A RECURRENT CASE OF PSEUDO-PSEUDO MEIGS SYNDROME RELATED TO SYSTEMIC LUPUS ERYTHEMATOSUS von RYAN, ALIXANDRA, KUTSCHE, WILLIAM, ODIGWE, CHIBUZO C

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Discussing the “Most Important Question of the 20th Century”: W. E. B. Du Bois and the ILO’s Efforts for a Regulation of “Native Labor” Politics, 1919–1926 von Kutsche, Fabiana, Lindner, Ulrike

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Imaging the influence of peripheral TRPV1-signaling on cerebral nociceptive processing applying fMRI-based graph theory in a resiniferatoxin rat model von Wank, Isabel, Kutsche, Lisa, Kreitz, Silke, Reeh, Peter, Hess, Andreas

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A RARE CAUSE OF COUGH AND WHEEZING: A CASE OF DIFFUSE IDIOPATHIC PULMONARY NEUROENDOCRINE CELL HYPERPLASIA IN A YOUNG WOMAN von KUTSCHE, WILLIAM, ODIGWE, CHIBUZO C, FUCICH, LEE, RYAN, ALIXANDRA

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ACUTE ONSET OF RIGHT LEG PARALYSIS: AN UNUSUAL PRESENTATION OF TYPE A AORTIC DISSECTION von WILSON, MICHAEL A, HARRIS, SHANNON K, KUTSCHE, WILLIAM

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BREAKING FREE FROM ANCHORING: A CASE REPORT von KHAN, SAMEER, KUTSCHE, WILLIAM, DOUTHIT, NATHAN, RASLAN, MAHA, CLASON, JOSHUA

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Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder von Harms, Frederike L., Kloth, Katja, Bley, Annette, Denecke, Jonas, Santer, René, Lessel, Davor, Hempel, Maja, Kutsche, Kerstin

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis von Kortüm, Fanny, Das, Soma, Flindt, Max, Morris-Rosendahl, Deborah J, Stefanova, Irina, Goldstein, Amy, Horn, Denise, Klopocki, Eva, Kluger, Gerhard, Martin, Peter, Rauch, Anita, Roumer, Agathe, Saitta, Sulagna, Walsh, Laurence E, Wieczorek, Dagmar, Uyanik, Gökhan, Kutsche, Kerstin, Dobyns, William B

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Effects of voluntary exercise on the expression of browning markers in visceral and subcutaneous fat tissue of normotensive and spontaneously hypertensive rats von Karadedeli, Meryem Sevval, Schreckenberg, Rolf, Kutsche, Hanna S., Schlüter, Klaus-Dieter

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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome von Kortüm, Fanny, Caputo, Viviana, Bauer, Christiane K, Stella, Lorenzo, Ciolfi, Andrea, Alawi, Malik, Bocchinfuso, Gianfranco, Flex, Elisabetta, Paolacci, Stefano, Dentici, Maria Lisa, Grammatico, Paola, Korenke, Georg Christoph, Leuzzi, Vincenzo, Mowat, David, Nair, Lal D V, Nguyen, Thi Tuyet Mai, Thierry, Patrick, White, Susan M, Dallapiccola, Bruno, Pizzuti, Antonio, Campeau, Philippe M, Tartaglia, Marco, Kutsche, Kerstin

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Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes von Kratz, C P, Franke, L, Peters, H, Kohlschmidt, N, Kazmierczak, B, Finckh, U, Bier, A, Eichhorn, B, Blank, C, Kraus, C, Kohlhase, J, Pauli, S, Wildhardt, G, Kutsche, K, Auber, B, Christmann, A, Bachmann, N, Mitter, D, Cremer, F W, Mayer, K, Daumer-Haas, C, Nevinny-Stickel-Hinzpeter, C, Oeffner, F, Schlüter, G, Gencik, M, Überlacker, B, Lissewski, C, Schanze, I, Greene, M H, Spix, C, Zenker, M

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Response to Calgani et al von Zenker, Martin, Kutsche, Kerstin

