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A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition Garbern, James Y.; Neumann, Manuela; Trojanowski, John Q.; Lee, Virginia M. -Y.; Feldman, Gerald; Norris, Joy W.; Friez, Michael J.; Schwartz, Charles E.; Stevenson, Roger; Sima, Anders A. F. 分享 收藏
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Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1 Sima, Anders A. F.; Pierson, Christopher R.; Woltjer, Randall L.; Hobson, Grace M.; Golden, Jeffrey A.; Kupsky, William J.; Schauer, Galen M.; Bird, Thomas D.; Skoff, Robert P.; Garbern, James Y. 分享 收藏
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Peripheral neuropathy caused by proteolipid protein gene mutations Garbern, JY; Cambi, F; Lewis, R; Shy, M; Sima, A; Kraft, G; Vallat, JM; Bosch, EP; Hodes, ME; Dlouhy, S; Raskind, W; Bird, T; Macklin, W; Kamholz, J 分享 收藏
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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease Parchi, P; Castellani, R; Capellari, S; Ghetti, B; Young, K; Chen, SG; Farlow, M; Dickson, DW; Sima, AAF; Trojanowski, JQ; Petersen, RB; Gambetti, P 分享 收藏
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference Foster, NL; Wilhelmsen, K; Sima, AAF; Jones, MZ; DAmato, CJ; Gilman, S; Spillantini, MG; Lynch, T; Mayeux, RP; Gaskell, PC; Hulette, CM; PericakVance, MA; WelshBohmer, KA; Dickson, DW; Heutink, P; Kros, J; vanSwieten, JC; Arwert, F; Ghetti, MB; Murrell, J; Lannfelt, L; Hutton, M; Jones, M; Phelps, CH; Snyder, DS; Oliver, E; Ball, MJ; Cummings, JL; Miller, BL; Katzman, R; Reed, L; Schelper, RL; Landska, DJ; Brun, A; Fink, JK; Kuhl, DE; Knopman, DS; Wszolek, Z; Miller, CA; Bird, TD; Lendon, C; Elechi, C 分享 收藏
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