| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult phenylketonuria outcome and management
|
Trefz, F.
|
|
2011
|
104 |
S |
p. S26-S30
5 p.
|
artikel
|
| 2 |
Cognitive, neurophysiological, neurological and psychosocial outcomes in early-treated PKU-patients: A start toward standardized outcome measurement across development
|
van Spronsen, F.J.
|
|
2011
|
104 |
S |
p. S45-S51
7 p.
|
artikel
|
| 3 |
Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies
|
Blau, Nenad
|
|
2011
|
104 |
S |
p. S2-S9
8 p.
|
artikel
|
| 4 |
Diurnal variations in blood phenylalanine of PKU infants under different feeding regimes
|
van Rijn, Margreet
|
|
2011
|
104 |
S |
p. S68-S72
5 p.
|
artikel
|
| 5 |
Does a lower carbohydrate protein substitute impact on blood phenylalanine control, growth and appetite in children with PKU?
|
Gokmen-Ozel, Hulya
|
|
2011
|
104 |
S |
p. S64-S67
4 p.
|
artikel
|
| 6 |
Editorial
|
Blau, Nenad
|
|
2011
|
104 |
S |
p. S1-
1 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2011
|
104 |
S |
p. IFC-
1 p.
|
artikel
|
| 8 |
Follow up of phenylketonuria patients
|
Demirkol, M.
|
|
2011
|
104 |
S |
p. S31-S39
9 p.
|
artikel
|
| 9 |
Neurological complications and behavioral problems in patients with phenylketonuria in a Follow-up Unit
|
González, María J.
|
|
2011
|
104 |
S |
p. S73-S79
7 p.
|
artikel
|
| 10 |
Nutrition in phenylketonuria
|
MacDonald, A.
|
|
2011
|
104 |
S |
p. S10-S18
9 p.
|
artikel
|
| 11 |
Optimized loading test to evaluate responsiveness to tetrahydrobiopterin (BH4) in Brazilian patients with phenylalanine hydroxylase deficiency
|
Nalin, Tatiéle
|
|
2011
|
104 |
S |
p. S80-S85
6 p.
|
artikel
|
| 12 |
Oxidative stress in phenylketonuric patients
|
Vargas, C.R.
|
|
2011
|
104 |
S |
p. S97-S99
3 p.
|
artikel
|
| 13 |
Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients
|
Rivera, Isabel
|
|
2011
|
104 |
S |
p. S86-S92
7 p.
|
artikel
|
| 14 |
Specific prebiotics in a formula for infants with Phenylketonuria
|
MacDonald, Anita
|
|
2011
|
104 |
S |
p. S55-S59
5 p.
|
artikel
|
| 15 |
Table of Contents
|
|
|
2011
|
104 |
S |
p. iii-iv
nvt p.
|
artikel
|
| 16 |
The G46S-hPAH mutant protein: A model to study the rescue of aggregation-prone PKU mutations by chaperones
|
Leandro, João
|
|
2011
|
104 |
S |
p. S40-S44
5 p.
|
artikel
|
| 17 |
The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: Evaluation of protocol and influence of baseline phenylalanine concentration
|
Anjema, K.
|
|
2011
|
104 |
S |
p. S60-S63
4 p.
|
artikel
|
| 18 |
The spectrum of phenylketonuria genotypes in the Armenian population: Identification of three novel mutant PAH alleles
|
Kostandyan, Natella
|
|
2011
|
104 |
S |
p. S93-S96
4 p.
|
artikel
|
| 19 |
Up to date knowledge on different treatment strategies for phenylketonuria
|
Bélanger-Quintana, Amaya
|
|
2011
|
104 |
S |
p. S19-S25
7 p.
|
artikel
|
| 20 |
Vitamin B12 deficiency and phenylketonuria
|
Walter, John H.
|
|
2011
|
104 |
S |
p. S52-S54
3 p.
|
artikel
|
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