Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures von JEN, J. C, WAN, J, PALOS, T. P, HOWARD, B. D, BALOH, R. W

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Primary episodic ataxias: diagnosis, pathogenesis and treatment von Jen, J.C., Graves, T.D., Hess, E.J., Hanna, M.G., Griggs, R.C., Baloh, R.W.

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Cerebellar infarction presenting isolated vertigo : Frequency and vascular topographical patterns von LEE, H, SOHN, S.-I, CHO, Y.-W, LEE, S.-R, AHN, B.-H, PARK, B.-R, BALOH, R. W

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Practice Parameter: Therapies for benign paroxysmal positional vertigo (an evidence-based review) : Report of the Quality Standards Subcommittee of the American Academy of Neurolog... von FIFE, T. D, IVERSON, D. J, LEMPERT, T, FURMAN, J. M, BALOH, R. W, TUSA, R. J, HAIN, T. C, HERDMAN, S, MORROW, M. J, GRONSETH, G. S

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A prospective study of cerebral white matter abnormalities in older people with gait dysfunction von WHITMAN, G. T, TANG, T, LIN, A, BALOH, R. W

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Clinical spectrum of episodic ataxia type 2 von Jen, J, Kim, G W, Baloh, R W

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Otolith dysfunction in vestibular neuritis Recovery pattern and a predictor of symptom recovery von KIM, H.-A, HONG, J.-H, LEE, H, YI, H.-A, LEE, S.-R, LEE, S.-Y, JANG, B.-C, AHN, B.-H, BALOH, R. W

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Clinical features and associated syndromes of mal de debarquement von Cha, Y.-H., Brodsky, J., Ishiyama, G., Sabatti, C., Baloh, R. W.

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Association of Benign Recurrent Vertigo and Migraine in 208 Patients von Cha, Y-H, Lee, H, Santell, LS, Baloh, RW

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The relevance of migraine in patients with Ménière's disease von Cha, Y.H., Brodsky, J., Ishiyama, G., Sabatti, C., Baloh, R.W.

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Neurotology of Migraine von Baloh, Robert W.

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Acute Vestibular Syndrome von Hotson, John R, Baloh, Robert W

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Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations von SICOTTE, N. L, SALAMON, G, BALOH, R. W, DELLER, T, JEN, J. C, SHATTUCK, D. W, HAGEMAN, N, RÜB, U, SALAMON, N, DRAIN, A. E, DEMER, J. L, ENGLE, E. C, ALGER, J. R

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Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission von JEN, J, WAN, J, GRAVES, M, YU, H, MOCK, A. F, COULIN, C. J, KIM, G, YUE, Q, PAPAZIAN, D. M, BALOH, R. W

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Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3 von Bosley, T M, Salih, M A M, Jen, J C, Lin, D D M, Oystreck, D, Abu-Amero, K K, MacDonald, D B, al Zayed, Z, al Dhalaan, H, Kansu, T, Stigsby, B, Baloh, R W

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CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics von WAN, J, KHANNA, R, SANDUSKY, M, PAPAZIAN, D. M, JEN, J. C, BALOH, R. W

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Vertigo von Baloh, Robert W

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Rotational vertebral artery occlusion: a clinical entity or various syndromes? von Brandt, T, Baloh, R W

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Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS) von JEN, J, COHEN, A. H, YUE, Q, STOUT, J. T, VINTERS, H. V, NELSON, S, BALOH, R. W

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Pontine and cerebellar atrophy correlate with clinical disability in SCA2 von YING, S. H, CHOI, S. I, PERLMAN, S. L, BALOH, R. W, ZEE, D. S, TOGA, A. W

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