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Serum glial fibrillary acidic protein: a neuromyelitis optica spectrum disorder biomarker.
Aktas, O. and Smith, M.A. and Rees, W.A. and Bennett, J.L. and She, D. and Katz, E. and Cree, B.A.C.
Annals of Neurology 89 (5): 895-910. May 2021

Assessing dysferlinopathy patients over three years with a new motor scale.
Jacobs, M. and James, M.K. and Lowes, L.P. and Alfano, L.N. and Eagle, M. and Lofra, R.M. and Moore, U. and Feng, J. and Rufibach, L.E. and Rose, K. and Duong, T. and Bello, L. and Pedrosa-Hernández, I. and Holsten, S. and Sakamoto, C. and Canal, A. and Práxedes, N.S.A. and Thiele, S. and Siener, C. and Vandevelde, B. and DeWolf, B. and Maron, E. and Guglieri, M. and Hogrel, J.Y. and Blamire, A.M. and Carlier, P.G. and Spuler, S. and Day, J.W. and Jones, K.J. and Bharucha-Goebel, D.X. and Salort-Campana, E. and Pestronk, A. and Walter, M.C. and Paradas, C. and Stojkovic, T. and Mori-Yoshimura, M. and Bravver, E. and Díaz-Manera, J. and Pegoraro, E. and Mendell, J.R. and Mayhew, A.G. and Straub, V.
Annals of Neurology 89 (5): 967-978. May 2021


Identifying progression in multiple sclerosis: new perspectives.
Filippi, M. and Preziosa, P. and Langdon, D. and Lassmann, H. and Paul, F. and Rovira, À. and Schoonheim, M.M. and Solari, A. and Stankoff, B. and Rocca, M.A.
Annals of Neurology 88 (3): 438-452. September 2020

Human cerebrospinal fluid monoclonal LGI1 autoantibodies increase neuronal excitability.
Kornau, H.C. and Kreye, J. and Stumpf, A. and Fukata, Y. and Parthier, D. and Sammons, R.P. and Imbrosci, B. and Kurpjuweit, S. and Kowski, A.B. and Fukata, M. and Prüss, H. and Schmitz, D.
Annals of Neurology 87 (3): 405-418. March 2020


Human gestational N-methyl-d-aspartate receptor autoantibodies impair neonatal murine brain function.
Jurek, B. and Chayka, M. and Kreye, J. and Lang, K. and Kraus, L. and Fidzinski, P. and Kornau, H.C. and Dao, L.M. and Wenke, N.K. and Long, M. and Rivalan, M. and Winter, Y. and Leubner, J. and Herken, J. and Mayer, S. and Mueller, S. and Boehm-Sturm, P. and Dirnagl, U. and Schmitz, D. and Kölch, M. and Prüss, H.
Annals of Neurology 86 (5): 656-670. November 2019

Optimal intereye difference thresholds by optical coherence tomography in multiple sclerosis: an international study.
Nolan, R.C. and Liu, M. and Akhand, O. and Calabresi, P.A. and Paul, F. and Petzold, A. and Balk, L. and Brandt, A.U. and Martínez-Lapiscina, E.H. and Saidha, S. and Villoslada, P. and Abu Al-Hassan, A. and Behbehani, R. and Frohman, E.M. and Frohman, T. and Havla, J. and Hemmer, B. and Jiang, H. and Knier, B. and Korn, T. and Leocani, L. and Papadopoulou, A. and Pisa, M. and Zimmermann, H. and Galetta, S.L. and Balcer, L.J.
Annals of Neurology 85 (5): 618-629. May 2019


Neuromyelitis optica: evaluation of 871 attacks and 1153 treatment courses.
Kleiter, I. and Gahlen, A. and Borisow, N. and Fischer, K. and Wernecke, K.D. and Wegner, B. and Hellwig, K. and Pache, F. and Ruprecht, K. and Havla, J. and Krumbholz, M. and Kümpfel, T. and Aktas, O. and Hartung, H.P. and Ringelstein, M. and Geis, C. and Kleinschnitz, C. and Berthele, A. and Hemmer, B. and Angstwurm, K. and Stellmann, J.P. and Schuster, S. and Stangel, M. and Lauda, F. and Tumani, H. and Mayer, C. and Zeltner, L. and Ziemann, U. and Linker, R. and Schwab, M. and Marziniak, M. and Bergh, F.T. and Hofstadt-van Oy, U. and Neuhaus, O. and Winkelmann, A. and Marouf, W. and Faiss, J. and Wildemann, B. and Paul, F. and Jarius, S. and Trebst, C.
Annals of Neurology 79 (2): 206-216. February 2016


