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Treatment of MOG antibody associated disorders: results of an international survey.
Whittam, D.H. and Karthikeayan, V. and Gibbons, E. and Kneen, R. and Chandratre, S. and Ciccarelli, O. and Hacohen, Y. and de Seze, J. and Deiva, K. and Hintzen, R.Q. and Wildemann, B. and Jarius, S. and Kleiter, I. and Rostasy, K. and Huppke, P. and Hemmer, B. and Paul, F. and Aktas, O. and Pröbstel, A.K. and Arrambide, G. and Tintore, M. and Amato, M.P. and Nosadini, M. and Mancardi, M.M. and Capobianco, M. and Illes, Z. and Siva, A. and Altintas, A. and Akman-Demir, G. and Pandit, L. and Apiwattankul, M. and Hor, J.Y. and Viswanathan, S. and Qiu, W. and Kim, H.J. and Nakashima, I. and Fujihara, K. and Ramanathan, S. and Dale, R.C. and Boggild, M. and Broadley, S. and Lana-Peixoto, M.A. and Sato, D.K. and Tenembaum, S. and Cabre, P. and Wingerchuk, D.M. and Weinshenker, B.G. and Greenberg, B. and Matiello, M. and Klawiter, E.C. and Bennett, J.L. and Wallach, A.I. and Kister, I. and Banwell, B.L. and Traboulsee, A. and Pohl, D. and Palace, J. and Leite, M.I. and Levy, M. and Marignier, R. and Solomon, T. and Lim, M. and Huda, S. and Jacob, A.
Journal of Neurology 367 (12): 3565-3577. December 2020


Can we predict cognitive decline after initial diagnosis of multiple sclerosis? Results from the German National early MS cohort (KKNMS).
Johnen, A. and Bürkner, P.C. and Landmeyer, N.C. and Ambrosius, B. and Calabrese, P. and Motte, J. and Hessler, N. and Antony, G. and König, I.R. and Klotz, L. and Hoshi, M.M. and Aly, L. and Groppa, S. and Luessi, F. and Paul, F. and Tackenberg, B. and Bergh, F.T. and Kümpfel, T. and Tumani, H. and Stangel, M. and Weber, F. and Bayas, A. and Wildemann, B. and Heesen, C. and Zettl, U.K. and Zipp, F. and Hemmer, B. and Meuth, S.G. and Gold, R. and Wiendl, H. and Salmen, A.
Journal of Neurology 266 (2): 386-397. February 2019


Optical coherence tomography for the diagnosis and monitoring of idiopathic intracranial hypertension.
Albrecht, P. and Blasberg, C. and Ringelstein, M. and Mueller, A.K. and Finis, D. and Guthoff, R. and Kadas, E.M. and Lagreze, W. and Aktas, O. and Hartung, H.P. and Paul, F. and Brandt, A.U. and Methner, A.
Journal of Neurology 264 (7): 1370-1380. July 2017


Importance of cerebrospinal fluid analysis in the era of McDonald 2010 criteria: a German-Austrian retrospective multicenter study in patients with a clinically isolated syndrome.
Huss, A.M. and Halbgebauer, S. and Öckl, P. and Trebst, C. and Spreer, A. and Borisow, N. and Harrer, A. and Brecht, I. and Balint, B. and Stich, O. and Schlegel, S. and Retzlaff, N. and Winkelmann, A. and Roesler, R. and Lauda, F. and Yildiz, O. and Voss, E. and Muche, R. and Rauer, S. and Bergh, F.T. and Otto, M. and Paul, F. and Wildemann, B. and Kraus, J. and Ruprecht, K. and Stangel, M. and Buttmann, M. and Zettl, U.K. and Tumani, H.
Journal of Neurology 263 (12): 2499-2504. December 2016

Efficacy of glatiramer acetate in neuromyelitis optica spectrum disorder: a multicenter retrospective study.
Ayzenberg, I. and Schöllhammer, J. and Hoepner, R. and Hellwig, K. and Ringelstein, M. and Aktas, O. and Kümpfel, T. and Krumbholz, M. and Trebst, C. and Paul, F. and Pache, F. and Obermann, M. and Zeltner, L. and Schwab, M. and Berthele, A. and Jarius, S. and Kleiter, I.
Journal of Neurology 263 (3): 575-582. March 2016

