John H.J. Wokke - Publications

Affiliations: 
Neurology Utrecht University, Utrecht, Netherlands 
Area:
Neuromuscular disorders
Website:
https://profs.library.uu.nl/index.php/profrec/getprofdata/2409/516/529/0

140 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 van der Beek NA, de Vries JM, Hagemans ML, Hop WC, Kroos MA, Wokke JH, de Visser M, van Engelen BG, Kuks JB, van der Kooi AJ, Notermans NC, Faber KG, Verschuuren JJ, Reuser AJ, van der Ploeg AT, et al. Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study. Orphanet Journal of Rare Diseases. 7: 88. PMID 23147228 DOI: 10.1186/1750-1172-7-88  0.309
2012 Wadman RI, Bosboom WM, van der Pol WL, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. 4: CD006282. PMID 22513940 DOI: 10.1002/14651858.Cd006282.Pub4  0.468
2012 Wadman RI, Bosboom WM, van der Pol WL, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. 4: CD006281. PMID 22513939 DOI: 10.1002/14651858.Cd006281.Pub4  0.472
2012 De Visser M, van der Kooi A, Linssen WHJP, Ginjaar I, Wokke J, Van Doorn P. Anoctamin 5 Mutations Are a Frequent Cause of Limb Girdle Muscular Dystrophy and of the Miyoshi-Type Muscular Dystrophy in the Netherlands (S15.005) Neurology. 78: S15.005-S15.005. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S15.005  0.341
2011 Wadman RI, Bosboom WM, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. CD006282. PMID 22161400 DOI: 10.1002/14651858.CD006282.pub3  0.396
2011 Wadman RI, Bosboom WM, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. CD006281. PMID 22161399 DOI: 10.1002/14651858.CD006281.pub3  0.401
2011 Visser NA, Braun KP, Leijten FS, van Nieuwenhuizen O, Wokke JH, van den Bergh WM. Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations. Journal of Neurology. 258: 218-22. PMID 20803213 DOI: 10.1007/S00415-010-5721-2  0.316
2011 Straver DC, van Asseldonk JT, Notermans NC, Wokke JH, van den Berg LH, Franssen H. Cold paresis in multifocal motor neuropathy. Journal of Neurology. 258: 212-7. PMID 20803025 DOI: 10.1007/S00415-010-5712-3  0.529
2011 Piepers S, Cobben JM, Sodaar P, Jansen MD, Wadman RI, Meester-Delver A, Poll-The BT, Lemmink HH, Wokke JH, van der Pol WL, van den Berg LH. Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 850-2. PMID 20551479 DOI: 10.1136/Jnnp.2009.200253  0.478
2010 Franssen H, Gebbink TA, Wokke JH, van den Berg LH, van Schelven LJ. Is cold paresis related to axonal depolarization? Journal of the Peripheral Nervous System : Jpns. 15: 227-37. PMID 21040145 DOI: 10.1111/J.1529-8027.2010.00275.X  0.508
2010 Niks EH, Kuks JB, Wokke JH, Veldman H, Bakker E, Verschuuren JJ, Plomp JJ. Pre- and postsynaptic neuromuscular junction abnormalities in musk myasthenia. Muscle & Nerve. 42: 283-8. PMID 20544919 DOI: 10.1002/Mus.21642  0.336
2010 Groen EJ, van Es MA, van Vught PW, Spliet WG, van Engelen-Lee J, de Visser M, Wokke JH, Schelhaas HJ, Ophoff RA, Fumoto K, Pasterkamp RJ, Dooijes D, Cuppen E, Veldink JH, van den Berg LH. FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. Archives of Neurology. 67: 224-30. PMID 20142531 DOI: 10.1001/Archneurol.2009.329  0.442
2009 Van Es MA, Van Vught PW, Veldink JH, Andersen PM, Birve A, Lemmens R, Cronin S, Van Der Kooi AJ, De Visser M, Schelhaas HJ, Hardiman O, Ragoussis I, Lambrechts D, Robberecht W, Wokke JH, et al. Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 10: 441-7. PMID 19922138 DOI: 10.3109/17482960802673042  0.45
2009 Sutedja NA, Veldink JH, Fischer K, Kromhout H, Heederik D, Huisman MH, Wokke JH, van den Berg LH. Exposure to chemicals and metals and risk of amyotrophic lateral sclerosis: a systematic review. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 10: 302-9. PMID 19922117 DOI: 10.3109/17482960802455416  0.426
2009 Maessen M, Veldink JH, Onwuteaka-Philipsen BD, de Vries JM, Wokke JH, van der Wal G, van den Berg LH. Trends and determinants of end-of-life practices in ALS in the Netherlands. Neurology. 73: 954-61. PMID 19770471 DOI: 10.1212/WNL.0b013e3181b87983  0.376
2009 Piepers S, Veldink JH, de Jong SW, van der Tweel I, van der Pol WL, Uijtendaal EV, Schelhaas HJ, Scheffer H, de Visser M, de Jong JM, Wokke JH, Groeneveld GJ, van den Berg LH. Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis. Annals of Neurology. 66: 227-34. PMID 19743466 DOI: 10.1002/Ana.21620  0.434
2009 van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, ... ... Wokke JH, et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nature Genetics. 41: 1083-7. PMID 19734901 DOI: 10.1038/Ng.442  0.421
