Apoptosis and neurologic disease von Honig, Lawrence S, Rosenberg, Roger N

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Category fluency in mild cognitive impairment: Reduced effect of practice in test-retest conditions von COOPER, D. B, LACRITZ, L. H, WEINER, M. F, ROSENBERG, R. N, CULLUM, C. M

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Diagnostic investigation of patients with chronic polyneuropathy: evaluation of a clinical guideline von Rosenberg, N R, Portegies, P, de Visser, M, Vermeulen, M

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Platelet APP isoform ratios correlate with declining cognition in AD von BASKIN, F, ROSENBERG, R. N, IYER, L, HYNAN, L, CULLUM, C. M

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Should coeliac disease be considered in the work up of patients with chronic peripheral neuropathy? von Rosenberg, N R, Vermeulen, M

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Correlation of statin-increased platelet APP ratios and reduced blood lipids in AD patients von BASKIN, F, ROSENBERG, R. N, FANG, X, HYNAN, L. S, MOORE, C. B, WEINER, M, VEGA, G. L

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The molecular and genetic basis of AD: the end of the beginning: the 2000 Wartenberg lecture von Rosenberg, R N

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Machado-Joseph disease: An autosomal dominant motor system degeneration von Rosenberg, Roger N.

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Alzheimer's disease and its Lewy body variant: a clinical analysis of postmortem verified cases von WEINER, M. F, RISSER, R. C, CULLUM, M, HONIG, L, WHITE, C. III, SPECIALE, S, ROSENBERG, R. N

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Follow up of patients with signs and symptoms of polyneuropathy not confirmed by electrophysiological studies von Rosenberg, N R, Slotema, C W, Hoogendijk, J E, Vermeulen, M

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DNA-Triplet Repeats and Neurologic Disease von Rosenberg, Roger N

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At jeopardy: the NIH as we know it von Rosenberg, R.N

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Unexplained delayed nerve impairment in leprosy after treatment von Rosenberg, N R, Faber, W R, Vermeulen, M

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Altered apolipoprotein E secretion in cytokine treated human astrocyte cultures von Baskin, Fred, Smith, George M, Fosmire, Jennifer A, Rosenberg, Roger N

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Warren A. Weinberg, M.D. Chair in Pediatric Neurology and Learning von Rosenberg, Roger N.

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Editorial Governance of the Journal of the American Medical Association: A Report von Rosenberg, Roger N, Anderson, Jr, E. Ratcliffe

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Autosomal dominant progressive syndrome of motor-speech loss without dementia von CHAPMAN, S. B, ROSENBERG, R. N, WEINER, M. F, SHOBE, A

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Autosomal dominant cerebellar phenotypes: The genotype has settled the issue von Rosenberg, Roger N

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Reporting clinical trials: full access to all the data von Rosenberg, R N, Aminoff, M, Boller, F, Sørenson, P S, Griggs, R C, Hachinski, V, Hallett, M, Johnson, R T, Kennard, C, Lang, A E, Lees, A J, Lisak, R, Newsom-Davis, J, Pedley, T A, Selzer, M E, Zochodne, D

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Reporting clinical trials: full access to all the data von Rosenberg, R N, Aminoff, M, Boller, F, Soelberg, P, Griggs, R C, Hachinski, V, Hallett, M, Johnson, R T, Kennard, C, Lang, A E, Lees, A J, Lisak, R, Newsom-Davis, J, Pedley, T A, Selzer, M E, Zochodne, D

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