Electrophysiological diagnosis of motor neuron disease and pure motor neuropathy P. BoucheNadine Le ForestierJean Claude Willer ENS review Pages: 520 - 525
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL M. MayerA. StraubeJ. Müller-Höcker Original communication Pages: 526 - 532
Nonenzymatic antioxidants of blood in multiple sclerosis Eszter KargPéter KlivényiLászló Vécsei Original communication Pages: 533 - 539
Primitive reflexes in a case-control study of patients with advanced human immunodeficiency virus type 1 I. W. Tremont-LukatsGilda M. TeixeiraDimas E. Hernández Original communication Pages: 540 - 543
Median nerve mononeuropathy in spondylotic cervical myelopathy: double crush syndrome? Josef BednaříkZdeněk KadaňkaStanislav Voháňka Original communication Pages: 544 - 551
Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy Michael DonaghyRobin Kennett Original communication Pages: 552 - 555
Troyer syndrome: a combination of central brain abnormality and motor neuron disease? Michaela Auer-GrumbachF. FazekasHans Peter Hartung Original communication Pages: 556 - 561
Problems in designing and recruiting to therapeutic trials in primary progressive multiple sclerosis Siobhan M. LearyValerie L. StevensonA. J. Thompson Original communication Pages: 562 - 568
Immunological effects of in vivo interferon-β1b treatment in ten patients with multiple sclerosis: a 1-year follow-up M. GelatiE. CorsiniA. Salmaggi Original communication Pages: 569 - 573
Apolipoprotein E and presenilin-1 genotypes in Huntington’s disease Marios PanasDimitrios AvramopoulosD. Vassilopoulos Original communication Pages: 574 - 577
Cardiovascular autonomic dysfunction in multiple sclerosis: correlation with orthostatic intolerance P. FlacheneckerAnnalaska WolfKarlheinz Reiners Original communication Pages: 578 - 586
Exploring differences between subgroups of multiple sclerosis patients in health-related quality of life L. PfenningsL. CohenHenk van der Ploeg Original communication Pages: 587 - 591
Transcranial Doppler detection of microembolic signals in patients with Behçet’s disease E. KumralDilek EvyapanKaan Balkir Original communication Pages: 592 - 595
Phenotypic variation of a new P0 mutation in genetically identical twins Wilson Marques Jr.Michael G. HannaN. W. Wood Original communication Pages: 596 - 599
Saccades and smooth pursuit in myotonic dystrophy S. ShaunakR. OrrellC. Kennard Original communication Pages: 600 - 606
Reductions in the bilateral parietal and occipital cerebral blood flow and metabolism in a patient with Marchiafava-Bignami disease M. SanoKenji IshiiMichio Senda Letter to the editors Pages: 607 - 608
Recurrent brain edema in ornithine-transcarbamylase deficiency Stefan SchwabStefan SchwarzGeorg F. Hoffmann Letter to the editors Pages: 609 - 611
Neurological involvement and quadricuspid aortic valve in a patient with Ehlers-Danlos syndrome M. T. DottiNicola De StefanoAntonio Federico Letter to the editors Pages: 612 - 613
Erythropoietin induced visual hallucinations after bone marrow transplantation M. J. van den BentG. M. J. BosJ. J. Cornelissen Letter to the editors Pages: 614 - 616
Toxic leukencephalopathy following “ecstasy” ingestion M. BertramThomas EgelhoffStefan Schwab Letter to the editors Pages: 617 - 618
Intrathecal baclofen for intractable spasticity in amyotrophic lateral sclerosis G. MarquardtRüdiger Lorenz Letter to the editors Pages: 619 - 620
Pathological yawning (chasm) associated with periodic leg movements in sleep: cure by levodopa Martin LeonhardtMichael AbeleM. Weller Letter to the editors Pages: 621 - 622
Acquired neuromyotonia: superiority of plasma exchange over high-dose intravenous human immunoglobulin J. S. P. van den BergB. G. M. van EngelenM. H. de Baets Letter to the editors Pages: 623 - 625