The complete European guidelines on phenylketonuria: diagnosis and treatment von van Wegberg, A M J, MacDonald, A, Ahring, K, Bélanger-Quintana, A, Blau, N, Bosch, A M, Burlina, A, Campistol, J, Feillet, F, Giżewska, M, Huijbregts, S C, Kearney, S, Leuzzi, V, Maillot, F, Muntau, A C, van Rijn, M, Trefz, F, Walter, J H, van Spronsen, F J

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PKU dietary handbook to accompany PKU guidelines von MacDonald, A., van Wegberg, A. M. J., Ahring, K., Beblo, S., Belanger-Quintana, A., Burlina, A., Campistol, J., Coskun, T., Feillet, F., Gizewska, M., Huijbregts, S. C., Leuzzi, V., Maillot, F., Muntau, A. C., Rocha, J. C., Romani, C., Trefz, F., van Spronsen, F. J.

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Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data von Trefz, K F, Muntau, A C, Kohlscheen, K M, Altevers, J, Jacob, C, Braun, S, Greiner, W, Jha, A, Jain, M, Alvarez, I, Lane, P, Schröder, C, Rutsch, F

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Correction to: PKU dietary handbook to accompany PKU guidelines von MacDonald, A, van Wegberg, A. M. J, Ahring, K, Beblo, S, Bélanger-Quintana, A, Burlina, A, Campistol, J, CoÅkun, T, Feillet, F, Giżewska, M, Huijbregts, S. C, Leuzzi, V, Maillot, F, Muntau, A. C, Rocha, J. C, Romani, C, Trefz, F, van Spronsen, F. J

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Hepatocyte Transplantation Using the Domino Concept in a Child with Tetrabiopterin Nonresponsive Phenylketonuria von Stéphenne, X., Debray, F. G., Smets, F., Jazouli, N., Sana, G., Tondreau, T., Menten, R., Goffette, P., Boemer, F., Schoos, R., Gersting, S. W., Najimi, M., Muntau, A. C., Goyens, P., Sokal, E. M.

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Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts von Taanman, Jan-Willem, Muddle, John R., Muntau, Ania C.

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Validation of MCADD newborn screening von Maier, EM, Pongratz, J, Muntau, AC, Liebl, B, Nennstiel-Ratzel, U, Busch, U, Fingerhut, R, Olgemöller, B, Roscher, AA, Röschinger, W

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Phenotype and genotype in 101 males with X-linked creatine transporter deficiency von van de Kamp, J M, Betsalel, O T, Mercimek-Mahmutoglu, S, Abulhoul, L, Grünewald, S, Anselm, I, Azzouz, H, Bratkovic, D, de Brouwer, A, Hamel, B, Kleefstra, T, Yntema, H, Campistol, J, Vilaseca, M A, Cheillan, D, D’Hooghe, M, Diogo, L, Garcia, P, Valongo, C, Fonseca, M, Frints, S, Wilcken, B, von der Haar, S, Meijers-Heijboer, H E, Hofstede, F, Johnson, D, Kant, S G, Lion-Francois, L, Pitelet, G, Longo, N, Maat-Kievit, J A, Monteiro, J P, Munnich, A, Muntau, A C, Nassogne, M C, Osaka, H, Ounap, K, Pinard, J M, Quijano-Roy, S, Poggenburg, I, Poplawski, N, Abdul-Rahman, O, Ribes, A, Arias, A, Yaplito-Lee, J, Schulze, A, Schwartz, C E, Schwenger, S, Soares, G, Sznajer, Y, Valayannopoulos, V, Van Esch, H, Waltz, S, Wamelink, M M C, Pouwels, P J W, Errami, A, van der Knaap, M S, Jakobs, C, Mancini, G M, Salomons, G S

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Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countries von Evers, R.A.F., van Wegberg, A.M.J., Ahring, K., Beblo, S., Bélanger-Quintana, A., Bosch, A.M., Burlina, A., Campistol, J., Coskun, T., Feillet, F., Giżewska, M., Huijbregts, S.C.J., Kearney, S., Langeveld, M., Leuzzi, V., Maillot, F., Muntau, A.C., Rocha, J.C., Romani, C., Trefz, F.K., MacDonald, A., van Spronsen, F.J.

