Macrophage Migration Inhibitory Factor in Major Depressive Disorder: A Multilevel Pilot Study by Swoboda, Caroline, Deloch, Lena, von Zimmermann, Claudia, Richter-Schmidinger, Tanja, Lenz, Bernd, Kornhuber, Johannes, Mühle, Christiane

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Fusion gene detection by RNA-sequencing complements diagnostics of acute myeloid leukemia and identifies recurring NRIP1-MIR99AHG rearrangements by Kerbs, Paul, Vosberg, Sebastian, Krebs, Stefan, Graf, Alexander, Blum, Helmut, Swoboda, Anja, Batcha, Aarif M N, Mansmann, Ulrich, Metzler, Dirk, Heckman, Caroline A, Herold, Tobias, Greif, Philipp A

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Rapid Cardiovascular Magnetic Resonance for Ischemic Heart Disease Investigation (RAPID-IHD) by Foley, James R.J., Richmond, Caroline, Fent, Graham J., Bissell, Malenka, Levelt, Eylem, Dall’armellina, Erica, Swoboda, Peter P., Plein, Sven, Greenwood, John P.

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Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1 by Schessl, Joachim, Taratuto, Ana L., Sewry, Caroline, Battini, Roberta, Chin, Steven S., Maiti, Baijayanta, Dubrovsky, Alberto L., Erro, Marcela G., Espada, Graciela, Robertella, Monica, Saccoliti, Maria, Olmos, Patricia, Bridges, Leslie R., Standring, Peter, Hu, Ying, Zou, Yaqun, Swoboda, Kathryn J., Scavina, Mena, Goebel, Hans-Hilmar, Mitchell, Christina A., Flanigan, Kevin M., Muntoni, Francesco, Bönnemann, Carsten G.

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Auditory frequency discrimination in developmental dyslexia: A meta‐analysis by Witton, Caroline, Swoboda, Katy, Shapiro, Laura R., Talcott, Joel B.

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Teaching cultural dexterity in surgical care: As essential to a surgeon's skill set as tying a knot by Ortega, Gezzer, Dacier, Brittany M., Dacier, Brittany M., Zárate Rodriguez, Jorge, Zárate Rodriguez, Jorge, Chun, Maria B.J., Chun, Maria B.J., Udyavar, N. Rhea, Allar, Benjamin G., Allar, Benjamin G., Green, Alexander R., Green, Alexander R., Haider, Adil H., Haider, Adil H., Smink, Douglas S., Atkinson, Rachel B., Barreiro-Rosado, Jeenn, Britt, L.D., Brittain, Molly A., Caldwell, Katharine, Chen, Annie, Demko, Caroline, Harrington, David T., Kent, Tara S., Olufajo, Olubode A., Lipsett, Pamela A., Lynch, Kenneth A., Mullen, John T., Ortega, Gezzer, Petrusa, Emil, Reidy, Emma, Sheu, Christina, Smink, Douglas S., Swoboda, Sandra M., Wilson, Lori L., Wise, Paul E.

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Distinct neurological disorders with ATP1A3 mutations by Heinzen, Erin L, Dr, Arzimanoglou, Alexis, MD, Brashear, Allison, Prof, Clapcote, Steven J, PhD, Gurrieri, Fiorella, Prof, Goldstein, David B, Prof, Jóhannesson, Sigurður H, Mikati, Mohamad A, Prof, Neville, Brian, Prof, Nicole, Sophie, PhD, Ozelius, Laurie J, PhD, Poulsen, Hanne, PhD, Schyns, Tsveta, PhD, Sweadner, Kathleen J, PhD, van den Maagdenberg, Arn, Prof, Vilsen, Bente, Prof

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Concordance of Resident and Patient Perceptions of Culturally Dexterous Patient Care Skills by Atkinson, Rachel B., Ortega, Gezzer, Green, Alexander R., Chun, Maria B.J., Harrington, David T., Lipsett, Pamela A., Mullen, John T., Petrusa, Emil, Reidy, Emma, Haider, Adil H., Smink, Douglas S.

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Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy by Wallgren-Pettersson, Carina, Pelin, Katarina, Hilpelä, Pirta, Donner, Kati, Porfirio, Berardino, Graziano, Claudio, Swoboda, Kathryn J., Fardeau, Michel, Urtizberea, J.Andoni, Muntoni, Francesco, Sewry, Caroline, Dubowitz, Victor, Iannaccone, Susan, Minetti, Carlo, Pedemonte, Marina, Seri, Marco, Cusano, Roberto, Lammens, Martin, Castagna-Sloane, Avril, Beggs, Alan H., Laing, Nigel G., de la Chapelle, Albert

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Combined Fmoc-Alloc strategy for a general SPPS of phosphoserine peptides; preparation of phosphorylation-dependent tau antisera by Shapiro, Gideon, Büchler, Dieter, Dalvit, Claudio, Frey, Peter, Fernández, Maria del Carmen, Gomez-Lor, Berta, Pombo-Villar, Esteban, Stauss, Urs, Swoboda, Robert, Waridel, Caroline

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