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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Mutations in the tail domain of DYNC1H1 cause dominant spinal: muscular atrophy von HARMS, M. B, ORI-MCKENNEY, K. M, MILLER, L. J, JANI-ACSADI, A, PESTRONK, A, SHY, M. E, MUNTONI, F, VALLEE, R. B, BALOH, R. H, SCOTO, M, TUCK, E. P, BELL, S, MA, D, MASI, S, ALLRED, P, AL-LOZI, M, REILLY, M. M

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C9orf72 is required for proper macrophage and microglial function in mice von O'Rourke, J. G., Bogdanik, L., Yáñez, A., Lall, D., Wolf, A. J., Muhammad, A. K. M. G., Ho, R., Carmona, S., Vit, J.P., Zarrow, J., Kim, K. J., Bell, S., Harms, M. B., Miller, T. M., Dangler, C. A., Underhill, D. M., Goodridge, H. S., Lutz, C. M., Baloh, R. H.

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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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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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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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Schwann cell mitochondrial metabolism supports long-term axonal survival and peripheral nerve function von Viader, Andreu, Golden, Judith P, Baloh, Robert H, Schmidt, Robert E, Hunter, Daniel A, Milbrandt, Jeffrey

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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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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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Dominant spinal muscular atrophy with lower extremity predominance: Linkage to 14q32 von HARMS, M. B, ALLRED, P, GARDNER, R, FERNANDES, J. A, FLORENCE, J, PESTRONK, A, AL-LOZI, M, BALOH, R. H

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

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Neurotology of Migraine von Baloh, Robert W.

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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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Vertigo von Baloh, Robert 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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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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