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Citation: O. Musumeci et al., Familial cerebellar ataxia with muscle coenzyme Q10 deficiency, NEUROLOGY, 56(7), 2001, pp. 849-855

Authors: Vladutiu, GD Slonim, AE

Citation: Gd. Vladutiu et Ae. Slonim, Combined biochemical and molecular diagnosis in blood of a common lipid myopathy, MUSCLE NERV, 23(11), 2000, pp. 1773-1775

Authors: Slonim, AE Bulone, L Damore, MB Goldberg, T Wingertzahn, MA McKinley, MJ

Citation: Ae. Slonim et al., A preliminary study of growth hormone therapy for Crohn's disease, N ENG J MED, 342(22), 2000, pp. 1633-1637

Authors: Slonim, AE Bulone, L Ritz, S Goldberg, T Chen, A Martiniuk, F

Citation: Ae. Slonim et al., Identification of two subtypes of infantile acid maltase deficiency, J PEDIAT, 137(2), 2000, pp. 283-285

Authors: Martiniuk, F Chen, A Donnabella, V Arvanitopoulos, E Slonim, AE Raben, N Plotz, P Rom, WN

Citation: F. Martiniuk et al., Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFRneg cell line, BIOC BIOP R, 276(3), 2000, pp. 917-923

Authors: Damore, ME Speiser, PW Slonim, AE New, MI Shanske, S Xia, WL Santorelli, FM DiMauro, S

Citation: Me. Damore et al., Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: Patient report and literature review, J PED END M, 12(2), 1999, pp. 207-213