Lee B - Search Results

1

Nutritional management of urea cycle disorders.

Singh RH, Rhead WJ, Smith W, Lee B, Sniderman King L, Summar M. Singh RH, et al. Among authors: lee b. Crit Care Clin. 2005 Oct;21(4 Suppl):S27-35. doi: 10.1016/j.ccc.2005.08.003. Crit Care Clin. 2005. PMID: 16227113 Review.

2

Urea-cycle disorders as a paradigm for inborn errors of hepatocyte metabolism.

Mian A, Lee B. Mian A, et al. Among authors: lee b. Trends Mol Med. 2002 Dec;8(12):583-9. doi: 10.1016/s1471-4914(02)02437-1. Trends Mol Med. 2002. PMID: 12470992 Review.

3

Differential utilization of systemic and enteral ammonia for urea synthesis in control subjects and ornithine transcarbamylase deficiency carriers.

Scaglia F, Marini J, Rosenberger J, Henry J, Garlick P, Lee B, Reeds P. Scaglia F, et al. Among authors: lee b. Am J Clin Nutr. 2003 Oct;78(4):749-55. doi: 10.1093/ajcn/78.4.749. Am J Clin Nutr. 2003. PMID: 14522733

4

Effect of alternative pathway therapy on branched chain amino acid metabolism in urea cycle disorder patients.

Scaglia F, Carter S, O'Brien WE, Lee B. Scaglia F, et al. Among authors: lee b. Mol Genet Metab. 2004 Apr;81 Suppl 1:S79-85. doi: 10.1016/j.ymgme.2003.11.017. Mol Genet Metab. 2004. PMID: 15050979

5

Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism.

Scaglia F, Brunetti-Pierri N, Kleppe S, Marini J, Carter S, Garlick P, Jahoor F, O'Brien W, Lee B. Scaglia F, et al. Among authors: lee b. J Nutr. 2004 Oct;134(10 Suppl):2775S-2782S; discussion 2796S-2797S. doi: 10.1093/jn/134.10.2775S. J Nutr. 2004. PMID: 15465784 Free article. Review.

6

Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency.

McBride KL, Miller G, Carter S, Karpen S, Goss J, Lee B. McBride KL, et al. Among authors: lee b. Pediatrics. 2004 Oct;114(4):e523-6. doi: 10.1542/peds.2004-0198. Pediatrics. 2004. PMID: 15466081

7

Unmasked adult-onset urea cycle disorders in the critical care setting.

Summar ML, Barr F, Dawling S, Smith W, Lee B, Singh RH, Rhead WJ, Sniderman King L, Christman BW. Summar ML, et al. Among authors: lee b. Crit Care Clin. 2005 Oct;21(4 Suppl):S1-8. doi: 10.1016/j.ccc.2005.05.002. Crit Care Clin. 2005. PMID: 16227111 Review.

8

Considerations in the difficult-to-manage urea cycle disorder patient.

Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith W, Summar ML. Lee B, et al. Crit Care Clin. 2005 Oct;21(4 Suppl):S19-25. doi: 10.1016/j.ccc.2005.05.001. Crit Care Clin. 2005. PMID: 16227112 Review.

9

Genetic counseling issues in urea cycle disorders.

Sniderman King L, Singh RH, Rhead WJ, Smith W, Lee B, Summar ML. Sniderman King L, et al. Among authors: lee b. Crit Care Clin. 2005 Oct;21(4 Suppl):S37-44. doi: 10.1016/j.ccc.2005.08.001. Crit Care Clin. 2005. PMID: 16227114 Review.

10

Urea cycle disorders: clinical presentation outside the newborn period.

Smith W, Kishnani PS, Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith M, Summar M. Smith W, et al. Among authors: lee b. Crit Care Clin. 2005 Oct;21(4 Suppl):S9-17. doi: 10.1016/j.ccc.2005.05.007. Crit Care Clin. 2005. PMID: 16227115 Review.

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