Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophy von DALI, C. I, HANSON, L. G, BARTON, N. W, FOGH, J, NAIR, N, LUND, A. M

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Quantitative analysis of epidermal innervation in Fabry disease von SCOTT, L. J. C, GRIFFIN, J. W, LUCIANO, C, BARTON, N. W, BANERJEE, T, CRAWFORD, T, MCARTHUR, J. C, TOURNAY, A, SCHIFFMANN, R

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Quantitative analysis of cerebral vasculopathy in patients with Fabry disease von CRUTCHFIELD, K. E, PATRONAS, N. J, DAMBROSIA, J. M, FREI, K. P, BANERJEE, T. K, BARTON, N. W, SCHIFFMANN, R

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Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease von Barton, Norman W, Brady, Roscoe O, Dambrosia, James M, Di Bisceglie, Adrian M, Doppelt, Samuel H, Hill, Suvimol C, Mankin, Henry J, Murray, Gary J, Parker, Robert I, Argoff, Charles E, Grewal, Raji P, Yu, Kian-Ti

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Risk factors for osteonecrosis in patients with Type 1 Gaucher's disease von RODRIGUE, S. W, ROSENTHAL, D. I, BARTON, N. W, ZURAKOWSKI, D, MANKIN, H. J

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Therapeutic Response to Intravenous Infusions of Glucocerebrosidase in a Patient with Gaucher Disease von Barton, Norman W., Furbish, F. Scott, Murray, Gary J., Garfield, Mark, Brady, Roscoe O.

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Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease von Schiffmann, Raphael, Heyes, Melvyn P., Aerts, J. M., Dambrosia, James M., Patterson, Marc C., DeGraba, Thomas, Parker, Colette C., Zirzow, Gregory C., Oliver, Katherine, Tedeschi, Gioacchino, Brady, Roscoe O., Barton, Norman W.

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Comparative Efficacy of Dose Regimens in Enzyme Replacement Therapy of Type I Gaucher Disease von Altarescu, G, Schiffmann, R, Parker, C.C, Moore, D.F, Kreps, C, Brady, R.O, Barton, N.W

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The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease von Altarescu, Gheona, Hill, Suvimol, Wiggs, Edyth, Jeffries, Neal, Kreps, Constance, Parker, Colette C., Brady, Roscoe O., Barton, Norman W., Schiffmann, Raphael

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Proton magnetic resonance spectroscopic imaging in the clinical evaluation of patients with Niemann-Pick type C disease von Tedeschi, G, Bonavita, S, Barton, N W, Bertolino, A, Frank, J A, Patronas, N J, Alger, J R, Schiffmann, R

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Gastrointestinal symptoms and delayed gastric emptying in Fabryʼs disease: Response to metoclopramide von ARGOFF, C E, BARTON, N W, BRADY, R O, ZIESSMAN, H A

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Management of Neutralizing Antibody to Ceredase in a Patient With Type 3 Gaucher Disease von Brady, Roscoe O, Murray, Gary J, Oliver, Katherine L, Leitman, Susan F, Sneller, Michael C, Fleisher, Thomas A, Barton, Norman W, Collaborators

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Leukodystrophy in patients with ovarian dysgenesis von Schiffmann, Raphael, Tedeschi, Gioacchino, Kinkel, R. Philip, Trapp, Bruce D., Frank, Joseph A., Kaneski, Christine R., Brady, Roscoe O., Barton, Norman W., Nelson, Lawrence, Yanovski, Jack A.

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Outcome of partial splenectomy for type I Gaucher disease von Zimran, A., Elstein, D., Schiffmann, R., Abrahamov, A., Goldberg, M., Bar-Maor, J.A., Brady, R.O., Guzzetta, P.C., Barton, N.W.

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Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination von Tedeschi, G, Schiffmann, R, Barton, N W, Shih, H H, Gospe, Jr, S M, Brady, R O, Alger, J R, Di Chiro, G

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Physiological characterization of neuropathy in Fabry's disease von Luciano, Carlos A., Russell, James W., Banerjee, Tapas K., Quirk, Jane M., Scott, Leland J.C., Dambrosia, James M., Barton, Norman W., Schiffmann, Raphael

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Dose-dependent responses to macrophage-targeted glucocerebrosidase in a child with Gaucher disease von Barton, Norman W., Brady, Roscoe O., Dambrosla, James M., Doppelt, Samuel H., Hill, Suvimol C., Holder, Carol A., Mankin, Henry J., Murray, Gary J., Zirzow, Gregory C., Parker, Robert I.

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Gaucher disease: a prototype for molecular medicine von Grabowski, Gregory A., Saal, Howard M., Wenstrup, Richard J., Barton, Norman W.

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Enzyme replacement therapy for Gaucher disease: skeletal responses to macrophage-targeted glucocerebrosidase von Rosenthal, D I, Doppelt, S H, Mankin, H J, Dambrosia, J M, Xavier, R J, McKusick, K A, Rosen, B R, Baker, J, Niklason, L T, Hill, S C

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Late onset globoid cell leukodystrophy von Grewal, R P, Petronas, N, Barton, N W

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