A Milestone in the Treatment of Ataxias: Approval of Omaveloxolone for Friedreich Ataxia von Subramony, S. H., Lynch, D. L.

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RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia von Zu, Tao, Liu, Yuanjing, Bañez-Coronel, Monica, Reid, Tammy, Pletnikova, Olga, Lewis, Jada, Miller, Timothy M, Harms, Matthew B, Falchook, Annet E, Subramony, S H, Ostrow, Lyle W, Rothstein, Jeffrey D, Troncoso, Juan C, Ranum, Laura P W

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New NBIA subtype: Genetic, clinical, pathologic, and radiographic features of MPAN von HOGARTH, Penelope, GREGORY, Allison, FOULDS, Nicola C, HAMMANS, Simon R, DESGUERRE, Isabelle, RODRIGUEZ, Diana, WILSON, Callum, DIEDRICH, Andrea, GREEN, Sarah, TRAN, Huong, REESE, Lindsay, WOLTJER, Randall L, KRUER, Michael C, HAYFLICK, Susan J, SANFORD, Lynn, WAGONER, Wendy, NATOWICZ, Marvin R, EGEL, Robert T, SUBRAMONY, S. H, GOLDMAN, Jennifer G, BERRY-KRAVIS, Elizabeth

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Frataxin analysis using triple quadrupole mass spectrometry: application to a large heterogeneous clinical cohort von Lynch, David R., Rojsajjakul, Teerapat, Subramony, S. H., Perlman, Susan L., Keita, Medina, Mesaros, Clementina, Blair, Ian A.

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SARA captures disparate progression and responsiveness in spinocerebellar ataxias von Petit, Emilien, Schmitz-Hübsch, Tanja, Coarelli, Giulia, Jacobi, Heike, Heinzmann, Anna, Figueroa, Karla P., Perlman, Susan L., Gomez, Christopher M., Wilmot, George R., Schmahmann, Jeremy D., Ying, Sarah H., Zesiewicz, Theresa A., Paulson, Henry L., Shakkottai, Vikram G., Bushara, Khalaf O., Kuo, Sheng-Han, Geschwind, Michael D., Xia, Guangbin, Pulst, Stefan M., Subramony, S. H., Ewenczyk, Claire, Brice, Alexis, Durr, Alexandra, Klockgether, Thomas, Ashizawa, Tetsuo, Tezenas du Montcel, Sophie

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Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed‐Start Analysis of the MOXIe Extension von Lynch, David R., Chin, Melanie P., Boesch, Sylvia, Delatycki, Martin B., Giunti, Paola, Goldsberry, Angie, Hoyle, J. Chad, Mariotti, Caterina, Mathews, Katherine D., Nachbauer, Wolfgang, O'Grady, Megan, Perlman, Susan, Subramony, S.H., Wilmot, George, Zesiewicz, Theresa, Meyer, Colin J.

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Subcutaneous IGF-1 is not beneficial in 2-year ALS trial von SORENSON, E. J, WINDBANK, A. J, FELDMAN, E, GLASS, J, GUTMANN, L, KATZ, J, KING, W, LUCIANO, C. A, MCCLUSKEY, L. F, NASH, S, NEWMAN, D. S, PASCUZZI, R. M, MANDREKAR, J. N, PIORO, E, SAMS, L. J, SCELSA, S, SIMPSON, E. P, SUBRAMONY, S. H, TIRYAKI, E, THORNTON, C. A, BAMLET, W. R, APPEL, S. H, ARMON, C, BARKHAUS, P. E, BOSCH, P, BOYLAN, K, DAVID, W. S

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Depression and clinical progression in spinocerebellar ataxias von Lo, Raymond Y, Figueroa, Karla P, Pulst, Stefan M, Perlman, Susan, Wilmot, George, Gomez, Christopher, Schmahmann, Jeremy, Paulson, Henry, Shakkottai, Vikram G, Ying, Sarah, Zesiewicz, Theresa, Bushara, Khalaf, Geschwind, Michael, Xia, Guangbin, Yu, Jui-Tsen, Lee, Lue-En, Ashizawa, Tetsuo, Subramony, S.H, 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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SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F von Ayhan, Fatma, Perez, Barbara A, Shorrock, Hannah K, Zu, Tao, Banez‐Coronel, Monica, Reid, Tammy, Furuya, Hirokazu, Clark, H Brent, Troncoso, Juan C, Ross, Christopher A, Subramony, SH, Ashizawa, Tetsuo, Wang, Eric T, Yachnis, Anthony T, Ranum, Laura PW

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Genome Modification Leads to Phenotype Reversal in Human Myotonic Dystrophy Type 1 Induced Pluripotent Stem Cell‐Derived Neural Stem Cells von Xia, Guangbin, Gao, Yuanzheng, Jin, Shouguang, Subramony, S.H., Terada, Naohiro, Ranum, Laura P.W., Swanson, Maurice S., Ashizawa, Tetsuo

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Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood von Sznajder, Łukasz J., Scotti, Marina M., Shin, Jihae, Taylor, Katarzyna, Ivankovic, Franjo, Nutter, Curtis A., Aslam, Faaiq N., Subramony, S. H., Ranum, Laura P. W., Swanson, Maurice S.

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Temporal Invariance in SCA6 Is Related to Smaller Cerebellar Lobule VI and Greater Disease Severity von Yacoubi, Basma, Casamento-Moran, Agostina, Burciu, Roxana G, Subramony, S H, Vaillancourt, David E, Christou, Evangelos A

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Generation of Human-Induced Pluripotent Stem Cells to Model Spinocerebellar Ataxia Type 2 In vitro von Xia, Guangbin, Santostefano, Katherine, Hamazaki, Takashi, Liu, Jilin, Subramony, S. H., Terada, Naohiro, Ashizawa, Tetsuo

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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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SPG7 and Impaired Emotional Communication von Zhang, Linwei, McFarland, Karen N., Subramony, S . H., Heilman, Kenneth M., Ashizawa, Tetsuo

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Long-term safety of dichloroacetate in congenital lactic acidosis von Abdelmalak, Monica, Lew, Alicia, Ramezani, Ryan, Shroads, Albert L., Coats, Bonnie S., Langaee, Taimour, Shankar, Meena N., Neiberger, Richard E., Subramony, S.H., Stacpoole, Peter W.

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Measuring Friedreich ataxia : Complementary features of examination and performance measures von LYNCH, D. R, FARMER, J. M, TSOU, A. Y, PERLMAN, S, SUBRAMONY, S. H, GOMEZ, C. M, ASHIZAWA, T, WILMOT, G. R, WILSON, R. B, BALCER, L. J

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Measuring the rate of progression in Friedreich ataxia: Implications for clinical trial design von Friedman, Lisa S., Farmer, Jennifer M., Perlman, Susan, Wilmot, George, Gomez, Christopher M., Bushara, Khalaf O., Mathews, Katherine D., Subramony, S. H., Ashizawa, Tetsuo, Balcer, Laura J., Wilson, Robert B., Lynch, David R.

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The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3 von Gan, Shi-Rui, Figueroa, Karla P., Xu, Hao-Ling, Perlman, Susan, Wilmot, George, Gomez, Christopher M., Schmahmann, Jeremy, Paulson, Henry, Shakkottai, Vikram G., Ying, Sarah H., Zesiewicz, Theresa, Bushara, Khalaf, Geschwind, Michael D., Xia, Guangbin, Subramony, S.H., Rosenthal, Liana, Ashizawa, Tetsuo, Pulst, Stefan M., Wang, Ning, Kuo, Sheng-Han

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