Ausgabe 2/2016
Inhalt (31 Artikel)
The full spectrum of ethical issues in the care of patients with ALS: a systematic qualitative review
F. Seitzer, H. Kahrass, G. Neitzke, D. Strech
Vestibular-evoked myogenic potentials in central vestibular disorders
Sun-Young Oh, Hyo-Jeong Kim, Ji-Soo Kim
The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies
Alexander Grimm, Maria Rasenack, Ioanna M. Athanasopoulou, Nele Maria Dammeier, Christina Lipski, Stefan Wolking, Debora Vittore, Bernhard F. Décard, Hubertus Axer
Prognostic value of trans-thoracic echocardiography in patients with acute stroke and atrial fibrillation: findings from the RAF study
Maurizio Paciaroni, Giancarlo Agnelli, Nicola Falocci, Valeria Caso, Cecilia Becattini, Simona Marcheselli, Christina Rueckert, Alessandro Pezzini, Loris Poli, Alessandro Padovani, Laszló Csiba, Lilla Szabó, Sung-Il Sohn, Tiziana Tassinari, Azmil H. Abdul-Rahim, Patrik Michel, Maria Cordier, Peter Vanacker, Suzette Remillard, Andrea Alberti, Michele Venti, Monica Acciarresi, Cataldo D’Amore, Maria Giulia Mosconi, Umberto Scoditti, Licia Denti, Giovanni Orlandi, Alberto Chiti, Gino Gialdini, Paolo Bovi, Monica Carletti, Alberto Rigatelli, Jukka Putaala, Turgut Tatlisumak, Luca Masotti, Gianni Lorenzini, Rossana Tassi, Francesca Guideri, Giuseppe Martini, Georgios Tsivgoulis, Kostantinos Vadikolias, Chrissoula Liantinioti, Francesco Corea, Massimo Del Sette, Walter Ageno, Maria Luisa De Lodovici, Giorgio Bono, Antonio Baldi, Sebastiano D’Anna, Simona Sacco, Antonio Carolei, Cindy Tiseo, Davide Imberti, Dorjan Zabzuni, Boris Doronin, Vera Volodina, Domenico Consoli, Franco Galati, Alessio Pieroni, Danilo Toni, Serena Monaco, Mario Maimone Baronello, Kristian Barlinn, Lars-Peder Pallesen, Jessica Kepplinger, Ulf Bodechtel, Johannes Gerber, Dirk Deleu, Gayane Melikyan, Faisal Ibrahim, Naveed Akhtar, Kennedy R. Lees
The clinical relevance of cerebral microbleeds in patients with cerebral ischemia and atrial fibrillation
Shamir Haji, Ryan Planchard, Adeel Zubair, Jonathan Graff-Radford, Charlotte Rydberg, Robert D. Brown Jr., Kelly D. Flemming
Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome: a slowly progressive disorder with stereotypical presentation
Daniele Cazzato, Eleonora Dalla Bella, Patrizia Dacci, Caterina Mariotti, Giuseppe Lauria
Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson’s disease
Giovanna Calandra-Buonaura, Andrea Doria, Giovanna Lopane, Pietro Guaraldi, Sabina Capellari, Paolo Martinelli, Pietro Cortelli, Manuela Contin
Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population
Turgut Tatlisumak, Jukka Putaala, Markus Innilä, Christian Enzinger, Tiina M. Metso, Sami Curtze, Bettina von Sarnowski, Alexandre Amaral-Silva, Gerhard Jan Jungehulsing, Christian Tanislav, Vincent Thijs, Arndt Rolfs, Bo Norrving, Franz Fazekas, Anu Suomalainen, Edwin H. Kolodny
Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation
Li Di, Hai Chen, Yuwei Da, Suobing Wang, Xin-Ming Shen
RETRACTED ARTICLE: Factors associated with post-stroke depression and fatigue: lesion location and coping styles
Changjuan Wei, Fang Zhang, Li Chen, Xiaofeng Ma, Nan Zhang, Junwei Hao
Predictors of outcome in HSV encephalitis
Tarun D. Singh, Jennifer E. Fugate, Sara Hocker, Eelco F. M. Wijdicks, Allen J. Aksamit Jr., Alejandro A. Rabinstein
Deep brain stimulation of the internal pallidum in Huntington’s disease patients: clinical outcome and neuronal firing patterns
Cécile Delorme, Alister Rogers, Brian Lau, Hélène Francisque, Marie-Laure Welter, Sara Fernandez Vidal, Jérôme Yelnik, Alexandra Durr, David Grabli, Carine Karachi
The relationship between the rate of brain volume loss during first 24 months and disability progression over 24 and 48 months in relapsing MS
