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PINK1 defect causes mitochondrial dysfunction, proteasomal deficit and alpha-synuclein aggregation in cell culture models of Parkinson's disease.
Liu W, Vives-Bauza C, Acín-Peréz- R, Yamamoto A, Tan Y, Li Y, Magrané J, Stavarache MA, Shaffer S, Chang S, Kaplitt MG, Huang XY, Beal MF, Manfredi G, Li C. Liu W, et al. Among authors: kaplitt mg. PLoS One. 2009;4(2):e4597. doi: 10.1371/journal.pone.0004597. Epub 2009 Feb 26. PLoS One. 2009. PMID: 19242547 Free PMC article.
Gene therapy for psychiatric disorders.
Gelfand Y, Kaplitt MG. Gelfand Y, et al. Among authors: kaplitt mg. World Neurosurg. 2013 Sep-Oct;80(3-4):S32.e11-8. doi: 10.1016/j.wneu.2012.12.028. Epub 2012 Dec 23. World Neurosurg. 2013. PMID: 23268195 Review.
Spectrum of ocular manifestations in CLN2-associated batten (Jansky-Bielschowsky) disease correlate with advancing age and deteriorating neurological function.
Orlin A, Sondhi D, Witmer MT, Wessel MM, Mezey JG, Kaminsky SM, Hackett NR, Yohay K, Kosofsky B, Souweidane MM, Kaplitt MG, D'Amico DJ, Crystal RG, Kiss S. Orlin A, et al. Among authors: kaplitt mg. PLoS One. 2013 Aug 28;8(8):e73128. doi: 10.1371/journal.pone.0073128. eCollection 2013. PLoS One. 2013. PMID: 24015292 Free PMC article. Clinical Trial.
Neurological deterioration in late infantile neuronal ceroid lipofuscinosis.
Worgall S, Kekatpure MV, Heier L, Ballon D, Dyke JP, Shungu D, Mao X, Kosofsky B, Kaplitt MG, Souweidane MM, Sondhi D, Hackett NR, Hollmann C, Crystal RG. Worgall S, et al. Among authors: kaplitt mg. Neurology. 2007 Aug 7;69(6):521-35. doi: 10.1212/01.wnl.0000267885.47092.40. Neurology. 2007. PMID: 17679671
123 results