Feuchtbaum L - Search Results

1

Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.

Gallant NM, Leydiker K, Tang H, Feuchtbaum L, Lorey F, Puckett R, Deignan JL, Neidich J, Dorrani N, Chang E, Barshop BA, Cederbaum SD, Abdenur JE, Wang RY. Gallant NM, et al. Among authors: feuchtbaum l. Mol Genet Metab. 2012 May;106(1):55-61. doi: 10.1016/j.ymgme.2012.02.007. Epub 2012 Feb 9. Mol Genet Metab. 2012. PMID: 22424739

2

Neural tube defect prevalence in California (1990-1994): eliciting patterns by type of defect and maternal race/ethnicity.

Feuchtbaum LB, Currier RJ, Riggle S, Roberson M, Lorey FW, Cunningham GC. Feuchtbaum LB, et al. Genet Test. 1999;3(3):265-72. doi: 10.1089/109065799316572. Genet Test. 1999. PMID: 10495925

3

Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the California experience.

Feuchtbaum LB, Currier RJ, Lorey FW, Cunningham GC. Feuchtbaum LB, et al. Prenat Diagn. 2000 Apr;20(4):293-9. doi: 10.1002/(sici)1097-0223(200004)20:4<293::aid-pd801>3.0.co;2-o. Prenat Diagn. 2000. PMID: 10740201

4

California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometry.

Feuchtbaum L, Lorey F, Faulkner L, Sherwin J, Currier R, Bhandal A, Cunningham G. Feuchtbaum L, et al. Pediatrics. 2006 May;117(5 Pt 2):S261-9. doi: 10.1542/peds.2005-2633E. Pediatrics. 2006. PMID: 16735252

5

The context and approach for the California newborn screening short- and long-term follow-up data system: preliminary findings.

Feuchtbaum L, Dowray S, Lorey F. Feuchtbaum L, et al. Genet Med. 2010 Dec;12(12 Suppl):S242-50. doi: 10.1097/GIM.0b013e3181fe5d66. Genet Med. 2010. PMID: 21150370 Free article.

6

Extremely high phenylalanine levels in a newborn on parenteral nutrition: phenylketonuria in the neonatal intensive care unit.

Lin HJ, Kwong AM, Carter JM, Ferreira BF, Austin MF, Devarajan K, Coleman RJ, Feuchtbaum LB, Lorey F, Jonas AJ. Lin HJ, et al. Among authors: feuchtbaum lb. J Perinatol. 2011 Jul;31(7):507-10. doi: 10.1038/jp.2010.207. J Perinatol. 2011. PMID: 21712831 Review.

7

Birth prevalence of disorders detectable through newborn screening by race/ethnicity.

Feuchtbaum L, Carter J, Dowray S, Currier RJ, Lorey F. Feuchtbaum L, et al. Genet Med. 2012 Nov;14(11):937-45. doi: 10.1038/gim.2012.76. Epub 2012 Jul 5. Genet Med. 2012. PMID: 22766612 Free article.

8

Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database.

Lam C, Carter JM, Cederbaum SD, Neidich J, Gallant NM, Lorey F, Feuchtbaum L, Wong DA. Lam C, et al. Among authors: feuchtbaum l. Mol Genet Metab. 2013 Dec;110(4):477-83. doi: 10.1016/j.ymgme.2013.09.006. Epub 2013 Sep 17. Mol Genet Metab. 2013. PMID: 24103308

9

Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.

Hinton CF, Mai CT, Nabukera SK, Botto LD, Feuchtbaum L, Romitti PA, Wang Y, Piper KN, Olney RS. Hinton CF, et al. Among authors: feuchtbaum l. Genet Med. 2014 Jun;16(6):484-90. doi: 10.1038/gim.2013.177. Epub 2013 Dec 5. Genet Med. 2014. PMID: 24310309 Free PMC article.

10

Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening.

Merritt JL 2nd, Vedal S, Abdenur JE, Au SM, Barshop BA, Feuchtbaum L, Harding CO, Hermerath C, Lorey F, Sesser DE, Thompson JD, Yu A. Merritt JL 2nd, et al. Among authors: feuchtbaum l. Mol Genet Metab. 2014 Apr;111(4):484-92. doi: 10.1016/j.ymgme.2014.01.009. Epub 2014 Jan 23. Mol Genet Metab. 2014. PMID: 24503138

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