• 427 Citations
  • 11 h-Index
19932018

Research output per year

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Publications

  • 427 Citations
  • 11 h-Index
  • 12 Article
  • 4 Review article
  • 1 Short survey
2018

Trisomies

Levy, P. A. & Marion, R. W., Feb 1 2018, In : Pediatrics in Review. 39, 2, p. 104-106 3 p.

Research output: Contribution to journalArticle

2016

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., Cameron, C. A., Hiner, S. J., Edick, M. J., Berry, S. A., Thomas, J., Dodge, M., Singh, R., Lakshman, S., Coakley, K., Stembridge, A., Russi, A. S., Phillips, E., Burton, B., Edano, C. & 62 others, Shrestha, S., Hoganson, G., Dwyer, L., Hainline, B., Romie, S., Hainline, S., Asamoah, A., Goodin, K., Rajakaruna, C., Jackson, K., Hamosh, A., Vernon, H., Smith, N., Ahmad, A., Lipinski, S., Feldman, G., Berry, S., Elsbecker, S., Bentler, K., Font-Montgomery, E., Peck, D., Pena, L. D. M., Koeberl, D. D., Jiang, Y. H., Kishnani, P. S., Rizzo, W., Dawson, M., Ambrose, N., Levy, P., Kronn, D., Fong, C. T., D'Aco, K., Hart, T., Erbe, R., Samons, M., Leslie, N., Powers, R., Bartholomew, D., Goff, M., vanCalcar, S., Hansen, J., Arnold, G., Vockley, J., Walsh-Vockley, C., Rhead, W., Dimmock, D., Engelking, P., Bird, C., Swan, A., Schwoerer, J. S., Henry, S., Narumanchi, T. C., Hummel, M., Wilkins, J., Davis-Keppen, L., Stein, Q., Loman, R., Cameron, C., Edick, M. J., Hiner, S. J., Justice, K. & Zhai, S., Sep 1 2016, In : Molecular Genetics and Metabolism. 119, 1-2, p. 75-82 8 p.

Research output: Contribution to journalArticle

5 Scopus citations

Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State

Wasserstein, M. P., Andriola, M., Arnold, G., Aron, A., Duffner, P., Erbe, R. W., Escolar, M. L., Estrella, L., Galvin-Parton, P., Iglesias, A., Kay, D. M., Kronn, D. F., Kurtzberg, J., Kwon, J. M., Langan, T. J., Levy, P. A., Naidich, T. P., Orsini, J. J., Pellegrino, J. E., Provenzale, J. M. & 2 others, Wenger, D. A. & Caggana, M., Dec 1 2016, In : Genetics in Medicine. 18, 12, p. 1235-1243 9 p.

Research output: Contribution to journalArticle

42 Scopus citations

Newborn screening for Krabbe disease in New York State: The first eight years' experience

Orsini, J. J., Kay, D. M., Saavedra-Matiz, C. A., Wenger, D. A., Duffner, P. K., Erbe, R. W., Biski, C., Martin, M., Krein, L. M., Nichols, M., Kurtzberg, J., Escolar, M. L., Adams, D. J., Arnold, G. L., Iglesias, A., Galvin-Parton, P., Kronn, D. F., Kwon, J. M., Levy, P. A., Pellegrino, J. E. & 3 others, Shur, N., Wasserstein, M. P. & Caggana, M., Mar 1 2016, In : Genetics in Medicine. 18, 3, p. 239-248 10 p.

Research output: Contribution to journalArticle

42 Scopus citations
2015

Newborn screening for X-linked adrenoleukodystrophy in New York State: Diagnostic protocol, surveillance protocol and treatment guidelines

Vogel, B. H., Bradley, S. E., Adams, D. J., D'Aco, K., Erbe, R. W., Fong, C., Iglesias, A., Kronn, D., Levy, P., Morrissey, M., Orsini, J., Parton, P., Pellegrino, J., Saavedra-Matiz, C. A., Shur, N., Wasserstein, M., Raymond, G. V. & Caggana, M., Apr 1 2015, In : Molecular Genetics and Metabolism. 114, 4, p. 599-603 5 p.

