Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine von Haghikia, Aiden, Jörg, Stefanie, Duscha, Alexander, Berg, Johannes, Manzel, Arndt, Waschbisch, Anne, Hammer, Anna, Lee, De-Hyung, May, Caroline, Wilck, Nicola, Balogh, Andras, Ostermann, Annika I., Schebb, Nils Helge, Akkad, Denis A., Grohme, Diana A., Kleinewietfeld, Markus, Kempa, Stefan, Thöne, Jan, Demir, Seray, Müller, Dominik N., Gold, Ralf, Linker, Ralf A.

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Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine von Haghikia, Aiden, Jörg, Stefanie, Duscha, Alexander, Berg, Johannes, Manzel, Arndt, Waschbisch, Anne, Hammer, Anna, Lee, De-Hyung, May, Caroline, Wilck, Nicola, Balogh, Andras, Ostermann, Annika I., Schebb, Nils Helge, Akkad, Denis A., Grohme, Diana A., Kleinewietfeld, Markus, Kempa, Stefan, Thöne, Jan, Demir, Seray, Müller, Dominik N., Gold, Ralf, Linker, Ralf A.

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The genetics of multiple sclerosis: An update 2010 von Hoffjan, Sabine, Akkad, Denis A.

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Competing endogenous RNA network crosstalk reveals novel molecular markers in colorectal cancer von Samir, Nehal, Matboli, Marwa, El‐Tayeb, Hanaa, El‐Tawdi, Ahmed, Hassan, Mohmed K., Waly, Amr, EL‐Akkad, Hesham A. E., Ramadan, Mohamed G., Al‐Belkini, Tarek N., El‐Khamisy, Sherif, El‐Asmar, Farid

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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease von Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa

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Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients von Akkad, D.A, Hoffjan, S, Petrasch-Parwez, E, Beygo, J, Gold, R, Epplen, J.T

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A handy review of carpal tunnel syndrome: From anatomy to diagnosis and treatment von Ghasemi-Rad, Mohammad, Nosair, Emad, Vegh, Andrea, Mohammadi, Afshin, Akkad, Adam, Lesha, Emal, Mohammadi, Mohammad Hossein, Sayed, Doaa, Davarian, Ali, Maleki-Miyandoab, Tooraj, Hasan, Anwarul

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Telomere length in small‐for‐gestational‐age babies von Akkad, A, Hastings, R, Konje, JC, Bell, SC, Thurston, H, Williams, B

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Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity von Akkad, Denis A, Olischewsky, Alexandra, Reiner, Franziska, Hellwig, Kerstin, Esser, Sarika, Epplen, Jörg T, Curk, Tomaz, Gold, Ralf, Haghikia, Aiden

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SOX9 duplication linked to intersex in deer von Kropatsch, Regina, Dekomien, Gabriele, Akkad, Denis A, Gerding, Wanda M, Petrasch-Parwez, Elisabeth, Young, Neil D, Altmüller, Janine, Nürnberg, Peter, Gasser, Robin B, Epplen, Jörg T

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mtDNA nt13708A variant increases the risk of multiple sclerosis von Yu, Xinhua, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A, Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I, Mørk, Sverre J, Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G, Myhr, Kjell-Morten, Epplen, Joerg T, Saarela, Janna, Ibrahim, Saleh M

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Ccdc66 null mutation causes retinal degeneration and dysfunction von GERDING, Wanda M, SCHREIBER, Sabrina, RÜLICKE, Thomas, IBRAHIM, Saleh, EPPLEN, Jörg T, PETRASCH-PARWEZ, Elisabeth, SCHULTE-MIDDELMANN, Tobias, DE CASTRO MARQUES, Andreia, ATORF, Jenny, AKKAD, Denis A, DEKOMIEN, Gabriele, KREMERS, Jan, DERMIETZEL, Rolf, GAL, Andreas

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Gender differences in final year medical students’ experience of teaching of intimate examinations: a questionnaire study von Akkad, A, Bonas, S, Stark, P

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Association of TNFAIP3 and TNFRSF1A variation with multiple sclerosis in a German case-control cohort von Hoffjan, S., Okur, A., Epplen, J. T., Wieczorek, S., Chan, A., Akkad, D. A.

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Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS von Schrewe, L, Lill, C M, Liu, T, Salmen, A, Gerdes, L A, Guillot-Noel, L, Akkad, D A, Blaschke, P, Graetz, C, Hoffjan, S, Kroner, A, Demir, S, Böhme, A, Rieckmann, P, ElAli, A, Hagemann, N, Hermann, D M, Cournu-Rebeix, I, Zipp, F, Kümpfel, T, Buttmann, M, Zettl, U K, Fontaine, B, Bertram, L, Gold, R, Chan, A

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ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease von Arning, Larissa, Monté, Didier, Hansen, Wiebke, Wieczorek, Stefan, Jagiello, Peter, Akkad, Denis A., Andrich, Jürgen, Kraus, Peter H., Saft, Carsten, Epplen, Jörg T.

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Myocyte-Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2–Mediated Myocarditis von Tucker, Nathan R., Chaffin, Mark, Bedi, Kenneth C., Papangeli, Irinna, Akkad, Amer-Denis, Arduini, Alessandro, Hayat, Sikander, Eraslan, Gökcen, Muus, Christoph, Bhattacharyya, Roby P., Stegmann, Christian M., Margulies, Kenneth B., Ellinor, Patrick T.

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IL28B polymorphisms are not associated with the response to interferon-beta in multiple sclerosis von Malhotra, S, Morcillo-Suárez, C, Brassat, D, Goertsches, R, Lechner-Scott, J, Urcelay, E, Fernández, O, Drulovic, J, García-Merino, A, Martinelli Boneschi, F, Chan, A, Vandenbroeck, K, Navarro, A, Bustamante, M.F, Río, J, Akkad, D.A, Giacalone, G, Sánchez, A.J, Leyva, L, Alvarez-Lafuente, R, Zettl, U.K, Oksenberg, J, Montalban, X, Comabella, M

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Multiple organ dysfunction after trauma von Cole, E, Gillespie, S, Vulliamy, P, Brohi, K, Akkad, H, Apostolidou, K, Ardley, R, Aylwin, C, Bassford, C, Bonner, S, Brooks, A, Cairns, T, Cecconi, M, Clark, F, Dempsey, G, Denison Davies, E, Docking, R, Eddlestone, J, Ellis, D, Evans, J, Galea, M, Healy, M, Horner, D, Howarth, R, Jansen, J, Jones, J, Kaye, C, Keep, J, Kerslake, D, Kilic, J, Leong, M, Martinson, V, McIldowie, B, Michael, S, Millo, J, Morgan, M, O'Leary, R, Oram, J, Ortiz-Ruiz De Gordoa, L, Porter, K, Raby, S, Service, J, Shaw, D, Smith, J D, Smith, N, Stotz, M, Thomas, E, Thomas, M, Vincent, A, Ward, G, Welters, I

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Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitis von Hoffjan, S, Beygo, J, Akkad, D.A, Parwez, Q, Petrasch-Parwez, E, Epplen, J.T

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