2009 Saris CG, Horvath S, van Vught PW, van Es MA, Blauw HM, Fuller TF, Langfelder P, DeYoung J, Wokke JH, Veldink JH, van den Berg LH, Ophoff RA. Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. Bmc Genomics. 10: 405. PMID 19712483 DOI: 10.1186/1471-2164-10-405  0.505
2009 Faber CG, Molenaar PC, Vles JS, Bonifati DM, Verschuuren JJ, van Doorn PA, Kuks JB, Wokke JH, Beeson D, De Baets M. AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands. Journal of Neurology. 256: 1719-23. PMID 19544078 DOI: 10.1007/S00415-009-5190-7  0.301
2009 Piepers S, van der Pol WL, Brugman F, Wokke JH, van den Berg LH. Natural history of SMA IIIb: muscle strength decreases in a predictable sequence and magnitude. Neurology. 72: 2057-8; author reply. PMID 19506238 DOI: 10.1212/01.wnl.0000349698.94744.1e  0.369
2009 Van den Berg-Vos RM, Visser J, Kalmijn S, Fischer K, de Visser M, de Jong V, de Haan RJ, Franssen H, Wokke JH, Van den Berg LH. A long-term prospective study of the natural course of sporadic adult-onset lower motor neuron syndromes. Archives of Neurology. 66: 751-7. PMID 19506135 DOI: 10.1001/Archneurol.2009.91  0.489
2009 Landers JE, Melki J, Meininger V, Glass JD, van den Berg LH, van Es MA, Sapp PC, van Vught PW, McKenna-Yasek DM, Blauw HM, Cho TJ, Polak M, Shi L, Wills AM, Broom WJ, ... ... Wokke JH, et al. Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 106: 9004-9. PMID 19451621 DOI: 10.1073/Pnas.0812937106  0.474
2009 Brugman F, Veldink JH, Franssen H, de Visser M, de Jong JM, Faber CG, Kremer BH, Schelhaas HJ, van Doorn PA, Verschuuren JJ, Bruyn RP, Kuks JB, Robberecht W, Wokke JH, van den Berg LH. Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes. Archives of Neurology. 66: 509-14. PMID 19364936 DOI: 10.1001/Archneurol.2009.19  0.534
2009 Faber CG, Notermans NC, Wokke JH, Franssen H. Entrapment in anti myelin-associated glycoprotein neuropathy. Journal of Neurology. 256: 620-4. PMID 19306083 DOI: 10.1007/S00415-009-0132-Y  0.366
2009 Brugman F, Scheffer H, Schelhaas HJ, Nillesen WM, Wokke JH, van de Warrenburg BP, van den Berg LH. Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. Journal of Neurology. 256: 824-6. PMID 19252810 DOI: 10.1007/S00415-009-5009-6  0.515
2009 Bosboom W, Vrancken AF, van den Berg LH, Wokke JH, Iannaccone ST. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. CD006282. PMID 19160275 DOI: 10.1002/14651858.CD006282.pub2  0.395
2009 Bosboom W, Vrancken AF, van den Berg LH, Wokke J, Iannaccone ST. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. CD006281. PMID 19160274 DOI: 10.1002/14651858.CD006281.pub2  0.414
2008 Wokke JH, Escolar DM, Pestronk A, Jaffe KM, Carter GT, van den Berg LH, Florence JM, Mayhew J, Skrinar A, Corzo D, Laforet P. Clinical features of late-onset Pompe disease: a prospective cohort study. Muscle & Nerve. 38: 1236-45. PMID 18816591 DOI: 10.1002/Mus.21025  0.497
2008 Brugman F, Scheffer H, Wokke JH, Nillesen WM, de Visser M, Aronica E, Veldink JH, van den Berg LH. Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes. Neurology. 71: 1500-5. PMID 18799786 DOI: 10.1212/01.wnl.0000319700.11606.21  0.418
2008 Piepers S, van den Berg LH, Brugman F, Scheffer H, Ruiterkamp-Versteeg M, van Engelen BG, Faber CG, de Visser M, van der Pol WL, Wokke JH. A natural history study of late onset spinal muscular atrophy types 3b and 4. Journal of Neurology. 255: 1400-4. PMID 18575920 DOI: 10.1007/S00415-008-0929-0  0.323
2008 Dierick I, Baets J, Irobi J, Jacobs A, De Vriendt E, Deconinck T, Merlini L, Van den Bergh P, Rasic VM, Robberecht W, Fischer D, Morales RJ, Mitrovic Z, Seeman P, Mazanec R, ... ... Wokke JH, et al. Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study. Brain : a Journal of Neurology. 131: 1217-27. PMID 18325928 DOI: 10.1093/Brain/Awn029  0.329
2008 Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, Franke L, Burbach JP, Wokke JH, Ophoff RA, van den Berg LH. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen. The Lancet. Neurology. 7: 319-26. PMID 18313986 DOI: 10.1016/S1474-4422(08)70048-6  0.411
2008 van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, Van den Bosch L, de Jong SW, de Jong V, Baas F, van't Slot R, Lemmens R, Schelhaas HJ, Birve A, Sleegers K, Van Broeckhoven C, ... ... Wokke JH, et al. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nature Genetics. 40: 29-31. PMID 18084291 DOI: 10.1038/Ng.2007.52  0.461
