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Browsing by Author Doorn, P.A. van
Showing results 1 to 15 of 15
| Full Text | Issue Date | Title | Author(s) | | 2012 | Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment | Eftimov, F.; Vermeulen, M; Doorn, P.A. van; Brusse, E.; Schaik, I.N. van, et al |
| 2011 | Screening for antecedent Campylobacter jejuni infections and anti-ganglioside antibodies in idiopathic neuralgic amyotrophy | Eijk, J.J.J. van; Alfen, N. van; Tio-Gillen, A.P.; Maas, Marijke; Herbrink, P., et al |
| 2011 | Selective digestive tract decontamination decreases time on ventilator in Guillain-Barre syndrome | Eyssen, M.E.; Doorn, P.A. van; Jacobs, B.C.; Steyerberg, E.W.; Voort, P.H. van der, et al |
| 2010 | Pulsed high-dose dexamethasone versus standard prednisolone treatment for chronic inflammatory demyelinating polyradiculoneuropathy (PREDICT study): a double-blind, randomised, controlled trial. | Schaik, I.N. van; Eftimov, F.; Doorn, P.A. van; Brusse, E.; Berg, L.H. van den, et al |
| 2010 | Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy | Cats, E.A.; Pol, W.L. van der; Piepers, S.; Franssen, H.; Jacobs, B.C., et al |
| 2009 | Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes. | Brugman, F.; Veldink, J.H.; Franssen, H.; Visser, M. de; Jong, J.M. de, et al |
| 2007 | Contribution of central and peripheral factors to residual fatigue in Guillain-Barre syndrome. | Garssen, M.P.; Schillings, M.L.; Doorn, P.A. van; Engelen, B.G.M. van; Zwarts, M.J. |
| 2007 | Ptosis as a feature of late-onset glycogenosis type II. Response to: Ravaglia S, Repetto A, De Filippi P, Danesino C. | Leen, W.; Groen, W.B.; Vos, A.M.C.; Cruysberg, J.R.M.; Doorn, P.A. van, et al |
| 2007 | Genetic polymorphisms of macrophage-mediators in Guillain-Barre syndrome. | Geleijns, K.; Emonts, M.; Laman, J.D.; Rijs, W. van; Doorn, P.A. van, et al |
| 2007 | The Dutch neuromuscular database CRAMP (Computer Registry of All Myopathies and Polyneuropathies): development and preliminary data. | Engelen, B.G.M. van; Veenendaal, H. van; Doorn, P.A. van; Faber, C.G.; Hoeven, J.H. van, et al |
| 2007 | TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations. | Seelaar, H.; Schelhaas, H.J.; Azmani, A.; Kusters, B.; Rosso, S., et al |
| 2006 | Ptosis as a feature of late-onset glycogenosis type II. | Groen, W.B.; Leen, W.G.; Vos, A.M.C.; Cruysberg, J.R.M.; Doorn, P.A. van, et al |
| 2005 | Inclusion body myositis Clinical features and clinical course of the disease in 64 patients. | Badrising, U.A.; Maat-Schieman, M.L.; Houwelingen, J.C. van; Doorn, P.A. van; Duinen, S.G. van, et al |
| 2004 | The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands. | Wirtz, P.W.; Dijk, J.G. van; Doorn, P.A. van; Engelen, B.G.M. van; Kooi, A.J. van der, et al |
| 2004 | Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk. | Hout, J.M. van den; Kamphoven, J.H.; Winkel, L.P.; Arts, W.F.M.; Klerk, J.B.C. de, et al |
Showing results 1 to 15 of 15
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