Ausgabe 11/2014
Inhalt (30 Artikel)
Deep brain stimulation in Parkinson’s disease: meta-analysis of randomized controlled trials
L. Perestelo-Pérez, A. Rivero-Santana, J. Pérez-Ramos, P. Serrano-Pérez, J. Panetta, P. Hilarion
Progressing haemorrhagic stroke: categories, causes, mechanisms and managements
Shiyu Chen, Liuwang Zeng, Zhiping Hu
Endolymphatic space size in patients with vestibular migraine and Ménière’s disease
Takafumi Nakada, Tadao Yoshida, Kenji Suga, Masahiro Kato, Hironao Otake, Ken Kato, Masaaki Teranishi, Michihiko Sone, Saiko Sugiura, Kayao Kuno, Ilmari Pyykkö, Shinji Naganawa, Hirohisa Watanabe, Gen Sobue, Tsutomu Nakashima
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort
P. E. Cohn-Hokke, T. H. Wong, P. Rizzu, G. Breedveld, W. M. van der Flier, P. Scheltens, F. Baas, P. Heutink, E. J. Meijers-Heijboer, J. C. van Swieten, Y. A. L. Pijnenburg
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, Alain Créange, Jérôme Franques, Stéphane Mathis, Emilien Delmont, Thierry Kuntzer, Jean-Pascal Lefaucheur, Jean Pouget, Karine Viala, Claude Desnuelle, Andoni Echaniz-Laguna, Francesco Rotolo, Jean-Philippe Camdessanché
A 2-year observational study of patients with relapsing-remitting multiple sclerosis converting to glatiramer acetate from other disease-modifying therapies: the COPTIMIZE trial
Tjalf Ziemssen, Ovidiu A. Bajenaru, Adriana Carrá, Nina de Klippel, João C. de Sá, Astrid Edland, Jette L. Frederiksen, Olivier Heinzlef, Klimentini E. Karageorgiou, Rafael H. Lander Delgado, Anne-Marie Landtblom, Miguel A. Macías Islas, Niall Tubridy, Yossi Gilgun-Sherki
Dopamine transporter availability in motor subtypes of de novo drug-naïve Parkinson’s disease
Marcello Moccia, Sabina Pappatà, Marina Picillo, Roberto Erro, Anna Rita Daniela Coda, Katia Longo, Carmine Vitale, Marianna Amboni, Arturo Brunetti, Giuseppe Capo, Marco Salvatore, Paolo Barone, Maria Teresa Pellecchia
The presence of dysautonomia in different subgroups of myasthenia gravis patients
Ana Nikolić, Stojan Perić, Tanja Nišić, Srdjan Popović, Miroljub Ilić, Vidosava Rakočević Stojanović, Dragana Lavrnić
Hippocampal damage and affective disorders after treatment of cerebral aneurysms
Maria Wostrack, Benjamin Friedrich, Katrin Hammer, Kathrin Harmening, Anne Stankewitz, Florian Ringel, Ehab Shiban, Tobias Boeckh-Behrens, Sascha Prothmann, Claus Zimmer, Bernhard Meyer, Annette Förschler, Yu-Mi Ryang
Non-convulsive status epilepticus after ischemic stroke: a hospital-based stroke cohort study
Vincenzo Belcastro, Simone Vidale, Gaetano Gorgone, Laura Rosa Pisani, Luigi Sironi, Marco Arnaboldi, Francesco Pisani
Clinical characteristics and outcome of intracerebral hemorrhage in young adults
Loes CA Rutten-Jacobs, Noortje AM Maaijwee, Renate M. Arntz, Hennie C. Schoonderwaldt, Lucille D. Dorresteijn, Ewoud J. van Dijk, Frank-Erik de Leeuw
New-onset psychiatric disorders after corticosteroid therapy in systemic lupus erythematosus: an observational case-series study
Katsuji Nishimura, Masako Omori, Eri Sato, Yasuhiro Katsumata, Takahisa Gono, Yasushi Kawaguchi, Masayoshi Harigai, Hisashi Yamanaka, Jun Ishigooka
Subcutaneous immunoglobulin in CIDP and MMN: a short-term nationwide study
Dario Cocito, Aristide Merola, Erdita Peci, Anna Mazzeo, Raffaella Fazio, Ada Francia, Paola Valentino, Rocco Liguori, Massimiliano Filosto, Gabriele Siciliano, Angelo Maurizio Clerici, Stefania Lelli, Girolama Alessandra Marfia, Giovanni Antonini, Ilaria Cecconi, Eduardo Nobile-Orazio, Leonardo Lopiano
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia
Ayelet Halevy, Israela Lerer, Rony Cohen, Liora Kornreich, Avinoam Shuper, Moria Gamliel, Bat-El Zimerman, Isam Korabi, Vardiella Meiner, Rachel Straussberg, Alexander Lossos
Heritability in frontotemporal dementia: more missing pieces?
