Disparities in Genetic Testing for Neurologic Disorders
Baldwin, Aaron, Copeland, Juliette, Azage, Meron, Dratch, Laynie, Johnson, Kelsey, Paul, Rachel A, Amado, Defne A, Baer, Michael, Deik, Andres, Elman, Lauren B, Guo, Michael, Hamedani, Ali G, Irwin, David J, Lasker, Aaron, Orthmann-Murphy, Jennifer, Quinn, Colin C, Tropea, Thomas F, Scherer, Steven S, Shinohara, Russell T, Hamilton, Roy H, Ellis, Colin A
Published in Neurology (26.03.2024)
Published in Neurology (26.03.2024)
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Journal Article
Enhancing Clinical Infrastructure for the Delivery of Intrathecal and Genetic Therapies: A Qalsody (Tofersen) Model for Patients With SOD1 -ALS
Morganroth, Jennifer, Bardakjian, Tanya M, Dratch, Laynie, Quinn, Colin C, Elman, Lauren B
Published in Neurology. Clinical practice (01.08.2024)
Published in Neurology. Clinical practice (01.08.2024)
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Charcot-Marie-Tooth Disease Associated With a Novel Mutation in MFN2 Presenting With Subacute Vision Loss
Li, Yafeng, Aleman, Tomas S, Quinn, Colin C, Xia, Tian, Miller, Charles G, Kim, Benjamin J, Tamhankar, Madhura A
Published in Journal of neuro-ophthalmology (01.03.2022)
Published in Journal of neuro-ophthalmology (01.03.2022)
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Journal Article
Teaching NeuroImages: Ganglion cyst causing pure sensory ulnar neuropathy at the wrist
Karam, Chafic, Quinn, Colin C, Paganoni, Sabrina, David, William S
Published in Neurology (21.08.2012)
Published in Neurology (21.08.2012)
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C9orf72 repeat expansions modify risk for secondary motor and cognitive-behavioral symptoms in behavioral-variant frontotemporal degeneration and amyotrophic lateral sclerosis
Spencer, Barbara E, Xie, Sharon X, Elman, Lauren, Quinn, Colin C, Amado, Defne, Baer, Michael, Lee, Edward B, Van Deerlin, Vivianna M, Dratch, Laynie, Massimo, Lauren, Irwin, David J, McMillan, Corey T
Published in medRxiv : the preprint server for health sciences (19.09.2024)
Published in medRxiv : the preprint server for health sciences (19.09.2024)
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