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Universal screening for congenital hearing loss.
Garganta C, Seashore MR. Garganta C, et al. Pediatr Ann. 2000 May;29(5):302-8. doi: 10.3928/0090-4481-20000501-09. Pediatr Ann. 2000. PMID: 10826325 No abstract available.
Metabolic evaluation of the sick neonate.
Garganta CL, Smith WE. Garganta CL, et al. Semin Perinatol. 2005 Jun;29(3):164-72. doi: 10.1053/j.semperi.2005.04.009. Semin Perinatol. 2005. PMID: 16114579 Review.
A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.
Arnold GL, Koeberl DD, Matern D, Barshop B, Braverman N, Burton B, Cederbaum S, Fiegenbaum A, Garganta C, Gibson J, Goodman SI, Harding C, Kahler S, Kronn D, Longo N. Arnold GL, et al. Among authors: garganta c. Mol Genet Metab. 2008 Apr;93(4):363-70. doi: 10.1016/j.ymgme.2007.11.002. Epub 2007 Dec 21. Mol Genet Metab. 2008. PMID: 18155630
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
Arnold GL, Van Hove J, Freedenberg D, Strauss A, Longo N, Burton B, Garganta C, Ficicioglu C, Cederbaum S, Harding C, Boles RG, Matern D, Chakraborty P, Feigenbaum A. Arnold GL, et al. Among authors: garganta c. Mol Genet Metab. 2009 Mar;96(3):85-90. doi: 10.1016/j.ymgme.2008.09.008. Epub 2009 Jan 20. Mol Genet Metab. 2009. PMID: 19157942 Free PMC article.
Newborn Screening for Glutaric Aciduria-II: The New England Experience.
Sahai I, Garganta CL, Bailey J, James P, Levy HL, Martin M, Neilan E, Phornphutkul C, Sweetser DA, Zytkovicz TH, Eaton RB. Sahai I, et al. Among authors: garganta cl. JIMD Rep. 2014;13:1-14. doi: 10.1007/8904_2013_262. Epub 2013 Nov 5. JIMD Rep. 2014. PMID: 24190796 Free PMC article.
30 results