Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36 von Hampshire, Daniel J, Roberts, Emma, Crow, Yanick, Bond, Jacquelyn, Mubaidin, Ammar, Wriekat, Abdul-Latif, Al-Din, Amir, Woods, C Geoffrey

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Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum von Mubaidin, A, Roberts, E, Hampshire, D, Dehyyat, M, Shurbaji, A, Mubaidien, M, Jamil, A, Al-Din, A, Kurdi, A, Woods, C G

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Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: a novel disorder or a new variant of Boucher-Neuhauser... von Jbour, A-K, Mubaidin, A F, Till, M, El-Shanti, H, Hadidi, A, Ajlouni, K M

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Alcohol with xylocaine for treatment of eyelid dystonia von Mubaidin, A. F.

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Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size von Bond, Jacquelyn, Scott, Sheila, Hampshire, Daniel J., Springell, Kelly, Corry, Peter, Abramowicz, Marc J., Mochida, Ganesh H., Hennekam, Raoul C.M., Maher, Eamonn R., Fryns, Jean-Pierre, Alswaid, Abdulrahman, Jafri, Hussain, Rashid, Yasmin, Mubaidin, Ammar, Walsh, Christopher A., Roberts, Emma, Woods, C. Geoffrey

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Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene von Middleton, L, Ohno, K, Christodoulou, K, Brengman, J, Milone, M, Neocleous, V, Serdaroğlu, P, Deymeer, F, Ozdemir, C, Mubaidin, A, Horany, K, Al-Shehab, A, Mavromatis, I, Mylonas, I, Tsingis, M, Zamba, E, Pantzaris, M, Kyriallis, K, Engel, A G

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Distal Hereditary Motor Neuronopathy of the Jerash Type von MIDDLETON, L. T., CHRISTODOULOU, K., MUBAIDIN, A., ZAMBA, E., TSINGIS, M., KYRIACOU, K., ABU-SHEIKH, S., KYRIAKIDES, T., NEOCLEOUS, V., GEORGIOU, D. M., EL-KHATEEB, M., AL-QUDAH, A., HORANY, K.

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Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation von Ververis, A, Dajani, R, Koutsou, P, Aloqaily, A, Nelson-Williams, C, Loring, E, Arafat, A, Mubaidin, AF, Horany, K, Bader, MB, Al-Baho, Y, Ali, B, Muhtaseb, A, DeSpenza, T, Al-Qudah, AA, Middleton, LT, Zamba-Papanicolaou, E, Lifton, R, Christodoulou, K

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Multiple sclerosis in Arabs in Jordan von Al-Din, A.S.Najim, El-Khateeb, M., Kurdi, A., Mubaidin, A., Wriekat, A., Al-Shehab, Ahmed, Khalil, Raida W.

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Distal Hereditary Motor Neuronopathy of the Jerash Type von MIDDLETON, L. T., CHRISTODOULOU, K., MUBAIDIN, A., ZAMBA, E., TSINGIS, M., KYRIACOU, K., ABU-SHEIKH, S., KYRIAKIDES, T., NEOCLEOUS, V., GEORGIOU, D. M., EL-KHATEEB, M., AL-QUDAN, A., HORANY, K.

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Signaling between the placenta and the uterus involving the mitogen-regulated protein/proliferins von Fang, Y, Lepont, P, Fassett, J T, Ford, S P, Mubaidin, A, Hamilton, R T, Nilsen-Hamilton, M

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Sixth nerve palsy and sphenoidal sinusitis von Mubaidin, A F, Hairi, M A

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Subdural hematoma complicating middle fossa arachnoid cyst von Mubaidin, A F, Shurbaji, A A

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A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12 von Christodoulou, Kyproula, Zamba, Eleni, Tsingis, Marios, Mubaidin, Amar, Horani, Khalid, Abu-Sheik, Salem, El-Khateeb, Mohammed, Kyriacou, Kyriacos, Kyriakides, Theodoros, Al-Qudah, Abdel-Karim, Middleton, Lefkos

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Distal Hereditary Motor Neuronopathy of the Jerash Type von Middleton, L T, Christodoulou, K, Mubaidin, A, Zamba, E, Tsingis, M, Kyriacou, K, Abu-Sheikh, S, Kyriakides, T, Neocleous, V, Georgiou, D M, El-Khateeb, M, Al-Qudah, A, Horany, K

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Epidemiology of multiple sclerosis in Arabs in Jordan: a comparative study between Jordanians and Palestinians von Najim Al-Din, Amir S., Kurdi, Ashraf, Mubaidin, Ammar, El-Khateeb, Mohammed, Khalil, Raida W., Wriekat, Abdel-Latif

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Distal Hereditary Motor Neuronopathy of the Jerash Type von Middleton, L T, Christodoulou, K, Mubaidin, A, Zamba, E, Tsingis, M, Kyriacou, K, Abu-Sheikh, S, Kyriakides, T, Neocleous, V, Georgiou, D M, El-Khateeb, M, Al-Qudan, A, Horany, K

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Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor ∈-subunit gene von MIDDLETON, L, OHNO, K, HORANY, K, AL-SHEHAB, A, MAVROMATIS, I, MYLONAS, I, TSINGIS, M, ZAMBA, E, PANTZARIS, M, KYRIALLIS, K, ENGEL, A. G, CHRISTODOULOU, K, BRENGMAN, J, MILONE, M, NEOCLEOUS, V, SERDAROGLU, P, DEYMEER, F, ÖZDEMIR, C, MUBAIDIN, A

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Autosomal recessive ataxia, slow eye movements and psychomotor retardation von Najim Al-Din, Amir S., Al-Kurdi, Ashraf, Dasouki, Majed, Wriekat, Abdul-Latif, Al-Khateeb, Mohammed, Mubaidin, Amar, Al-Hiari, Mohmad

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Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum von Mubaidin, A, Roberts, E, Hampshire, D, Dheyyat, M, Shurbaji, A, Mubaidin, M, Jamil, A, Din, A, Kurdi, A, Woods, C.G

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