Rare variants in GABA(A) receptor genes in Rolandic epilepsy and related syndromes.
Reinthaler, E.M. and Dejanovic, B. and Lal, D. and Semtner, M. and Merkler, Y. and Reinhold, A. and Pittrich, D.A. and Hotzy, C. and Feucht, M. and Steinboeck, H. and Gruber-Sedlmayr, U. and Ronen, G. and Neophytou, B. and Geldner, J. and Haberlandt, E. and Muhle, H. and Ikram, M.A. and van Duijn, CM. and Uitterlinden, A.G. and Hofman, A. and Altmueller, J. and Kawalia, A. and Toliat, M.R. and Nuernberg, P. and Lerche, H. and Nothnagel, M. and Thiele, H. and Sander, T. and Meier, J.C. and Schwarz, G. and Neubauer, B.A. and Zimprich, F.
Annals of Neurology 77 (6): 972-986. June 2015


Functional and structural brain changes in anti-N-methyl-D-aspartate receptor encephalitis.
Finke, C. and Kopp, U.A. and Scheel, M. and Pech, L.M. and Soemmer, C. and Schlichting, J. and Leypoldt, F. and Brandt, A.U. and Wuerfel, J. and Probst, C. and Ploner, C.J. and Prüss, H. and Paul, F.
Annals of Neurology 74 (2): 284-296. August 2013


No cerebrocervical venous congestion in patients with multiple sclerosis.
Doepp, F. and Paul, F. and Valdueza, J.M. and Schmierer, K. and Schreiber, S.J.
Annals of Neurology 68 (2): 173-183. August 2010

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.
Knoblauch, H. and Geier, C. and Adams, S. and Budde, B. and Rudolph, A. and Zacharias, U. and Schulz-Menger, J. and Spuler, A. and Yaou, R.B. and Nuernberg, P. and Voit, T. and Bonne, G. and Spuler, S.
Annals of Neurology 67 (1): 136-140. January 2010


Lower motor neuron loss in multiple sclerosis and experimental autoimmune encephalomyelitis.
Vogt, J. and Paul, F.E. and Aktas, O. and Mueller-Wielsch, K. and Doerr, J. and Doerr, S. and Bharathi, B.S. and Glumm, R. and Schmitz, C. and Steinbusch, H. and Raine, C.S. and Tsokos, M. and Nitsch, R. and Zipp, F.
Annals of Neurology 66 (3): 310-322. September 2009


Dysferlin-deficient muscular dystrophy features amyloidosis.
Spuler, S. and Carl, M. and Zabojszcza, J. and Straub, V. and Bushby, K. and Moore, S.A. and Baehring, S. and Wenzel, K. and Vinkemeier, U. and Rocken, C.
Annals of Neurology 63 (3): 323-328. March 2008


Low stability of huntington muscle mitochondria against Ca2+ in R6/2 mice.
Gizatullina, Z.Z. and Lindenberg, K.S. and Harjes, P. and Chen, Y. and Kosinski, C.M. and Landwehrmeyer, B.G. and Ludolph, A.C. and Striggow, F. and Zierz, S. and Gellerich, F.N.
Annals of Neurology 59 (2): 407-411. February 2006


Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy.
Tauer, U. and Lorenz, S. and Lenzen, K.P. and Heils, A. and Muhle, H. and Gresch, M. and Neubauer, B.A. and Waltz, S. and Rudolf, G. and Mattheisen, M. and Strauch, K. and Schmitz, B. and Stephani, U. and Sander, T.
Annals of Neurology 57 (6): 866-873. 1 January 2005


Imaging-guided convection-enhanced delivery and gene therapy of glioblastoma.
Voges, J. and Reszka, R. and Gossmann, A. and Dittmar, C. and Richter, R. and Garlip, G. and Kracht, L. and Coenen, H.H. and Sturm, V. and Wienhard, K. and Heiss, W.D. and Jacobs, A.H.
Annals of Neurology 54 (4): 479-487. October 2003

Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia.
Bunse, M. and Bit-Avragim, N. and Riefflin, A. and Perrot, A. and Schmidt, O. and Kreuz, F.R. and Dietz, R. and Jung, W.I. and Osterziel, K.J.
Annals of Neurology 53 : 121-123. 1 January 2003


Neuroplasticity in old age: sustained fivefold induction of hippocampal neurogenesis by long-term environmental enrichment.
Kempermann, G. and Gast, D. and Gage, F.H.
Annals of Neurology 52 (2): 135-143. August 2002


Amyloid myopathy: an underdiagnosed entity.
Spuler, S. and Emslie-Smith, A. and Engel, A.G.
Annals of Neurology 43 (6): 719-728. June 1998


SMI-31 immunoreactivity in inclusion body myositis.
Spuler, S. and Engel, A.G.
Annals of Neurology 42 (5): 815. November 1997


The phenotypic spectrum related to the human epilepsy susceptibility gene ejm1.
Sander, T. and Hildmann, T. and Janz, D. and Wienker, T.F. and Neitzel, H. and Bianchi, A. and Bauer, G. and Sailer, U. and Berek, K. and Schmitz, B. and Beckmannagetta, G.
Annals of Neurology 38 (2): 210-217. 1 January 1995

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