12.07.2016)
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