Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutations von Werner, Klaus G.E., MD, PhD, Morel, Chantal F., MD, Kirton, Adam, MD, Benseler, Susanne M., MD, Shoffner, John M., MD, Addis, Jane B.L., BSc, Robinson, Brian H., PhD, Burrowes, Delilah M., MD, Blaser, Susan I., MD, Epstein, Leon G., MD, Feigenbaum, Annette S.J., MD

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MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation von Connolly, Barbara S., Feigenbaum, Annette S.J., Robinson, Brian H., Dipchand, Anne I., Simon, David K., Tarnopolsky, Mark A.

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Screening for Carriers of Tay-Sachs Disease among Ashkenazi Jews: A Comparison of DNA-Based and Enzyme-Based Tests von Triggs-Raine, Barbara L, Feigenbaum, Annette S.J, Natowicz, Marvin, Skomorowski, Marie-Anne, Schuster, Sheldon M, Clarke, Joe T.R, Mahuran, Don J, Kolodny, Edwin H, Gravel, Roy A

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