Feedback learning and behavior problems after pediatric traumatic brain injury von Königs, M., van Heurn, L. W. E., Vermeulen, R. J., Goslings, J. C., Luitse, J. S. K., Poll-Thé, B. T., Beelen, A., van der Wees, M., Kemps, R. J. J. K., Catsman-Berrevoets, C. E., Luman, M., Oosterlaan, J.

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Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation von Stam, A H, Luijckx, G-J, Poll-Thé, B T, Ginjaar, I B, Frants, R R, Haan, J, Ferrari, M D, Terwindt, G M, van den Maagdenberg, A M J M

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Prognostic factors after a first attack of inflammatory CNS demyelination in children von NEUTEBOOM, R. F, BOON, M, POLL-THE, B. T, DE RIJK-VAN ANDEL, J. F, VERRIPS, A, HINTZEN, R. Q, CATSMAN BERREVOETS, C. E, VLES, J. S, GOOSKENS, R. H, STROINK, H, VERMEULEN, R. J, ROTTEVEEL, J. J, KETELSLEGERS, I. A, PEETERS, E

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The unfolding clinical spectrum of POLG mutations von Blok, M J, van den Bosch, B J, Jongen, E, Hendrickx, A, de Die-Smulders, C E, Hoogendijk, J E, Brusse, E, de Visser, M, Poll-The, B T, Bierau, J, de Coo, I F, Smeets, H J

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‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes von Bramswig, Nuria C., Ockeloen, C. W., Czeschik, J. C., van Essen, A. J., Pfundt, R., Smeitink, J., Poll-The, B. T., Engels, H., Strom, T. M., Wieczorek, D., Kleefstra, T., Lüdecke, H.-J.

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MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata von BAMS-MENGERINK, A. M, MAJOIE, C. B. L. M, DURAN, M, WANDERS, R. J. A, VAN HOVE, J, SCHEURER, C. D, BARTH, P. G, POLL-THE, B. T

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Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study von de Mol, C. L., Wong, Y. Y. M., van Pelt, E. D., Ketelslegers, I. A., Bakker, D. P., Boon, M., Braun, K. P. J., van Dijk, K. G. J., Eikelenboom, M. J., Engelen, M., Geleijns, K., Haaxma, C. A., Niermeijer, J. M. F., Niks, E. H., Peeters, E. A. J., Peeters-Scholte, C. M. P. C. D., Poll-The, B. T., Portier, R. P., de Rijk-van Andel, J. F., Samijn, J. P. A., Schippers, H. M., Snoeck, I. N., Stroink, H., Vermeulen, R. J., Verrips, A., Visscher, F., Vles, J. S. H., Willemsen, M. A. A. P., Catsman-Berrevoets, C. E., Hintzen, R. Q., Neuteboom, R. F.

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Development and validation of a severity scoring system for Zellweger spectrum disorders von Klouwer, F.C.C., Meester‐Delver, A., Vaz, F.M., Waterham, H.R., Hennekam, R.C.M., Poll‐The, B.T.

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Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D von Frenkel, J., Houten, S. M., Waterham, H. R., Wanders, R. J. A., Rijkers, G. T., Duran, M., Kuijpers, T. W., van Luijk, W., Poll‐The, B. T., Kuis, W.

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Sequential MR Imaging Changes in Nonketotic Hyperglycinemia von Mourmans, J, Majoie, C.B.L.M, Barth, P.G, Duran, M, Akkerman, E.M, Poll-The, B.T

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Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology von Aronica, E, van Kempen, A A M W, van der Heide, M, Poll-The, B T, van Slooten, H J, Troost, D, Rozemuller-Kwakkel, J M

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Renal Fanconi syndrome with ultrastructural defects in lysinuric protein intolerance von Benninga, M. A, Lilien, M, de Koning, T. J, Duran, M, Versteegh, F. G. A, Goldschmeding, R, Poll-The, B. T

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Congenital microcephaly and seizures due to 3‐phosphoglycerate dehydrogenase deficiency: Outcome of treatment with amino acids von De Koning, T. J., Duran, M., Maldergem, L. Van, Pineda, M., Dorland, L., Gooskens, R., Jaeken, J., Poll‐The, B. T.

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Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation von Cleary, M. A., Dorland, L., Koning, T. J., Poll‐The, B. T., Duran, M., Mandell, R., Shih, V. E., Berger, R., Olpin, S. E., Besley, G. T. N.

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Isolated and contiguous glycerol kinase gene disorders: A review von Sjarif, D. R., Ploos van Amstel, J. K., Duran, M., Beemer, F. A., Poll‐The, B. T.

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Phenotype of adult Refsum disease due to a defect in peroxin 7 von HORN, M. A, VAN DEN BRINK, D. M, WANDERS, R. J. A, DURAN, M, POLL-THE, B. T, TALLAKSEN, C. M. E, STOKKE, O. H, MOSER, H, SKJELDAL, O. H

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The metabolism of phytanic acid and pristanic acid in man: A review von Verhoeven, N. M., Wanders, R. J. A., Poll‐The, B. T., Saudubray, J.‐M., Jakobs, C.

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Normal very‐long‐chain fatty acids in peroxisomal D‐bifunctional protein deficiency: A diagnostic pitfall von Soorani‐Lunsing, R. J., Spronsen, F. J., Stolte‐Dijkstra, I., Wanders, R. J., Ferdinandusse, S., Waterham, H. R., Poll‐The, B. T., Rake, J. P.

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The eye as a window to inborn errors of metabolism von Poll‐The, B. T., Maillette De Buy Wenniger‐Prick, L. J., Barth, P. G., Duran, M.

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Increasing fat in the diet does not improve muscle performance in patients with mitochondrial myopathy due to complex I deficiency von Meer, K., Roef, M. J., Klerk, J. B. C., Bakker, H. D., Smit, G. P. A., Poll‐The, B. T.

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