Urinary dopamine in aromatic L-amino acid decarboxylase deficiency: The unsolved paradox von Wassenberg, T., Willemsen, M.A.A.P., Geurtz, P.B.H., Lammens, M., Verrijp, K., Wilmer, M., Lee, W.T., Wevers, R.A., Verbeek, M.M.

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Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis von Willemsen, Michèl A., Verbeek, Marcel M., Kamsteeg, Erik-Jan, de Rijk-van Andel, Johanneke F., Aeby, Alec, Blau, Nenad, Burlina, Alberto, Donati, Maria A., Geurtz, Ben, Grattan-Smith, Padraic J., Haeussler, Martin, Hoffmann, Georg F., Jung, Hans, de Klerk, Johannis B., van der Knaap, Marjo S., Kok, Fernando, Leuzzi, Vincenzo, de Lonlay, Pascale, Megarbane, Andre, Monaghan, Hugh, Renier, Willy O., Rondot, Pierre, Ryan, Monique M., Seeger, Jürgen, Smeitink, Jan A., Steenbergen-Spanjers, Gerry C., Wassmer, Evangeline, Weschke, Bernhard, Wijburg, Frits A., Wilcken, Bridget, Zafeiriou, Dimitrios I., Wevers, Ron A.

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Aromatic l-amino acid decarboxylase enzyme activity in deficient patients and heterozygotes von Verbeek, M.M., Geurtz, P.B.H., Willemsen, M.A.A.P., Wevers, R.A.

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MLP02 Aromatic L-amino acid decarboxylase enzyme activity in deficient patients and heterozygotes von Verbeek, M.M, Geurtz, B, Willemsen, M.A, Wevers, R.A

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L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiency von DE RIJK-VAN ANDEL, J. F, GABREËLS, F. J. M, GEURTZ, B, STEENBERGEN-SPANJERS, G. C. H, VAN DEN HEUVEL, L. P. W. J, SMEITINK, J. A. M, WEVERS, R. A

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A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC) von Wevers, R. A., Rijk‐van Andel, J. F., Bräutigam, C., Geurtz, B., Heuvel, L. P. W. J., Steenbergen‐Spanjers, G. C. H., Smeitink, J. A. M., Hoffmann, G. F., Gabreëls, F. J. M.

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The Paradox of Hyperdopaminuria in Aromatic l-Amino Acid Deficiency Explained von Wassenberg, Tessa, Monnens, Leo A. H., Geurtz, Ben P. B. H., Wevers, Ron A., Verbeek, Marcel M., Willemsen, Michèl A. A. P.

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Monoamine oxidase A activity in fibroblasts as a functional confirmation of MAOA variants von Peters, Tessa M. A., Lammerts van Bueren, Irma, Geurtz, Ben P.B.H., Coene, Karlien L. M., Leeuw, Nicole, Brunner, Han G., Jónsson, Jón J., Willemsen, Michèl A. A. P., Wevers, Ron A., Verbeek, Marcel M.

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Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis von Willemsen, M A, Verbeek, M M, Kamsteeg, E J, de Rijk-van Andel, J F, Aeby, A, Blau, N, Burlina, A, Donati, M A, Geurtz, B, Grattan-Smith, P J, Haeussler, M, Hoffmann, G F, Jung, H, de Klerk, J B, van der Knaap, M S, Kok, F, Leuzzi, V, de Lonlay, P, Megarbane, A, Monaghan, H, Renier, W O, Rondot, P, Ryan, M M, Seeger, J, Smeitink, J A, Steenbergen-Spanjers, G C, Wassmer, E, Weschke, B, Wijburg, F A, Wilcken, B, Zafeiriou, D I, Wevers, R A

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Spinal cord injury-induced immunodeficiency is mediated by a sympathetic-neuroendocrine adrenal reflex von Prüss, Harald, Tedeschi, Andrea, Thiriot, Aude, Lynch, Lydia, Loughhead, Scott M, Stutte, Susanne, Mazo, Irina B, Kopp, Marcel A, Brommer, Benedikt, Blex, Christian, Geurtz, Laura-Christin, Liebscher, Thomas, Niedeggen, Andreas, Dirnagl, Ulrich, Bradke, Frank, Volz, Magdalena S, DeVivo, Michael J, Chen, Yuying, von Andrian, Ulrich H, Schwab, Jan M

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Nosocomial bloodstream infections due to Candida spp. in the USA: species distribution, clinical features and antifungal susceptibilities von Wisplinghoff, Hilmar, Ebbers, Jenny, Geurtz, Lea, Stefanik, Danuta, Major, Yvette, Edmond, Michael B, Wenzel, Richard P, Seifert, Harald

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The sex difference of plasma homovanillic acid is unaffected by cross-sex hormone administration in transsexual subjects von Giltay, Erik J, Kho, King H, Blansjaar, Ben A, Verbeek, Marcel M, Geurtz, P Ben H, Geleijnse, Johanna M, Gooren, Louis J G

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MDO04 Paroxysmal dopa-responsive dystonia and sepiapterine reductase deficiecy von Verbeek, M.M, Lagerwerf, A.J, Geurtz, B.P.H, Abeling, N, Thoeny, B, Blau, N, Zafeiriou, D

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De Gids. Jaargang 132 von [tijdschrift] Gids, De

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