Second Cistron in CACNA1A Gene Encodes a Transcription Factor Mediating Cerebellar Development and SCA6 von Du, Xiaofei, Wang, Jun, Zhu, Haipeng, Rinaldo, Lorenzo, Lamar, Kay-Marie, Palmenberg, Ann C., Hansel, Christian, Gomez, Christopher M.

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The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability von Hekman, Katherine E, Gomez, Christopher M

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Neurochemical abnormalities in premanifest and early spinocerebellar ataxias von Joers, James M., Deelchand, Dinesh K., Lyu, Tianmeng, Emir, Uzay E., Hutter, Diane, Gomez, Christopher M., Bushara, Khalaf O., Eberly, Lynn E., Öz, Gülin

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Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits von Velázquez‐Pérez, Luis, Rodriguez‐Labrada, Roberto, González‐Garcés, Yasmani, Arrufat‐Pie, Eduardo, Torres‐Vega, Reidenis, Medrano‐Montero, Jacqueline, Ramirez‐Bautista, Beatriz, Vazquez‐Mojena, Yaimeé, Auburger, Georg, Horak, Fay, Ziemann, Ulf, Gomez, Christopher M.

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Pontine stroke in a patient with Chronic Progressive External Ophthalmoplegia (CPEO): a case report von Eliyan, Yazan, Rezania, Kourosh, Gomez, Christopher M, Seibert, Kaitlin

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HER2 c-Terminal Fragments Are Expressed via Internal Translation of the HER2 mRNA von Godfrey, Jack D, Hejazi, Daniel, Du, Xiaofei, Wei, Cenfu, Rao, Eshaan, Gomez, Christopher M

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Characterization of a chronic cough in cerebellar ataxia, neuropathy, vestibular areflexia syndrome von Tatineni, Swetha, Jarrouj, George, Gomez, Christopher M., Baird, Brandon J.

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Overexpression of the autism candidate gene Cyfip1 pathologically enhances olivo-cerebellar signaling in mice von Busch, Silas E, Simmons, Dana H, Gama, Eric, Du, Xiaofei, Longo, Francesco, Gomez, Christopher M, Klann, Eric, Hansel, Christian

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Dystonia and ataxia progression in spinocerebellar ataxias von Kuo, Pei-Hsin, Gan, Shi-Rui, Wang, Jie, Lo, Raymond Y., Figueroa, Karla P., Tomishon, Darya, Pulst, Stefan M., Perlman, Susan, Wilmot, George, Gomez, Christopher M., Schmahmann, Jeremy D., Paulson, Henry, Shakkottai, Vikram G., Ying, Sarah H., Zesiewicz, Theresa, Bushara, Khalaf, Geschwind, Michael D., Xia, Guangbin, Subramony, S.H., Ashizawa, Tetsuo, Kuo, Sheng-Han

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CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity von Perez, Barbara A, Shorrock, Hannah K, Banez‐Coronel, Monica, Zu, Tao, Romano, Lisa EL, Laboissonniere, Lauren A, Reid, Tammy, Ikeda, Yoshio, Reddy, Kaalak, Gomez, Christopher M, Bird, Thomas, Ashizawa, Tetsuo, Schut, Lawrence J, Brusco, Alfredo, Berglund, J Andrew, Hasholt, Lis F, Nielsen, Jorgen E, Subramony, SH, Ranum, Laura PW

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Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels von Watase, Kei, Barrett, Curtis F, Miyazaki, Taisuke, Ishiguro, Taro, Ishikawa, Kinya, Hu, Yuanxin, Unno, Toshinori, Sun, Yaling, Kasai, Sayumi, Watanabe, Masahiko, Gomez, Christopher M, Mizusawa, Hidehiro, Tsien, Richard W, Zoghbi, Huda Y

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The Initial Symptom and Motor Progression in Spinocerebellar Ataxias von Luo, Lan, Wang, Jie, Lo, Raymond Y, Figueroa, Karla P, Pulst, Stefan M, Kuo, Pei-Hsin, Perlman, Susan, Wilmot, George, Gomez, Christopher M, Schmahmann, Jeremy D., Paulson, Henry, Shakkottai, Vikram G, Ying, Sarah H, Zesiewicz, Theresa, Bushara, Khalaf, Geschwind, Michael, Xia, Guangbin, Subramony, S H, Ashizawa, Tetsuo, Kuo, Sheng-Han

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Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean von Rodríguez-Labrada, Roberto, Martins, Ana Carolina, Magaña, Jonathan J., Vazquez-Mojena, Yaimeé, Medrano-Montero, Jacqueline, Fernandez-Ruíz, Juan, Cisneros, Bulmaro, Teive, Helio, McFarland, Karen N., Saraiva-Pereira, Maria Luiza, Cerecedo-Zapata, César M., Gomez, Christopher M., Ashizawa, Tetsuo, Velázquez-Pérez, Luis, Jardim, Laura Bannach

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Cerebrospinal Fluid Biomarkers in Spinocerebellar Ataxia: A Pilot Study von Brouillette, Ashley M., Gomez, Christopher M., Öz, Gülin

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Hereditary Cerebellar Ataxia Progressively Impairs Force Adaptation During Goal-Directed Arm Movements von Maschke, Matthias, Gomez, Christopher M, Ebner, Timothy J, Konczak, Jurgen

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A non-synonymous single nucleotide polymorphism in SIRT6 predicts neurological severity in Friedreich ataxia von Rodden, Layne N., Rummey, Christian, Dong, Yi Na, Lagedrost, Sarah, Regner, Sean, Brocht, Alicia, Bushara, Khalaf, Delatycki, Martin B., Gomez, Christopher M., Mathews, Katherine, Murray, Sarah, Perlman, Susan, Ravina, Bernard, Subramony, S. H., Wilmot, George, Zesiewicz, Theresa, Bolotta, Alessandra, Domissy, Alain, Jespersen, Christine, Ji, Baohu, Soragni, Elisabetta, Gottesfeld, Joel M., Lynch, David R.

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The cerebellum in health and disease von Gomez, Christopher M.

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Distinct Neurochemical Profiles of Spinocerebellar Ataxias 1, 2, 6, and Cerebellar Multiple System Atrophy von Öz, Gülin, Iltis, Isabelle, Hutter, Diane, Thomas, William, Bushara, Khalaf O., Gomez, Christopher M.

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Stable respiratory activity requires both P/Q-type and N-type voltage-gated calcium channels von Koch, Henner, Zanella, Sebastien, Elsen, Gina E, Smith, Lincoln, Doi, Atsushi, Garcia, 3rd, Alfredo J, Wei, Aguan D, Xun, Randy, Kirsch, Sarah, Gomez, Christopher M, Hevner, Robert F, Ramirez, Jan-Marino

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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13) von Figueroa, Karla P, Waters, Michael F, Garibyan, Vartan, Bird, Thomas D, Gomez, Christopher M, Ranum, Laura P W, Minassian, Natali A, Papazian, Diane M, Pulst, Stefan M

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