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Journal of Neurology

Issue 7/2000

Content (25 Articles)

LETTER TO THE EDITORS

Persistent facial myokymia: an autoimmune aetiology?

Paul Maddison, Angela Vincent, Kerry Mills, Chris Fursdon Davis

ORIGINAL COMMUNICATION

Dopamine transporter binding in Gilles de la Tourette syndrome

Kirsten R. Müller-Vahl, Georg Berding, Thomas Brücke, Hans Kolbe, Geerd J. Meyer, Heinz Hundeshagen, Reinhard Dengler, Wolfram H. Knapp, Hinderk M. Emrich

ENS REVIEW

Management of vestibular disorders

Thomas Brandt

ORIGINAL COMMUNICATION

MRI and motor evoked potential findings in nondisabled multiple sclerosis patients with and without symptoms of fatique

Bruno Colombo, Filippo Martinelli Boneschi, Paolo Rossi, Marco Rovaris, Luca Maderna, Massimo Filippi, Giancarlo Comi

REVIEW

The two faces of Alzheimer's disease

W. A. van Gool, P. Eikelenboom

ORIGINAL COMMUNICATION

Significantly increased prevalence of factor V Leiden in patients with dural arteriovenous fistulas

Jürgen A. Kraus, Bettina K. Stüper, Hans-C. Nahser, Thomas Klockgether, Peter Berlit

ORIGINAL COMMUNICATION

Comparison of second lumbrical and interosseus latencies with standard measures of median nerve function across the carpal tunnel: a prospective study of 450 hands

Wolfgang N. Löscher, Michaela Auer-Grumbach, Eugen Trinka, Gunther Ladurner, Hans-Peter Hartung

ORIGINAL COMMUNICATION

Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy

H. B. Ginjaar, A. J. van der Kooi, H. Ceelie, A. L. J. Kneppers, M. van Meegen, P. G. Barth, H. F. M. Busch, J. H. J. Wokke, L. V. B. Anderson, C. G. Bönnemann, M. Jeanpierre, P. A. Bolhuis, A. F. M. Moorman, M. de Visser, E. Bakker, G. J. B. v. Ommen

ORIGINAL COMMUNICATION

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis

Ludo Vanopdenbosch, Bénédicte Dubois, Marie-Béatrice D'Hooghe, Françoise Meire, Herwig Carton

ORIGINAL COMMUNICATION

Differential response to corticosteroid therapy of MRI findings and clinical manifestations in spinal cord sarcoidosis

Haruki Koike, Ken-ichiro Misu, Keizo Yasui, Takashi Kameyama, Tetsuo Ando, Tsutomu Yanagi, Gen Sobue

LETTER TO THE EDITORS

Recurrent transverse myelitis with unusual long-standing Gd-DTPA enhancement

Antonio García-Merino, María Rosario Blasco

LETTER TO THE EDITORS

Lamotrigine in trigeminal neuralgia secondary to multiple sclerosis

Massimo Leandri, Gianluigi Lunardi, Matilde Inglese, Michélle Messmer-Uccelli, Gian Luigi Mancardi, Alberto Gottlieb, Claudio Solaro

LETTER TO THE EDITORS

Anti-Hu-associated paraneoplastic sensory neuropathy and breast cancer

Siraj Bechich, Francesc Graus, Adrià Arboix, Albert Isidro, Margarita Martí, Francesc Rosell

LETTER TO THE EDITORS

Parkinson's disease misdiagnosed as multiple system atrophy by sphincter electromyography

C. Colosimo, M. Inghilleri, K. R. Chaudhuri

LETTER TO THE EDITORS

Elevation in anti-GQ1b, anti-GT1a, and anti-GT1b IgG antibodies in postinfectious acute ataxic neuropathy with oropharyngeal palsy but without ophthalmolplegia

Keiko Kamakura, Ken-ichi Kaida, Susumu Kusunoki, Norikazu Miyamoto, Jun Fukuda, Kazuo Motoyoshi

LETTER TO THE EDITORS

Akinetic mutism from frontal lobe damage responding to levodopa

Onofre Combarros, Jon Infante, José Berciano

LETTER TO THE EDITORS

Cauda equina syndrome as the isolated presentation of sarcoidosis

Kamal K. Verma, Arthur D. Forman, Gregory N. Fuller, Mazen M. Dimachkie, Francine J. Vriesendorp

LETTER TO THE EDITORS

An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder)

Ozden Sanal, Leman Yel, Turkan Kucukali, Enid Gilbert-Barnes, Marc Tardieu, Ilhan Tezcan, Fugen Ersoy, Ayse Metin, Genevieve de Saint Basile

PIONEERS IN NEUROLOGY

Adolf Strümpell (1853–1925)

Frank J. Erbguth, Bernhard Neundörfer