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Journal of Neurology

Ausgabe 4/2013

Inhalt (41 Artikel)

Review

The chain of care enabling tPA treatment in acute ischemic stroke: a comprehensive review of organisational models

Maarten M. H. Lahr, Gert-Jan Luijckx, Patrick C. A. J. Vroomen, Durk-Jouke van der Zee, Erik Buskens

Original Communication

Quantitative MRI and loss of free ambulation in Duchenne muscular dystrophy

Arne Fischmann, Patricia Hafner, Monika Gloor, Maurice Schmid, Andrea Klein, Urs Pohlman, Tanja Waltz, Rocio Gonzalez, Tanja Haas, Oliver Bieri, Dirk Fischer

Original Communication

Global functional connectivity reveals highly significant differences between the vegetative and the minimally conscious state

Boris Kotchoubey, Susanne Merz, Simone Lang, Alexandra Markl, Friedemann Müller, Tao Yu, Christian Schwarzbauer

Original Communication

MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1

Vincent Huin, Francis Vasseur, Susanna Schraen-Maschke, Claire-Marie Dhaenens, Patrick Devos, Kathy Dupont, Nicolas Sergeant, Luc Buée, Arnaud Lacour, Hélène Hofmann-Radvanyi, Bernard Sablonnière

Original Communication

Olfactory bulb volume in patients with temporal lobe epilepsy

Thomas Hummel, Sophia Henkel, Simona Negoias, José R. B. Galván, Vasyl Bogdanov, Peter Hopp, Susanne Hallmeyer-Elgner, Johannes Gerber, Ulrike Reuner, Antje Haehner

Original Communication

Normal pressure hydrocephalus or progressive supranuclear palsy? A clinicopathological case series

Nadia K. Magdalinou, Helen Ling, James D. Shand Smith, Jonathan M. Schott, Laurence D. Watkins, Andrew J. Lees

Original Communication

Cerebral white matter changes are associated with abnormalities on neurological examination in non-disabled elderly: the LADIS study

Anna Poggesi, Alida Gouw, Wiesje van der Flier, Giovanni Pracucci, Hugues Chabriat, Timo Erkinjuntti, Franz Fazekas, José M. Ferro, Michael Hennerici, Peter Langhorne, John T. O’Brien, Marieke C. Visser, Lars-Olof Wahlund, Gunhild Waldemar, Anders Wallin, Philip Scheltens, Domenico Inzitari, Leonardo Pantoni

Original Communication

A nurse-led self-management intervention for people who attend emergency departments with epilepsy: the patients’ view

Adam J. Noble, Myfanwy Morgan, Cheryl Virdi, Leone Ridsdale

Original Communication

MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy

Igor N. Petrovic, Antonio Martin-Bastida, Luke Massey, Helen Ling, Sean S. O’Sullivan, David R. Williams, Janice L. Holton, Tamas Revesz, James W. Ironside, Andrew J. Lees, Laura Silveira-Moriyama

Original Communication

Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia

Valerija S. Dobričić, Nikola D. Kresojević, Marina V. Svetel, Milena Z. Janković, Igor N. Petrović, Aleksandra D. Tomić, Ivana V. Novaković, Vladimir S. Kostić

Original Communication

Prognostic value of early epileptic seizures on mortality and functional disability in acute stroke: the Dijon Stroke Registry (1985–2010)

Bello Hamidou, Corine Aboa-Eboulé, Jérôme Durier, Agnès Jacquin, Martine Lemesle-Martin, Maurice Giroud, Yannick Béjot

Original Communication

Aneurysmal subarachnoid hemorrhage in elderly patients: long-term outcome and prognostic factors in an interdisciplinary treatment approach

Karsten Schöller, Maike Massmann, Gertraud Markl, Mathias Kunz, Gunther Fesl, Hartmut Brückmann, Thomas Pfefferkorn, Jörg-Christian Tonn, Christian Schichor

Original Communication

Peripheral neuropathy as initial manifestation of primary systemic vasculitides

Joachim Wolf, Verena Schmitt, Frederic Palm, Armin J. Grau, Raoul Bergner

Original Communication

Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation

Henriette J. Tschampa, Horst Urbach, Susanne Greschus, Wolfram S. Kunz, Cornelia Kornblum

Original Communication

Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study

D. Martino, A. Gajos, V. Gallo, L. Cif, P. Coubes, M. Tinazzi, S. A. Schneider, M. Fiorio, G. Zorzi, N. Nardocci, Y. Ben-Shlomo, M. J. Edwards, K. P. Bhatia

Original Communication

Clinical and imaging correlates of EEG patterns in hospitalized patients with encephalopathy

Raoul Sutter, Robert D. Stevens, Peter W. Kaplan

Original Communication

The applause sign in cortical and cortical-subcortical dementia

Valeria Isella, Francesco Rucci, Debora Traficante, Cristina Mapelli, Francesca Ferri, Ildebrando M. Appollonio

Original Communication

Multivariate classification of patients with Alzheimer’s and dementia with Lewy bodies using high-dimensional cortical thickness measurements: an MRI surface-based morphometric study

Alexander V. Lebedev, E. Westman, M. K. Beyer, M. G. Kramberger, C. Aguilar, Z. Pirtosek, D. Aarsland

