Installation of the soft X-ray multi-camera tomography system (XMCTS) in the Wendelstein 7-X stellarator von Brandt, C., Broszat, T., Thomsen, H., Laube, R., Marquardt, M., Franz, P., Schülke, M., Sieber, T., Weißflog, S.

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Soft x-ray tomography measurements in the Wendelstein 7-X stellarator von Brandt, C, Schilling, J, Thomsen, H, Broszat, T, Laube, R, Schröder, T, Andreeva, T, Beurskens, M N A, Bozhenkov, S A, Brunner, K J, Card, A, Cordes, C, Damm, H, Fuchert, G, Gallowski, K, Gutzmann, R, Knauer, J, Laqua, H P, Marquardt, M, Nelde, Ph, Neuner, U, Pasch, E, Rahbarnia, K, Recknagel, J, Schülke, M, Scott, E R, Sieber, T

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Upgrades of edge, divertor and scrape-off layer diagnostics of W7‐X for OP1.2 von Hathiramani, D., Ali, A., Anda, G., Barbui, T., Biedermann, C., Charl, A., Chauvin, D., Czymek, G., Dhard, C.P., Drewelow, P., Dudek, A., Effenberg, F., Ehrke, G., Endler, M., Ennis, D.A., Fellinger, J., Ford, O., Freundt, S., Gradic, D., Grosser, K., Harris, J., Hölbe, H., Jakubowski, M.W., Knaup, M., Kocsis, G., König, R., Krause, M., Kremeyer, T., Kornejew, P., Krychowiak, M., Lambertz, H.T., Jenzsch, H., Mayer, M., Mohr, S., Neubauer, O., Otte, M., Perseo, V., Pilopp, D., Rudischhauser, L., Schmitz, O., Schweer, B., Schülke, M., Stephey, L., Szepesi, T., Terra, A., Toth, M., Wenzel, U., Wurden, G.A., Zoletnik, S., Pedersen, T. Sunn

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Axial myopathy in a patient with a heterozygous MSTN mutation von Voermans, N, Kusters, B, Rooy, J, Dieks, R, van Engelen, B, Kamsteeg, E, Schülke, M

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Critically Ill Patients With Icu-Acquired Weakness Show Reduced Density of Myosin in Electron Microscope Early After Onset of Critical Illness von Rathke, T, Wollersheim, T, Krebs, M, Schülke, M, Weber-Carstens, S

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CONGENITAL MYOPATHIES: GENERAL AND RYR1 von Schülke, M., Stenzel, W., Schwarz, M., Goebel, H.

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CONGENITAL MYOPATHIES: GENERAL AND RYR1: P.39Congenital cytoplasmic body myopathy – a nosological clarification von Schülke, M., Stenzel, W., Schwarz, M., Goebel, H.

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T.P.3.08 Clinical trial of epigallocatechin-3-gallate in Duchenne muscular dystrophy von von Moers, A, Paul, F, Schülke, M, Ohlraum, S, Nakae, Y, Dorchies, O.M, Ruegg, U.T

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Ambient Assistive Technologies (AAT): socio-technology as a powerful tool for facing the inevitable sociodemographic challenges? von Schülke, Astrid M, Plischke, Herbert, Kohls, Niko B

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Prolonged Grief Disorder in the Next of Kin of Adult Patients Who Die During or After Admission to Intensive Care von Rodríguez Villar, Sancho, LMS, Sánchez Casado, Marcelino, LMS, PhD, Prigerson, Holly G., MD, PhD, Mesa García, Silvia, NS, Rodríguez Villar, María, NS, Hortigüela Martín, Victoria A., LMS, Marco Schulke, Carlos M., LMS, Barrientos Vega, Rafael, LMS, Quintana, Manolo, LMS, PhD

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PP03.1 – 3059: Mutations in ECHS1: A defect in a multifunctional enzyme causing a mitochondrial disorder von Freisinger, P, Haack, T.B, Kölker, S, Schülke-Gerstenfeld, M, Mayr, J, Klopstock, T, Rodenburg, R, Trollmann, R, Nuoffer, J.M, Sperl, W, Taylpr, R, Krägeloh-Mann, I, Meitinger, T, Prokisch, H

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513P Deposition of MAC and IgG subclasses at the neuromuscular junction in LRP4+ myasthenia gravis von Hoffmann, S., Meisel, A., Brokamp, K., Helmig, L., Schülke-Gerstenfeld, M., Rückert, J., Pumberger, M., Schömig, F., Ruck, T., Pawlitzki, M., Stenzel, W., Preusse, C.

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Recessive mutation in EXOSC9 disrupts the exosome complex resulting in a novel form of cerebellar hypoplasia/atrophy with early motor neuronopathy von Donkervoort, S., Müller, J., Knierim, E., Bharucha-Goebel, D., Dyack, S., Burns, D., Hu, Y., Baker, L., Ezzo, D., Scavina, M., Foley, A., Schülke, M., Bönnemann, C.

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NG.O.13 - Recessive mutation in EXOSC9 disrupts the exosome complex resulting in a novel form of cerebellar hypoplasia/atrophy with early motor neuronopathy von Donkervoort, S., Müller, J., Knierim, E., Bharucha-Goebel, D., Dyack, S., Burns, D., Hu, Y., Baker, L., Ezzo, D., Scavina, M., Foley, A., Schülke, M., Bönnemann, C.

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G.P.102 - Axial myopathy in a patient with a heterozygous MSTN mutation von Voermans, N., Kusters, B., Rooy, J., Dieks, R., van Engelen, B., Kamsteeg, E., Schülke, M.

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Drei neue Arten der Tachinus fimbriatus-Gruppe vom Emei Shan (China, Sichuan) und ein neues Synonym (Coleoptera: Staphylinidae: Tachyporinae) von M. Schülke

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A novel mutation L1425P in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE). Mutation in brief no. 230. Online von Peters, H, Hess, D, Fahsold, R, Schülke, M

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Technology development of the soft X-ray tomography system in Wendelstein 7-X stellarator von Schülke, M., Cardella, A., Hathiramani, D., Mettchen, S., Thomsen, H., Weißflog, S., Zacharias, D.

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A novel mutation L1425p in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE) von Peters, Hartmut, Hess, D., Fahsold, R., Schülke, M.

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A Rare Variant of Guillain-Barré Syndrome with Acute Motor Axonal Neuropathy (AMAN) in a Caucasian Boy von Nagdyman, N., Behse, F., Schülke, M.

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