Mitochondrial Medicine and the Neurodegenerative Mitochondriopathies

by Swerdlow, Russell H.
Published 2009

Mitochondrial Manipulation and the Quest for Alzheimer's Treatments

by Swerdlow, Russell H.
Published 2015

Mitochondria and Parkinson's Disease

by Simon, David K., Chu, Charleen T., Swerdlow, Russell H.
Published 2011

Cytoplasmic hybrid (cybrid) cell lines as a practical model for mitochondriopathies

by Wilkins, Heather M., Carl, Steven M., Swerdlow, Russell H.
Published 2014

Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects

by Swerdlow, Russell H., Bothwell, Rebecca, Hutfles, Lewis, Burns, Jeffrey M., Reed, Gregory A.
Published 2016

Bioenergetic Dysfunction and Inflammation in Alzheimer’s Disease: A Possible Connection

by Wilkins, Heather M., Carl, Steven M., Greenlief, Alison C. S., Festoff, Barry W., Swerdlow, Russell H.
Published 2014

Mitochondrial Haplotypes Associated with Biomarkers for Alzheimer’s Disease

by Ridge, Perry G., Koop, Andre, Maxwell, Taylor J., Bailey, Matthew H., Swerdlow, Russell H., Kauwe, John S. K., Honea, Robyn A.
Published 2013

Altered neurochemical profile after traumatic brain injury: 1H-MRS biomarkers of pathological mechanisms

by Harris, Janna L, Yeh, Hung-Wen, Choi, In-Young, Lee, Phil, Berman, Nancy E, Swerdlow, Russell H, Craciunas, Sorin C, Brooks, William M
Published 2012

Mitochondrial metabolism in Parkinson's disease impairs quality control autophagy by hampering microtubule-dependent traffic

by Arduíno, Daniela M., Raquel Esteves, A., Cortes, Luísa, Silva, Diana F., Patel, Bindi, Grazina, Manuela, Swerdlow, Russell H., Oliveira, Catarina R., Cardoso, Sandra M.
Published 2012

GRK5 Deficiency Leads to Selective Basal Forebrain Cholinergic Neuronal Vulnerability

by He, Minchao, Singh, Prabhakar, Cheng, Shaowu, Zhang, Qiang, Peng, Wei, Ding, XueFeng, Li, Longxuan, Liu, Jun, Premont, Richard T., Morgan, Dave, Burns, Jeffery M., Swerdlow, Russell H., Suo, William Z.
Published 2016

Mutations in the colony stimulating factor 1 receptor (CSF1R) cause hereditary diffuse leukoencephalopathy with spheroids

by Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M., Rutherford, Nicola J., Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely, Adamson, Jennifer, Kouri, Naomi, Sundal, Christina, Shuster, Elizabeth A., Aasly, Jan, MacKenzie, James, Roeber, Sigrun, Kretzschmar, Hans A., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Cairns, Nigel J., Ghetti, Bernardino, Spina, Salvatore, Garbern, James, Tselis, Alexandros C., Uitti, Ryan, Das, Pritam, Van Gerpen, Jay A., Meschia, James F., Levy, Shawn, Broderick, Daniel F., Graff-Radford, Neill, Ross, Owen A., Miller, Bradley B., Swerdlow, Russell H., Dickson, Dennis W., Wszolek, Zbigniew K.
Published 2011