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

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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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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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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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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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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2 , encoding a lysosomal type 5 P-type ATPase von Al-Din, Amir, Hillmer, Axel M, Gründemann, Jan, Goebel, Ingrid, Woods, C Geoffrey, Stiller, Barbara, Wriekat, Abdul-Latif, Heimbach, André, Mubaidin, Ammar F, Behrens, Maria I, Cid, L Pablo, Karsak, Meliha, Ramirez, Alfredo, Kubisch, Christian, Liss, Birgit, Hampshire, Dan, Roeper, Jochen

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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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Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature : D-CHRAMPS syndrome von HIYASAT, Dana, DEHYYAT, Munir A, AJLOUNI, Saleh, MUBAIDIN, Ammar F, TILL, Maha, HADIDI, Azmi, EL-SHANTI, Hatem, AJLOUNI, Kamel M

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Multiple sclerosis simulating brain tumor von Shurbaji, Amer A, Dehayyat, Munir A, Abu-Ruman, Imad A, Mubaidin, Ammar F

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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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Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: "D-CHRAMPS syndrome" von Hiyasat, Dana, Dehyyat, Munir A, Ajlouni, Saleh, Mubaidin, Ammar F, Till, Maha, Hadidi, Azmi, El-Shanti, Hatem, Ajlouni, Kamel M

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