MERRF Classification: Implications for Diagnosis and Clinical Trials von Finsterer, Josef, Zarrouk-Mahjoub, Sinda, Shoffner, John M.

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Oxidative phosphorylation defects and Alzheimer's disease von Shoffner, J M

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Response to ‘‘The Appalling Poling Saga’’ von Shoffner, John M.

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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain von Mecocci, Patrizia, MacGarvey, Usha, Kaufman, Allan E., Koontz, Deborah, Shoffner, John M., Wallace, Douglas C., Beal, M. Flint

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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age von Corral-Debrinski, Marisol, Horton, Terzah, Lott, Marie T, Shoffner, John M, Flint Beal, M, Wallace, Douglas C

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Tau Pathology in a Family with Dementia and a P301L Mutation in Tau von Mirra, Suzanne S, Murrell, Jill R, Gearing, Marla, Spillantini, Maria G, Goedert, Michel, Crowther, R Anthony, Levey, Allan I, Jones, Randi, Green, Joanne, Shoffner, John M, Wainer, Bruce H, Schmidt, Marie L, Trojanowski, John Q, Ghetti, Bernardino

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Maternal inheritance and the evaluation of oxidative phosphorylation diseases von Shoffner, John M

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Mitochondrial DNA Variants Observed in Alzheimer Disease and Parkinson Disease Patients von Shoffner, John M., Brown, Michael D., Torroni, Antonio, Lott, Marie T., Cabell, Margaret F., Mirra, Suzanne S., Beal, M.Flint, Yang, Chi-Chuan, Gearing, Marla, Salvo, Rino, Watts, Ray L., Juncos, Jorge L., Hansen, Lawrence A., Crain, Barbara J., Fayad, Michel, Reckord, Calvin L., Wallace, Douglas C.

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Abnormalities in Gastrointestinal Motility Are Associated With Diseases of Oxidative Phosphorylation in Children von Chitkara, Denesh K, Nurko, Samuel, Shoffner, John M, Buie, Timothy, Flores, Alejandro

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Conflict of Interest Statement Concerning “Developmental Regression and Mitochondrial Dysfunction in a Child With Autism” von Frye, Richard E., Zimmerman, Andrew W., Shoffner, John M.

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Mitochondrial DNA mutations in human degenerative diseases and aging von Wallace, Douglas C., Shoffner, John M., Trounce, Ian, Brown, Michael D., Ballinger, Scott W., Corral-Debrinski, Marisol, Horton, Terzah, Jun, Albert S., Lott, Marie T.

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Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation von Shoffner, John M., Brown, Michael D., Stugard, Carol, June, Albert S., Pollock, Stephen, Haas, Richard H., Kaufman, Allan, Koontz, Deborah, Kim, Yoon, Graham, Jennifer R., Smith, Edwin, Dixon, John, Wallace, Douglas C.

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Mitochondrial oxidative phosphorylation defects in parkinson's disease von Shoffner, John M., Watts, Ray L., Juncos, Jorge L., Torroni, Antonio, Wallace, Douglas C.

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Rod Photoreceptor Function in Children With Mitochondrial Disorders von Cooper, Linda L, Hansen, Ronald M, Darras, Basil T, Korson, Mark, Dougherty, Frances E, Shoffner, John M, Fulton, Anne B

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Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction von Wallace, D C, Lott, M T, Lezza, A M, Seibel, P, Voljavec, A S, Shoffner, J M

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Siblings With Leukoencephalopathy von Breningstall, Galen N., MD, Shoffner, John, MD, Patterson, Richard J., MD

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An Introduction: Oxidative Phosphorylation Diseases von Shoffner, John M.

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Oxidative Phosphorylation Disease Diagnosis von Shoffner, John M.

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Insulin resistance associated with maternally inherited diabetes and deafness von Gebhart, Suzanne S.P., Shoffner, John M., Koontz, Deborah, Kaufman, Allan, Wallace, Douglas

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Oxidative phosphorylation defect associated with primary adrenal insufficiency von North, Kathryn, Korson, Mark S., Krawiecki, Nicolas, Shoffner, John M., Holm, Ingrid A.

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