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Results:
1-11
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Results: 11
Authors:
Levy, HL
Guldberg, P
Guttler, F
Hanley, WB
Matalon, R
Rouse, BM
Trefz, E
Azen, C
Allred, EN
de la Cruz, F
Koch, R
Citation: Hl. Levy et al., Congenital heart disease in maternal phenylketonuria: Report from the Maternal PKU Collaborative Study, PEDIAT RES, 49(5), 2001, pp. 636-642
Authors:
Acosta, PB
Matalon, K
Castiglioni, L
Rohr, FJ
Wenz, E
Austin, V
Azen, C
Citation: Pb. Acosta et al., Intake of major nutrients by women in the Maternal Phenylketonuria (MPKU) Study and effects on plasma phenylalanine concentrations, AM J CLIN N, 73(4), 2001, pp. 792-796
Authors:
Koch, R
Hanley, W
Levy, H
Matalon, R
Rouse, B
Trefz, F
Guttler, F
Azen, C
Friedman, E
Platt, L
de la Cruz, F
Citation: R. Koch et al., Maternal phenylketonuria: An international study, MOL GEN MET, 71(1-2), 2000, pp. 233-239
Authors:
Koch, R
Friedman, E
Azen, C
Hanley, W
Levy, H
Matalon, R
Rouse, B
Trefz, F
Waisbren, S
Michals-Matalon, K
Acosta, P
Guttler, F
Ullrich, K
Platt, L
de la Cruz, F
Citation: R. Koch et al., The international collaborative study of maternal phenylketonuria: status report 1998, EUR J PED, 159, 2000, pp. S156-S160
Authors:
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
Citation: Se. Waisbren et al., Outcome at age 4 years in offspring of women with maternal phenylketonuria- The maternal PKU collaborative study, J AM MED A, 283(6), 2000, pp. 756-762
Maternal phenylketonuria syndrome: Congenital heart defects, microcephaly,and developmental outcomes
Authors:
Rouse, B
Matalon, R
Koch, R
Azen, C
Levy, H
Hanley, W
Trefz, F
de la Cruz, F
Citation: B. Rouse et al., Maternal phenylketonuria syndrome: Congenital heart defects, microcephaly,and developmental outcomes, J PEDIAT, 136(1), 2000, pp. 57-61
Authors:
Platt, LD
Koch, R
Hanley, WB
Levy, HL
Matalon, R
Rouse, B
Trefz, F
de la Cruz, F
Guttler, F
Azen, C
Friedman, EG
Citation: Ld. Platt et al., The International Study of Pregnancy Outcome in Women with Maternal Phenylketonuria: Report of a 12-year study, AM J OBST G, 182(2), 2000, pp. 326-333
Authors:
Koch, R
Friedman, E
Azen, C
Hanley, W
Levy, H
Matalon, R
Rouse, B
Trefz, F
Waisbren, S
Michals-Matalon, K
Acosta, P
Guttler, F
Ullrich, K
Platt, L
de la Cruz, F
Citation: R. Koch et al., The international collaborative study of maternal phenylketonuria status report 1998, MENT RET D, 5(2), 1999, pp. 117-121
Authors:
Matalon, KM
Acosta, P
Azen, C
Matalon, R
Citation: Km. Matalon et al., Congenital heart disease in maternal phenylketonuria: Effects of blood phenylalanine and nutrient intake, MENT RET D, 5(2), 1999, pp. 122-124
Authors:
Guttler, F
Azen, C
Guldberg, P
Romstad, A
Hanley, WB
Levy, HL
Matalon, R
Rouse, BM
Trefz, F
de la Cruz, F
Koch, R
Citation: F. Guttler et al., Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: Report from the Maternal Phenylketonuria Collaborative Study, PEDIATRICS, 104(2), 1999, pp. 258-262
Authors:
Carmel, R
Green, R
Jacobsen, DW
Rasmussen, K
Florea, M
Azen, C
Citation: R. Carmel et al., Serum cobalamin, homocysteine, and methylmalonic acid concentrations in a multiethnic elderly population: ethnic and sex differences in cobalamin andmetabolite abnormalities, AM J CLIN N, 70(5), 1999, pp. 904-910
Risultati:
1-11
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