Publications by authors named "Hatem Murad"

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Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia.
Norah Alharbi, Rawan Matar, Edward Cupler, Hindi Al-Hindi, Hatem Murad

Front Neurosci· February 2022

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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Hatem Murad

Am J Hum Genet· October 2019

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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Hatem Murad

Am J Hum Genet· June 2019

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LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.
Saeed A Bohlega, Sarah Alfawaz, Hussam Abou-Al-Shaar, Hindi N Al-Hindi, Hatem N Murad

Acta Myol· September 2018

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Clinical and genetic features of anoctaminopathy in Saudi Arabia.
Saeed Bohlega, Dorothy M Monies, Ahmad A Abulaban, Hatem N Murad, Hindi N Alhindi

Neurosciences (Riyadh)· April 2015

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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T.
Salma M Wakil, Khushnooda Ramzan, Rula Abuthuraya, Samya Hagos, Haya Al-Dossari, Hatem Murad

Gene· February 2014

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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.
Salma M Wakil, Hatem N Murad, Batoul M Baz, Samiya T Hagos, Rana A Al-Amr

Neurosciences (Riyadh)· January 2012

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Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula.
Saeed Bohlega, Adel Al-Jishi, Carol Dobson-Stone, Luca Rampoldi, Parthasarathi Saha, Hatem Murad

Mov Disord· April 2003

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