Ausgabe 10/2012
Inhalt (42 Artikel)
Seizures and epilepsy in herpes simplex virus encephalitis: current concepts and future directions of pathogenesis and management
Johann Sellner, Eugen Trinka
Recognition and diagnosis of sleep disorders in Parkinson’s disease
Maartje Louter, Willemijn C. C. A. Aarden, Joy Lion, Bastiaan R. Bloem, Sebastiaan Overeem
SPECT-DTPA as a tool for evaluating the blood–brain barrier in post-stroke seizures
Ronit Gilad, Yair Lampl, Anda Eilam, Mona Boaz, Mordechai Loyberboim
Modified ASPECTS for DWI including deep white matter lesions predicts subsequent intracranial hemorrhage
Hiroyuki Kawano, Teruyuki Hirano, Makoto Nakajima, Yuichiro Inatomi, Toshiro Yonehara, Makoto Uchino
Impact of cystatin C levels on infarct size and hemorrhage volume in acute cerebral stroke
Dongfang Xiao, Hailong Liu, Hong Zhang, Yumin Luo
Nociceptive pathway function is normal in cervical dystonia: a study using laser-evoked potentials
Michele Tinazzi, Massimiliano Valeriani, Giovanna Squintani, Federica Corrà, Serena Recchia, Giovanni Defazio, Alfredo Berardelli
The spectrum of clinicopathological features in pure autonomic neuropathy
Haruki Koike, Rina Hashimoto, Minoru Tomita, Yuichi Kawagashira, Masahiro Iijima, Shigeru Koyano, Takayuki Momoo, Hiroyuki Yuasa, Shigehisa Mitake, Mana Higashihara, Kenichi Kaida, Daisuke Yamamoto, Shin Hisahara, Shun Shimohama, Yoshiharu Nakae, Ken Johkura, Steven Vernino, Gen Sobue
Diagnostic and ethical challenges in disorders of consciousness and locked-in syndrome: a survey of German neurologists
Katja Kuehlmeyer, Eric Racine, Nicole Palmour, Eva Hoster, Gian Domenico Borasio, Ralf J. Jox
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta, Fabrizio Rinaldi, Alessandra Morgante, Bjarne Udd, Olayinka Raheem, Sini Penttilä, Tiina Suominen, Laura V. Renna, Valeria Sansone, Enrico Bugiardini, Giuseppe Novelli, Giovanni Meola
Effect of stem cell transplantation for B-cell malignancies on disease course of associated polyneuropathy
A. C. J. Stork, W. L. van der Pol, D. van Kessel, H. M. Lokhorst, N. C. Notermans
Elevated plasma homocysteine levels in patients with multiple sclerosis are associated with male gender
Stefano Zoccolella, Carla Tortorella, Pietro Iaffaldano, Vita Direnzo, Mariangela D’Onghia, Damiano Paolicelli, Paolo Livrea, Maria Trojano
Early biomarkers for post-stroke cognitive impairment
Lai Qian, Lidong Ding, Liqun Cheng, Xiaolei Zhu, Hui Zhao, Jiali Jin, Dening Guan, Bing Zhang, Xuemei Chen, Yun Xu
In vivo assessment of retinal neuronal layers in multiple sclerosis with manual and automated optical coherence tomography segmentation techniques
Michaela A. Seigo, Elias S. Sotirchos, Scott Newsome, Aleksandra Babiarz, Christopher Eckstein, E’Tona Ford, Jonathan D. Oakley, Stephanie B. Syc, Teresa C. Frohman, John N. Ratchford, Laura J. Balcer, Elliot M. Frohman, Peter A. Calabresi, Shiv Saidha
Presymptomatic genetic testing in CADASIL
S. Reyes, A. Kurtz, D. Hervé, E. Tournier-Lasserve, H. Chabriat
Prevalence and phenomenology of eye tics in Gilles de la Tourette syndrome
Davide Martino, Andrea E. Cavanna, Mary M. Robertson, Michael Orth
Outcome of MRI-based intravenous thrombolysis in carotid-T occlusion
Christoph Beck, Bastian Cheng, Anna Krützelmann, Michael Rosenkranz, Christian Gerloff, Jens Fiehler, Götz Thomalla
Intracerebral mass lesion diagnosed as cryptococcoma in a patient with sarcoidosis, a rare opportunistic manifestation induced by immunosuppression with corticosteroids
Alexander Jung, Catharina Korsukewitz, Tanja Kuhlmann, Malte Richters, Bernhard Fischer, Thomas Niederstadt, Wolfgang Fegeler, Jens Minnerup, Peter Young, Ingo W. Husstedt
Can we overcome the ‘clinico-radiological paradox’ in multiple sclerosis?