2007 Van Den Berg LH, Franssen H, Van Asseldonk JT, Van Den Berg-Vos RM, Wokke JH. Chapter 12 Multifocal and other motor neuropathies. Handbook of Clinical Neurology. 82: 229-45. PMID 18808897 DOI: 10.1016/S0072-9752(07)80015-7  0.513
2007 Sutedja NA, Veldink JH, Fischer K, Kromhout H, Wokke JH, Huisman MH, Heederik DJ, Van den Berg LH. Lifetime occupation, education, smoking, and risk of ALS. Neurology. 69: 1508-14. PMID 17923612 DOI: 10.1212/01.wnl.0000277463.87361.8c  0.333
2007 van Es MA, Van Vught PW, Blauw HM, Franke L, Saris CG, Andersen PM, Van Den Bosch L, de Jong SW, van 't Slot R, Birve A, Lemmens R, de Jong V, Baas F, Schelhaas HJ, Sleegers K, ... ... Wokke JH, et al. ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. The Lancet. Neurology. 6: 869-77. PMID 17827064 DOI: 10.1016/S1474-4422(07)70222-3  0.487
2007 Brugman F, Eymard-Pierre E, van den Berg LH, Wokke JH, Gauthier-Barichard F, Boespflug-Tanguy O. Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene. Neurology. 69: 702-4. PMID 17698795 DOI: 10.1212/01.wnl.0000267322.48364.76  0.371
2007 Piepers S, Van Den Berg-Vos R, Van Der Pol WL, Franssen H, Wokke J, Van Den Berg L. Mycophenolate mofetil as adjunctive therapy for MMN patients: A randomized, controlled trial Brain. 130: 2004-2010. PMID 17626040 DOI: 10.1093/Brain/Awm144  0.526
2007 Niermeijer JM, Eurelings M, van der Linden MW, Lokhorst HM, Franssen H, Fischer K, Teunissen LL, van den Berg LH, Schobben F, Wokke JH, Notermans NC. Intermittent cyclophosphamide with prednisone versus placebo for polyneuropathy with IgM monoclonal gammopathy. Neurology. 69: 50-9. PMID 17606880 DOI: 10.1212/01.wnl.0000265055.28218.cc  0.379
2007 Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Wokke JH, de Jong JM, Holman R, de Haan RJ, de Visser M. Disease course and prognostic factors of progressive muscular atrophy. Archives of Neurology. 64: 522-8. PMID 17420313 DOI: 10.1001/archneur.64.4.522  0.444
2007 Wokke JH. Fatigue is part of the burden of neuromuscular diseases. Journal of Neurology. 254: 948-9. PMID 17325819 DOI: 10.1007/S00415-006-0436-0  0.348
2007 Sutedja NA, Sinke RJ, Van Vught PW, Van der Linden MW, Wokke JH, Van Duijn CM, Njajou OT, Van der Schouw YT, Veldink JH, Van den Berg LH. The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population. Archives of Neurology. 64: 63-7. PMID 17210810 DOI: 10.1001/Archneur.64.1.63  0.452
2007 van Sorge NM, Yuki N, Jansen MD, Nishimoto Y, Susuki K, Wokke JH, van de Winkel JG, van den Berg LH, van der Pol WL. Leukocyte and complement activation by GM1-specific antibodies is associated with acute motor axonal neuropathy in rabbits. Journal of Neuroimmunology. 182: 116-23. PMID 17161468 DOI: 10.1016/J.Jneuroim.2006.10.005  0.69
2007 van Sorge NM, Yuki N, Koga M, Susuki K, Jansen MD, van Kooten C, Wokke JH, van de Winkel JG, van der Pol WL, van den Berg LH. Ganglioside-specific IgG and IgA recruit leukocyte effector functions in Guillain-Barré syndrome. Journal of Neuroimmunology. 182: 177-84. PMID 17156858 DOI: 10.1016/J.Jneuroim.2006.10.015  0.684
2007 Veldink JH, Kalmijn S, Groeneveld GJ, Wunderink W, Koster A, de Vries JH, van der Luyt J, Wokke JH, Van den Berg LH. Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 367-71. PMID 16648143 DOI: 10.1136/jnnp.2005.083378  0.344
2006 Piepers S, van den Berg JP, Kalmijn S, van der Pol WL, Wokke JH, Lindeman E, van den Berg LH. Effect of non-invasive ventilation on survival, quality of life, respiratory function and cognition: a review of the literature. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 7: 195-200. PMID 17127557 DOI: 10.1080/14660820500514974  0.46
2006 Van Asseldonk JT, Van den Berg LH, Wieneke GH, Wokke JH, Franssen H. Criteria for conduction block based on computer simulation studies of nerve conduction with human data obtained in the forearm segment of the median nerve. Brain : a Journal of Neurology. 129: 2447-60. PMID 16923956 DOI: 10.1093/brain/awl197  0.424
2006 Van Asseldonk JT, Van den Berg LH, Kalmijn S, Van den Berg-Vos RM, Polman CH, Wokke JH, Franssen H. Axon loss is an important determinant of weakness in multifocal motor neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 77: 743-7. PMID 16705197 DOI: 10.1136/jnnp.2005.064816  0.45
