Zobrazeno 1 - 10
of 344
pro vyhledávání: '"J.H.J. Wokke"'
Autor:
Willy M. Nillesen, L. H. van den Berg, J.H.J. Wokke, Frans Brugman, M. de Visser, Hans Scheffer, J. H. Veldink, Eleonora Aronica
Publikováno v:
Neurology, 71, 1500-5
Neurology, 71, 19, pp. 1500-5
Neurology, 71(19), 1500-1505. Lippincott Williams and Wilkins
Neurology, 71, 19, pp. 1500-5
Neurology, 71(19), 1500-1505. Lippincott Williams and Wilkins
Objective: To investigate the frequency of autosomal recessive paraplegin mutations in patients with sporadic adult-onset upper motor neuron (UMN) syndromes. Methods: We analyzed the paraplegin gene in 98 Dutch patients with a sporadic adult-onset UM
Publikováno v:
Brain. 129:2447-2460
The finding of conduction block (CB) on nerve conduction studies supports the diagnosis of potentially treatable immune-mediated neuropathies. CB in a number of axons may result in reduction of the compound muscle action potential (CMAP) on proximal
Autor:
J.H.J. Wokke, S. Kalmijn, H. Franssen, R. M. Van den Berg-Vos, C H Polman, L. H. van den Berg, J.T.H. van Asseldonk
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 77:743-747
Background: Multifocal motor neuropathy (MMN) is characterised by asymmetrical weakness and muscle atrophy, in the arms more than the legs, without sensory loss. Despite a beneficial response to treatment with intravenous immunoglobulins (IVIg), weak
Autor:
M. Eurelings, J.H.J. Wokke, R. Fijnheer, H M Lokhorst, Nicolette C. Notermans, J.M.F. Niermeijer, H. Franssen
Publikováno v:
Neurology, 67(11), 2076-2079. Lippincott Williams and Wilkins
We studied the efficacy of fludarabine in 16 patients with immunoglobulin M monoclonal gammopathy of unknown significance polyneuropathy in a prospective uncontrolled trial. The modified Rankin scale improved in 5/16 patients, all of whom had a demye
Autor:
Henny H. Lemmink, Jan H. Veldink, J.H.J. Wokke, Geert Jan Groeneveld, C. Lummen, L. H. van den Berg, Hans Scheffer, A. H. Van der Hout, S. Kalmijn
Publikováno v:
Neurology, 65(6), 820-825. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 65, 820-825
Neurology, 65, 6, pp. 820-825
Neurology, 65, 820-825
Neurology, 65, 6, pp. 820-825
Item does not contain fulltext BACKGROUND: ALS is believed to be multifactorial in origin with modifying genes affecting its clinical expression. Childhood-onset spinal muscular atrophy (SMA) is an autosomal recessive disorder of motor neurons, cause
Publikováno v:
Brain. 128:880-891
The diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP) is based on clinical and laboratory results and on features of demyelination found in nerve conduction studies. The criteria that are currently used to reveal demyelinative slo
Autor:
J. P. Van den Berg, S. Kalmijn, J. H. Veldink, M.M. van der Graaff, Eline Lindeman, J.H.J. Wokke, M. de Visser, L. H. van den Berg
Publikováno v:
Neurology, 65(8), 1264-1267. Lippincott Williams and Wilkins
Objective: To examine the effect of multidisciplinary ALS care on the quality-of-life (QoL) in patients with ALS and their caregivers. Methods: In a cross-sectional study, 208 patients with ALS and their caregivers were interviewed. QoL was assessed
Publikováno v:
Brain. 125:1875-1886
We performed a long-term follow-up study of 11 patients with multifocal motor neuropathy (MMN) who received maintenance treatment with intravenous immunoglobulins (IVIg). Patients were treated initially with one full course of IVIg (0.4 g/kg for 5 da
Autor:
L. H. van den Berg, J.H.J. Wokke, W. M. J. Bosboom, T. Logtenberg, I. Mollee, L.D. Sasker, J. Jansen
Publikováno v:
Neurology. 56:74-81
Objective: To investigate the utilization of T-cell receptor (TCR) variable (V) regions in infiltrates of sural nerve biopsies of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) and vasculitic neuropathy. Background: The presen
Publikováno v:
Muscle & Nerve. 23:73-79
In order to define diagnostic criteria for the demyelinating polyneuropathy associated with monoclonal gammopathy of undetermined significance (MGUS), we compared 30 patients with idiopathic chronic inflammatory demyelinating polyneuropathy (CIDP) wi