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Items: 1 to 20 of 141

1.

Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study.

Levy HL, Guldberg P, Güttler F, Hanley WB, Matalon R, Rouse BM, Trefz F, Azen C, Allred EN, de la Cruz F, Koch R.

Pediatr Res. 2001 May;49(5):636-42.

PMID:
11328945
2.

Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome.

Güttler F, Azen C, Guldberg P, Romstad A, Hanley WB, Levy HL, Matalon R, Rouse BM, Trefz F, de la Cruz F, Koch R.

Pediatrics. 2003 Dec;112(6 Pt 2):1530-3.

PMID:
14654659
3.

Maternal phenylketonuria: a metabolic teratogen.

Levy HL, Ghavami M.

Teratology. 1996 Mar;53(3):176-84. Review.

PMID:
8761885
4.

Nutrient intake and congenital heart defects in maternal phenylketonuria.

Michals-Matalon K, Platt LD, Acosta P P, Azen C, Walla CA.

Am J Obstet Gynecol. 2002 Aug;187(2):441-4.

PMID:
12193940
5.

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.

J Pediatr. 2000 Jan;136(1):57-61.

PMID:
10636975
6.

Phenylketonuria: variable phenotypic outcomes of the R261Q mutation and maternal PKU in the offspring of a healthy homozygote.

Kleiman S, Vanagaite L, Bernstein J, Schwartz G, Brand N, Elitzur A, Woo SL, Shiloh Y.

J Med Genet. 1993 Apr;30(4):284-8.

7.

[The maternal phenylketonuria syndrom--still current problem].

Didycz B, Domagała L, Pietrzyk JJ.

Przegl Lek. 2009;66(1-2):4-10. Polish.

PMID:
19485248
8.

Maternal phenylketonuria: an international study.

Koch R, Hanley W, Levy H, Matalon R, Rouse B, Trefz F, Guttler F, Azen C, Friedman E, Platt L, de la Cruz F.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):233-9. Review.

PMID:
11001815
9.

Role of nutrition in pregnancy with phenylketonuria and birth defects.

Matalon KM, Acosta PB, Azen C.

Pediatrics. 2003 Dec;112(6 Pt 2):1534-6.

PMID:
14654660
10.
11.

Pregnancy experiences in the woman with mild hyperphenylalaninemia.

Levy HL, Waisbren SE, Güttler F, Hanley WB, Matalon R, Rouse B, Trefz FK, de la Cruz F, Azen CG, Koch R.

Pediatrics. 2003 Dec;112(6 Pt 2):1548-52.

PMID:
14654663
12.

The international study of pregnancy outcome in women with maternal phenylketonuria: report of a 12-year study.

Platt LD, Koch R, Hanley WB, Levy HL, Matalon R, Rouse B, Trefz F, de la Cruz F, Güttler F, Azen C, Friedman EG.

Am J Obstet Gynecol. 2000 Feb;182(2):326-33.

PMID:
10694332
13.

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.

JAMA. 2000 Feb 9;283(6):756-62.

PMID:
10683054
14.

Maternal phenylketonuria: report from the United Kingdom Registry 1978-97.

Lee PJ, Ridout D, Walter JH, Cockburn F.

Arch Dis Child. 2005 Feb;90(2):143-6.

15.

Effects of untreated maternal phenylketonuria and hyperphenylalaninemia on the fetus.

Levy HL, Waisbren SE.

N Engl J Med. 1983 Nov 24;309(21):1269-74.

PMID:
6633585
16.

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.

Acta Paediatr Suppl. 1994 Dec;407:111-9.

PMID:
7766945
17.

Maternal phenylketonuria in Western Australia: pregnancy outcomes and developmental outcomes in offspring.

Ng TW, Rae A, Wright H, Gurry D, Wray J.

J Paediatr Child Health. 2003 Jul;39(5):358-63.

PMID:
12887666
18.
19.

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.

Pediatrics. 1999 Aug;104(2 Pt 1):258-62.

PMID:
10429004
20.

Maternal non-phenylketonuric mild hyperphenylalaninemia.

Levy HL, Waisbren SE, Lobbregt D, Allred E, Leviton A, Koch R, Hanley WB, Rouse B, Matalon R, de la Cruz F.

Eur J Pediatr. 1996 Jul;155 Suppl 1:S20-5.

PMID:
8828603
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