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Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact von Toncheva, A. A., Potaczek, D. P., Schedel, M., Gersting, S. W., Michel, S., Krajnov, N., Gaertner, V. D., Klingbeil, J. M., Illig, T., Franke, A., Winkler, C., Hohlfeld, J. M., Vogelberg, C., Berg, A., Bufe, A., Heinzmann, A., Laub, O., Rietschel, E., Simma, B., Genuneit, J., Muntau, A. C., Kabesch, M.

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Fish oil supplementation improves visual evoked potentials in children with phenylketonuria von BEBLO, S, REINHARDT, H, MUNTAU, A. C, MUELLER-FELBER, W, ROSCHER, A. A, KOLETZKO, B

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Clinical Course, Early Diagnosis, Treatment, and Prevention of Disease in Glutaryl-CoA Dehydrogenase Deficiency von Hoffmann, G. F., Athanassopoulos, S., Burlina, A. B., Duran, M., Klerk, J. B., Lehnert, W., Leonard, J. V., Monavari, A. A., Müller, E., Muntau, A. C., Naughten, E. R., Plecko-Starting, B., Superti-Furga, A., Zschocke, J., Christensen, E.

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Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: Two novel cases von Linnebank, M., Lagler, F., Muntau, A. C., Röschinger, W., Olgemöller, B., Fowler, B., Koch, H. G.

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The challenges of managing coexistent disorders with phenylketonuria: 30 cases von MacDonald, A., Ahring, K., Almeida, M.F., Belanger-Quintana, A., Blau, N., Burlina, A., Cleary, M., Coskum, T., Dokoupil, K., Evans, S., Feillet, F., Giżewska, M., Gokmen Ozel, H., Lotz-Havla, A.S., Kamieńska, E., Maillot, F., Lammardo, A.M., Muntau, A.C., Puchwein-Schwepcke, A., Robert, M., Rocha, J.C., Santra, S., Skeath, R., Strączek, K., Trefz, F.K., van Dam, E., van Rijn, M., van Spronsen, F., Vijay, S.

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D‐2‐Hydroxyglutaric aciduria: Further clinical delineation von der Knaap, M. S., Jakobs, C., Hoffmann, G. F., Duran, M., Muntau, A. C., Schweitzer, S., Kelley, R. I., Parrot‐Roulaud, F., Amiel, J., De Lonlay, P., Rabier, D., Eeg‐Olofsson, O.

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T-cell-depleted peripheral blood stem cell transplantation for α-mannosidosis von ALBERT, M. H, SCHUSTER, F, SCHMID, I, PETERS, C, SCHULZE, S, PONTZ, B. F, MUNTAU, A. C, RÖSCHINGER, W, STACHEL, D. K, ENDERS, A, HAAS, R. J

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Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle von Röschinger, Wulf, Muntau, Ania C, Duran, Marinus, Dorland, Lambertus, IJlst, Lodewijk, Wanders, Ronald J.A, Roscher, Adelbert A

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Niemann-Pick Type C-2 Disease: Identification by Analysis of Plasma Cholestane-3β,5α,6β-Triol and Further Insight into the Clinical Phenotype von Reunert, J., Lotz-Havla, A. S., Polo, G., Kannenberg, F., Fobker, M., Griese, M., Mengel, E., Muntau, A. C., Schnabel, P., Sommerburg, O., Borggraefe, I., Dardis, A., Burlina, A. P., Mall, M. A., Ciana, G., Bembi, B., Burlina, A. B., Marquardt, T.

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Combined D-2- and L-2-Hydroxyglutaric Aciduria with Neonatal Onset Encephalopathy: A Third Biochemical Variant of 2-Hydroxyglutaric Aciduria? von Muntau, Ania C., Röschinger, W., Merkenschlager, A., van der Knaap, M. S., Jakobs, C., Duran, M., Hoffmann, G. F., Roscher, A. A.

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Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G von Muntau, Ania C., Mayerhofer, Peter U., Paton, Barbara C., Kammerer, Stefan, Roscher, Adelbert A.

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