Research output: Contribution to journalArticle

41 Scopus citations
2012

Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening

Arnold, G. L., Salazar, D., Neidich, J. A., Suwannarat, P., Graham, B. H., Lichter-Konecki, U., Bosch, A. M., Cusmano-Ozog, K., Enns, G., Wright, E. L., Lanpher, B. C., Owen, N. N., Lipson, M. H., Cerone, R., Levy, P., Wong, L. J. C. & Dezsofi, A., Aug 2012, In : Molecular Genetics and Metabolism. 106, 4, p. 439-441 3 p.

Research output: Contribution to journalArticle

13 Scopus citations
2010

An overview of newborn screening

Levy, P. A., Sep 1 2010, In : Journal of Developmental and Behavioral Pediatrics. 31, 7, p. 622-631 10 p.

Research output: Contribution to journalReview article

35 Scopus citations

Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State

Arnold, G. L., Saavedra-Matiz, C. A., Galvin-Parton, P. A., Erbe, R., DeVincentis, E., Kronn, D., Mofidi, S., Wasserstein, M., Pellegrino, J. E., Levy, P. A., Adams, D. J., Nichols, M. & Caggana, M., Mar 1 2010, In : Molecular Genetics and Metabolism. 99, 3, p. 263-268 6 p.

Research output: Contribution to journalArticle

36 Scopus citations
2009

Enzyme replacement therapy in the home setting for mucopolysaccharidosis vi: A survey of patient characteristics and physicians' early findings in the united states

Tifft, C., Proud, V., Levy, P., DeMarco, K., Nicely, H. & Turbeville, S., Jan 1 2009, In : Journal of Infusion Nursing. 32, 1, p. 45-52 8 p.

Research output: Contribution to journalArticle

6 Scopus citations

Inborn errors of metabolism: Part 2: Specific disorders

Levy, P. A., Apr 1 2009, In : Pediatrics in review. 30, 4, p. e22-e28

Research output: Contribution to journalShort survey

15 Scopus citations

Inborn errors of metabolism: Part 1: Overview

Levy, P. A., Apr 1 2009, In : Pediatrics in review. 30, 4, p. 131-138 8 p.

Research output: Contribution to journalReview article

20 Scopus citations

Newborn Screening for Krabbe Disease: the New York State Model

Duffner, P. K., Caggana, M., Orsini, J. J., Wenger, D. A., Patterson, M. C., Crosley, C. J., Kurtzberg, J., Arnold, G. L., Escolar, M. L., Adams, D. J., Andriola, M. R., Aron, A. M., Ciafaloni, E., Djukic, A., Erbe, R. W., Galvin-Parton, P., Helton, L. E., Kolodny, E. H., Kosofsky, B. E., Kronn, D. F. & 8 others, Kwon, J. M., Levy, P. A., Miller-Horn, J., Naidich, T. P., Pellegrino, J. E., Provenzale, J. M., Rothman, S. J. & Wasserstein, M. P., Apr 1 2009, In : Pediatric Neurology. 40, 4, p. 245-252 8 p.

Research output: Contribution to journalReview article

139 Scopus citations
1998

Amniotic bands.

Levy, P. A., Jul 1998, In : Pediatrics in review / American Academy of Pediatrics. 19, 7, 1 p.

Research output: Contribution to journalReview article

17 Scopus citations

The advantage of phenylalanine to tyrosine ratio for the early detection of phenylketonuria

Levy, P. A., Miller, J. B. & Shapira, E., Feb 23 1998, In : Clinica Chimica Acta. 270, 2, p. 177-181 5 p.

Research output: Contribution to journalArticle

11 Scopus citations
1994

The awareness of chromosomal disarrangements in the evaluation of child psychiatry patients

Levy, P. A., Dalton, R. & Shapira, E., Jun 1994, In : Child Psychiatry and Human Development. 25, 4, p. 281-287 7 p.

Research output: Contribution to journalArticle

1 Scopus citations
1993

Heterogeneity and Variability of Inborn Errors of Metabolism

Levy, P. A. & Shapira, E., Mar 1993, In : American Journal of Diseases of Children. 147, 3, p. 265-266 2 p.

Research output: Contribution to journalArticle

3 Scopus citations

State of the Art of Biochemical Genetics

Levy, P. & Shapira, E., Nov 1993, In : American Journal of Diseases of Children. 147, 11, p. 1153-1158 6 p.

Research output: Contribution to journalArticle

1 Scopus citations