Thermal hysteresis and its impact on the efficiency of first-order caloric materials von Hess, T., Maier, L. M., Bachmann, N., Corhan, P., Schäfer-Welsen, O., Wöllenstein, J., Bartholomé, K.

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Module Geometry and Contact Resistance of Thermoelectric Generators Analyzed by Multiphysics Simulation von Ebling, D., Bartholomé, K., Bartel, M., Jägle, M.

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Modelling cascaded caloric refrigeration systems that are based on thermal diodes or switches von Hess, T., Maier, L.M., Corhan, P., Schäfer–Welsen, O., Wöllenstein, J., Bartholomé, K.

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Method to characterize a thermal diode in saturated steam atmosphere von Maier, L. M., Hess, T., Kaube, A., Corhan, P., Fitger, A., Bachmann, N., Schäfer-Welsen, O., Wöllenstein, J., Bartholomé, K.

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Phenomenological model for a first-order magnetocaloric material von Hess, T., Vogel, C., Maier, L.M., Barcza, A., Vieyra, H.P., Schäfer-Welsen, O., Wöllenstein, J., Bartholomé, K.

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Thermoelectric efficiency of (1 - x)(GeTe) x(Bi2Se0.2Te2.8) and implementation into highly performing thermoelectric power generators von Koenig, J, Winkler, M, Dankwort, T, Hansen, A-L, Pernau, H-F, Duppel, V, Jaegle, M, Bartholomé, K, Kienle, L, Bensch, W

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Design principles of a bacterial signalling network von Kollmann, Markus, Løvdok, Linda, Bartholomé, Kilian, Timmer, Jens, Sourjik, Victor

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Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene von Knappskog, Per M., Flatmark, Torgeir, Mallet, Jacques, Lūdecke, Barbara, Bartholomé, Klaus

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A Simple Sb2Te3 Back-Contact Process for CdTe Solar Cells von Siepchen, B., Späth, B., Drost, C., Krishnakumar, V., Kraft, C., Winkler, M., König, J., Bartholomé, K., Peng, S.

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A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome von LÜDECKE, B, DWORNICZAK, B, BARTHOLOME, K

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Phase synchronization from noisy univariate signals von ROSSBERG, A. G, BARTHOLOME, K, VOSS, H. U, TIMMER, J

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A splice mutation in the GTP cyclohydrolase I gene causes dopa‐responsive dystonia by exon skipping von Skrygan, M., Bartholomé, B., Bonafé, L., Blau, N., Bartholomé, K.

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Recessively Inherited L-DOPA-Responsive Parkinsonism In Infancy Caused by A Point Mutation (L205p) in the Tyrosine Hydroxylase Gene von Lüdecke, Barbara, Knappskog, Per M., Clayton, Peter T., Surtees, Robert A. H., Clelland, James D., Heales, Simon J. R., Brand, Michael P., Bartholomé, Klaus, Flatmark, Torgeir

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Estimation of gene induction enables a relevance-based ranking of gene sets von Bartholomé, Kilian, Kreutz, Clemens, Timmer, Jens

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Mis-sense mutation of α1-antichymotrypsin gene associated with chronic lung disease von POLLER, W, FABER, J.-P, SCHOLZ, S, WEIDINGER, S, BARTHOLOME, K, OLEK, K, ERIKSSON, S

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Aberrant splicing of phenylalanine hydroxylase mRNA: The major cause for phenylketonuria in parts of southern Europe von Dworniczak, B., Aulehla-Scholz, C., Kalaydjieva, L., Bartholomé, K., Grudda, K., Horst, J.

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Frequent sequence variant in the human tyrosine hydroxylase gene von LÜBECKE, B, BARTHOLOME, K

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Mis-sense mutation of α 1-antichymotrypsin gene associated with chronic lung disease von Poller, W, Faber, J.-P, Scholz, S, Weidinger, S, Bartholomé, K, Olek, K, Eriksson, S

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Sequence variant of the human cathepsin G gene von LÜDECKE, B, POLLER, W, OLEK, K, BARTHOLOME, K

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Phenylalanine hydroxylase gene: Novel missense mutation in exon 7 causing severe phenylketonuria von Dworniczak, Bernd, Grudda, Klaus, Stümper, Judith, Bartholomé, Klaus, Aulehla-Scholz, Christa, Horst, Jürgen

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