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Sea-Anemone Toxin ATX-II Elicits A-Fiber-Dependent Pain and Enhances Resurgent and Persistent Sodium Currents in Large Sensory Neurons von Klinger, Alexandra B, Eberhardt, Mirjam, Link, Andrea S, Namer, Barbara, Kutsche, Lisa K, Schuy, E Theresa, Sittl, Ruth, Hoffmann, Tali, Alzheimer, Christian, Huth, Tobias, Carr, Richard W, Lampert, Angelika

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HIDDEN TREASURES: AN INCIDENTAL FINDING OF WORSENING CONGESTIVE HEART FAILURE WITH POINT OF CARE ULTRASOUND von KHAN, SAMEER, KUTSCHE, WILLIAM, DOUTHIT, NATHAN, NICKOLS, JORDAN, CLASON, JOSHUA, RASLAN, MAHA

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes von Endele, Sabine, Rosenberger, Georg, Geider, Kirsten, Popp, Bernt, Tamer, Ceyhun, Stefanova, Irina, Milh, Mathieu, Kortum, Fanny, Fritsch, Angela, Pientka, Friederike K, Hellenbroich, Yorck, Kalscheuer, Vera M, Kohlhase, Jurgen, Moog, Ute, Rappold, Gudrun, Rauch, Anita, Ropers, Hans-Hilger, von Spiczak, Sarah, Tonnies, Holger, Villeneuve, Nathalie, Villard, Laurent, Zabel, Bernhard, Zenker, Martin, Laube, Bodo, Reis, Andre, Wieczorek, Dagmar, Van Maldergem, Lionel, Kutsche, Kerstin

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Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing von Nayak, Shalini S., Schneeberger, Pauline E., Patil, Siddaramappa J., Arun, Karegowda M., Suresh, Pujar V., Kiran, Viralam S., Siddaiah, Sateesh, Maiya, Shreesha, Venkatachalagupta, Shrikanth K., Kausthubham, Neethukrishna, Kortüm, Fanny, Rau, Isabella, Wey-Fabrizius, Alexandra, Van Den Heuvel, Lotte, Meester, Josephina, Van Laer, Lut, Shukla, Anju, Loeys, Bart, Girisha, Katta M., Kutsche, Kerstin

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A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl−/H+-Exchanger, Causes Early-Onset Neurodegeneration von Polovitskaya, Maya M., Barbini, Carlo, Martinelli, Diego, Harms, Frederike L., Cole, F. Sessions, Calligari, Paolo, Bocchinfuso, Gianfranco, Stella, Lorenzo, Ciolfi, Andrea, Niceta, Marcello, Rizza, Teresa, Shinawi, Marwan, Sisco, Kathleen, Johannsen, Jessika, Denecke, Jonas, Carrozzo, Rosalba, Wegner, Daniel J., Kutsche, Kerstin, Tartaglia, Marco, Jentsch, Thomas J.

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Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K + channelopathies von Gripp, Karen W, Smithson, Sarah F, Scurr, Ingrid J, Baptista, Julia, Majumdar, Anirban, Pierre, Germaine, Williams, Maggie, Henderson, Lindsay B, Wentzensen, Ingrid M, McLaughlin, Heather, Leeuwen, Lisette, Simon, Marleen E H, van Binsbergen, Ellen, Dinulos, Mary Beth P, Kaplan, Julie D, McRae, Anne, Superti-Furga, Andrea, Good, Jean-Marc, Kutsche, Kerstin

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Novel biallelic variants expand the SLC5A6-related phenotypic spectrum von Holling, Tess, Nampoothiri, Sheela, Tarhan, Bedirhan, Schneeberger, Pauline E, Vinayan, Kollencheri Puthenveettil, Yesodharan, Dhanya, Roy, Arun Grace, Radhakrishnan, Periyasamy, Alawi, Malik, Rhodes, Lindsay, Girisha, Katta Mohan, Kang, Peter B, Kutsche, Kerstin

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Fundamental Approaches to Software Engineering: 5th International Conference, FASE 2002, Held As Part of the Joint European Conferences on Theory and Practice of Software, ETAPS 20... von Kutsche, Ralf-Detlef, Weber, Herbert

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