Peripheral Monocytes of Obese Women Display Increased Chemokine Receptor Expression and Migration Capacity von Krinninger, P, Ensenauer, R, Ehlers, K, Rauh, K, Stoll, J, Krauss-Etschmann, S, Hauner, H, Laumen, H

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PROCEDE D'ELIMINATION DE CHARGES CONTENANT DE L'AZOTE A PARTIR D'EAU von P. ENSENAUER, G.E. KURZMANN

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FILTRI SOMMERSI PER LA CONTEMPO RANEA DEPURAZIONE DISINFEZIONE E OZONIZZAZIONE DELL ACQUA von KURZMANN G, ENSENAUER P

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Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients von Ensenauer, Regina E., Adeyinka, Adewale, Flynn, Heather C., Michels, Virginia V., Lindor, Noralane M., Dawson, D. Brian, Thorland, Erik C., Lorentz, Cindy Pham, Goldstein, Jennifer L., McDonald, Marie T., Smith, Wendy E., Simon-Fayard, Elba, Alexander, Alan A., Kulharya, Anita S., Ketterling, Rhett P., Clark, Robin D., Jalal, Syed M.

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FILTRE DE SEDIMENTATION POUR LA PURIFICATION LA DESINFECTION ET L'OZONISATION SIMULTANEES DE L'EAU von P. ENSENAUER, G.E. KURZMANN

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Impact of the n-6:n-3 long-chain PUFA ratio during pregnancy and lactation on offspring neurodevelopment: 5-year follow-up of a randomized controlled trial von Brei, C, Stecher, L, Brunner, S, Ensenauer, R, Heinen, F, Wagner, P D, Hermsdörfer, J, Hauner, H

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Identification and characterization of new long chain Acyl-CoA dehydrogenases von He, Miao, Pei, Zhengtong, Mohsen, Al-Walid, Watkins, Paul, Murdoch, Geoffrey, Van Veldhoven, Paul P., Ensenauer, Regina, Vockley, Jerry

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Use of guidelines improves the neurological outcome in glutaric aciduria type I von Heringer, Jana, Boy, S. P. Nikolas, Ensenauer, Regina, Assmann, Birgit, Zschocke, Johannes, Harting, Inga, Lücke, Thomas, Maier, Esther M., Mühlhausen, Chris, Haege, Gisela, Hoffmann, Georg F., Burgard, Peter, Kölker, Stefan

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DISPOSITIVO PER LA MISURAZIONE DEL POTENZIALE DI OSSIRIDUZIONE DI MEZZI LIQUIDI von HORN R, KURZMANN G, SEIBERLING D, ENSENAUER P

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INSTRUMENT DE MESURE DE POTENTIEL D'OXYDO-REDUCTION D'AGENTS LIQUIDES von D. SEIBERLING, R. HORN, P. ENSENAUER, G.E. KURZMANN

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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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GAMT deficiency : Features, treatment, and outcome in an inborn error of creatine synthesis von MERCIMEK-MAHMUTOGLU, S, STOECKLER-IPSIROGLU, S, ITEM, C. B, LEUZZI, V, MARQUARDT, I, MÜHL, A, SAELKE-KELLERMANN, R. A, SALOMONS, G. S, SCHULZE, A, SURTEES, R, VAN DER KNAAP, M. S, VASCONCELOS, R, ADAMI, A, VERHOEVEN, N. M, VILARINHO, L, WILICHOWSKI, E, JAKOBS, C, APPLETON, R, CALDEIRA ARAUJO, H, DURAN, M, ENSENAUER, R, FERNANDEZ-ALVAREZ, E, GARCIA, P, GROLIK, C

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Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients von Grünert, Sarah C, Müllerleile, Stephanie, De Silva, Linda, Barth, Michael, Walter, Melanie, Walter, Kerstin, Meissner, Thomas, Lindner, Martin, Ensenauer, Regina, Santer, René, Bodamer, Olaf A, Baumgartner, Matthias R, Brunner-Krainz, Michaela, Karall, Daniela, Haase, Claudia, Knerr, Ina, Marquardt, Thorsten, Hennermann, Julia B, Steinfeld, Robert, Beblo, Skadi, Koch, Hans-Georg, Konstantopoulou, Vassiliki, Scholl-Bürgi, Sabine, van Teeffelen-Heithoff, Agnes, Suormala, Terttu, Sperl, Wolfgang, Kraus, Jan P, Superti-Furga, Andrea, Schwab, Karl Otfried, Sass, Jörn Oliver

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A Common Mutation Is Associated with a Mild, Potentially Asymptomatic Phenotype in Patients with Isovaleric Acidemia Diagnosed by Newborn Screening von Ensenauer, Regina, Vockley, Jerry, Willard, Jan-Marie, Huey, Joseph C., Sass, Jörn Oliver, Edland, Steven D., Burton, Barbara K., Berry, Susan A., Santer, René, Grünert, Sarah, Koch, Hans-Georg, Marquardt, Iris, Rinaldo, Piero, Hahn, Sihoun, Matern, Dietrich

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Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience von Kölker, Stefan, Boy, S.P. Nikolas, Heringer, Jana, Müller, Edith, Maier, Esther M., Ensenauer, Regina, Mühlhausen, Chris, Schlune, Andrea, Greenberg, Cheryl R., Koeller, David M., Hoffmann, Georg F., Haege, Gisela, Burgard, Peter

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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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2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene von Ofman, Rob, Jos Ruiter, P.N., Feenstra, Marike, Duran, Marinus, Bwee Poll-The, Tien, Zschocke, Johannes, Ensenauer, Regina, Lehnert, Willy, Sass, Jörn Oliver, Sperl, Wolfgang, Ronald Wanders, J.A.

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Clinical variability in 3-hydroxy-2-methylbutyryl-coa dehydrogenase deficiency von Ensenauer, Regina, Niederhoff, Helmut, Ruiter, Jos P. N., Wanders, Ronald J. A., Schwab, K. Otfried, Brandis, Matthias, Lehnert, Willy

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Genotypic differences of MCAD deficiency in the Asian population: Novel genotype and clinical symptoms preceding newborn screening notification von Ensenauer, Regina, Winters, Jennifer L., Parton, Patricia A., Kronn, David F., Kim, Jong-Won, Matern, Dietrich, Rinaldo, Piero, Hahn, Si Houn

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Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome von Beysen, Diane, De Jaegere, Sarah, Amor, David, Bouchard, Philippe, Christin-Maitre, Sophie, Fellous, Marc, Touraine, Philippe, Grix, Arthur W, Hennekam, Raoul, Meire, Françoise, Oyen, Nina, Wilson, Louise C, Barel, Dalit, Clayton-Smith, Jill, de Ravel, Thomy, Decock, Christian, Delbeke, Patricia, Ensenauer, Regina, Ebinger, Friedrich, Gillessen-Kaesbach, Gabriele, Hendriks, Yvonne, Kimonis, Virginia, Laframboise, Rachel, Laissue, Paul, Leppig, Kathleen, Leroy, Bart P, Miller, David T, Mowat, David, Neumann, Luitgard, Plomp, Astrid, Van Regemorter, Nicole, Wieczorek, Dagmar, Veitia, Reiner A, De Paepe, Anne, De Baere, Elfride

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