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Damage of the lateral geniculate nucleus in MS: assessing the missing node of the visual pathway.
Papadopoulou, A. and Gaetano, L. and Pfister, A. and Altermatt, A. and Tsagkas, C. and Morency, F. and Brandt, A.U. and Hardmeier, M. and Chakravarty, M.M. and Descoteaux, M. and Kappos, L. and Sprenger, T. and Magon, S.
Neurology 92 (19): e2240-e2249. 7 May 2019

Assessment of disease progression in dysferlinopathy: a 1-year cohort study.
Moore, U. and Jacobs, M. and James, M.K. and Mayhew, A.G. and Fernandez-Torron, R. and Feng, J. and Cnaan, A. and Eagle, M. and Bettinson, K. and Rufibach, L.E. and Lofra, R.M. and Blamire, A.M. and Carlier, P.G. and Mittal, P. and Lowes, L.P. and Alfano, L. and Rose, K. and Duong, T. and Berry, K.M. and Montiel-Morillo, E. and Pedrosa-Hernández, I. and Holsten, S. and Sanjak, M. and Ashida, A. and Sakamoto, C. and Tateishi, T. and Yajima, H. and Canal, A. and Ollivier, G. and Decostre, V. and Mendez, J.B. and Sánchez-Aguilera Praxedes, N. and Thiele, S. and Siener, C. and Shierbecker, J. and Florence, J.M. and Vandevelde, B. and DeWolf, B. and Hutchence, M. and Gee, R. and Prügel, J. and Maron, E. and Hilsden, H. and Lochmüller, H. and Grieben, U. and Spuler, S. and Tesi Rocha, C. and Day, J.W. and Jones, K.J. and Bharucha-Goebel, D.X. and Salort-Campana, E. and Harms, M. and Pestronk, A. and Krause, S. and Schreiber-Katz, O. and Walter, M.C. and Paradas, C. and Hogrel, J.Y. and Stojkovic, T. and Takeda, S. and Mori-Yoshimura, M. and Bravver, E. and Sparks, S. and Díaz-Manera, J. and Bello, L. and Semplicini, C. and Pegoraro, E. and Mendell, J.R. and Bushby, K. and Straub, V.
Neurology 92 (5): e461-e474. 29 January 2019


Racial differences in neuromyelitis optica spectrum disorder.
Kim, S.H. and Mealy, M.A. and Levy, M. and Schmidt, F. and Ruprecht, K. and Paul, F. and Ringelstein, M. and Aktas, O. and Hartung, H.P. and Asgari, N. and Tsz-Ching, J.L. and Siritho, S. and Prayoonwiwat, N. and Shin, H.J. and Hyun, J.W. and Han, M. and Leite, M.I. and Palace, J. and Kim, H.J.
Neurology 91 (22): e2089-e2099. 27 November 2018

Golgin A4 in CSF and granulovacuolar degenerations of patients with Alzheimer disease.
Kork, F. and Jankowski, J. and Goswami, A. and Weis, J. and Brook, G. and Yamoah, A. and Anink, J. and Aronica, E. and Fritz, S. and Huck, C. and Schipke, C. and Peters, O. and Tepel, M. and Noels, H. and Jankowski, V.
Neurology 91 (19): e1799-e1808. 6 November 2018

Venoplasty in MS: Therapeutic intervention without any evidence.
Paul, F. and Wattjes, M.P.
Neurology 91 (18): 815-816. 30 October 2018


High risk of postpartum relapses in neuromyelitis optica spectrum disorder.
Klawiter, E.C. and Bove, R. and Elsone, L. and Alvarez, E. and Borisow, N. and Cortez, M. and Mateen, F. and Mealy, M.A. and Sorum, J. and Mutch, K. and Tobyne, S.M. and Ruprecht, K. and Buckle, G. and Levy, M. and Wingerchuk, D. and Paul, F. and Cross, A.H. and Jacobs, A. and Chitnis, T. and Weinshenker, B.
Neurology 89 (22): 2238-2244. 28 November 2017


The APOSTEL recommendations for reporting quantitative optical coherence tomography studies.
Cruz-Herranz, A. and Balk, L.J. and Oberwahrenbrock, T. and Saidha, S. and Martinez-Lapiscina, E.H. and Lagreze, W.A. and Schuman, J.S. and Villoslada, P. and Calabresi, P. and Balcer, L. and Petzold, A. and Green, A.J. and Paul, F. and Brandt, A.U. and Albrecht, P.
Neurology 86 (24): 2303-2309. 14 June 2016


