Long‐term edaravone efficacy in amyotrophic lateral sclerosis: Post‐hoc analyses of Study 19 (MCI186‐19) von Shefner, Jeremy, Heiman‐Patterson, Terry, Pioro, Erik P., Wiedau‐Pazos, Martina, Liu, Shawn, Zhang, Jeffrey, Agnese, Wendy, Apple, Stephen

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Categorization of the amyotrophic lateral sclerosis population via the clinical determinant of post‐onset ΔFS for study design and medical practice von Ludolph, Albert C., Corcia, Philippe, Desnuelle, Claude, Heiman‐Patterson, Terry, Mora, Jesus S., Mansfield, Colin D., Couratier, Philippe

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease von Alexander, Guillermo M, Heiman-Patterson, Terry D, Bearoff, Frank, Sher, Roger B, Hennessy, Laura, Terek, Shannon, Caccavo, Nicole, Cox, Gregory A, Philip, Vivek M, Blankenhorn, Elizabeth A

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Primary lateral sclerosis (PLS) functional rating scale: PLS‐specific clinimetric scale von Mitsumoto, Hiroshi, Chiuzan, Codruta, Gilmore, Madison, Zhang, Yuan, Simmons, Zachary, Paganoni, Sabrina, Kisanuki, Yasushi Y., Zinman, Lorne, Jawdat, Omar, Sorenson, Eric, Floeter, Mary Kay, Pioro, Erik P., Fernandes Filho, J. Americo M., Heitzman, Daragh, Fournier, Christina Nicole, Oskarsson, Bjorn, Heiman‐Patterson, Terry, Maragakis, Nicholas, Joyce, Nanette, Hayat, Ghazala, Nations, Sharon, Scelsa, Stephen, Walk, David, Elman, Lauren, Hupf, Jonathan, McHale, Brittany

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Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial von Wills, Anne-Marie, Dr, Hubbard, Jane, RD, Macklin, Eric A, PhD, Glass, Jonathan, Prof, Tandan, Rup, Prof, Simpson, Ericka P, MD, Brooks, Benjamin, Prof, Gelinas, Deborah, MD, Mitsumoto, Hiroshi, Prof, Mozaffar, Tahseen, Prof, Hanes, Gregory P, MD, Ladha, Shafeeq S, MD, Heiman-Patterson, Terry, Prof, Katz, Jonathan, MD, Lou, Jau-Shin, MD, Mahoney, Katy, BA, Grasso, Daniela, BA, Lawson, Robert, BS, Yu, Hong, MS, Cudkowicz, Merit, Prof

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Hereditary spastic paraplegia: gain-of-function mechanisms revealed by new transgenic mouse von Qiang, Liang, Piermarini, Emanuela, Muralidharan, Hemalatha, Yu, Wenqian, Leo, Lanfranco, Hennessy, Laura E, Fernandes, Silvia, Connors, Theresa, Yates, Philip L, Swift, Michelle, Zholudeva, Lyandysha V, Lane, Michael A, Morfini, Gerardo, Alexander, Guillermo M, Heiman-Patterson, Terry D, Baas, Peter W

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Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease von Heiman-Patterson, Terry D, Blankenhorn, Elizabeth P, Sher, Roger B, Jiang, Juliann, Welsh, Priscilla, Dixon, Meredith C, Jeffrey, Jeremy I, Wong, Philip, Cox, Gregory A, Alexander, Guillermo M

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Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III von Kaufmann, Petra, Thompson, John L.P., Levy, Gilberto, Buchsbaum, Richard, Shefner, Jeremy, Krivickas, Lisa S., Katz, Jonathan, Rollins, Yvonne, Barohn, Richard J., Jackson, Carlayne E., Tiryaki, Ezgi, Lomen-Hoerth, Catherine, Armon, Carmel, Tandan, Rup, Rudnicki, Stacy A., Rezania, Kourosh, Sufit, Robert, Pestronk, Alan, Novella, Steven P., Heiman-Patterson, Terry, Kasarskis, Edward J., Pioro, Erik P., Montes, Jacqueline, Arbing, Rachel, Vecchio, Darleen, Barsdorf, Alexandra, Mitsumoto, Hiroshi, Levin, Bruce

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Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges von Jerath, Nivedita U., Mankodi, Ami, Crawford, Thomas O., Grunseich, Christopher, Baloui, Hasna, Nnamdi‐Emeratom, Chioma, Schindler, Alice B., Heiman‐Patterson, Terry, Chrast, Roman, Shy, Michael E.

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Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosis von Deitch, Jeffrey S, Alexander, Guillermo M, Bensinger, Andrew, Yang, Steven, Jiang, Juliann T, Heiman-Patterson, Terry D

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Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686] von Brooks, Benjamin Rix, Heiman-Patterson, Terry, Wiedau-Pazos, Martina, Liu, Shawn, Zhang, Jeffrey, Apple, Stephen

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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy von Ajroud-Driss, Senda, Fecto, Faisal, Ajroud, Kaouther, Lalani, Irfan, Calvo, Sarah E., Mootha, Vamsi K., Deng, Han-Xiang, Siddique, Nailah, Tahmoush, Albert J., Heiman-Patterson, Terry D., Siddique, Teepu

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease von Guillermo M. Alexander, Terry D. Heiman-Patterson, Frank Bearoff, Roger B. Sher, Laura Hennessy, Shannon Terek, Nicole Caccavo, Gregory A. Cox, Vivek M. Philip, Elizabeth A. Blankenhorn

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Evaluation of Gastrointestinal Symptoms in an ALS Cohort (P10-8.007) von Empeno, Rizamarie, Furey, John, Heiman-Patterson, Terry

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A Review of Economic Studies of Amyotrophic Lateral Sclerosis (ALS) in the United States (P3-8.015) von Gautam, Anudeeta, Hollin, Ilene, Heiman-Patterson, Terry

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NIPPV: a treatment for ALS whose time has come von Heiman-Patterson, Terry D, Miller, Robert G

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Deep hypothermic circulatory arrest: I. Effects of cooling on electroencephalogram and evoked potentials von Stecker, Mark M, Cheung, Albert T, Pochettino, Alberto, Kent, Glenn P, Patterson, Terry, Weiss, Stuart J, Bavaria, Joseph E

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A Retrospective Review of Radicava Experience Across US ALS Centers (5056) von Heiman-Patterson, Terry, Furey, John, Yuen, Ezri

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Evaluation of Gastrointestinal Symptoms in an ALS Cohort (P3-13.004) von Empeno, Rizamarie, Naveed, Omer, Furey, John, Heiman-Patterson, Terry

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Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia von Fink, John K, Zhao, Xinping, Alvarado, David, Rainier, Shirley, Lemons, Rosemary, Hedera, Peter, Weber, Christian H, Tukel, Turgut, Apak, Memnune, Heiman-Patterson, Terry, Ming, Lei, Bui, Melanie

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