Journal ArticleDOI
A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)
N. H. Wadia,R. K. Swami +1 more
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This article is published in Brain.The article was published on 1971-01-01. It has received 166 citations till now. The article focuses on the topics: Spinocerebellar Degenerations.read more
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Journal ArticleDOI
Late onset cerebello-pontomesencephalic degeneration
Amir S. Najim Al-Din,Ali G.H. Al-Zuhair,Mahmoud K. Al-Salem,Khalid Eid Al-Nassar,Mohammed A. Rudwan,Salah Khafaja,Tawfiq Hamawi +6 more
TL;DR: Electron microscopic muscle studies revealed abnormal distribution and form of the mitochondria, probably being the ultrastructural basis of the pathologic changes in a neurological syndrome as that described here has not been reported before.
Book ChapterDOI
Slow Saccadic Eye Movements in Neurological Patients
TL;DR: The conditions in which slow saccadic eye movements can be found in normal subjects and neurological patients are discussed.
Posted ContentDOI
Antagonistic roles for ataxin-2 structured and disordered domains in rnp condensation
Amanjot Singh,Joern Huelsmeier,Arvind Reddy Kandi,Sai Shruti Pothapragada,Jens Hillebrand,Arnas Petrauskas,Khushboo Agrawal,Krishnan Rt,Devasena Thiagarajan,K. VijayRaghavan,Mani Ramaswami,Mani Ramaswami,Baskar Bakthavachalu +12 more
TL;DR: It is shown that Atx2 preferentially interacts with AU-rich elements (AREs) in 3’UTRs and plays a broad role in stabilization of identified target mRNAs and interaction with its targets is dependent on the cIDR domain required for neuronal-granule formation.
Book ChapterDOI
Eye Movements in Autosomal Dominant Spinocerebellar Ataxias
Alessandra Rufa,Francesca Rosini +1 more
TL;DR: In this chapter, the goal is to elucidate the eye movement abnormalities in autosomal-dominant spinocerebellar ataxias through a systematic review of the literature.
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