Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations von Akawi, NA, Al-Gazali, L, Ali, BR

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Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients von Ali, BR, Xu, H, Akawi, NA, John, A, Karuvantevida, NS, Langer, R, Al-Gazali, L, Leitinger, B

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Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patients von Moselhy, H, Eapen, V, Akawi, NA, Younis, A, Salih, B, Othman, AR, Yousef, S, Clarke, RA, Ali, BR

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Antiandrogenic activity of Ruta graveolens L in male Albino rats with emphasis on sexual and aggressive behavior von Khouri, Nabil Azar, El-Akawi, Zeyad

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