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498 results

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Page 1
Expanded newborn screening identifies maternal primary carnitine deficiency.
Schimmenti LA, Crombez EA, Schwahn BC, Heese BA, Wood TC, Schroer RJ, Bentler K, Cederbaum S, Sarafoglou K, McCann M, Rinaldo P, Matern D, di San Filippo CA, Pasquali M, Berry SA, Longo N. Schimmenti LA, et al. Among authors: pasquali m. Mol Genet Metab. 2007 Apr;90(4):441-5. doi: 10.1016/j.ymgme.2006.10.003. Epub 2006 Nov 28. Mol Genet Metab. 2007. PMID: 17126586
Genotype-phenotype correlation in primary carnitine deficiency.
Rose EC, di San Filippo CA, Ndukwe Erlingsson UC, Ardon O, Pasquali M, Longo N. Rose EC, et al. Among authors: pasquali m. Hum Mutat. 2012 Jan;33(1):118-23. doi: 10.1002/humu.21607. Epub 2011 Oct 11. Hum Mutat. 2012. PMID: 21922592 Free PMC article.
Newborn screening and inborn errors of metabolism.
Pasquali M, Longo N. Pasquali M, et al. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):1-2. doi: 10.1002/ajmg.c.30290. Epub 2011 Feb 10. Am J Med Genet C Semin Med Genet. 2011. PMID: 21337697 No abstract available.
Carnitine transport and fatty acid oxidation.
Longo N, Frigeni M, Pasquali M. Longo N, et al. Among authors: pasquali m. Biochim Biophys Acta. 2016 Oct;1863(10):2422-35. doi: 10.1016/j.bbamcr.2016.01.023. Epub 2016 Jan 29. Biochim Biophys Acta. 2016. PMID: 26828774 Free PMC article. Review.
Prospective identification by neonatal screening of patients with guanidinoacetate methyltransferase deficiency.
Hart K, Rohrwasser A, Wallis H, Golsan H, Shao J, Anderson T, Wang X, Szabo-Fresnais N, Morrissey M, Kay DM, Wojcik M, Galvin-Parton PA, Longo N, Caggana M, Pasquali M. Hart K, et al. Among authors: pasquali m. Mol Genet Metab. 2021 Sep-Oct;134(1-2):60-64. doi: 10.1016/j.ymgme.2021.07.012. Epub 2021 Jul 29. Mol Genet Metab. 2021. PMID: 34389248
498 results