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Page 1
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'.
Hanley WB, Azen C, Koch R, Michals-Matalon K, Matalon R, Rouse B, Trefz F, Waisbren S, de la Cruz F. Hanley WB, et al. Among authors: michals matalon k. J Inherit Metab Dis. 2004;27(6):711-23. doi: 10.1023/B:BOLI.0000045758.86492.54. J Inherit Metab Dis. 2004. PMID: 15505376
Large neutral amino acids in the treatment of phenylketonuria (PKU).
Matalon R, Michals-Matalon K, Bhatia G, Grechanina E, Novikov P, McDonald JD, Grady J, Tyring SK, Guttler F. Matalon R, et al. Among authors: michals matalon k. J Inherit Metab Dis. 2006 Dec;29(6):732-8. doi: 10.1007/s10545-006-0395-8. Epub 2006 Sep 21. J Inherit Metab Dis. 2006. PMID: 16988900
Response of patients with phenylketonuria in the US to tetrahydrobiopterin.
Matalon R, Michals-Matalon K, Koch R, Grady J, Tyring S, Stevens RC. Matalon R, et al. Among authors: michals matalon k. Mol Genet Metab. 2005 Dec;86 Suppl 1:S17-21. doi: 10.1016/j.ymgme.2005.06.024. Epub 2005 Sep 6. Mol Genet Metab. 2005. PMID: 16143554 Clinical Trial.
Response of phenylketonuria to tetrahydrobiopterin.
Michals-Matalon K, Bhatia G, Guttler F, Tyring SK, Matalon R. Michals-Matalon K, et al. J Nutr. 2007 Jun;137(6 Suppl 1):1564S-1567S; discussion 1573S-1575S. doi: 10.1093/jn/137.6.1564S. J Nutr. 2007. PMID: 17513426 Free article.
Biopterin responsive phenylalanine hydroxylase deficiency.
Matalon R, Koch R, Michals-Matalon K, Moseley K, Surendran S, Tyring S, Erlandsen H, Gamez A, Stevens RC, Romstad A, Møller LB, Guttler F. Matalon R, et al. Genet Med. 2004 Jan-Feb;6(1):27-32. doi: 10.1097/01.gim.0000108840.17922.a7. Genet Med. 2004. PMID: 14726806 Clinical Trial.
28 results