Arterial intima-media thickness in children heterozygous for familial hypercholesterolaemia von Wiegman, Albert, de Groot, Eric, Hutten, Barbara A, Rodenburg, Jessica, Gort, Johan, Bakker, Henk D, Sijbrands, Eric JG, Kastelein, John JP

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Efficacy and Safety of Statin Therapy in Children With Familial Hypercholesterolemia: A Randomized Controlled Trial von Wiegman, Albert, Hutten, Barbara A, de Groot, Eric, Rodenburg, Jessica, Bakker, Henk D, Büller, Harry R, Sijbrands, Eric J. G, Kastelein, John J. P

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Early statin therapy restores endothelial function in children with familial hypercholesterolemia von de Jongh, Saskia, Lilien, Marc R, op’t Roodt, Jos, Stroes, Erik S.G, Bakker, Henk D, Kastelein, John J.P

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The Natural Course of Infantile Pompe's Disease: 20 Original Cases Compared With 133 Cases From the Literature von van den Hout, Hannerieke M. P, Hop, Wim, van Diggelen, Otto P, Smeitink, Jan A. M, Smit, G. Peter A, Poll-The, Bwee-Tien T, Bakker, Henk D, Loonen, M. Christa B, de Klerk, Johannis B. C, Reuser, Arnold J. J, van der Ploeg, Ans T

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Efficacy and safety of statin therapy in children with familial hypercholesterolemia: A randomized, double-blind, placebo-controlled trial with simvastatin von DE JONGH, Saskia, OSE, Leiv, STEPANAVAGE, Michael, SAPRE, Aditi, GUMBINER, Barry, MERCURI, Michele, VAN TROTSENBURG, A. S, BAKKER, Henk D, KASTELEIN, John J. P, SZAMOSI, Tamas, GAGNE, Claude, LAMBERT, M, SCOTT, Russell, PERRON, P, DOBBELAERE, Dries, SABORIO, M, TUOHY, Mary B

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Family history and cardiovascular risk in familial hypercholesterolemia: Data in more than 1000 children von WIEGMAN, Albert, RODENBURG, Jessica, DE JONGH, Saskia, DEFESCHE, Joep C, BAKKER, Henk D, KASTELEIN, John J. P, SIJBRANDS, Eric J. G

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Living With Classical Galactosemia: Health-Related Quality of Life Consequences von Bosch, Annet M, Grootenhuis, Martha A, Bakker, Henk D, Heijmans, Hugo S.A, Wijburg, Frits A, Last, Bob F

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Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseases von Asfaw, Befekadu, Ledvinová, Jana, Dobrovolńy, Robert, Bakker, Henk D, Desnick, Robert J, van Diggelen, Otto P, de Jong, Jan G N, Kanzaki, Tamotsu, Chabas, Amparo, Maire, Irene, Conzelmann, Ernst, Schindler, Detlev

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Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion von Morten, Karl J, Ashley, Neil, Wijburg, Frits, Hadzic, Nedim, Parr, Jeremy, Jayawant, Sandeep, Adams, Susan, Bindoff, Laurence, Bakker, Henk D, Mieli-Vergani, Giorgina, Zeviani, Massimo, Poulton, Joanna

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Family history of cardiovascular events and endothelial dysfunction in children with familial hypercholesterolemia von de Jongh, Saskia, Lilien, Marc R., Bakker, Henk D., Hutten, Barbara A., Kastelein, John J.P., Stroes, Erik S.G.

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Sepiapterin reductase deficiency an autosomal recessive DOPA-responsive dystonia von Abeling, Nico G., Duran, Marinus, Bakker, Henk D., Stroomer, Lida, Thöny, Beat, Blau, Nenad, Booij, Jan, Poll-The, Bwee Tien

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Identification of novel mutations in classical galactosemia von Bosch, Annet M., IJlst, Lodewijk, Oostheim, Wendy, Mulders, Joyce, Bakker, Henk D., Wijburg, Frits A., Wanders, Ronald J.A., Waterham, Hans R.

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The Apolipoprotein ε4 Allele Confers Additional Risk in Children with Familial Hypercholesterolemia von Wiegman, Albert, Sijbrands, Eric J G, Rodenburg, Jessica, Defesche, Joep C, de Jongh, Saskia, Bakker, Henk D, Kastelein, John J P

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Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: no association with neuroaxonal dystrophy? von Bakker, H D, de Sonnaville, M L, Vreken, P, Abeling, N G, Groener, J E, Keulemans, J L, van Diggelen, O P

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Steady-state pharmacokinetics of pravastatin in children with familial hypercholesterolaemia von Wiersma, Heleen E, Wiegman, Albert, Koopmans, Richard P, Bakker, Henk D, Kastelein, John J P, van Boxtel, Chris J

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Differences in the Phenotype Between Children With Familial Defective Apolipoprotein B-100 and Familial Hypercholesterolemia von Pimstone, Simon N, Defesche, Joep C, Clee, Susanne M, Bakker, Henk D, Hayden, Michael R, Kastelein, John J.P

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Phenylketonuria and glycogen storage disease type III in sibs of one family von Yilmazer, Tuncay, van Gennip, Albert H, Abeling, Nico G G M, Ozalp, Imran, Coşkun, Turgay, Bakker, Henk D

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Mutations in the Liver Glycogen Phosphorylase Gene ( PYGL) Underlying Glycogenosis Type VI (Hers Disease) von Burwinkel, Barbara, Bakker, Henk D., Herschkovitz, Eliezer, Moses, Shimon W., Shin, Yoon S., Kilimann, Manfred W.

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Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease von Bakker, Henk D., Scholte, Hans R., Dingemans, Koert P., Spelbrink, Johannes N., Wijburg, Frits A., Coby, Van den Bogert

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Living with classical galactosemia: health-related quality of life consequences von Bosch, Annet M, Grootenhuis, Martha A, Bakker, Henk D, Heijmans, Hugo S.A, Wijburg, Frits A, Last, Bob F

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