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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Nat Genet. 2006 Oct;38(10):1184-91. doi: 10.1038/ng1884. Epub 2006 Sep 10.
Nat Genet. 2006.
PMID: 16964263
Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36.
Hampshire DJ, Roberts E, Crow Y, Bond J, Mubaidin A, Wriekat AL, Al-Din A, Woods CG.
Hampshire DJ, et al. Among authors: wriekat al.
J Med Genet. 2001 Oct;38(10):680-2. doi: 10.1136/jmg.38.10.680.
J Med Genet. 2001.
PMID: 11584046
Free PMC article.
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Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome.
Najim al-Din AS, Wriekat A, Mubaidin A, Dasouki M, Hiari M.
Najim al-Din AS, et al. Among authors: wriekat a.
Acta Neurol Scand. 1994 May;89(5):347-52. doi: 10.1111/j.1600-0404.1994.tb02645.x.
Acta Neurol Scand. 1994.
PMID: 8085432
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Multiple sclerosis in Arabs in Jordan.
al-Din AS, el-Khateeb M, Kurdi A, Mubaidin A, Wriekat A, al-Shehab A, Khalil RW.
al-Din AS, et al. Among authors: wriekat a, al shehab a.
J Neurol Sci. 1995 Aug;131(2):144-9. doi: 10.1016/0022-510x(95)00092-g.
J Neurol Sci. 1995.
PMID: 7595639
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Risk factors of aseptic intracranial venous occlusive disease.
Najim al-Din AS, Mubaidin A, Wriekat AL, Alqam M.
Najim al-Din AS, et al. Among authors: wriekat al.
Acta Neurol Scand. 1994 Dec;90(6):412-6. doi: 10.1111/j.1600-0404.1994.tb02750.x.
Acta Neurol Scand. 1994.
PMID: 7892760
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Autosomal recessive ataxia, slow eye movements and psychomotor retardation.
Najim al-Din AS, al-Kurdi A, Dasouki M, Wriekat AL, al-Khateeb M, Mubaidin A, al-Hiari M.
Najim al-Din AS, et al. Among authors: wriekat al.
J Neurol Sci. 1994 Jun;124(1):61-6. doi: 10.1016/0022-510x(94)90011-6.
J Neurol Sci. 1994.
PMID: 7931423
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Epidemiology of multiple sclerosis in Arabs in Jordan: a comparative study between Jordanians and Palestinians.
Najim Al-Din AS, Kurdi A, Mubaidin A, El-Khateeb M, Khalil RW, Wriekat AL.
Najim Al-Din AS, et al. Among authors: wriekat al.
J Neurol Sci. 1996 Feb;135(2):162-7. doi: 10.1016/0022-510x(95)00276-8.
J Neurol Sci. 1996.
PMID: 8867073
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