Issue 8/2015
Content (28 Articles)
Diagnosis and differential diagnosis of MSA: boundary issues
Han-Joon Kim, Beom S. Jeon, Kurt A. Jellinger
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia
M. J. Keogh, H. Steele, K. Douroudis, A. Pyle, J. Duff, R. Hussain, T. Smertenko, H. Griffin, M. Santibanez-Koref, R. Horvath, P. F. Chinnery
Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014
Akihiko Ueda, Mitsuharu Ueda, Akihito Nagatoshi, Teruyuki Hirano, Takaaki Ito, Nobutaka Arai, Eiichiro Uyama, Kota Mori, Masaaki Nakamura, Satoru Shinriki, Katsuyoshi Ikeda, Yukio Ando
Gaze holding deficits discriminate early from late onset cerebellar degeneration
Alexander A. Tarnutzer, K. P. Weber, B. Schuknecht, D. Straumann, S. Marti, G. Bertolini
Neuroimaging evidence of gray and white matter damage and clinical correlates in progressive supranuclear palsy
Maria Cristina Piattella, N. Upadhyay, M. Bologna, E. Sbardella, F. Tona, A. Formica, N. Petsas, A. Berardelli, P. Pantano
Treatment and outcome of children and adolescents with N-methyl-d-aspartate receptor encephalitis
Anastasia Zekeridou, Evgenia Karantoni, Aurélien Viaccoz, François Ducray, Cyril Gitiaux, Frédéric Villega, Kumaran Deiva, Veronique Rogemond, Elodie Mathias, Géraldine Picard, Marc Tardieu, Jean-Christophe Antoine, Jean-Yves Delattre, Jerome Honnorat
Tailored care for somatoform vertigo/dizziness: study protocol for a randomised controlled trial evaluating integrative group psychotherapy
Claas Lahmann, P. Henningsen, M. Dieterich, K. Radziej, G. Schmid
Progression of subcortical atrophy and iron deposition in multiple system atrophy: a comparison between clinical subtypes
Jae-Hyeok Lee, Tae-Hyung Kim, Chi-Woong Mun, Tae-Hyoung Kim, Yong-Hee Han
Normalization of sensorimotor integration by repetitive transcranial magnetic stimulation in cervical dystonia
S. Zittel, R. C. Helmich, C. Demiralay, A. Münchau, T. Bäumer
Olfactory dysfunction in neuromyelitis optica spectrum disorders
Lin-Jie Zhang, Ning Zhao, Ying Fu, Da-Qi Zhang, Jing Wang, Wen Qin, Ningnannan Zhang, Kristofer Wood, Yaou Liu, Chunshui Yu, Fu-Dong Shi, Li Yang
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland
Boglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, Sinead M. Murphy, John McHugh, Michael Alexander, Richard Wells, Joanna Davies, David Hilton-Jones, Hanns Lochmüller, Patrick Chinnery, Rita Horvath
Magnetization transfer ratio in lesions rather than normal-appearing brain relates to disability in patients with multiple sclerosis
Michael Amann, Athina Papadopoulou, Michaela Andelova, Stefano Magon, Nicole Mueller-Lenke, Yvonne Naegelin, Christoph Stippich, Ernst Wilhelm Radue, Oliver Bieri, Ludwig Kappos, Till Sprenger
Eye-tracking controlled cognitive function tests in patients with amyotrophic lateral sclerosis: a controlled proof-of-principle study
Jürgen Keller, Martin Gorges, Hannah T. Horn, Helena E. A. Aho-Özhan, Elmar H. Pinkhardt, Ingo Uttner, Jan Kassubek, Albert C. Ludolph, Dorothée Lulé
Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency
Sarah Doss, Jan Leo Rinnenthal, Tanja Schmitz-Hübsch, Alexander U. Brandt, Sebastian Papazoglou, Silke Lux, Stephan Maul, Jens Würfel, Matthias Endres, Thomas Klockgether, Martina Minnerop, Friedemann Paul
Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life
Etienne Allart, Anne Benoit, Anne Blanchard-Dauphin, Vincent Tiffreau, André Thevenon, Hélène Zephir, Olivier Outteryck, Arnaud Lacour, Patrick Vermersch
Unchanged gastric emptying and visceral perception in early Parkinson's disease after a high caloric test meal
L. Epprecht, S. R. Schreglmann, O. Goetze, D. Woitalla, C. R. Baumann, D. Waldvogel
Ambiguous value of anti-ganglioside IgM autoantibodies in Guillain-Barré syndrome and its variants
Michiaki Koga, Masaki Takahashi, Keiko Yokoyama, Takashi Kanda
Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations
Tobias Lindig, Benjamin Bender, Till-Karsten Hauser, Sarah Mang, Daniel Schweikardt, Uwe Klose, Kathrin N. Karle, Rebecca Schüle, Ludger Schöls, Tim W. Rattay
Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation
Georgios Koutsis, David Lynch, Andreea Manone, Georgia Karadima, Mary M. Reilly, Henry Houlden, Marios Panas
Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation
Georgios Koutsis, David Lynch, Andreea Manole, Georgia Karadima, Mary M. Reilly, Henry Houlden, Marios Panas
Functional dizziness: diagnostic keys and differential diagnosis
Thomas Brandt, Doreen Huppert, Michael Strupp, Marianne Dieterich
Radiotherapy treatment of sialorrhea in patients with amyotrophic lateral sclerosis requiring non-invasive ventilation
Maria del Mar Amador, Avi Assouline, Jésus Gonzalez-Bermejo, Pierre-François Pradat
Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies
Alejandro Horga, Ellen Cottenie, Pedro J. Tomaselli, Ricard Rojas-García, Maria Salvado, Liliana Villarreal-Pérez, Josep Gamez, Celedonio Márquez-Infante, Henry Houlden, Mary M. Reilly
Hereditary spastic paraplegia type 11 with a very late onset
Anna Rubegni, Eugenia Storti, Alessandra Tessa, Antonio Federico, Filippo M. Santorelli
Progress in Huntington’s disease: the search for markers of disease onset and progression
Sarah Mason, Roger A. Barker