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Search Results - Murad, Hatem N
Search Results - Murad, Hatem N
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LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
by
BOHLEGA, SAEED A.
,
ALFAWAZ, SARAH
,
ABOU-AL-SHAAR, HUSSAM
,
AL-HINDI, HINDI N.
,
MURAD, HATEM N.
,
BOHLEGA, MOHAMED S.
,
MEYER, BRIAN F.
,
MONIES, DOROTA
Published in
Acta myologica
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Clinical and genetic features of anoctaminopathy in Saudi Arabia
by
Bohlega, Saeed
,
Monies, Dorothy M
,
Abulaban, Ahmad A
,
Murad, Hatem N
,
Alhindi, Hindi N
,
Meyer, Brian F
Published in
Neurosciences (Riyadh, Saudi Arabia)
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Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants
by
Zaki, Osama K
,
Priya Doss C, George
,
Ali, Salsabil A
,
Murad, Ghadeer G
,
Elashi, Shaima A
,
Ebnou, Maryam S A
,
Kumar D, Thirumal
,
Khalifa, Ola
,
Gamal, Radwa
,
El Abd, Heba S A
,
Nasr, Bilal N
,
Zayed, Hatem
Published in
Human molecular genetics
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Design and Fabrication of Waveguide Slot Antenna Using 3D Printing for 5G Application
by
Hanoosh, Hatem O.
,
Rahim, M. K. A.
,
Murad, N. A.
,
Hussein, Yaqdhan M.
Published in
Applied Computational Electromagnetics Society journal
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Multi-Beams Waveguide Slot Antennas at X-Band for Wireless Communications Systems
by
Hanoosh, Hatem Oday
,
Rahim, M K A
,
Murad, N A
,
Yaqdhan Mahmood Hussein
Published in
Applied Computational Electromagnetics Society journal
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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
by
Wakil, Salma M.
,
Ramzan, Khushnooda
,
Abuthuraya, Rula
,
Hagos, Samya
,
Al-Dossari, Haya
,
Al-Omar, Rana
,
Murad, Hatem
,
Chedrawi, Aziza
,
Al-Hassnan, Zuhair N.
,
Finsterer, Josef
,
Bohlega, Saeed
Published in
Gene
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