Kerstin Hackmack, Martin Weygandt, Jens Wuerfel, Caspar F. Pfueller, Judith Bellmann-Strobl, Friedemann Paul, John-Dylan Haynes
Correlates of tumor development in patients with myotonic dystrophy
Maya Das, Richard T. Moxley III, James E. Hilbert, William B. Martens, Lisa Letren, Mark H. Greene, Shahinaz M. Gadalla
Characteristics of late-onset myasthenia gravis
Saša A. Živković, Paula R. Clemens, David Lacomis
Hypoglycemic encephalopathy: a case series and literature review on outcome determination
Jens Witsch, Hermann Neugebauer, Julia Flechsenhar, Eric Jüttler
Comparison of clinical characteristics between familial and non-familial early onset Alzheimer’s disease
Simantini J. Karve, John M. Ringman, Albert S. Lee, Kevin O. Juarez, Mario F. Mendez
Neurological disorder screening in the elderly in low-income countries
Felicity Dewhurst, Matthew J. Dewhurst, Golda Orega, William K. Gray, William Howlett, Naomi Warren, Eric Aris, Richard W. Walker
Clinical assessment of deficits after SAH: hasty neurosurgeons and accurate neurologists
Christian Fung, Jürgen Beck, Lara Lauber, René Müri, Andreas Raabe, Thomas Nyffeler
Age-dependent differences in cervical artery dissection
Tiina M. Metso, Stéphanie Debette, Caspar Grond-Ginsbach, Stefan T. Engelter, Didier Leys, Tobias Brandt, Alessandro Pezzini, Anna Bersano, Manja Kloss, Vincent Thijs, Philippe A. Lyrer, Turgut Tatlisumak, Antti J. Metso
Adolf von Strümpell: a key yet neglected protagonist of neurology
Birk Engmann, Armin Wagner, Steinberg Holger
Computer mouse-related dystonia: a novel presentation of task-specific dystonia
Keisuke Suzuki, Masatsugu Takano, Kenichi Hashimoto, Ayaka Numao, Toshiki Nakamura, Hideki Sakuta, Koichi Hirata
Fear of heights in ancient China
Matthias Bauer, Doreen Huppert, Thomas Brandt
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis
Chiara Briani, Tiziana Cavallaro, Sergio Ferrari, Federica Taioli, Sara Calamelli, Laura Verga, Fausto Adami, Gian Maria Fabrizi
Multiple cerebral infarctions related to famotidine-induced eosinophilia
Chi-Shun Wu, Sheng-Feng Sung, Show-Hwa Tong, Cheung-Ter Ong
POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening study
Matthis Synofzik, Julia Schicks, Karin Srulijes, Claudia Schulte, Franziska Schiele, Daniela Berg, Ludger Schöls
Adult-onset Alexander disease with an R66Q mutation in GFAP presented with severe vocal cord paralysis during sleep
Ayumi Hida, Hiroyuki Ishiura, Noritoshi Arai, Hisayo Fukuoka, Kanehiro Hasuo, Jun Goto, Yoshikazu Uesaka, Shoji Tsuji, Sousuke Takeuchi
Lower motor neuron disease caused by a novel FUS/TLS gene frameshift mutation
Makoto Hara, Masayuki Minami, Satoshi Kamei, Naoki Suzuki, Masaaki Kato, Masashi Aoki
Erdheim–Chester disease presenting with an intramedullary spinal cord lesion
Charalampos Tzoulis, Ivar Otto Gjerde, Eirik Søfteland, Gesche Neckelmann, Eivind Strøm, Olav Karsten Vintermyr, Lisbeth Sviland, Martin Biermann
Neurological involvement during legionellosis, look beyond the lung
Donato Sauchelli, Gennaro De Pascale, Giancarlo Scoppettuolo, Giovanni Frisullo, Daniela Bernardo, Cristina Cuccagna, Mario Tumbarello, Massimo Antonelli, Serenella Servidei
Breastfeeding and multiple sclerosis relapses: a meta-analysis
Julia Pakpoor, Giulio Disanto, Melanie V. Lacey, Kerstin Hellwig, Gavin Giovannoni, Sreeram V. Ramagopalan
Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease
Koji Fujita, Tatsuhiko Yuasa, Osamu Watanabe, Yukitoshi Takahashi, Shuji Hashiguchi, Katsuhito Adachi, Yuishin Izumi, Ryuji Kaji
Interconnections in superior temporal cortex revealed by musicogenic seizure propagation
Z. Irene Wang, Kazutaka Jin, Yosuke Kakisaka, Richard C. Burgess, Jorge A. Gonzalez-Martinez, Shuang Wang, Susumu Ito, John C. Mosher, Stephen Hantus, Andreas V. Alexopoulos
Clinical neurogenetics: recent advances
Davide Pareyson, Ettore Salsano