Douglas R. Jeffery, Elisabetta Verdun Di Cantogno, Shannon Ritter, Daniela Piani Meier, Ernst-Wilhelm Radue, William Camu
Domain-specific versus generalized cognitive screening in acute stroke
Nele Demeyere, M. J. Riddoch, E. D. Slavkova, K. Jones, I. Reckless, P. Mathieson, G. W. Humphreys
Pseudobulbar affect (PBA) in an incident ALS cohort: results from the Apulia registry (SLAP)
Rosanna Tortelli, Massimiliano Copetti, Simona Arcuti, Marianna Tursi, Annalisa Iurillo, Maria Rosaria Barulli, Rosa Cortese, Rosa Capozzo, Eustachio D’Errico, Benoit Marin, Isabella Laura Simone, Giancarlo Logroscino
Rituximab in paediatric onset multiple sclerosis: a case series
Jonatan Salzer, Jan Lycke, Ronny Wickström, Hans Naver, Fredrik Piehl, Anders Svenningsson
Efficacy of fingolimod is superior to injectable disease modifying therapies in second-line therapy of relapsing remitting multiple sclerosis
Stefan Braune, M. Lang, A. Bergmann
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia
N. Schwarz, A. Hahn, T. Bast, S. Müller, H. Löffler, S. Maljevic, E. Gaily, I. Prehl, S. Biskup, T. Joensuu, A.-E. Lehesjoki, B. A. Neubauer, H. Lerche, U. B. S. Hedrich
Brief intervention by general practitioners for medication-overuse headache, follow-up after 6 months: a pragmatic cluster-randomised controlled trial
Espen Saxhaug Kristoffersen, Jørund Straand, Kjersti Grøtta Vetvik, Jūratė Šaltytė Benth, Michael Bjørn Russell, Christofer Lundqvist
Onset of clinical and MRI efficacy occurs early after fingolimod treatment initiation in relapsing multiple sclerosis
Ludwig Kappos, Ernst-Wilhelm Radue, Peter Chin, Shannon Ritter, Davorka Tomic, Fred Lublin
NEFL N98S mutation: another cause of dominant intermediate Charcot–Marie–Tooth disease with heterogeneous early-onset phenotype
José Berciano, Kristien Peeters, Antonio García, Tomás López-Alburquerque, Elena Gallardo, Arantxa Hernández-Fabián, Ana L. Pelayo-Negro, Els De Vriendt, Jon Infante, Albena Jordanova
Isolated new onset ‘atypical’ optic neuritis in the NMO clinic: serum antibodies, prognoses and diagnoses at follow-up
L. Piccolo, M. Woodhall, G. Tackley, M. Juryńczyk, Y. Kong, J. Domingos, R. Gore, A. Vincent, P. Waters, M. I. Leite, J. Palace
Progressive supranuclear palsy: progression and survival
Julieta E. Arena, Stephen D. Weigand, Jennifer L. Whitwell, Anhar Hassan, Scott D. Eggers, Günter U. Höglinger, Irene Litvan, Keith A. Josephs
Clinical features and differential diagnosis of flail arm syndrome
Annemarie Hübers, Viviane Hildebrandt, Susanne Petri, Katja Kollewe, Andreas Hermann, Alexander Storch, Frank Hanisch, Stephan Zierz, Angela Rosenbohm, Albert C. Ludolph, Johannes Dorst
Defining the phenotype of restless legs syndrome/Willis–Ekbom disease (RLS/WED): a clinical and polysomnographic study
Fabrizio Rinaldi, Andrea Galbiati, Sara Marelli, Maria Cusmai, Alessandro Gasperi, Alessandro Oldani, Marco Zucconi, Alessandro Padovani, Luigi Ferini Strambi
Improvement of lateral axial dystonia following prismatic correction of oculomotor control disorders in Parkinson’s disease
Marco Santilli, Michele Meglio, Sara Varanese, Francesco Lena, Ennio Iezzi, Giovanni Grillea, Nicola Modugno
Paraneoplastic opsoclonus and cerebellar ataxia related to anti-Ma2 antibody: a case report
Nicolas Mélé, Charlotte Hautefort, Alain Toledano, Jean-Yves Delattre, Dimitri Psimaras
New ways of looking at an old disease: the reimagination of epilepsy
Clinton J. Mitchell, Neil P. Robertson
Erratum to: The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegia
Grant Guthrie, Gerald Pfeffer, Maura Bailie, Karen Bradshaw, Andrew C. Browning, Rita Horvath, Patrick F. Chinnery, Patrick Yu-Wai-Man