How instability in virtual economies of mobile digital games drives and ruins profit von Lohse, P.

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Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges von Kuemmerle-Deschner, J B, Verma, D, Endres, T, Broderick, L, de Jesus, A A, Hofer, F, Blank, N, Krause, K, Rietschel, C, Horneff, G, Aksentijevich, I, Lohse, P, Goldbach-Mansky, R, Hoffman, H M, Benseler, S M

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Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone von Staub, J., Pfannschmidt, N., Strohal, R., Braun-Falco, M., Lohse, P., Goerdt, S., Leverkus, M.

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Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts von Löffler, W., Lohse, P., Weihmayr, T., Widenmayer, W.

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Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor von Bork, K., Wulff, K., Hardt, J., Witzke, G., Lohse, P.

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Brief Report: Clinical and Molecular Phenotypes of Low‐Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges von Kuemmerle‐Deschner, J. B., Verma, D., Endres, T., Broderick, L., Jesus, A. A., Hofer, F., Blank, N., Krause, K., Rietschel, C., Horneff, G., Aksentijevich, I., Lohse, P., Goldbach‐Mansky, R., Hoffman, H. M., Benseler, S. M.

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Varieties of work‐based higher education: France, Germany and the United States compared von Graf, Lukas, Lohse, Anna P., Bernhard, Nadine

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Data Augmentation for SAR Sea Ice and Water Classification Based on Per-Class Backscatter Variation With Incidence Angle von Wang, Qiang, Lohse, Johannes P., Doulgeris, Anthony P., Eltoft, Torbjorn

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MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes von Wittkowski, Helmut, Kuemmerle-Deschner, Jasmin B, Austermann, Judith, Holzinger, Dirk, Goldbach-Mansky, Raphaela, Gramlich, Katharina, Lohse, Peter, Jung, Thomas, Roth, Johannes, Benseler, Susanne M, Foell, Dirk

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Chronology of Glacial Advances and Deglaciation in the Encierro River Valley (29° Lat. S), Southern Atacama Desert, Based on Geomorphological Mapping and Cosmogenic 10Be Exposure A... von Aguilar, G., Riquelme, R., Lohse, P., Cabré, A., García, J.-L.

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Genetics of cryopyrin-associated periodic syndrome von Kümmerle-Deschner, J B, Lohse, P

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Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine von Hepping, N, Griese, M, Lohse, P, Garbe, W, Lange, L

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Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics von Lainka, Elke, Neudorf, Ulrich, Lohse, Peter, Timmann, Christian, Stojanov, Silvia, Huss, Kristina, von Kries, Rudiger, Niehues, Tim

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease von Török, H-P, Glas, J, Tonenchi, L, Lohse, P, Müller-Myhsok, B, Limbersky, O, Neugebauer, C, Schnitzler, F, Seiderer, J, Tillack, C, Brand, S, Brünnler, G, Jagiello, P, Epplen, J T, Griga, T, Klein, W, Schiemann, U, Folwaczny, M, Ochsenkühn, T, Folwaczny, C

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Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children von Lainka, E., Neudorf, U., Lohse, P., Timmann, C., Bielak, M., Stojanov, S., Huss, K., von Kries, R., Niehues, T.

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Conditions for cross-border policy transfer and cooperation: Analysing differences between higher education and vocational training von Graf, Lukas, Lohse, Anna P.

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Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrom... von Stojanov, S, Dejaco, C, Lohse, P, Huss, K, Duftner, C, Belohradsky, B H, Herold, M, Schirmer, M

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Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population von Lainka, E., Bielak, M., Lohse, P., Timmann, C., Stojanov, S., von Kries, R., Niehues, T., Neudorf, U.

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Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis von Griese, M, Brasch, F, Aldana, VR, Cabrera, MM, Goelnitz, U, Ikonen, E, Karam, BJ, Liebisch, G, Linder, MD, Lohse, P, Meyer, W, Schmitz, G, Pamir, A, Ripper, J, Rolfs, A, Schams, A, Lezana, FJ

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Polymorphisms in the ACE and PAI‐1 genes are associated with recurrent spontaneous miscarriages von Buchholz, T., Lohse, P., Rogenhofer, N., Kosian, E., Pihusch, R., Thaler, C.J.

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