Learning From the Exception and Not the Rule: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype von Fournier, Christina N

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Considerations for Amyotrophic Lateral Sclerosis (ALS) Clinical Trial Design von Fournier, Christina N.

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AIMing for Better Tools to Track Disease Progression von Fournier, Christina N.

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Unintended Consequences of Approving Unproven Treatments—Hope, Hype, or Harm? von Glass, Jonathan D, Fournier, Christina N

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Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS Clinic von Brand, David, Polak, Meraida, Glass, Jonathan D., Fournier, Christina N.

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Development and Validation of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) von Fournier, Christina N, Bedlack, Richard, Quinn, Colin, Russell, James, Beckwith, Diane, Kaminski, Kathleen H, Tyor, William, Hertzberg, Vicki, James, Virginia, Polak, Meraida, Glass, Jonathan D

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Chinese validation of the Rasch‐Built Overall Amyotrophic Lateral Sclerosis Disability Scale von Sun, Can, Fournier, Christina N., Ye, Shan, Zhang, Nan, Ma, Yan, Fan, Dongsheng

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Tau deposition in the spinal cord is not specific for CTE-ALS von Fournier, Christina N., Gearing, Marla, Glass, Jonathan D.

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The gut microbiome and neuroinflammation in amyotrophic lateral sclerosis? Emerging clinical evidence von Fournier, Christina N., Houser, Madelyn, Tansey, Malú G., Glass, Jonathan D., Hertzberg, Vicki Stover

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Head injury does not alter disease progression or neuropathologic outcomes in ALS von Fournier, Christina N, Gearing, Marla, Upadhyayula, Saila R, Klein, Mitch, Glass, Jonathan D

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Reader response: Pathologic Thr 175 tau phosphorylation in CTE and CTE with ALS von Glass, Jonathan D, Fournier, Christina N, Gearing, Marla

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Infection rate, mortality and characteristics of veterans with amyotrophic lateral sclerosis with COVID‐19 von Galea, Marinella D., Galea, Vincent P., Eberhart, Adam C., Patwa, Huned S., Howard, Ileana, Fournier, Christina N., Bedlack, Richard S.

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Longitudinal comparison of the self‐entry Amyotrophic Lateral Sclerosis Functional Rating Scale‐Revised (ALSFRS‐RSE) and Rasch‐Built Overall Amyotrophic Lateral Sclerosis Disabilit... von Johnson, Stephen A., Burke, Katherine M., Scheier, Zoe A., Keegan, Mackenzie A., Clark, Alison P., Chan, James, Fournier, Christina N., Berry, James D.

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TDP-43 cytoplasmic inclusion formation is disrupted in C9orf72-associated amyotrophic lateral sclerosis/frontotemporal lobar degeneration von Lee, Samuel M, Asress, Seneshaw, Hales, Chadwick M, Gearing, Marla, Vizcarra, Juan C, Fournier, Christina N, Gutman, David A, Chin, Lih-Shen, Li, Lian, Glass, Jonathan D

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ANNA-1 (anti-Hu) associated sensory neuronopathy with malignant mixed mullerian tumor von Fournier, Christina N., Kalra, Aarti, Lachance, Daniel H., Zarwan, Corinne, Srinivasan, Jayashri

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Rehabilitation is [still] necessary to optimize function in neuromuscular disorders von Omura, Jaclyn, Stratton, Anne, Fournier, Christina, Howard, Ileana

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Rehabilitation is still necessary to optimize function in neuromuscular disorders von Omura, Jaclyn, Stratton, Anne, Fournier, Christina, Howard, Ileana

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Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS Clinic von Brand, David, Polak, Meraida, Glass, Jonathan D., Fournier, Christina N.

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Application of Rasch Analysis for Measurement of Disability in Multiple Sclerosis (P9-3.018) von Azad, Nadia, Tarr, Andrew, Fournier, Christina, Tyor, William

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Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS Clinic von Brand, David, Polak, Meraida, Glass, Jonathan D., Fournier, Christina N.

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