2005 Van Vught PW, Sutedja NA, Veldink JH, Koeleman BP, Groeneveld GJ, Wijmenga C, Uitdehaag BM, de Jong JM, Baas F, Wokke JH, Van den Berg LH. Lack of association between VEGF polymorphisms and ALS in a Dutch population. Neurology. 65: 1643-5. PMID 16301496 DOI: 10.1212/01.Wnl.0000184514.39853.56  0.371
2005 Wokke JH, van den Berg LH. A way out of the maze: Campylobacter jejuni gene polymorphisms define Guillain-Barré syndrome. Neurology. 65: 1350-1. PMID 16275819 DOI: 10.1212/01.Wnl.0000185127.89668.7A  0.513
2005 Van den Berg JP, Kalmijn S, Lindeman E, Veldink JH, de Visser M, Van der Graaff MM, Wokke JH, Van den Berg LH. Multidisciplinary ALS care improves quality of life in patients with ALS. Neurology. 65: 1264-7. PMID 16247055 DOI: 10.1212/01.wnl.0000180717.29273.12  0.37
2005 Brugman F, Wokke JH, Scheffer H, Versteeg MH, Sistermans EA, van den Berg LH. Spastin mutations in sporadic adult-onset upper motor neuron syndromes. Annals of Neurology. 58: 865-9. PMID 16240363 DOI: 10.1002/Ana.20652  0.514
2005 Losen M, Stassen MH, Martínez-Martínez P, Machiels BM, Duimel H, Frederik P, Veldman H, Wokke JH, Spaans F, Vincent A, De Baets MH. Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis. Brain : a Journal of Neurology. 128: 2327-37. PMID 16150851 DOI: 10.1093/Brain/Awh612  0.312
2005 Veldink JH, Kalmijn S, Van der Hout AH, Lemmink HH, Groeneveld GJ, Lummen C, Scheffer H, Wokke JH, Van den Berg LH. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS. Neurology. 65: 820-5. PMID 16093455 DOI: 10.1212/01.wnl.0000174472.03292.dd  0.419
2005 Beekman R, van den Berg LH, Franssen H, Visser LH, van Asseldonk JT, Wokke JH. Ultrasonography shows extensive nerve enlargements in multifocal motor neuropathy. Neurology. 65: 305-7. PMID 16043806 DOI: 10.1212/01.wnl.0000169179.67764.30  0.43
2005 Erdmann PG, van Meeteren NL, Kalmijn S, Wokke JH, Helders PJ, van den Berg LH. Functional health status of patients with chronic inflammatory neuropathies. Journal of the Peripheral Nervous System : Jpns. 10: 181-9. PMID 15958129 DOI: 10.1111/J.1085-9489.2005.0010208.X  0.487
2005 Brugman F, Wokke JH, Vianney de Jong JM, Franssen H, Faber CG, Van den Berg LH. Primary lateral sclerosis as a phenotypic manifestation of familial ALS. Neurology. 64: 1778-9. PMID 15911810 DOI: 10.1212/01.WNL.0000162033.47893.F7  0.402
2005 Van Asseldonk JT, Franssen H, Van den Berg-Vos RM, Wokke JH, Van den Berg LH. Multifocal motor neuropathy. The Lancet. Neurology. 4: 309-19. PMID 15847844 DOI: 10.1016/S1474-4422(05)70074-0  0.556
2005 van Sorge NM, van der Pol WL, Jansen MD, Geleijns KP, Kalmijn S, Hughes RA, Rees JH, Pritchard J, Vedeler CA, Myhr KM, Shaw C, van Schaik IN, Wokke JH, van Doorn PA, Jacobs BC, et al. Severity of Guillain-Barré syndrome is associated with Fc gamma Receptor III polymorphisms. Journal of Neuroimmunology. 162: 157-64. PMID 15833371 DOI: 10.1016/J.Jneuroim.2005.01.016  0.691
2005 Groeneveld GJ, Beijer C, Veldink JH, Kalmijn S, Wokke JH, van den Berg LH. Few adverse effects of long-term creatine supplementation in a placebo-controlled trial. International Journal of Sports Medicine. 26: 307-13. PMID 15795816 DOI: 10.1055/s-2004-817917  0.384
2005 Van Asseldonk JT, Van den Berg LH, Kalmijn S, Wokke JH, Franssen H. Criteria for demyelination based on the maximum slowing due to axonal degeneration, determined after warming in water at 37 degrees C: diagnostic yield in chronic inflammatory demyelinating polyneuropathy. Brain : a Journal of Neurology. 128: 880-91. PMID 15689367 DOI: 10.1093/brain/awh375  0.451
2005 Veldink JH, Kalmijn S, Groeneveld GJ, Titulaer MJ, Wokke JH, van den Berg LH. Physical activity and the association with sporadic ALS. Neurology. 64: 241-5. PMID 15668420 DOI: 10.1212/01.WNL.0000149513.82332.5C  0.369
2004 Groeneveld GJ, van Muiswinkel FL, de Leeuw van Weenen J, Blauw H, Veldink JH, Wokke JH, van den Berg LH, Bär PR. CGP 3466B has no effect on disease course of (G93A) mSOD1 transgenic mice. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 5: 220-5. PMID 15799550 DOI: 10.1080/14660820410019530  0.43
2004 Groeneveld GJ, van der Tweel I, Wokke JH, van den Berg LH. Sequential designs for clinical trials in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 5: 202-7. PMID 15799547  0.347
2004 Veldink JH, Van den Berg LH, Wokke JH. The future of motor neuron disease: the challenge is in the genes. Journal of Neurology. 251: 491-500. PMID 15083302 DOI: 10.1007/S00415-004-0322-6  0.507
