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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A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias von STRUPP, M, KALLA, R, LEHMANN-HORN, F, JURKAT-ROTT, K, BRANDT, T, JEN, J. C, JAHN, K, CLAASSEN, J, ADRION, C, MANSMANN, U, KLOPSTOCK, T, FREILINGER, T, NEUGEBAUER, H, SPIEGEL, R, DICHGANS, M

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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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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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Prolonged hemiplegic episodes in children due to mutations in ATP1A2 von Jen, J C, Klein, A, Boltshauser, E, Cartwright, M S, Roach, E S, Mamsa, H, 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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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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Different effects of strenuous exercise and moderate exercise on platelet function in men von JONG-SHYAN WANG, JEN, C. J, HSIUE-CHING KUNGH, LI-JEN LIN, TZUEN-REN HSIUE, HSIUN-ING CHEN

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Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy von JEN, J. C, WANG, H, LEE, H, SABATTI, C, TRENT, R, HANNIGAN, I, BRANTBERG, K, HALMAGYI, G. M, NELSON, S. F, BALOH, R. W

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Episodic vertical oscillopsia with progressive gait ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13q von Cha, Y H, Lee, H, Jen, J C, Kattah, J C, Nelson, S F, Baloh, R W

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Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene von Yue, Qing, Jen, Joanna C., Nelson, Stanley F., Baloh, Robert W.

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Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia von JEN, J. C, LEE, H, CHA, Y. H, NELSON, S. F, BALOH, R. W

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A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism von Blanco-Arias, Patricia, Einholm, Anja P., Mamsa, Hafsa, Concheiro, Carla, Gutiérrez-de-Terán, Hugo, Romero, Jesús, Toustrup-Jensen, Mads S., Carracedo, Ángel, Jen, Joanna C., Vilsen, Bente, Sobrido, María-Jesús

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Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia von Jen, Joanna C, Yue, Qing, Karrim, Juliana, Nelson, Stanley F, Baloh, Robert W

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Compulsive exercise acutely upregulates rat hippocampal brain-derived neurotrophic factor von Huang, A M, Jen, C J, Chen, H F, Yu, L, Kuo, Y M, Chen, H I

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Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformation von WATERS, M. F, SHIELDS, D. C, MARTIN, N. A, BALOH, R. W, JEN, J. C

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Effects of chronic exercise and deconditioning on platelet function in women von Wang, Jong-Shyan, Jen, Chauying J, Chen, Hsiun-Ing

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Endothelial [Ca(2+)](i) signaling during transmigration of polymorphonuclear leukocytes von Su, W H, Chen, H I, Huang, J P, Jen, C J

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Chronic Consumption of Raw But Not Boiled Welsh Onion Juice Inhibits Rat Platelet Function von Chen, Jia-Huey, Chen, Hsiun-ing, Tsai, Shun-Jen, Jen, Chauying J.

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Effects of Exercise Training and Deconditioning on Platelet Function in Men von Wang, Jong-shyan, Jen, Chauying J, Chen, Hsiun-ing

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