Iridodonesis as a cause of recurrent vertigo.
Kunte, H. and Paul, F. and Pache, F. and Doerr, J. and Bellmann-Strobl, J. and Harms, L. and Kronenberg, G.
Neurology 85 (15): 1353. 13 October 2015

Retinal pathology in Susac syndrome detected by spectral-domain optical coherence tomography.
Ringelstein, M. and Albrecht, P. and Kleffner, I. and Bühn, B. and Harmel, J. and Müller, A.K. and Finis, D. and Guthoff, R. and Bergholz, R. and Duning, T. and Krämer, M. and Paul, F. and Brandt, A. and Oberwahrenbrock, T. and Mikolajczak, J. and Wildemann, B. and Jarius, S. and Hartung, H.P. and Aktas, O. and Dörr, J.
Neurology 85 (7): 610-618. 18 August 2015

Retinal pathology in idiopathic moyamoya angiopathy detected by optical coherence tomography.
Albrecht, P. and Blasberg, C. and Lukas, S. and Ringelstein, M. and Müller, A.K. and Harmel, J. and Kadas, E.M. and Finis, D. and Guthoff, R. and Aktas, O. and Hartung, H.P. and Paul, F. and Brandt, A.U. and Berlit, P. and Methner, A. and Kraemer, M.
Neurology 85 (6): 521-527. 11 August 2015

Pushing the boundaries of neuromyelitis optica: Does antibody make the disease?
Kister, I. and Paul, F.
Neurology 85 (2): 118-119. 14 July 2015

Subjective cognitive decline is related to CSF biomarkers of AD in patients with MCI.
Wolfsgruber, S. and Jessen, F. and Koppara, A. and Kleineidam, L. and Schmidtke, K. and Froelich, L. and Kurz, A. and Schulz, S. and Hampel, H. and Heuser, I. and Peters, O. and Reischies, F.M. and Jahn, H. and Luckhaus, C. and Huell, M. and Gertz, H.J. and Schroeder, J. and Pantel, J. and Rienhoff, O. and Ruether, E. and Henn, F. and Wiltfang, J. and Maier, W. and Kornhuber, J. and Wagner, M.
Neurology 84 (12): 1261-1268. 24 March 2015

MRI characteristics of neuromyelitis optica spectrum disorder: An international update.
Kim, H.J. and Paul, F. and Lana-Peixoto, M.A. and Tenembaum, S. and Asgari, N. and Palace, J. and Klawiter, E.C. and Sato, D.K. and de Seze, J. and Wuerfel, J. and Banwell, B.L. and Villoslada, P. and Saiz, A. and Fujihara, K. and Kim, S.H.
Neurology 84 (11): 1165-1173. 17 March 2015


The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.
Hooli, B.V. and Parrado, A.R. and Mullin, K. and Yip, W.K. and Liu, T. and Roehr, J.T. and Qiao, D. and Jessen, F. and Peters, O. and Becker, T. and Ramirez, A. and Lange, C. and Bertram, L. and Tanzi, R.E.
Neurology 83 (15): 1353-1358. 7 October 2014

Dynamic formation of macular microcysts independent of vitreous traction changes.
Brandt, A.U. and Oberwahrenbrock, T. and Kadas, E.M. and Lagrèze, W.A. and Paul, F.
Neurology 83 (1): 73-77. 1 July 2014


T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients.
Balint, B. and Haas, J. and Schwarz, A. and Jarius, S. and Fürwentsches, A. and Engelhardt, K. and Bussmann, C. and Ebinger, F. and Fritzsching, B. and Paul, F. and Seidel, U. and Vlaho, S. and Huppke, P. and Gärtner, J. and Wildemann, B.
Neurology 81 (9): 784-792. 27 August 2013

Bilateral vertebral artery dissection, agenesis of both ICAs, and connective tissue aberrations.
Lill, C.M. and Guenther-Kunkel, K. and Hoch, H. and Paul, F. and Grond-Ginsbach, C. and Hausser, I. and Zipp, F.
Neurology 80 (15): 1442-1443. 9 April 2013


