Koch R - Search Results

1

Phenylketonuria in adulthood: a collaborative study.

Koch R, Burton B, Hoganson G, Peterson R, Rhead W, Rouse B, Scott R, Wolff J, Stern AM, Guttler F, Nelson M, de la Cruz F, Coldwell J, Erbe R, Geraghty MT, Shear C, Thomas J, Azen C. Koch R, et al. J Inherit Metab Dis. 2002 Sep;25(5):333-46. doi: 10.1023/a:1020158631102. J Inherit Metab Dis. 2002. PMID: 12408183 Clinical Trial.

2

The Maternal Phenylketonuria International Study: 1984-2002.

Koch R, Hanley W, Levy H, Matalon K, Matalon R, Rouse B, Trefz F, Güttler F, Azen C, Platt L, Waisbren S, Widaman K, Ning J, Friedman EG, de la Cruz F. Koch R, et al. Pediatrics. 2003 Dec;112(6 Pt 2):1523-9. Pediatrics. 2003. PMID: 14654658 Clinical Trial.

3

Intellectual development in 12-year-old children treated for phenylketonuria.

Azen CG, Koch R, Friedman EG, Berlow S, Coldwell J, Krause W, Matalon R, McCabe E, O'Flynn M, Peterson R, et al. Azen CG, et al. Among authors: koch r. Am J Dis Child. 1991 Jan;145(1):35-9. doi: 10.1001/archpedi.1991.02160010037012. Am J Dis Child. 1991. PMID: 1985428 Clinical Trial.

4

A preliminary report of the collaborative study of maternal phenylketonuria in the United States and Canada.

Koch R, Hanley W, Levy H, Matalon R, Rouse B, Dela Cruz F, Azen C, Gross Friedman E. Koch R, et al. J Inherit Metab Dis. 1990;13(4):641-50. doi: 10.1007/BF01799519. J Inherit Metab Dis. 1990. PMID: 2122127 Clinical Trial.

5

The international collaborative study of maternal phenylketonuria: status report 1994.

Koch R, Levy HL, Matalon R, Rouse B, Hanley WB, Trefz F, Azen C, Friedman EG, de la Cruz F, Güttler F, et al. Koch R, et al. Acta Paediatr Suppl. 1994 Dec;407:111-9. doi: 10.1111/j.1651-2227.1994.tb13468.x. Acta Paediatr Suppl. 1994. PMID: 7766945 Clinical Trial.

6

Maternal PKU Collaborative Study: pregnancy outcome and postnatal head growth.

Matalon R, Michals K, Azen C, Friedman E, Koch R, Rouse B, Hanley WB, de la Cruz F. Matalon R, et al. Among authors: koch r. J Inherit Metab Dis. 1994;17(3):353-5. doi: 10.1007/BF00711828. J Inherit Metab Dis. 1994. PMID: 7807951 Clinical Trial. No abstract available.

7

The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993.

Koch R, Levy HL, Matalon R, Rouse B, Hanley W, Azen C. Koch R, et al. Am J Dis Child. 1993 Nov;147(11):1224-30. doi: 10.1001/archpedi.1993.02160350098015. Am J Dis Child. 1993. PMID: 8237918 Clinical Trial.

8

Summary of findings from the United States Collaborative Study of children treated for phenylketonuria.

Azen C, Koch R, Friedman E, Wenz E, Fishler K. Azen C, et al. Among authors: koch r. Eur J Pediatr. 1996 Jul;155 Suppl 1:S29-32. doi: 10.1007/BF03036507. Eur J Pediatr. 1996. PMID: 8828605 Clinical Trial.

9

The relationship of genotype to phenotype in phenylalanine hydroxylase deficiency.

Koch R, Fishler K, Azen C, Guldberg P, Güttler F. Koch R, et al. Biochem Mol Med. 1997 Apr;60(2):92-101. doi: 10.1006/bmme.1997.2577. Biochem Mol Med. 1997. PMID: 9169088

10

Neonatal neurological assessment of offspring in maternal phenylketonuria.

Waisbren SE, Chang P, Levy HL, Shifrin H, Allred E, Azen C, de la Cruz F, Hanley W, Koch R, Matalon R, Rouse B. Waisbren SE, et al. Among authors: koch r. J Inherit Metab Dis. 1998 Feb;21(1):39-48. doi: 10.1023/a:1005359313883. J Inherit Metab Dis. 1998. PMID: 9501268

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