Phenylketonuria by van Spronsen, Francjan J., Blau, Nenad, Harding, Cary, Burlina, Alberto, Longo, Nicola, Bosch, Annet M.

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O 2 Activation by Metal Surfaces: Implications for Bonding and Reactivity on Heterogeneous Catalysts by Montemore, Matthew M, van Spronsen, Matthijs A, Madix, Robert J, Friend, Cynthia M

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The ReactorAFM: non-contact atomic force microscope operating under high-pressure and high-temperature catalytic conditions by Roobol, S B, Cañas-Ventura, M E, Bergman, M, van Spronsen, M A, Onderwaater, W G, van der Tuijn, P C, Koehler, R, Ofitserov, A, van Baarle, G J C, Frenken, J W M

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Brain dysfunction in phenylketonuria: Is phenylalanine toxicity the only possible cause? by van Spronsen, F. J, Hoeksma, Marieke, Reijngoud, Dirk-Jan

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Long-term dietary intervention with low Phe and/or a specific nutrient combination improve certain aspects of brain functioning in phenylketonuria (PKU) by Bruinenberg, Vibeke M, van Vliet, Danique, van der Goot, Els, Counotte, Danielle S, Kuhn, Mirjam, van Spronsen, Francjan J, van der Zee, Eddy A

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Impact of Phenylketonuria on the Serum Metabolome and Plasma Lipidome: A Study in Early-Treated Patients by Weerd, Jorine C van der, Wegberg, Annemiek M J van, Boer, Theo S, Engelke, Udo F H, Coene, Karlien L M, Wevers, Ron A, Bakker, Stephan J L, Blaauw, Pim de, Groen, Joost, Spronsen, Francjan J van, Heiner-Fokkema, M Rebecca

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Meta-analyses of cognitive functions in early-treated adults with phenylketonuria by Romani, Cristina, Olson, Andrew, Aitkenhead, Lynne, Baker, Lucy, Patel, Dhanesha, Spronsen, Francjan Van, MacDonald, Anita, Wegberg, Annemiek van, Huijbregts, Stephan

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Dried blood spot versus venous blood sampling for phenylalanine and tyrosine by van Vliet, Kimber, van Ginkel, Wiggert G, van Dam, Esther, de Blaauw, Pim, Koehorst, Martijn, Kingma, Hermi A, van Spronsen, Francjan J, Heiner-Fokkema, M Rebecca

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Patient's thoughts and expectations about centres of expertise for PKU by van Wegberg, A M J, MacDonald, A, Abeln, D, Hagedorn, T S, Lange, E, Trefz, F, van Vliet, D, van Spronsen, F J

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The increasing importance of LNAA supplementation in phenylketonuria at higher plasma phenylalanine concentrations by van Vliet, D., van der Goot, E., van Ginkel, W.G., van Faassen, H.J.R., de Blaauw, P., Kema, I.P., Heiner-Fokkema, M.R., van der Zee, E.A., van Spronsen, F.J.

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Glycomacropeptide: long-term use and impact on blood phenylalanine, growth and nutritional status in children with PKU by Daly, A, Evans, S, Chahal, S, Santra, S, Pinto, A, Jackson, R, Gingell, C, Rocha, J, Van Spronsen, F J, MacDonald, A

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Fluctuations in phenylalanine concentrations in phenylketonuria: A review of possible relationships with outcomes by Cleary, Maureen, Trefz, Friedrich, Muntau, Ania C., Feillet, François, van Spronsen, Francjan J., Burlina, Alberto, Bélanger-Quintana, Amaya, Giżewska, Maria, Gasteyger, Christoph, Bettiol, Esther, Blau, Nenad, MacDonald, Anita

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Inherited metabolic diseases and pregnancy by Spronsen, F.J., Smit, G.P.A., Erwich, J.J.H.M.

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Optimising amino acid absorption: essential to improve nitrogen balance and metabolic control in phenylketonuria by MacDonald, Anita, Singh, Rani H., Rocha, Júlio César, van Spronsen, Francjan J.

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Long-Term Outcomes and Practical Considerations in the Pharmacological Management of Tyrosinemia Type 1 by van Ginkel, Willem G., Rodenburg, Iris L., Harding, Cary O., Hollak, Carla E. M., Heiner-Fokkema, M. Rebecca, van Spronsen, Francjan J.

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The clinical relevance of novel biomarkers as outcome parameter in adults with phenylketonuria by Wegberg, A. M. J., Weerd, J. C., Engelke, U. F. H., Coene, K. L. M., Jahja, R., Bakker, S. J. L., Huijbregts, S. C. J., Wevers, R. A., Heiner‐Fokkema, M. R., Spronsen, F. J.

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Metabolic control during the neonatal period in phenylketonuria: associations with childhood IQ by Liemburg, Geertje B., Huijbregts, Stephan C. J., Rutsch, Frank, Feldmann, Reinhold, Jahja, Rianne, Weglage, Josef, Och, Ulrike, Burgerhof, Johannes G. M., van Spronsen, Francjan J.

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Long‐term safety of sapropterin in paediatric and adult individuals with phenylalanine hydroxylase deficiency: Final results of the Kuvan® Adult Maternal Paediatric European Regist... by Feillet, François, Arnoux, Jean‐Baptiste, Delgado, María Bueno, Burlina, Alberto, Chabrol, Brigitte, Kucuksayrac, Ece, Lagler, Florian B., Muntau, Ania C., Olsson, David, Paci, Sabrina, Rutsch, Frank, Spronsen, Francjan J.

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Consensus guidelines for the diagnosis and management of isolated sulfite oxidase deficiency and molybdenum cofactor deficiencies by Schwahn, Bernd C., Spronsen, Francjan, Misko, Albert, Pavaine, Julija, Holmes, Victoria, Spiegel, Ronen, Schwarz, Guenter, Wong, Flora, Horman, Alistair, Pitt, James, Sass, Jörn Oliver, Lubout, Charlotte

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The first European guidelines on phenylketonuria: Usefulness and implications for BH4 responsiveness testing by Evers, Roeland A. F., Wegberg, Annemiek M. J., Anjema, Karen, Lubout, Charlotte M. A., Dam, Esther, Vliet, Danique, Blau, Nenad, Spronsen, Francjan J.

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