Thuy LP - Search Results

1

Thuy LP, Sweetman L, Nyhan WL. Thuy LP, et al. Clin Chim Acta. 1991 Oct 31;202(3):191-7. doi: 10.1016/0009-8981(91)90049-i. Clin Chim Acta. 1991. PMID: 1814646

2

Prenatal diagnosis of holocarboxylase synthetase deficiency by assay of the enzyme in chorionic villus material followed by prenatal treatment.

Thuy LP, Jurecki E, Nemzer L, Nyhan WL. Thuy LP, et al. Clin Chim Acta. 1999 Jun 15;284(1):59-68. doi: 10.1016/s0009-8981(99)00053-4. Clin Chim Acta. 1999. PMID: 10437643

3

High voltage electrophoresis of amino acids in urine containing ampicillin.

Thuy LP, Nyhan WL. Thuy LP, et al. Clin Biochem. 1993 Oct;26(5):389-90. doi: 10.1016/0009-9120(93)90115-m. Clin Biochem. 1993. PMID: 8299209

4

A screening method for cystine and homocystine in urine.

Thuy LP, Nyhan WL. Thuy LP, et al. Clin Chim Acta. 1992 Oct 30;211(3):175-9. doi: 10.1016/0009-8981(92)90193-t. Clin Chim Acta. 1992. PMID: 1458612 No abstract available.

5

A new quantitative assay for glycosaminoglycans.

Thuy LP, Nyhan WL. Thuy LP, et al. Clin Chim Acta. 1992 Nov 16;212(1-2):17-26. doi: 10.1016/0009-8981(92)90134-c. Clin Chim Acta. 1992. PMID: 1486678

6

Transport of the biotin dietary derivative biocytin (N-biotinyl-L-lysine) in rat small intestine.

Said HM, Thuy LP, Sweetman L, Schatzman B. Said HM, et al. Among authors: thuy lp. Gastroenterology. 1993 Jan;104(1):75-80. doi: 10.1016/0016-5085(93)90837-3. Gastroenterology. 1993. PMID: 8419264

7

Prenatal diagnosis and treatment of holocarboxylase synthetase deficiency.

Thuy LP, Belmont J, Nyhan WL. Thuy LP, et al. Prenat Diagn. 1999 Feb;19(2):108-12. doi: 10.1002/(sici)1097-0223(199902)19:2<108::aid-pd476>3.0.co;2-e. Prenat Diagn. 1999. PMID: 10215065

8

Deficiency of biotinyl-AMP synthetase activity in fibroblasts of patients with holocarboxylase synthetase deficiency.

Morita J, Thuy LP, Sweetman L. Morita J, et al. Among authors: thuy lp. Mol Genet Metab. 1998 Aug;64(4):250-5. doi: 10.1006/mgme.1998.2700. Mol Genet Metab. 1998. PMID: 9758715

9

Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.

Tuchman M, Berry SA, Thuy LP, Nyhan WL. Tuchman M, et al. Among authors: thuy lp. Pediatrics. 1993 Mar;91(3):664-6. Pediatrics. 1993. PMID: 8441580 No abstract available.

10

Management of a patient with holocarboxylase synthetase deficiency.

Van Hove JL, Josefsberg S, Freehauf C, Thomas JA, Thuy le P, Barshop BA, Woontner M, Mock DM, Chiang PW, Spector E, Meneses-Morales I, Cervantes-Roldán R, León-Del-Río A. Van Hove JL, et al. Mol Genet Metab. 2008 Dec;95(4):201-5. doi: 10.1016/j.ymgme.2008.09.006. Epub 2008 Oct 29. Mol Genet Metab. 2008. PMID: 18974016 Free PMC article.

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