Distinct lesion morphology at 7-T MRI differentiates neuromyelitis optica from multiple sclerosis.
Sinnecker, T. and Doerr, J. and Pfueller, C.F. and Harms, L. and Ruprecht, K. and Jarius, S. and Brueck, W. and Niendorf, T. and Wuerfel, J. and Paul, F.
Neurology 79 (7): 708-714. 14 August 2012

IgA NMDA receptor antibodies are markers of synaptic immunity in slow cognitive impairment.
Pruess, H. and Hoeltje, M. and Maier, N. and Gomez, A. and Buchert, R. and Harms, L. and Ahnert-Hilger, G. and Schmitz, D. and Terborg, C. and Kopp, U. and Klingbeil, C. and Probst, C. and Kohler, S. and Schwab, J.M. and Stoecker, W. and Dalmau, J. and Wandinger, K.P.
Neurology 78 (22): 1743-1753. 29 May 2012

Biomarker validation of a cued recall memory deficit in prodromal Alzheimer disease.
Wagner, M. and Wolf, S. and Reischies, F.M. and Daerr, M. and Wolfsgruber, S. and Jessen, F. and Popp, J. and Maier, W. and Huell, M. and Froelich, L. and Hampel, H. and Perneczky, R. and Peters, O. and Jahn, H. and Luckhaus, C. and Gertz, H.J. and Schroeder, J. and Pantel, J. and Lewczuk, P. and Kornhuber, J. and Wiltfang, J.
Neurology 78 (6): 379-386. 7 February 2012


Venous drainage in multiple sclerosis: A combined MRI and ultrasound study.
Doepp, F. and Wuerfel, J.T. and Pfueller, C.F. and Valdueza, J.M. and Petersen, D. and Paul, F. and Schreiber, S.J.
Neurology 77 (19): 1745-1751. 8 November 2011


Clinical features of facioscapulohumeral muscular dystrophy 2.
de Greef, J.C. and Lemmers, R.J. and Camano, P. and Day, J.W. and Sacconi, S. and Dunand, M. and van Engelen, B.G. and Kiuru-Enari, S. and Padberg, G.W. and Rosa, A.L. and Desnuelle, C. and Spuler, S. and Tarnopolsky, M. and Venance, S.L. and Frants, R.R. and van der Maarel, S.M. and Tawil, R.
Neurology 75 (17): 1548-1554. 26 October 2010


Poor PASAT performance correlates with MRI contrast enhancement in multiple sclerosis.
Bellmann-Strobl, J. and Wuerfel, J. and Aktas, O. and Doerr, J. and Wernecke, K.D. and Zipp, F. and Paul, F.
Neurology 73 (20): 1624-1627. 17 November 2009

Severe cardiac failure in a patient with multiple sclerosis following low-dose mitoxantrone treatment.
Doerr, J. and Bitsch, A. and Schmailzl, K.J. and Chan, A. and von Ahsen, N. and Hummel, M. and Varon, R. and Lill, C.M. and Vogel, H.P. and Zipp, F. and Paul, F.
Neurology 73 (12): 991-993. 22 September 2009


Celiac antibodies in the diagnostic workup of white matter lesions.
Paul, F. and Pfueller, C.F. and Wuerfel, J.T. and Egerer, K. and Tanczos, B. and Baumgart, D.C. and Zipp, F.
Neurology 71 (3): 223-225. 15 July 2008


Autoimmune autonomic ganglionopathy: IgG effects on ganglionic acetylcholine receptor current.
Wang, Z. and Lowden, P.A. and Jordan, J. and Freeman, R. and Gibbons, C.H. and Schroeder, C. and Sandroni, P. and Vernino, S.
Neurology 68 (22): 1917-1921. 29 May 2007

Classifications and treatment responses in chronic immune-mediated demyelinating polyneuropathy.
Tackenberg, B. and Luenemann, J.D. and Steinbrecher, A. and Rothenfusser-Korber, E. and Sailer, M. and Brueck, W. and Schock, S. and Zschenderlein, R. and Zipp, F. and Sommer, N.
Neurology 68 (19): 1622-1629. 8 May 2007

Muscle and nerve pathology in Dunnigan familial partial lipodystrophy.
Spuler, S. and Kalbhenn, T. and Zabojszcza, J. and van Landeghem, F.K. and Ludtke, A. and Wenzel, K. and Koehnlein, M. and Schuelke, M. and Luedemann, L. and Schmidt, H.H.
Neurology 68 (9): 677-683. 27 February 2007

