R
Robert W. Baloh
Researcher at University of California, Los Angeles
Publications - 319
Citations - 17485
Robert W. Baloh is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Vestibular system & Vestibulo–ocular reflex. The author has an hindex of 71, co-authored 306 publications receiving 16363 citations.
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Journal ArticleDOI
Benign positional vertigo: clinical and oculographic features in 240 cases
TL;DR: The clinical and oculographic features in 240 patients with benign positional vertigo (BPV) are consistent with a peripheral, posterior semicircular canal origin of BPV.
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Quantitative measurement of saccade amplitude, duration, and velocity.
TL;DR: A method for rapid, accurate measurement of saccade amplitude, duration, and velocity (average and maximum) was developed as a functional test of the extraocular motor system, and the two constants of this equation adequately characterized the relationship between saccades amplitude and velocity and permitted rapid statistical comparison between normal and abnormal subjects.
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Coding and Noncoding Variation of the Human Calcium-Channel β4-Subunit Gene CACNB4 in Patients with Idiopathic Generalized Epilepsy and Episodic Ataxia
Andrew Escayg,Michel De Waard,David D. Lee,Delphine Bichet,Peter Wolf,Thomas Mayer,Janine L. Johnston,Robert W. Baloh,Thomas Sander,Miriam H. Meisler +9 more
TL;DR: Eight noncoding single-nucleotide substitutions, two of which are present at polymorphic frequency, and a previously unrecognized first intron of CACNB4 that interrupts exon 1 at codon 21 are described, which may be considered candidate disease mutations.
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Cerebellar infarction presenting isolated vertigo: frequency and vascular topographical patterns.
TL;DR: Cerebellar infarction simulating vestibular neuritis is more common than previously thought and early recognition of the pseudo-vestibul neuritis of vascular cause may allow specific management.
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C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Anna Richards,Arn M. J. M. van den Maagdenberg,Joanna C. Jen,David J. Kavanagh,Paula Bertram,Dirk Spitzer,M. Kathryn Liszewski,Maria Louise Barilla-Labarca,Gisela M. Terwindt,Yumi Kasai,Michael D. McLellan,Mark Gilbert Grand,Kaate R J Vanmolkot,Boukje de Vries,Jijun Wan,Michael J. Kane,Hafsa Mamsa,Ruth Schäfer,Anine H. Stam,Joost Haan,Paulus T. V. M. de Jong,Paulus T. V. M. de Jong,Caroline W. Storimans,Mary J. van Schooneveld,J. A. Oosterhuis,Andreas Gschwendter,Martin Dichgans,Katya E. Kotschet,Suzanne Hodgkinson,Todd A. Hardy,Martin B. Delatycki,Rula A. Hajj-Ali,Parul H. Kothari,Stanley F. Nelson,Rune R. Frants,Robert W. Baloh,Michel D. Ferrari,John P. Atkinson +37 more
TL;DR: Heterozygous C-terminal frameshift mutations in TREX1 retain exonuclease activity but lose normal perinuclear localization, which has implications for the maintenance of vascular integrity in the degenerative cerebral microangiopathies leading to stroke and dementias.