Status of diagnostic approaches to AQP4-IgG seronegative NMO and NMO/MS overlap syndromes.
Juryńczyk, M. and Weinshenker, B. and Akman-Demir, G. and Asgari, N. and Barnes, D. and Boggild, M. and Chaudhuri, A. and D'hooghe, M. and Evangelou, N. and Geraldes, R. and Illes, Z. and Jacob, A. and Kim, H.J. and Kleiter, I. and Levy, M. and Marignier, R. and McGuigan, C. and Murray, K. and Nakashima, I. and Pandit, L. and Paul, F. and Pittock, S. and Selmaj, K. and de Sèze, J. and Siva, A. and Tanasescu, R. and Vukusic, S. and Wingerchuk, D. and Wren, D. and Leite, I. and Palace, J.
Journal of Neurology 263 (1): 140-149. January 2016


Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.
Doss, S. and Rinnenthal, J.L. and Schmitz-Hübsch, T. and Brandt, A.U. and Papazoglou, S. and Lux, S. and Maul, S. and Würfel, J. and Endres, M. and Klockgether, T. and Minnerop, M. and Paul, F.
Journal of Neurology 262 (8): 1927-1935. August 2015

Very late-onset neuromyelitis optica spectrum disorder beyond the age of 75.
Krumbholz, M. and Hofstadt-van Oy, U. and Angstwurm, K. and Kleiter, I. and Jarius, S. and Paul, F. and Aktas, O. and Buchholz, G. and Kern, P. and Straube, A. and Kümpfel, T.
Journal of Neurology 262 (5): 1379-1384. May 2015


Detailing intra-lesional venous lumen shrinking in multiple sclerosis investigated by sFLAIR MRI at 7-T.
Mueller, K. and Kuchling, J. and Doerr, J. and Harms, L. and Ruprecht, K. and Niendorf, T. and Wuerfel, J. and Paul, F. and Sinnecker, T.
Journal of Neurology 261 (10): 2032-2036. October 2014

Update on the diagnosis and treatment of neuromyelitis optica: recommendations of the Neuromyelitis Optica Study Group (NEMOS).
Trebst, C. and Jarius, S. and Berthele, A. and Paul, F. and Schippling, S. and Wildemann, B. and Borisow, N. and Kleiter, I. and Aktas, O. and Kümpfel, T.
Journal of Neurology 261 (1): 1-16. January 2014


Dynamics of saccade parameters in multiple sclerosis patients with fatigue.
Finke, C. and Pech, L.M. and Soemmer, C. and Schlichting, J. and Stricker, S. and Endres, M. and Ostendorf, F. and Ploner, C.J. and Brandt, A.U. and Paul, F.
Journal of Neurology 259 (12): 2656-2663. December 2012

Can we overcome the 'clinico-radiological paradox' in multiple sclerosis?
Hackmack, K. and Weygandt, M. and Wuerfel, J. and Pfueller, C.F. and Bellmann-Strobl, J. and Paul, F. and Haynes, J.D.
Journal of Neurology 259 (10): 2151-2160. October 2012


Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values.
Gong, M. and Rueschendorf, F. and Marx, P. and Schulz, H. and Kraft, H.G. and Huebner, N. and Koennecke, H.C.
Journal of Neurology 257 (8): 1240-1245. August 2010


Neuromyelitis and more: the unfolding spectrum of aquaporin 4-related neurological diseases.
Aktas, O. and Hartung, H.P.
Journal of Neurology 256 (11): 1906-1908. November 2009


Bell's palsy: combined treatment of famciclovir and prednisone is superior to prednisone alone.
Minnerop, M. and Herbst, M. and Fimmers, R. and Matz, B. and Klockgether, T. and Wuellner, U.
Journal of Neurology 255 (11): 1726-1730. November 2008


A new LMNA mutation causing limb girdle muscular dystrophy 1B.
Spuler, S. and Geier, C. and Osterziel, K.J. and Gutberlet, M. and Genschel, J. and Lehmann, T.N. and Zinn-Justin, S. and Gilquin, B. and Schmidt, H.
Journal of Neurology 252 (5): 621-623. May 2005

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