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UPD1p indicates the presence of MPL W515L mutation in RARS-T, a mechanism analogous to UPD9p and JAK2 V617F mutation.
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Gait apraxia in multiple sclerosis.
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Gait apraxia in multiple sclerosis.
Abou Zeid NE, Weinshenker BG, Keegan BM. Gait apraxia in multiple sclerosis. Can J Neurol Sci. 2009 Sep; 36(5):562-5.
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PubMed
subject areas
Adult
Age of Onset
Aged
Disability Evaluation
Disease Progression
Female
Gait Apraxia
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Multiple Sclerosis
Oligoclonal Bands
Retrospective Studies
authors with profiles
Nuhad E. Abou Zeid MD