Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy von Wraith, J. Edmond, Scarpa, Maurizio, Beck, Michael, Bodamer, Olaf A., De Meirleir, Linda, Guffon, Nathalie, Meldgaard Lund, Allan, Malm, Gunilla, Van der Ploeg, Ans T., Zeman, Jiri

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Mucopolysaccharidosis type II in females: Case report and review of literature von Tuschl, Karin, Gal, Andreas, Paschke, Eduard, Kircher, Susanne, Bodamer, Olaf A.

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Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU) von Huemer, M., Simma, B., Mayr, D., Möslinger, D., Mühl, A., Schmid, I., Ulmer, H., Bodamer, O.A.

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Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency von KÜLKENS, S, HARTING, I, SAUER, S, ZSCHOCKE, J, HOFFMANN, G. F, GRUBER, S, BODAMER, O. A, KÖLKER, S

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Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism von Stromberger, C., Bodamer, O. A., Stöckler‐Ipsiroglu, S.

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Prenatal and postnatal treatment in cobalamin C defect von Huemer, Martina, Simma, Burkhard, Fowler, Brian, Suormala, Terttu, Bodamer, Olaf A., Sass, Jörn Oliver

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Analysis of guanidinoacetate and creatine by isotope dilution electrospray tandem mass spectrometry von Bodamer, Olaf A, Bloesch, Shannon M, Gregg, Anthony R, Stockler-Ipsiroglu, Silvia, O'Brien, William E

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Rapid analysis of total plasma homocysteine by tandem mass spectrometry von Tuschl, Karin, Bodamer, Olaf A., Erwa, Wolfgang, Mühl, Adolf

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Creatine metabolism in combined methylmalonic aciduria and homocystinuria von Bodamer, Olaf A., Sahoo, Trilochan, Beaudet, Arthur L., O'Brien, William E., Bottiglieri, Teodoro, Stöckler-Ipsiroglu, Sylvia, Wagner, Conrad, Scaglia, Fernando

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Central nervous system malformations in oral-facial-digital syndrome, type 1 von Holub, Margareta, Potocki, Lorraine, Bodamer, Olaf A.

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Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome? von HOLUB, M, BODAMER, O. A, ITEM, C, MÜHL, A, POLLAK, A, STÖCKLER-IPSIROGLU, S

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Use of Denaturing HPLC to Provide Efficient Detection of Mutations Causing Familial Hypercholesterolemia von Bodamer, Olaf A, Bercovich, Dan, Schlabach, Michael, Ballantyne, Christie, Zoch, Daniele, Beaudet, Arthur L

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Recurrent acroparaesthesia during febrile infections von Bodamer, OA, Ratschmann, R, Paschke, E, Voigtländer, T, Stockler-Ipsiroglu, S

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Practical Management of Combined Methylmalonicaciduria and Homocystinuria von Smith, Debra L., Bodamer, Olaf A.

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Nuclear magnetic resonance spectroscopy in glutaryl‐CoA dehydrogenase deficiency von Bodamer, O. A., Gruber, S., StÖckler‐Ipsiroglu, S.

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Analysis of Acylcarnitine Ester for Neonatal Screening of Inborn Errors of Metabolism Using Tandem Mass-spectrometry von Bodamer, Olaf A., Mühl, Adolf

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Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type I von Crone, J, Möslinger, D, Bodamer, OA, Schima, W, Huber, WD, Holme, E, Ipsiroglu, S Stöckler

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Fabry disease defined von Stromberger, C., Bodamer, Olaf A.

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l-alanine supplementation in late infantile glycogen storage disease type II von Bodamer, Olaf A, Haas, Dorothea, Hermans, Monique M, Reuser, Arnold J, Hoffmann, Georg F

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Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia von Tuschl, K, Meyer, E, Valdivia, LE, Zhao, N, Dadswell, C, Abdul-Sada, A, Hung, CY, Simpson, MA, Chong, WK, Jacques, TS, Woltjer, RL, Eaton, S, Gregory, A, Sanford, L, Kara, E, Houlden, H, Cuno, SM, Prokisch, H, Valletta, L, Tiranti, V, Younis, R, Maher, ER, Spencer, J, Straatman-Iwanowska, A, Gissen, P, Selim, LA, Pintos-Morell, G, Coroleu-Lletget, W, Mohammad, SS, Yoganathan, S, Dale, RC, Thomas, M, Rihel, J, Bodamer, OA, Enns, CA, Hayflick, SJ, Clayton, PT, Mills, PB, Kurian, MA, Wilson, SW

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