Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7 von Rüb, Udo, Schöls, Ludger, Paulson, Henry, Auburger, Georg, Kermer, Pawel, Jen, Joanna C, Seidel, Kay, Korf, Horst-Werner, Deller, Thomas

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Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria von Steffen, Janos, Vashisht, Ajay A, Wan, Jijun, Jen, Joanna C, Claypool, Steven M, Wohlschlegel, James A, Koehler, Carla M

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Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia von Wan, Jijun, Steffen, Janos, Yourshaw, Michael, Mamsa, Hafsa, Andersen, Erik, Rudnik-Schöneborn, Sabine, Pope, Kate, Howell, Katherine B, McLean, Catriona A, Kornberg, Andrew J, Joseph, Jörg, Lockhart, Paul J, Zerres, Klaus, Ryan, Monique M, Nelson, Stanley F, Koehler, Carla M, Jen, Joanna C

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Impaired K+ binding to glial glutamate transporter EAAT1 in migraine von Kovermann, Peter, Hessel, Margarita, Kortzak, Daniel, Jen, Joanna C., Koch, Johannes, Fahlke, Christoph, Freilinger, Tobias

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Hereditary Episodic Ataxias von Jen, Joanna C.

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Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration von Wan, Jijun, Yourshaw, Michael, Mamsa, Hafsa, Rudnik-Schöneborn, Sabine, Menezes, Manoj P, Hong, Ji Eun, Leong, Derek W, Senderek, Jan, Salman, Michael S, Chitayat, David, Seeman, Pavel, von Moers, Arpad, Graul-Neumann, Luitgard, Kornberg, Andrew J, Castro-Gago, Manuel, Sobrido, María-Jesús, Sanefuji, Masafumi, Shieh, Perry B, Salamon, Noriko, Kim, Ronald C, Vinters, Harry V, Chen, Zugen, Zerres, Klaus, Ryan, Monique M, Nelson, Stanley F, Jen, Joanna C

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Surveying physical therapists' understanding of benign paroxysmal positional vertigo von Harrell, Regan G., Hart, Rebecca, Jen, Joanna C., Whitney, Susan L.

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Late-onset episodic ataxia associated with SLC1A3 mutation von Choi, Kwang-Dong, Jen, Joanna C, Choi, Seo Young, Shin, Jin-Hong, Kim, Hyang-Sook, Kim, Hyo-Jung, Kim, Ji-Soo, Choi, Jae-Hwan

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Two cases of rheumatoid meningitis von Magaki, Shino, Chang, Edward, Hammond, Robert R., Yang, Isaac, Mackenzie, Ian R. A., Chou, Benedict T., Choi, Soo I., Jen, Joanna C., Pope, Whitney B., Bell, David A., Vinters, Harry V.

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CANVAS with cerebellar/sensory/vestibular dysfunction from RFC1 intronic pentanucleotide expansion von Paisán-Ruiz, Coro, Jen, Joanna C

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Mutations of EXOSC3/Rrp40p associated with neurological diseases impact ribosomal RNA processing functions of the exosome in S. cerevisiae von Gillespie, Abby, Gabunilas, Jason, Jen, Joanna C, Chanfreau, Guillaume F

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Recent advances in the genetics of recurrent vertigo and vestibulopathy von Jen, Joanna C

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Comment: Challenges in defining the clinical spectrum of neurogenetic disorders von Jen, Joanna C

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Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations von Stam, Anine H, Kothari, Parul H, Shaikh, Aisha, Gschwendter, Andreas, Jen, Joanna C, Hodgkinson, Suzanne, Hardy, Todd A, Hayes, Michael, Kempster, Peter A, Kotschet, Katya E, Bajema, Ingeborg M, van Duinen, Sjoerd G, Maat-Schieman, Marion L C, de Jong, Paulus T V M, de Smet, Marc D, de Wolff-Rouendaal, Didi, Dijkman, Greet, Pelzer, Nadine, Kolar, Grant R, Schmidt, Robert E, Lacey, JoAnne, Joseph, Daniel, Fintak, David R, Grand, M Gilbert, Brunt, Elizabeth M, Liapis, Helen, Hajj-Ali, Rula A, Kruit, Mark C, van Buchem, Mark A, Dichgans, Martin, Frants, Rune R, van den Maagdenberg, Arn M J M, Haan, Joost, Baloh, Robert W, Atkinson, John P, Terwindt, Gisela M, Ferrari, Michel D

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Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation von GRAVES, Tracey D, CHA, Yoon-Hee, HAHN, Angelika F, BAROHN, Richard, SALAJEGHEH, Mohammed K, GRIGGS, Robert C, BUNDY, Brian N, JEN, Joanna C, BALOH, Robert W, HANNA, Michael G

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Lesion evolution and neurodegeneration in RVCL-S: A monogenic microvasculopathy von Ford, Andria L., Chin, Victoria W., Fellah, Slim, Binkley, Michael M., Bodin, Allie M., Balasetti, Vamshi, Taiwo, Yewande, Kang, Peter, Lin, Doris, Jen, Joanna C., Grand, M. Gilbert, Bogacki, Madonna, Liszewski, M. Kathryn, Hourcade, Dennis, Chen, Yasheng, Hassenstab, Jason, Lee, Jin-Moo, An, Hongyu, Miner, Jonathan J., Atkinson, John P.

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Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life von Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.

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Episodic Ataxia Type 1: Natural History and Effect on Quality of Life von Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.

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Familial Episodic Ataxia von Jen, Joanna C., Baloh, Robert W.

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TREX1 is expressed by microglia in normal human brain and increases in regions affected by ischemia von Kothari, Parul H., Kolar, Grant R., Jen, Joanna C., Hajj‐Ali, Rula, Bertram, Paula, Schmidt, Robert E., Atkinson, John P.

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