Issue 7/2008
Content (33 Articles)
Prevalence and prognostic impact of microembolic signals in arterial sources of embolism
M. A. Ritter, R. Dittrich, N. Thoenissen, E. B. Ringelstein, D. G. Nabavi
Hypothyroidism and cerebral vein thrombosis – a possible association
A. R. Peralta, P. Canhão
Variations in functioning and disability in multiple sclerosis
C. Ytterberg, S. Johansson, M. Andersson, L. Widén Holmqvist, L. von Koch
Is screening for urinary porphobilinogen useful among patients with acute polyneuropathy or encephalopathy?
E. Pischik, V. Kazakov, R. Kauppinen
N-terminal pro-brain natriuretic peptide (NT-proBNP) release in children with vagus nerve stimulation
M. Rauchenzauner, E. Haberlandt, M. Ortler, T. Tatarczyk, M. Laimer, E. Trinka, G. Luef
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation
E. Gallardo, K. G. Claeys, E. Nelis, A. García, A. Canga, O. Combarros, V. Timmerman, P. De Jonghe, J. Berciano
The renin-angiotensin-aldosterone system in cerebral small vessel disease
D. Brenner, J. Labreuche, F. Pico, P. Scheltens, O. Poirier, F. Cambien, P. Amarenco
Enhanced corticomotor excitability with dynamic fatiguing exercise of the lower limb in multiple sclerosis
G. W. Thickbroom, P. Sacco, D. L. Faulkner, A. G. Kermode, F. L. Mastaglia
Identification of internuclear ophthalmoplegia signs in multiple sclerosis patients
M. Jozefowicz-Korczynska, M. Łukomski, A. Pajor
Acute stroke unit care and early neurological deterioration in ischemic stroke
Jaume Roquer, Ana Rodríguez-Campello, Meritxell Gomis, Jordi Jiménez-Conde, Elisa Cuadrado-Godia, Rosa Vivanco, Eva Giralt, Maria Sepúlveda, Claustre Pont-Sunyer, Gracia Cucurella, Angel Ois
A series of patients with subpial hemorrhage: Clinical manifestation, neuroradiological presentation and therapeutic implications
P. Roth, C. Happold, G. Eisele, T. Nägele, M. Weller, A. R. Luft
A multifactorial prognostic index in multiple sclerosis
J. Mandrioli, P. Sola, R. Bedin, M. Gambini, E. Merelli
Sleep-wake cycle and effects of cabergoline monotherapy in de novo Parkinson’s disease patients
F. Placidi, F. Izzi, A. Romigi, P. Stanzione, M. G. Marciani, L. Brusa, F. Sperli, S. Galati, P. Pasqualetti, M. Pierantozzi
Clinical features and associated syndromes of mal de debarquement
Y.-H. Cha, J. Brodsky, G. Ishiyama, C. Sabatti, R. W. Baloh
Valvular heart disease in patients with Parkinson’s disease treated with pergolide. Course following treatment modifications
D. Dupuy, J. P. Lesbre, P. Gérard, M. Andrejak, O. Godefroy
Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations
Knut Brockmann, Steffi Dreha-Kulaczewski, Peter Dechent, Carsten Bönnemann, Gunther Helms, Marten Kyllerman, Wolfgang Brück, Jens Frahm, Kathrin Huehne, Jutta Gärtner, Bernd Rautenstrauss
Effects of subthalamic nucleus stimulation on striatal dopaminergic transmission in patients with Parkinson’s disease within one-year follow-up
S. Hesse, K. Strecker, D. Winkler, J. Luthardt, C. Scherfler, A. Reupert, C. Oehlwein, H. Barthel, J.-P. Schneider, F. Wegner, P. Meyer, J. Meixensberger, O. Sabri, J. Schwarz
Accelerated forgetting in subjects with memory complaints
F. Manes, C. Serrano, M. L. Calcagno, J. Cardozo, J. Hodges
Parkinsonian patients show impaired predictive smooth pursuit
J. Ladda, P. Valkovič, T. Eggert, A. Straube
Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy
C. Cagnoli, A. Brussino, E. Di Gregorio, P. Caroppo, S. Stola, E. Dragone, M. Ferrone, S. Padovan, N. Migone, L. Orsi, A. Brusco
Association of superficial siderosis of the central nervous system and low pressure headache
D. Holle, I. E. Sandalcioglu, E. R. Gizewski, S. Asgari, D. Timmann, H. C. Diener, C. Weimar
Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation
A. Jiménez-Huete, J. Bernar, H. Miyajima, Y. Takahashi, J. Álvarez-Linera, O. Franch, M. S. van der Knaap
Paraneoplastic vasculitic neuropathy related to carcinoid tumor
S. Ashok Muley, K. Brown, G. J. Parry
An infected arachnoid cyst in an elderly patient
V. Sivaraman, A. Au-Yeung, S. Brew, A. W. McEvoy, R. Greenwood
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy
A. Tessa, G. Silvestri, M. F. de Leva, A. Modoni, P. S. Denora, M. Masciullo, M. T. Dotti, C. Casali, M. A. B. Melone, A. Federico, A. Filla, F. M. Santorelli
Successful treatment of hyperventilation-induced nystagmus in vestibular schwannoma with oxcarbacepine
G. Ahle, W. Visser, A. Juergens, U. Schlegel
Disjunctive saccadesduring smooth pursuit eye movements in ocular myasthenia gravis
T. Sander, A. Sprenger, B. Machner, H. Rambold, C. Helmchen
Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity
T. D. Graves, M. G. Hanna
Relative frequency of VGKC and ‘classical’ paraneoplastic antibodies in patients with limbic encephalitis
S. Jarius, L. A. Hoffmann, O. Stich, L. Clover, S. Rauer, A. Vincent, R. Voltz
A case of eosinophilic meningitis in Germany
S. Kirsch, P. Dekumyoy, T. Löscher, R. L. Haberl
Neurogenetics: T1 level translational research, myopathies and moyamoya disease
Michael Strupp