2004 Vrancken AF, Notermans NC, Jansen GH, Wokke JH, Said G. Progressive idiopathic axonal neuropathy--a comparative clinical and histopathological study with vasculitic neuropathy. Journal of Neurology. 251: 269-78. PMID 15015005 DOI: 10.1007/S00415-004-0275-9  0.355
2004 Beekman R, Schoemaker MC, Van Der Plas JP, Van Den Berg LH, Franssen H, Wokke JH, Uitdehaag BM, Visser LH. Diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow. Neurology. 62: 767-73. PMID 15007128 DOI: 10.1212/01.WNL.0000113733.62689.0D  0.34
2004 Groeneveld GJ, Van Kan HJ, Kalmijn S, Veldink JH, Guchelaar HJ, Wokke JH, Van den Berg LH. Riluzole serum concentrations in patients with ALS: associations with side effects and symptoms. Neurology. 61: 1141-3. PMID 14581684 DOI: 10.1212/01.WNL.0000090459.76784.49  0.415
2004 Eurelings M, van den Berg LH, Wokke JH, Franssen H, Vrancken AF, Notermans NC. Increase of sural nerve T cells in progressive axonal polyneuropathy and monoclonal gammopathy. Neurology. 61: 707-9. PMID 12963771 DOI: 10.1212/01.WNL.0000078103.71192.40  0.448
2003 Van Den Berg-Vos RM, Van Den Berg LH, Visser J, de Visser M, Franssen H, Wokke JH. The spectrum of lower motor neuron syndromes. Journal of Neurology. 250: 1279-92. PMID 14648143 DOI: 10.1007/S00415-003-0235-9  0.368
2003 Visser J, Mans E, de Visser M, van den Berg-Vos RM, Franssen H, de Jong JM, van den Berg LH, Wokke JH, de Haan RJ. Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndrome. Neuromuscular Disorders : Nmd. 13: 744-50. PMID 14561498 DOI: 10.1016/S0960-8966(03)00135-4  0.358
2003 Reagan P, Hurst R, Cook L, Zylicz Z, Otlowski M, Veldink JH, van den Berg LH, Wokke JH. Physician-assisted death: dying with dignity? The Lancet. Neurology. 2: 637-43. PMID 14505588 DOI: 10.1016/S1474-4422(03)00536-2  0.469
2003 van den Berg JP, Kalmijn S, Lindeman E, Wokke JH, van den Berg LH. Rehabilitation care for patients with ALS in The Netherlands. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 4: 186-90. PMID 13129805 DOI: 10.1080/Aml.4.3.186.190  0.474
2003 Teunissen LL, Notermans NC, Franssen H, Van Engelen BG, Baas F, Wokke JH. Disease course of Charcot-Marie-Tooth disease type 2: a 5-year follow-up study. Archives of Neurology. 60: 823-8. PMID 12810486 DOI: 10.1001/Archneur.60.6.823  0.323
2003 van Sorge NM, van den Berg LH, Geleijns K, van Strijp JA, Jacobs BC, van Doorn PA, Wokke JH, van de Winkel JG, Leusen JH, van der Pol WL. Anti-GM1 IgG antibodies induce leukocyte effector functions via Fcgamma receptors. Annals of Neurology. 53: 570-9. PMID 12730990 DOI: 10.1002/Ana.10503  0.674
2003 van den Berg-Vos RM, Visser J, Franssen H, de Visser M, de Jong JM, Kalmijn S, Wokke JH, van den Berg LH. Sporadic lower motor neuron disease with adult onset: classification of subtypes. Brain : a Journal of Neurology. 126: 1036-47. PMID 12690044 DOI: 10.1093/Brain/Awg117  0.532
2003 Groeneveld GJ, Veldink JH, van der Tweel I, Kalmijn S, Beijer C, de Visser M, Wokke JH, Franssen H, van den Berg LH. A randomized sequential trial of creatine in amyotrophic lateral sclerosis. Annals of Neurology. 53: 437-45. PMID 12666111 DOI: 10.1002/Ana.10554  0.494
2003 Van Asseldonk JT, Van den Berg LH, Van den Berg-Vos RM, Wieneke GH, Wokke JH, Franssen H. Demyelination and axonal loss in multifocal motor neuropathy: distribution and relation to weakness. Brain : a Journal of Neurology. 126: 186-98. PMID 12477706 DOI: 10.1093/Brain/Awg019  0.523
2003 van der Meulen MF, van Wichen DF, van Blokland WT, van den Berg LH, Wokke JH, Hoogendijk JE, de Weger RA. Evidence for heterogeneity of T cell expansion in polymyositis and inclusion body myositis. Journal of Neuroimmunology. 133: 198-204. PMID 12446023 DOI: 10.1016/S0165-5728(02)00363-6  0.512
2002 Van den Berg-Vos RM, Franssen H, Wokke JH, Van den Berg LH. Multifocal motor neuropathy: long-term clinical and electrophysiological assessment of intravenous immunoglobulin maintenance treatment. Brain : a Journal of Neurology. 125: 1875-86. PMID 12135977 DOI: 10.1093/Brain/Awf193  0.538
2002 Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Vogels OJ, Wokke JH, de Jong JM, de Visser M. Mimic syndromes in sporadic cases of progressive spinal muscular atrophy. Neurology. 58: 1593-6. PMID 12058084 DOI: 10.1212/Wnl.58.11.1593  0.555
