COVID-19 versus SARS: A comparative review von Keshta, Ahmed S., Mallah, Saad I., Al Zubaidi, Khaled, Ghorab, Omar K., Keshta, Mohamed S., Alarabi, Dalal, Abousaleh, Mohammad A., Salman, Mustafa Thaer, Taha, Omer E., Zeidan, Anas A., Elsaid, Mahmoud F., Tang, Patrick

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Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant von Abdel Aleem, Alice, Elsaid, Mahmoud F., Chalhoub, Nader, Chakroun, Almahdi, Mohamed, Khalid A.S., AlShami, Rana, Kuzu, Omer, Mohamed, Reem B., Ibrahim, Khalid, AlMudheki, Noora, Osman, Omar, Ross, M. Elizabeth, ELalamy, Osama

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NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup von Elsaid, Mahmoud F, Ibrahim, Khalid, Chalhoub, Nader, Elsotouhy, Ahmed, El Mudehki, Noora, Abdel Aleem, Alice

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Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy von Lakhani, Shenela, Doan, Ryan, Almureikhi, Mariam, Partlow, Jennifer N, Al Saffar, Muna, Elsaid, Mahmoud F, Alaaraj, Nada, James Barkovich, A, Walsh, Christopher A, Ben-Omran, Tawfeg, MD, FRCPC, FCCMG

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Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance von Kumar, Pankaj, Al-Shafai, Mashael, Al Muftah, Wadha Ahmed, Chalhoub, Nader, Elsaid, Mahmoud F, Aleem, Alice Abdel, Suhre, Karsten

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Oculo-ectodermal syndrome: A case report and further delineation of the syndrome von Habib, Fajish, Elsaid, Mahmoud F, Salem, Khalid Yacout, Ibrahim, Khalid Omer, Mohamed, Khalid

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Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum von Elsaid, Mahmoud F., Kamel, Hussein, Chalhoub, Nader, Aziz, Nahla Abdel, Ibrahim, Khalid, Ben-Omran, Tawfeg, George, Binu, Al-Dous, Eman, Mohamoud, Yasmin, Malek, Joel A., Ross, M. Elizabeth, Aleem, Alice Abdel

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New subtype of familial intracranial calcification in a mother and two children von Elsaid, Mahmoud F., Crow, Yanick J., Livingston, John H., Ben-Omran, Tawfeg

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Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency? von Elsaid, Mahmoud F, Bener, Abdulbari, Lindner, Martin, Alzyoud, Mahmoud, Shahbek, Noora, Abdelrahman, Mohammed O, Abdoh, Ghassan, Bessisso, Mohammed S, Zschocke, Johannes, Hoffmann, Georg F

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Acute bacterial meningitis in Qatar von ELSAID, Mahmoud F, FLAMERZI, Aminaa, BESSISSO, Mohammed S, ELSHAFIE, Sittana S

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Pattern of headache in school children in the State of Qatar von BESSISSO, Mohammed S, BENER, Abdulbari, ELSAID, Mahmoud F, AL-KHALAF, Fawzia A, HUZAIMA, Khalid A

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Clinical presentation of acute bacterial meningitis in Qatar von Elsaid, Mahmoud F, Alsoub, Hussam, Bessisso, Mohammed S, Janahi, Mohammad A, Elshafie, Sittana S, Flamerzi, Amina A, Abdulla, Mahmoud I

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Clinico-Radiological Correlation in Children with Ataxia Telangiectasia in Qatar von Ehlayel, Mohammad, Elsaid, Mahmoud F., Shami, Rana, Salem, Khalid, Bener, Abdulbari

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Recurrence risk after a first febrile convulsion von BESSISSO, Mohamed S, ELSAID, Mahmoud F, ALKHALAF, Fawzia A, ALMULA, Naama A, KADOMI, Najeh K, ZEIDAN, Safwan H, AZZAM, Ms. Samir B, SWIED, Hani A, SHAHBIEK, Noora I, ABUHAZEMMA, Khalid J, ABU-SHAHIN, Ahmad M

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Are heterocygotes for classical homocystinuria at risk of vitamin B 12 and folic acid deficiency? von Elsaid, Mahmoud F., Bener, Abdulbari, Lindner, Martin, Alzyoud, Mahmoud, Shahbek, Noora, Abdelrahman, Mohammed O., Abdoh, Ghassan, Bessisso, Mohammed S., Zschocke, Johannes, Hoffmann, Georg F.

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Sandhoff disease (GM2 gangliosidoses) in a premature patient with bronchopulmonary dysplasia von ABDUL-WAHAB, Atiqa, BESSISSO, Mohammed S, ELSAID, Mahmoud F

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Sandhoff disease (GM2 gangliosidoses) in a premature patient with bronchopulmonary dysplasia von Abdul-Wahab, Atiqa, Bessisso, Mohammed S, Elsaid, Mahmoud F

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Oculo-ectodermal syndrome: A case report and further delineation of the syndrome von Habib, Fajish, Elsaid, Mahmoud F, Salem, Khalid Yacout, Ibrahim, Khalid Omer, Mohamed, Khalid

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Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum von Elsaid, Mahmoud F, Kamel, Hussein, Chalhoub, Nader, Aziz, Nahla Abdel, Ibrahim, Khalid, Ben-Omran, Tawfeg, George, Binu, Al-Dous, Eman, Mohamoud, Yasmin, Malek, Joel A, Ross, M Elizabeth, Aleem, Alice Abdel

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Fabrication of novel coral reef-like nanostructured ZnFeNiCo2S4 on Ni foam as an electrode material for battery-type supercapacitors von Elsaid, Mahmoud A.M., Hassan, Ahmed A., Sayed, Ahmed Z., Ashmawy, Ashraf M., Waheed, Abdelaziz F., Mohamed, Saad G.

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