Kieren Po, Felicity V. C. Leslie, Natalie Gracia, Lauren Bartley, John B. J. Kwok, Glenda M. Halliday, John R. Hodges, James R. Burrell
NADPH oxidase (NOX2) activity is a modifier of survival in ALS
Giuseppe Marrali, Federico Casale, Paolina Salamone, Giuseppe Fuda, Cristiana Caorsi, Antonio Amoroso, Maura Brunetti, Gabriella Restagno, Marco Barberis, Davide Bertuzzo, Antonio Canosa, Cristina Moglia, Andrea Calvo, Adriano Chiò
Thinking about the end of life: a common issue for patients with Huntington’s disease
Suzanne J. Booij, Aad Tibben, Dick P. Engberts, Johan Marinus, Raymund A. C. Roos
ANO10 mutations cause ataxia and coenzyme Q10 deficiency
Andrea Balreira, Veronika Boczonadi, Emanuele Barca, Angela Pyle, Boglarka Bansagi, Marie Appleton, Claire Graham, Iain P. Hargreaves, Vedrana Milic Rasic, Hanns Lochmüller, Helen Griffin, Robert W. Taylor, Ali Naini, Patrick F. Chinnery, Michio Hirano, Catarina M. Quinzii, Rita Horvath
Spinal axis imaging in non-aneurysmal subarachnoid hemorrhage: a prospective cohort study
Menno R. Germans, Bert A. Coert, Charles B. L. M. Majoie, René van den Berg, Dagmar Verbaan, W. Peter Vandertop
Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD)
Anna De Rosa, Claudia Carducci, Carla Carducci, Silvio Peluso, Maria Lieto, Andrea Mazzella, Francesco Saccà, Vincenzo Brescia Morra, Sabina Pappatà, Vincenzo Leuzzi, Giuseppe De Michele
Concomitant accumulation of α-synuclein and TDP-43 in a patient with corticobasal degeneration
Satoshi Yamashita, Naomi Sakashita, Taro Yamashita, Nozomu Tawara, Masayoshi Tasaki, Kensuke Kawakami, Yoshihiro Komohara, Yukio Fujiwara, Masashi Kamikawa, Takenobu Nakagawa, Teruyuki Hirano, Yasushi Maeda, Masato Hasegawa, Motohiro Takeya, Yukio Ando
Rare variant of unknown significance in POLG1 and diagnostic dilemma
Pankaj Prasun
Intraventricular hemorrhage in reversible cerebral vasoconstriction syndrome
Duncan Wilson, Charles R. Marshall, Thomas Solbach, Laurence Watkins, David J. Werring
X-linked agammaglobulinemia with hearing impairment, dystonia-parkinsonism, and progressive neurodegeneration
Aloysius Domingo, Thomas G. P. M. Schmidt, Ela Barcelon, Marissa Lukban, Ana Westenberger, Christine Klein
Visual hallucinations: an unusual manifestation of sporadic Creutzfeldt–Jakob disease termed the ‘Heidenhain variant’
R. Gooriah, B. E. A. Dafalla, S. Tun, T. C. Venugopalan, K. K. Lwin
Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation
Andreas C. Themistocleous, Robin Kennett, Masud Husain, Jacqueline Palace, Simon Mead, David L. H. Bennett
Inherited disorders of the neuromuscular junction: an update
Pedro M. Rodríguez Cruz, Jacqueline Palace, David Beeson
Ernest-Charles Lasègue (1816–1883)
Behnam Dalfardi, Golnoush Sadat Mahmoudi Nezhad
Hugo Karl Liepmann (1863–1925)
Behnam Dalfardi, Golnoush Sadat Mahmoudi Nezhad