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Publications for David F. Kronn david_kronn@nymc.edu

NYMC School of Medicine

  • Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., . . Kronn, D. (2016). 221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the inborn errors of metabolism collaborative. Molecular Genetics and Metabolism, 119(1-2), 75-82. doi:10.1016/j.ymgme.2016.07.002

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  • Hahn, S., Pena, L., Day, J. W., Gambello, M., Gibson, J. B., Kronn, D., . . . Pompe ADVANCE Study Consortium. (2016). 52-week efficacy and safety profile of alglucosidase alfa produced at 4000 liter scale in US patients with Pompe disease: ADVANCE, a phase 4 open-label prospective study. Molecular Genetics and Metabolism, 117(2), S54. doi:10.1016/j.ymgme.2015.12.281

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  • Kishnani, P. S., Day, J. W., Gambello, M., Gibson, J. B., Hillman, R., Kronn, D., . . . Pompe ADVANCE Study Consortium. (2016). Clinical characteristics and genotypes in the ADVANCE baseline dataset, a comprehensive cohort of US children and youth with pompe disease. Molecular Genetics and Metabolism, 117(2), S68. doi:10.1016/j.ymgme.2015.12.323

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  • Kishnani, P. S., Hahn, S., Day, J. W., Gambello, M. J., Gibson, J. B., Kronn D., . . . Pompe ADVANCE Study Consortium. (2016). Infusion-associated reactions and immunogenicity in the advance study of alglucosidase alfa produced at 4000 L scale in patients with Pompe disease. Molecular Genetics and Metabolism, 117(3), 265. This material can be found here.

  • Kronn, D., Gottesdiener, L., Marrero-Stein, V., Stein, M., & Banikazemi, M. (2016). Infantile onset Pompe disease: Sibling cases in the pre-newborn screening era. Molecular Genetics and Metabolism, 117(3), 266-267. This material can be found here.

  • Mofidi, S., & Kronn, D. (2016). Recurrent infection induces apparent liver failure in a female with chrullinemia type 1. Molecular Genetics and Metabolism, 117(3), 272. This material can be found here.

  • Vogel, B. H., Bradley, S. E., Adams, D. J., D'Aco, K., Erbe, R. W., Fong, C., . . . Kronn, D. (2015). Newborn screening for X-linked adrenoleukodystrophy in New York State: Diagnostic protocol, surveillance protocol and treatment guidelines. Molecular Genetics and Metabolism, 114(4), 599-603. doi:10.1016/j.ymgme.2015.02.002

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