2002 Veldink JH, Wokke JH, van der Wal G, Vianney de Jong JM, van den Berg LH. Euthanasia and physician-assisted suicide among patients with amyotrophic lateral sclerosis in the Netherlands. The New England Journal of Medicine. 346: 1638-44. PMID 12023997 DOI: 10.1056/Nejmsa012739  0.48
2002 Van den Berg-Vos RM, Franssen H, Visser J, de Visser M, de Haan RJ, Wokke JH, Van den Berg LH. Disease severity in multifocal motor neuropathy and its association with the response to immunoglobulin treatment. Journal of Neurology. 249: 330-6. PMID 11993534 DOI: 10.1046/J.1529-8027.2002.02032_4.X  0.539
2002 Oey PL, Vos PE, Wieneke GH, Wokke JH, Blankestijn PJ, Karemaker JM. Subtle involvement of the sympathetic nervous system in amyotrophic lateral sclerosis. Muscle & Nerve. 25: 402-8. PMID 11870718 DOI: 10.1002/Mus.10049  0.331
2002 Bosboom WM, van den Berg LH, Franssen H, Giesbergen PC, Flach HZ, van Putten AM, Veldman H, Wokke JH. Diagnostic value of sural nerve demyelination in chronic inflammatory demyelinating polyneuropathy. Brain : a Journal of Neurology. 124: 2427-38. PMID 11701597 DOI: 10.1093/BRAIN/124.12.2427  0.442
2001 Eurelings M, Notermans NC, Franssen H, Van Es HW, Ramos LM, Wokke JH, van den Berg LH. MRI of the brachial plexus in polyneuropathy associated with monoclonal gammopathy. Muscle & Nerve. 24: 1312-8. PMID 11562910 DOI: 10.1002/Mus.1149  0.514
2001 van der Meulen MF, Hoogendijk JE, Moons KG, Veldman H, Badrising UA, Wokke JH. Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositis. Neuromuscular Disorders : Nmd. 11: 447-51. PMID 11404115 DOI: 10.1016/S0960-8966(00)00219-4  0.329
2001 Van den Berg-Vos RM, Van den Berg LH, Jansen GH, Parton M, Shaw CE, Hesseling-Janssen AL, Wokke JH. Hereditary pure lower motor neuron disease with adult onset and rapid progression. Journal of Neurology. 248: 290-6. PMID 11374093 DOI: 10.1007/S004150170203  0.509
2001 Veldink JH, van den Berg LH, Cobben JM, Stulp RP, De Jong JM, Vogels OJ, Baas F, Wokke JH, Scheffer H. Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 56: 749-52. PMID 11274309  0.43
2001 Eurelings M, Moons KG, Notermans NC, Sasker LD, De Jager AE, Wintzen AR, Wokke JH, Van den Berg LH. Neuropathy and IgM M-proteins: prognostic value of antibodies to MAG, SGPG, and sulfatide. Neurology. 56: 228-33. PMID 11160960 DOI: 10.1212/WNL.56.2.228  0.407
2001 Bosboom WM, Van den Berg LH, Mollee I, Sasker LD, Jansen J, Wokke JH, Logtenberg T. Sural nerve T-cell receptor Vbeta gene utilization in chronic inflammatory demyelinating polyneuropathy and vasculitic neuropathy. Neurology. 56: 74-81. PMID 11148239 DOI: 10.1212/WNL.56.1.74  0.664
2001 Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, et al. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy. Journal of Neurology. 247: 524-9. PMID 10993494 DOI: 10.1007/S004150070151  0.308
2001 Teunissen LL, Notermans NC, Jansen GH, Banga JD, Veldman H, Wokke JH. Thickness of endoneurial vessel basal lamina area in chronic idiopathic axonal polyneuropathy. Acta Neuropathologica. 100: 445-50. PMID 10985705 DOI: 10.1007/S004010000193  0.32
2000 Weijnen FG, van der Bilt A, Wokke JH, Kuks JB, van der Glas HW, Bosman F. Maximal bite force and surface EMG in patients with myasthenia gravis. Muscle & Nerve. 23: 1694-9. PMID 11054747 DOI: 10.1002/1097-4598(200011)23:11<1694::Aid-Mus4>3.0.Co;2-H  0.345
2000 van der Kooi AJ, Visser MC, Rosenberg N, van den Berg-Vos R, Wokke JH, Bakker E, de Visser M. Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 114-6. PMID 10864616 DOI: 10.1136/Jnnp.69.1.114  0.327
2000 van der Pol WL, van den Berg LH, Scheepers RH, van der Bom JG, van Doorn PA, van Koningsveld R, van den Broek MC, Wokke JH, van de Winkel JG. IgG receptor IIa alleles determine susceptibility and severity of Guillain-Barré syndrome. Neurology. 54: 1661-5. PMID 10762510 DOI: 10.1212/WNL.54.8.1661  0.424
2000 Reijneveld JC, Notermans NC, Linssen WH, Wokke JH. Benign prognosis in idiopathic hyper-CK-emia. Muscle & Nerve. 23: 575-9. PMID 10716769 DOI: 10.1002/(Sici)1097-4598(200004)23:4<575::Aid-Mus17>3.0.Co;2-5  0.37
2000 Weijnen FG, van der Bilt A, Wokke JH, Kuks JB, van der Glas HW, Bosman F. What's in a smile?: Quantification of the vertical smile of patients with myasthenia gravis. Journal of the Neurological Sciences. 173: 124-8. PMID 10675656 DOI: 10.1016/S0022-510X(99)00319-6  0.355
2000 Van den Berg-Vos RM, Van den Berg LH, Franssen H, Vermeulen M, Witkamp TD, Jansen GH, van Es HW, Kerkhoff H, Wokke JH. Multifocal inflammatory demyelinating neuropathy: a distinct clinical entity? Neurology. 54: 26-32. PMID 10636121 DOI: 10.1212/WNL.54.1.26  0.46
