Next-generation sequencing for detection of mutations associated with rare disorders in patients meeting diagnostic criteria for primary progressive multiple sclerosis von Weisfeld-Adams, J.D, Ludtke, A, Scott, S.A, Katzsand, I, Naik, H, Linderman, M.D, Paizan-Ruiz, C, Wasserstein, M.P, Shi, L, Brandt, T, McGraw, C.A, Kornreich, R, Farrell, C, Schadt, E.E, Lublin, F.D, Oksenberg, J.S

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Cerebral glucose metabolism in adults with early treated classic phenylketonuria von Wasserstein, M.P., Snyderman, S.E., Sansaricq, C., Buchsbaum, M.S.

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Whole-genome sequencing holds the key to the success of gene-targeted therapies von Vockley, J., Aartsma-Rus, A., Cohen, J.L., Cowsert, L.M., Howell, R.R., Yu, T.W., Wasserstein, M.P., Defay, T.

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Fabry Disease (α-Galactosidase A Deficiency): Renal Involvement and Enzyme Replacement Therapy von Desnick, R.J., Wasserstein, M.P., Banikazemi, M.

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