VEXAS-Syndrom – Erfolg der multidisziplinären Zusammenarbeit von Ferincz, V., Hackner, K., Kopetzky, G., Schöls, K., Wegscheider, C., Mihalcz, A., Maieron, A.

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Fallbericht und Review: Symmetrische Gelenkschwellung bedeutet nicht automatisch Arthritis von Ferincz, V., Schöls, K., Leeb, B. F., Maieron, A.

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Breast milk of atopic mothers provides their infants with normal amounts of w-6-fatty acids von Schroten, H., Schöls, K., Melnik, B., VonKries, R., Wahn, V., Biggemann, B.

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Perceived stress mediates the effect of yoga on quality of life and disease activity in ulcerative colitis. Secondary analysis of a randomized controlled trial von Koch, Anna K., Schöls, Margarita, Langhorst, Jost, Dobos, Gustav, Cramer, Holger

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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy von Syrbe, Steffen, Hedrich, Ulrike B S, Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S, Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S, Arslan, Mutluay, Serratosa, José M, Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C, Hoffman-Zacharska, Dorota, Korff, Christian M, Weber, Yvonne G, Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K, Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M, Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R

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Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis von Ehnert, Sabrina, Hauser, Stefan, Hengel, Holger, Höflinger, Philip, Schüle, Rebecca, Lindig, Tobias, Baets, Jonathan, Deconinck, Tine, de Jonghe, Peter, Histing, Tina, Nüssler, Andreas K., Schöls, Ludger, Rattay, Tim W.

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Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights von Rüb, U., Bürk, K., Timmann, D., den Dunnen, W., Seidel, K., Farrag, K., Brunt, E., Heinsen, H., Egensperger, R., Bornemann, A., Schwarzacher, S., Korf, H.-W., Schöls, L., Bohl, J., Deller, T.

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The Predictive Validity of the Tilburg Frailty Indicator: Disability, Health Care Utilization, and Quality of Life in a Population at Risk von Gobbens, Robbert J. J, van Assen, Marcel A. L. M, Luijkx, Katrien G, Schols, Jos M. G. A

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Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3 von Garcia‐Moreno, Hector, Prudencio, Mercedes, Thomas‐Black, Gilbert, Solanky, Nita, Jansen‐West, Karen R., Hanna AL‐Shaikh, Rana, Heslegrave, Amanda, Zetterberg, Henrik, Santana, Magda M., Pereira de Almeida, Luis, Vasconcelos‐Ferreira, Ana, Januário, Cristina, Infante, Jon, Faber, Jennifer, Klockgether, Thomas, Reetz, Kathrin, Raposo, Mafalda, Ferreira, Ana F., Lima, Manuela, Schöls, Ludger, Synofzik, Matthis, Hübener‐Schmid, Jeannette, Puschmann, Andreas, Gorcenco, Sorina, Wszolek, Zbigniew K., Petrucelli, Leonard, Giunti, Paola

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Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia von Pellerin, David, Danzi, Matt C., Wilke, Carlo, Renaud, Mathilde, Fazal, Sarah, Dicaire, Marie-Josée, Scriba, Carolin K., Ashton, Catherine, Yanick, Christopher, Beijer, Danique, Rebelo, Adriana, Rocca, Clarissa, Jaunmuktane, Zane, Sonnen, Joshua A., Larivière, Roxanne, Genís, David, Molina Porcel, Laura, Choquet, Karine, Sakalla, Rawan, Provost, Sylvie, Robertson, Rebecca, Allard-Chamard, Xavier, Tétreault, Martine, Reiling, Sarah J., Nagy, Sara, Nishadham, Vikas, Purushottam, Meera, Vengalil, Seena, Bardhan, Mainak, Nalini, Atchayaram, Chen, Zhongbo, Mathieu, Jean, Massie, Rami, Chalk, Colin H., Lafontaine, Anne-Louise, Evoy, François, Rioux, Marie-France, Ragoussis, Jiannis, Boycott, Kym M., Dubé, Marie-Pierre, Duquette, Antoine, Houlden, Henry, Ravenscroft, Gianina, Laing, Nigel G., Lamont, Phillipa J., Saporta, Mario A., Schüle, Rebecca, Schöls, Ludger, La Piana, Roberta, Synofzik, Matthis, Zuchner, Stephan, Brais, Bernard

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Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients von Schlipf, NA, Schüle, R, Klimpe, S, Karle, KN, Synofzik, M, Schicks, J, Riess, O, Schöls, L, Bauer, P

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Quantitative Assessment of Brain Stem and Cerebellar Atrophy in Spinocerebellar Ataxia Types 3 and 6: Impact on Clinical Status von EICHLER, L, BELLENBERG, B, HAHN, H. K, KÖSTER, O, SCHÖLS, L, LUKAS, C

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High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia von BEETZ, C, NYGREN, A. O. H, OTTO, S, SCHÜLE, R, SCHÖLS, L, SPERFELD, A.-D, WITTE, O. W, DEUFEL, T, SCHICKEL, J, AUER-GRUMBACH, M, BÜRK, K, HEIDE, G, KASSUBEK, J, KLIMPE, S, KLOPSTOCK, T, KREUZ, F

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Consensus Paper: Management of Degenerative Cerebellar Disorders von Ilg, W., Bastian, A. J., Boesch, S., Burciu, R. G., Celnik, P., Claaßen, J., Feil, K., Kalla, R., Miyai, I., Nachbauer, W., Schöls, L., Strupp, M., Synofzik, M., Teufel, J., Timmann, D.

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Human Milk Oligosaccharides in Colostrum and Mature Milk of Chinese Mothers: Lewis Positive Secretor Subgroups von Elwakiel, M, Hageman, J. A, Wang, W, Szeto, I. M, van Goudoever, J. B, Hettinga, K. A, Schols, H. A

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A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system von Khundadze, Mukhran, Kollmann, Katrin, Koch, Nicole, Biskup, Christoph, Nietzsche, Sandor, Zimmer, Geraldine, Hennings, J Christopher, Huebner, Antje K, Symmank, Judit, Jahic, Amir, Ilina, Elena I, Karle, Kathrin, Schöls, Ludger, Kessels, Michael, Braulke, Thomas, Qualmann, Britta, Kurth, Ingo, Beetz, Christian, Hübner, Christian A

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Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content von Solbach, K, Kraff, O, Minnerop, M, Beck, A, Schöls, L, Gizewski, E R, Ladd, M E, Timmann, D

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“Ears of the lynx” sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers von Rattay, Tim W., Schöls, Ludger, Zeltner, Lena, Rohrschneider, Wiltrud K., Ernemann, Ulrike, Lindig, Tobias

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Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian Authority von Mayer, Anja K., Balousha, Ghassan, Sharkia, Rajech, Mahajnah, Muhammad, Ayesh, Suhail, Schulze, Martin, Buchert, Rebecca, Zobor, Ditta, Azem, Abdussalam, Schoels, Ludger, Bauer, Peter, Wissinger, Bernd

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The 2015 Dutch food-based dietary guidelines von Kromhout, D, Spaaij, C J K, de Goede, J, Weggemans, R M

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