Original Communication

Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene

Francesco Saccà, Angela Marsili, Giorgia Puorro, Antonella Antenora, Chiara Pane, Alessandra Tessa, Pasquale Scoppettuolo, Claudia Nesti, Vincenzo Brescia Morra, Giuseppe De Michele, Filippo M. Santorelli, Alessandro Filla

Original Communication

Diffusion tensor imaging reveals widespread white matter abnormalities in children and adolescents with myotonic dystrophy type 1

Jeffrey R. Wozniak, Bryon A. Mueller, Christopher J. Bell, Ryan L. Muetzel, Kelvin O. Lim, John W. Day

Original Communication

Patients with rest-tremor and scans with ipsilateral dopaminergic deficit

Maria Aguirregomozcorta, Maria Stamelou, Angelo Antonini, Petra Schwingenschuh, Liz Prvulovich, Mark J. Edwards, John C. Dickson, Kailash P. Bhatia

Original Communication

MRI outcomes with cladribine tablets for multiple sclerosis in the CLARITY study

Giancarlo Comi, Stuart D. Cook, Gavin Giovannoni, Kottil Rammohan, Peter Rieckmann, Per Soelberg Sørensen, Patrick Vermersch, Anthony C. Hamlett, Vissia Viglietta, Steven J. Greenberg

Original Communication

A family with IVIg-responsive Charcot–Marie–Tooth disease

Yasuo Miki, Masahiko Tomiyama, Rie Haga, Haruo Nishijima, Chieko Suzuki, Aiichiro Kurihara, Kazuhiro Sugimoto, Akihiro Hashiguchi, Hiroshi Takashima, Masayuki Baba

Letter to the Editors

Lithium neurotoxicity mimicking rapidly progressive dementia

Andrea Mignarri, Elena Chini, Alessandra Rufa, Raffaele Rocchi, Antonio Federico, Maria Teresa Dotti

Letter to the Editors

Bipolar affective disorder preceding frontotemporal dementia in a patient with C9ORF72 mutation: is there a genetic link between these two disorders?

Gianluca Floris, Giuseppe Borghero, Antonino Cannas, Francesca Di Stefano, Maria R. Murru, Daniela Corongiu, Stefania Cuccu, Stefania Tranquilli, Maria G. Marrosu, Adriano Chiò, Francesco Marrosu

Letter to the Editors

From anti-GAD to ataxia with ocular motor apraxia type 2: through the looking glass

Louise-Laure Mariani, Bertrand Degos, Jérôme Honnorat, Paul Trouillas, Magali Rabin, Michel Koenig, Mathieu Anheim

Letter to the Editors

Vertebral body infarction revealed by diffusion-weighted magnetic resonance imaging

Makoto Kobayashi, Tetsuya Kanai

Letter to the Editors

Giant serpentine aneurysm of the anterior cerebral artery mimicking frontotemporal dementia

Christopher Kobylecki, Alexander Gerhard, Jennifer C. Thompson, David Hughes, Kieran O’Driscoll

Letter to the Editors

Unmasking of incipient amyotrophic lateral sclerosis by botulinum toxin therapy

Louisa Kent, Paul Davies, Robin Kennett, Sunil Wimalaratna, Richard Kerr, Martin R. Turner, Kevin Talbot

Letter to the Editors

Successful treatment of CANOMAD with IVIg and rituximab

Wolfgang N. Löscher, Alexander Woertz, Monika Wallnöfer, Julia V. Wanschitz, Gerhard Luef

Letter to the Editors

An exceptional case of MSA-P

Thomas Foki, Suna Steininger, Gregor Kasprian, Gregor K. Wenning, Elisabeth Fertl, Walter Pirker

Letter to the Editors

Hashimoto’s encephalopathy associated with an elevated intrathecal IgG4 level

Yasushi Hosoi, Satoshi Kono, Tatsuhiro Terada, Takashi Konishi, Hiroaki Miyajima

Letter to the Editors

Early-onset familial Alzheimer’s disease related to presenilin 1 mutation resembling autosomal dominant spinocerebellar ataxia

Pedro Braga-Neto, José Luiz Pedroso, Helena Alessi, Paulo Victor Sgobbi de Souza, Paulo Henrique Ferreira Bertolucci, Orlando Graziani Povoas Barsottini

Short Commentary

Charles Bonnet syndrome: two case reports and review of the literature

Alberto Lerario, Andrea Ciammola, Barbara Poletti, Floriano Girotti, Vincenzo Silani

Journal Club

Antibody mediated encephalitis

Gillian Ingram, Neil P. Robertson

Pioneers in Neurology

Sir Charles Symonds (1890–1978)

J. van Gijn

Erratum

Erratum to: Functional consequences of a section of the anterior part of the body of the corpus callosum: evidence from an interhemispheric transcallosal approach

Johann Peltier, Martine Roussel, Yasmina Gerard, Maryse Lassonde, Hervé Deramond, Daniel Le Gars, Louis De Beaumont, Olivier Godefroy

Erratum

Erratum to: Bell’s palsy

Martina Minnerop, Martin Herbst, Rolf Fimmers, Pavlina Kaabar, Bertfried Matz, Thomas Klockgether, Ullrich Wüllner

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