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Muscle & Nerve|March 15, 2000
Diagnosis of ulnar neuropathy: a new approachK Merlevede, P Theys, J van HeesJournal of Neurology|January 1, 1983
Clinical parameters and intrathecal IgG synthesis as prognostic features in multiple sclerosis. Part IE Verjans, P Theys, P Delmotte, et al.Journal of Neurology|January 1, 1981
Short-term intensive cyclophosphamide treatment in multiple sclerosis. A retrospective controlled studyP Theys, F Gosseye-Lissoir, P Ketelaer, et al.Clinical Neurology and Neurosurgery|February 1, 1994
Pregnancy and multiple sclerosis: the influence on long term disabilityP Verdru, P Theys, M B D'Hooghe, et al.Acta Neurologica Belgica|August 10, 2000
Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis populationV Thijs, E Peeters, P Theys, et al.Journal of the Neurological Sciences|March 1, 1996
Pathological findings in a patient with amyotrophic lateral sclerosis and multifocal motor neuropathy with conduction blockB Veugelers, P Theys, M Lammens, et al.American Journal of Medical Genetics|April 9, 1996
Lujan-Fryns syndrome in the differential diagnosis of schizophreniaM De Hert, D Steemans, P Theys, et al.Archives of Neurology|January 1, 1996
Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activityW Robberecht, T Aguirre, L Van den Bosch, et al.Annals of Neurology|June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsiesD Verhalle, A Löfgren, E Nelis, et al.Journal of Neurochemistry|January 1, 1994
Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosisW Robberecht, P Sapp, M K Viaene, et al.Pageof 2