Gestational diabetes predicts the risk of childhood overweight and abdominal circumference independent of maternal obesity von Nehring, I., Chmitorz, A., Reulen, H., von Kries, R., Ensenauer, R.

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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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Effects of suboptimal or excessive gestational weight gain on childhood overweight and abdominal adiposity: results from a retrospective cohort study von Ensenauer, R, Chmitorz, A, Riedel, C, Fenske, N, Hauner, H, Nennstiel-Ratzel, U, von Kries, R

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Hyperargininemia due to arginase I deficiency: the original patients and their natural history, and a review of the literature von Schlune, A, vom Dahl, S, Häussinger, D, Ensenauer, R, Mayatepek, E

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Peri-conceptional obesogenic exposure induces sex-specific programming of disease susceptibilities in adult mouse offspring von Dahlhoff, M., Pfister, S., Blutke, A., Rozman, J., Klingenspor, M., Deutsch, M.J., Rathkolb, B., Fink, B., Gimpfl, M., Hrabě de Angelis, M., Roscher, A.A., Wolf, E., Ensenauer, R.

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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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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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Prediction of excessive gestational weight gain from week-specific cutoff values: a cohort study von Knabl, J, Riedel, C, Gmach, J, Ensenauer, R, Brandlhuber, L, Rasmussen, K M, Schiessl, B, von Kries, R

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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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Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle von Ensenauer, R, Thiel, T, Schwab, K.O, Tacke, U, Stöckler-Ipsiroglu, S, Schulze, A, Hennig, J, Lehnert, W

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Perinatale Programmierung des Typ-2-Diabetes von Ensenauer, R, Hucklenbruch-Rother, E, Brüll, V, Dötsch, J

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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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Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation von Babovic‐Vuksanovic, Dusica, Jenkins, S.C., Ensenauer, R., Newman, D.C., Jalal, S.M.

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3‐Methylglutaconyl‐CoA hydratase deficiency: A new patient with speech retardation as the leading sign von Ensenauer, R., Müller, C. B., Schwab, K. O., Gibson, K. M., Brandis, M., Lehnert, W.

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Human Acyl-CoA Dehydrogenase-9 Plays a Novel Role in the Mitochondrial β-Oxidation of Unsaturated Fatty Acids von Ensenauer, Regina, He, Miao, Willard, Jan-Marie, Goetzman, Eric S., Corydon, Thomas J., Vandahl, Brian B., Mohsen, Al-Walid, Isaya, Grazia, Vockley, Jerry

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Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle von ENSENAUER, R

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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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Pregnancy and infants' outcome: nutritional and metabolic implications von Berti, C, Cetin, I, Agostoni, C, Desoye, G, Devlieger, Roland, Emmett, P.M, Ensenauer, R, Hauner, H, Herrera, E, Hoesli, I, Krauss-Etschmann, S, Olsen, S.F, Schaefer-Graf, U, Schiessl, B, Symonds, M.E, Koletzko, B

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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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