1999 Bosboom WM, Van den Berg LH, De Boer L, Van Son MJ, Veldman H, Franssen H, Logtenberg T, Wokke JH. The diagnostic value of sural nerve T cells in chronic inflammatory demyelinating polyneuropathy. Neurology. 53: 837-45. PMID 10489051 DOI: 10.1212/WNL.53.4.837  0.658
1999 Wokke JH, Van den Berg LH. New hope for patients with pure lower motor neuron syndromes. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 6. PMID 10369813 DOI: 10.1136/JNNP.67.1.6  0.427
1998 Van den Berg LH, Franssen H, Wokke JH. The long-term effect of intravenous immunoglobulin treatment in multifocal motor neuropathy. Brain : a Journal of Neurology. 421-8. PMID 9549518 DOI: 10.1093/BRAIN/121.3.421  0.463
1998 van den Berg LH, Franssen H, Van Doorn PA, Wokke JH. Intravenous immunoglobulin treatment in lower motor neuron disease associated with highly raised anti-GM1 antibodies. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 674-7. PMID 9408114 DOI: 10.1136/jnnp.63.5.674  0.461
1997 Van Es HW, Van den Berg LH, Franssen H, Witkamp TD, Ramos LM, Notermans NC, Feldberg MA, Wokke JH. Magnetic resonance imaging of the brachial plexus in patients with multifocal motor neuropathy. Neurology. 48: 1218-24. PMID 9153446 DOI: 10.1212/WNL.48.5.1218  0.423
1997 van Dijk GW, Wokke JH, Notermans NC, van den Berg LH, Bär PR. Indications for an immune-mediated etiology of idiopathic sensory neuronopathy. Journal of Neuroimmunology. 74: 165-72. PMID 9119970 DOI: 10.1016/S0165-5728(96)00225-1  0.329
1997 Wokke JH, van Dijk GW. Sensory neuropathies including painful and toxic neuropathies. Journal of Neurology. 244: 209-21. PMID 9112589 DOI: 10.1007/S004150050075  0.318
1997 Van den Berg LH, Lokhorst H, Wokke JH. Pulsed high-dose dexamethasone is not effective in patients with multifocal motor neuropathy. Neurology. 48: 1135. PMID 9109920 DOI: 10.1212/WNL.48.4.1135  0.403
1997 Weijnen F, van der Bilt A, van der Glas H, Bosman F, Wokke J. Oral muscle functions in patients with myasthenia gravis Neuromuscular Disorders. 7: 451-452. DOI: 10.1016/S0960-8966(97)87263-X  0.326
1996 van der Kooi AJ, Barth PG, Busch HF, de Haan R, Ginjaar HB, van Essen AJ, van Hooff LJ, Höweler CJ, Jennekens FG, Jongen P, Oosterhuis HJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, et al. The clinical spectrum of limb girdle muscular dystrophy. A survey in The Netherlands. Brain : a Journal of Neurology. 119: 1471-80. PMID 8931572 DOI: 10.1093/Brain/119.5.1471  0.567
1996 Notermans NC, Lokhorst HM, Franssen H, Van der Graaf Y, Teunissen LL, Jennekens FG, Van den Berg LH, Wokke JH. Intermittent cyclophosphamide and prednisone treatment of polyneuropathy associated with monoclonal gammopathy of undetermined significance. Neurology. 47: 1227-33. PMID 8909434 DOI: 10.1212/Wnl.47.5.1227  0.646
1996 Notermans NC, Wokke JH, van den Berg LH, van der Graaf Y, Franssen H, Teunissen LL, Lokhorst HM. Chronic idiopathic axonal polyneuropathy. Comparison of patients with and without monoclonal gammopathy. Brain : a Journal of Neurology. 421-7. PMID 8800937 DOI: 10.1093/BRAIN/119.2.421  0.477
1996 Jennekens FG, de Visser M, Wintzen AR, Wokke JH. [For the present Duchenne' disease should not be treated with prednisone]. Nederlands Tijdschrift Voor Geneeskunde. 140: 1109-11. PMID 8692335  0.5
1996 Wokke JH, van den Berg LH, van Schaik JP. Sixth nerve palsy from a CNS lesion in chronic inflammatory demyelinating polyneuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 60: 695-6. PMID 8648345 DOI: 10.1136/jnnp.60.6.695  0.389
1995 Van den Berg LH, Franssen H, Wokke JH. Improvement of multifocal motor neuropathy during long-term weekly treatment with human immunoglobulin. Neurology. 45: 987-8. PMID 7746420 DOI: 10.1212/WNL.45.5.987  0.413
1995 Van den Berg LH, Mollee I, Wokke JH, Logtenberg T. Increased frequencies of HPRT mutant T lymphocytes in patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy: further evidence for a role of T cells in the etiopathogenesis of peripheral demyelinating diseases. Journal of Neuroimmunology. 58: 37-42. PMID 7730448 DOI: 10.1016/0165-5728(94)00185-Q  0.634
1995 Van den Berg LH, Kerkhoff H, Oey PL, Franssen H, Mollee I, Vermeulen M, Jennekens FG, Wokke JH. Treatment of multifocal motor neuropathy with high dose intravenous immunoglobulins: a double blind, placebo controlled study. Journal of Neurology, Neurosurgery, and Psychiatry. 59: 248-52. PMID 7673950 DOI: 10.1136/Jnnp.59.3.248  0.629
