Trefz F - Search Results

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: trefz f. J Inherit Metab Dis. 2004;27(6):711-23. doi: 10.1023/B:BOLI.0000045758.86492.54. J Inherit Metab Dis. 2004. PMID: 15505376

2

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. Among authors: trefz f. 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.

3

Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKU.

Lichter-Konecki U, Rupp A, Konecki DS, Trefz FK, Schmidt H, Burgard P. Lichter-Konecki U, et al. Among authors: trefz fk. J Inherit Metab Dis. 1994;17(3):362-5. doi: 10.1007/BF00711831. J Inherit Metab Dis. 1994. PMID: 7807954 Clinical Trial. No abstract available.

4

Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.

Guldberg P, Levy HL, Hanley WB, Koch R, Matalon R, Rouse BM, Trefz F, de la Cruz F, Henriksen KF, Güttler F. Guldberg P, et al. Among authors: trefz f. Am J Hum Genet. 1996 Jul;59(1):84-94. Am J Hum Genet. 1996. PMID: 8659548 Free PMC article.

5

The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sample.

Friedman EG, Koch R, Azen C, Levy H, Hanley W, Matalon R, Rouse B, Trefz F, de la Cruz F. Friedman EG, et al. Among authors: trefz f. Eur J Pediatr. 1996 Jul;155 Suppl 1:S158-61. doi: 10.1007/pl00014236. Eur J Pediatr. 1996. PMID: 8828635

6

Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994.

Koch R, Levy H, Hanley W, Matalon R, Rouse B, Trefz F, de la Cruz F. Koch R, et al. Among authors: trefz f. Eur J Pediatr. 1996 Jul;155 Suppl 1:S162-4. doi: 10.1007/pl00014238. Eur J Pediatr. 1996. PMID: 8828636

7

Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelae.

Rouse B, Azen C, Koch R, Matalon R, Hanley W, de la Cruz F, Trefz F, Friedman E, Shifrin H. Rouse B, et al. Among authors: trefz f. Am J Med Genet. 1997 Mar 3;69(1):89-95. doi: 10.1002/(sici)1096-8628(19970303)69:1<89::aid-ajmg17>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9066890

8

Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study.

Güttler F, Azen C, Guldberg P, Romstad A, Hanley WB, Levy HL, Matalon R, Rouse BM, Trefz F, de la Cruz F, Koch R. Güttler F, et al. Among authors: trefz f. Pediatrics. 1999 Aug;104(2 Pt 1):258-62. doi: 10.1542/peds.104.2.258. Pediatrics. 1999. PMID: 10429004

9

Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomes.

Rouse B, Matalon R, Koch R, Azen C, Levy H, Hanley W, Trefz F, de la Cruz F. Rouse B, et al. Among authors: trefz f. J Pediatr. 2000 Jan;136(1):57-61. doi: 10.1016/s0022-3476(00)90050-7. J Pediatr. 2000. PMID: 10636975

10

Outcome at age 4 years in offspring of women with maternal phenylketonuria: the Maternal PKU Collaborative Study.

Waisbren SE, Hanley W, Levy HL, Shifrin H, Allred E, Azen C, Chang PN, Cipcic-Schmidt S, de la Cruz F, Hall R, Matalon R, Nanson J, Rouse B, Trefz F, Koch R. Waisbren SE, et al. Among authors: trefz f. JAMA. 2000 Feb 9;283(6):756-62. doi: 10.1001/jama.283.6.756. JAMA. 2000. PMID: 10683054

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