Familial effects on the clinical course of multiple sclerosis.
Hensiek, A.E. and Seaman, S.R. and Barcellos, L.F. and Oturai, A. and Eraksoi, M. and Cocco, E. and Vecsei, L. and Stewart, G. and Dubois, B. and Bellman-Strobl, J. and Leone, M. and Andersen, O. and Bencsik, K. and Booth, D. and Celius, E.G. and Harbo, H.F. and Hauser, S.L. and Heard, R. and Hillert, J. and Myhr, K.M. and Marrosu, M.G. and Oksenberg, J.R. and Rajda, C. and Sawcer, S.J. and Sorensen, P.S. and Zipp, F. and Compston, D.A.S.
Neurology 68 (5): 376-383. 30 January 2007


Blockade of chemokine signaling in patients with multiple sclerosis.
Zipp, F. and Hartung, H.P. and Hillert, J. and Schimrigk, S. and Trebst, C. and Stangel, M. and Infante-Duarte, C. and Jakobs, P. and Wolf, C. and Sandbrink, R. and Pohl, C. and Filippi, M.
Neurology 67 (10): 1880-1883. 28 November 2006


Osmosensitive mechanisms contribute to the water drinking-induced pressor response in humans.
Lipp, A. and Tank, J. and Franke, G. and Arnold, G. and Luft, F.C. and Jordan, J.
Neurology 65 : 905-907. 27 September 2005

An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures.
Straussberg, R. and Basel-Vanagaite, L. and Kivity, S. and Dabby, R. and Cirak, S. and Nuernberg, P. and Voit, T. and Mahajnah, M. and Inbar, D. and Saifi, G.M. and Lupski, J.R. and Delague, V. and Megarbane, A. and Richter, A. and Leshinsky, E. and Berkovic, S.F.
Neurology 64 (1): 142-144. 1 January 2005


Inhibition of thrombus formation by low-dose acetylsalicylic acid, dipyridamole, and their combination in a model of platelet-vessel wall interaction.
Mueller, T.H.
Neurology 57 : S8-S11. 1 January 2001


Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance.
Plassart-Schiess, E. and Gervais, A. and Eymard, B. and Lagueny, A. and Pouget, J. and Warter, J.M. and Fardeau, M. and Jentsch, T.J. and Fontaine, B.
Neurology 50 (4): 1176-1179. April 1998

Unexpected sarcolemmal complement membrane attack complex deposits on nonnecrotic muscle fibers in muscular dystrophies.
Spuler, S. and Engel, A.G.
Neurology 50 (1): 41-46. 1 January 1998


Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
Sander, T. and Bockenkamp, B. and Hildmann, T. and Blasczyk, R. and Kretz, R. and Wienker, T.F. and Volz, A. and Schmitz, B. and Beckmannagetta, G. and Riess, O. and Epplen, J.T. and Janz, D. and Ziegler, A.
Neurology 49 (3): 842-847. 1 September 1997


Comparison of triple dose versus standard dose gadolinium-DTPA for detection of MRI enhancing lesions in patients with MS.
Filippi, M. and Yousry, T. and Campi, A. and Kandziora, C. and Colombo, B. and Voltz, R. and Martinelli, V. and Spuler, S. and Bressi, S. and Scotti, G. and Comi, G.
Neurology 46 (2): 379-384. February 1996


The role of autoimmune T lymphocytes in the pathogenesis of multiple sclerosis.
Hohlfeld, R. and Meinl, E. and Weber, F. and Zipp, F. and Schmidt, S. and Sotgiu, S. and Goebels, N. and Voltz, R. and Spuler, S. and Iglesias, A.
Neurology 45 (6 Suppl 6): S33-S38. June 1995

Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.
Sander, T. and Janz, D. and Ramel, C. and Ross, C.A. and Paschen, W. and Hildmann, T. and Wienker, T.F. and Bianchi, A. and Bauer, G. and Sailer, U. and Berek, K. and Neitzel, H. and Volz, A. and Ziegler, A. and Schmitz, B. and Beckmannagetta, G.
Neurology 45 (9): 1713-1720. 1 January 1995


Cecile and Oskar Vogt. On the occasion of her 75th and his 80th birthday.
Haymaker, W.
Neurology 1 (3): 179-218. May 1951

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