Propionic acidemia: neonatal versus selective metabolic screening von Grünert, S. C., Müllerleile, S., de Silva, L., Barth, M., Walter, M., Walter, K., Meissner, T., Lindner, M., Ensenauer, R., Santer, R., Bodamer, O. A., Baumgartner, M. R., Brunner-Krainz, M., Karall, D., Haase, C., Knerr, I., Marquardt, T., Hennermann, J. B., Steinfeld, R., Beblo, S., Koch, H. G., Konstantopoulou, V., Scholl-Bürgi, S., van Teeffelen-Heithoff, A., Suormala, T., Sperl, W., Kraus, J. P., Superti-Furga, A., Schwab, K. O., Sass, J. O.

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Cyclophosphamide is a highly effective and safe induction therapy in chronic periaortitis: a long-term follow-up of 35 patients with chronic periaortitis von Binder, M, Uhl, M, Wiech, T, Kollert, F, Thiel, J, Sass, J O, Walker, U A, Peter, H H, Warnatz, K

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Mutation analysis in 54 propionic acidemia patients von Kraus, J. P., Spector, E., Venezia, S., Estes, P., Chiang, P. W., Creadon-Swindell, G., Müllerleile, S., de Silva, L., Barth, M., Walter, M., Walter, K., Meissner, T., Lindner, M., Ensenauer, R., Santer, R., Bodamer, O. A., Baumgartner, M. R., Brunner-Krainz, M., Karall, D., Haase, C., Knerr, I., Marquardt, T., Hennermann, J. B., Steinfeld, R., Beblo, S., Koch, H. G., Konstantopoulou, V., Scholl-Bürgi, S., van Teeffelen-Heithoff, A., Suormala, T., Ugarte, M., Sperl, W., Superti-Furga, A., Schwab, K. O., Grünert, S. C., Sass, J. O.

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Propionic Acidemia Revisited: A Workshop Report von Sass, J. O., Hofmann, M., Skladal, D., Mayatepek, E., Schwahn, B., Sperl, W.

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Neurological findings in aminoacylase 1 deficiency von SASS, J. O, OLBRICH, H, MOHR, V, HART, C, WOLDSETH, B, KRYWAWYCH, S, BJURULF, B, LAKHANI, P. K, BUCHDAHL, R. M, OMRAN, H

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Isobutyryl‐CoA dehydrogenase deficiency: Isobutyrylglycinuria and ACAD8 gene mutations in two infants von Sass, J. O., Sander, S., Zschocke, J.

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L-2-Hydroxyglutaric aciduria: Identification of ten novel mutations in the L2HGDH gene von Sass, J. O., Jobard, F., Topçu, M., Mahfoud, A., Werlé, E., Cure, S., Al-Sannaa, N., Alshahwan, S. A., Bataillard, M., Cimbalistiene, L., Grolik, C., Kemmerich, V., Omran, H., Sztriha, L., Tabache, M., Fischer, J.

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Possible Genotype-Phenotype Correlations in Children with Mild Clinical Course of Canavan Disease von Tacke, U., Olbrich, H., Sass, J. O., Fekete, A., Horvath, J., Ziyeh, S., Kleijer, W. J., Rolland, M.-O., Fisher, S., Payne, S., Vargiami, E., Zafeiriou, D. I., Omran, H.

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Quantitation of total homocysteine in human plasma by derivatization to its N(O,S)-propoxycarbonyl propyl ester and gas chromatography–mass spectrometry analysis von Oliver Sass, Jörn, Endres, Wolf

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The relation of cerebrospinal fluid and plasma glycine levels in propionic acidaemia, a ‘ketotic hyperglycinaemia’ von Scholl-Bürgi, S., Korman, S. H., Applegarth, D. A., Karall, D., Lillquist, Y., Heinz-Erian, P., Davidson, A. G. F., Haberlandt, E., Sass, J. O.

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Trichothiodystrophy: quantification of cysteine in human hair and nails by application of sodium azide-dependent oxidation to cysteic acid von SASS, J. O, SKLADAL, D, ZELGER, B, ROMANI, N, UTERMANN, B

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Hypohomocysteinaemia and highly increased proportion of S‐sulfonated plasma transthyretin in molybdenum cofactor deficiency von Sass, J. O., Kishikawa, M., Puttinger, R., Reiss, J., Erwa, W., Shimizu, A., Sperl, W.

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Odd-numbered long-chain fatty acids in propionic acidaemia von SPERL, W, MURR, C, SKLADAL, D, SASS, J. O, SUORMALA, T, BAUMGARTNER, R, WENDEL, U

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Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serum[S] von Janzen, N., Sander, S., Terhardt, M., Das, A.M., Sass, J.O., Kraetzner, R., Rosewich, H., Peter, M., Sander, J.

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Paronychia with Pyogenic Granuloma in a Child Treated with Indinavir: The Retinoid-Mediated Side Effect Theory Revisited von Sass, J.O., Jakob-Sölder, B., Heitger, A., Tzimas, G., Sarcletti, M.

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Peripheral neuropathy in a patient with d-2-hydroxyglutaric aciduria von Haliloglu, G., Temucin, C. M., Oguz, K. K., Celiker, A., Coskun, T., Sass, J. O., Fischer, J., Topcu, M.

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Mechanisms of brain injury in infantile child abuse von Sass, JO, Crazzolara, R, Heinz-Erian, P

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Treatment of neonatal hyperammonaemia von Sass, JO, Sperl, W, Bachmann, C

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Plasma concentrations and renal clearance of orotic acid in argininosuccinic acid synthetase deficiency von SASS, J. O, SKLADAL, D

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Human isotretinoin metabolism during indinavir therapy von Sass, J O, Padberg, J

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