1995 Wokke JH, Ausems MG, van den Boogaard MJ, Ippel EF, van Diggelene O, Kroos MA, Boer M, Jennekens FG, Reuser AJ, Ploos van Amstel HK. Genotype-phenotype correlation in adult-onset acid maltase deficiency. Annals of Neurology. 38: 450-4. PMID 7668832 DOI: 10.1002/Ana.410380316  0.588
1994 Harms L, Bock A, JÄnisch W, Valdueza J, Weber J, Link I, De Keyser J, Goossens A, Wilczak N, Vedeler C, Bjorge L, Uvestad E, Conti G, Williams K, Ginsberg L, ... ... Wokke JH, ... ... Wokke JH, et al. Fourth meeting of the European Neurological Society 25-29 June 1994 Barcelona, Spain : Abstracts of Symposia and free communications. Journal of Neurology. 241: 1-164. PMID 26553063 DOI: 10.1007/Bf02333089  0.45
1994 Notermans NC, Franssen H, Wieneke GH, Wokke JH. Temperature dependence of nerve conduction and EMG in neuropathy associated with gammopathy. Muscle & Nerve. 17: 516-22. PMID 8159182 DOI: 10.1002/Mus.880170508  0.337
1994 Notermans NC, Wokke JH, Franssen H, Vermeulen M, Busch HF, Jennekens FG. [Course of chronic idiopathic polyneuropathy during middle age and older: 2-year follow-up study]. Nederlands Tijdschrift Voor Geneeskunde. 138: 1281-5. PMID 8022510  0.582
1994 Notermans NC, Wokke JH, Lokhorst HM, Franssen H, van der Graaf Y, Jennekens FG. Polyneuropathy associated with monoclonal gammopathy of undetermined significance. A prospective study of the prognostic value of clinical and laboratory abnormalities. Brain : a Journal of Neurology. 117: 1385-93. PMID 7820574 DOI: 10.1093/Brain/117.6.1385  0.578
1994 Notermans NC, Wokke JH, van der Graaf Y, Franssen H, van Dijk GW, Jennekens FG. Chronic idiopathic axonal polyneuropathy: a five year follow up. Journal of Neurology, Neurosurgery, and Psychiatry. 57: 1525-7. PMID 7798984 DOI: 10.1136/Jnnp.57.12.1525  0.569
1994 van Dijk G, Wokke J, Notermans N, Bär P. Serum from patients with idiopathic sensory neuronopathy inhibits neurite outgrowth from embryonic dorsal root ganglia Journal of Neuroimmunology. 54: 157. DOI: 10.1016/0165-5728(94)90290-9  0.312
1994 Van den Berg L, Wokke J, Mollee I, Logtenberg T. In vivo frequency of mutant T cells in Guillain Barre syndrome and chronic inflammatory demyelinating polyneuropathy Journal of Neuroimmunology. 54: 152. DOI: 10.1016/0165-5728(94)90262-3  0.581
1993 van den Berg LH, Lankamp CL, de Jager AE, Notermans NC, Sodaar P, Marrink J, de Jong HJ, Bär PR, Wokke JH. Anti-sulphatide antibodies in peripheral neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 1164-8. PMID 8229027 DOI: 10.1136/jnnp.56.11.1164  0.453
1993 Notermans NC, Wokke JH, Franssen H, van der Graaf Y, Vermeulen M, van den Berg LH, Bär PR, Jennekens FG. Chronic idiopathic polyneuropathy presenting in middle or old age: a clinical and electrophysiological study of 75 patients. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 1066-71. PMID 7691991 DOI: 10.1136/Jnnp.56.10.1066  0.658
1992 Hesselmans LF, Jennekens FG, Kartman J, Wokke JH, de Visser M, Klaver-Krol EG, DeBaets M, Spaans F, Veldman H. Secondary changes of the motor endplate in Lambert-Eaton myasthenic syndrome: a quantitative study. Acta Neuropathologica. 83: 202-6. PMID 1557950 DOI: 10.1007/Bf00308480  0.547
1992 Notermans N, Wokke J, Franssen H, van der Graaf Y, Vermeulen M, van den Berg H, Jennekens F. 12. Chronic idiopathic neuropathy Clinical Neurology and Neurosurgery. 94: 83. DOI: 10.1016/0303-8467(92)90157-X  0.494
1990 Jansen C, Jennekens FG, Wokke JH, Leppink GJ, Wijnne HJ. Lip-length and snout indices: methods for quantitative assessment of peri-oral facial muscle strength. Journal of the Neurological Sciences. 97: 133-42. PMID 2401893 DOI: 10.1016/0022-510X(90)90212-6  0.572
1990 Wokke JH, Jennekens FG, van den Oord CJ, Veldman H, Smit LM, Leppink GJ. Morphological changes in the human end plate with age. Journal of the Neurological Sciences. 95: 291-310. PMID 2358822 DOI: 10.1016/0022-510X(90)90076-Y  0.564
1989 Wokke JH, Van den Oord CJ, Leppink GJ, Jennekens FG. Perisynaptic satellite cells in human external intercostal muscle: a quantitative and qualitative study. The Anatomical Record. 223: 174-80. PMID 2712344 DOI: 10.1002/Ar.1092230209  0.554
1989 Wokke JH, Jennekens FG, Molenaar PC, Van den Oord CJ, Oen BS, Busch HF. Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibs. Neurology. 39: 648-54. PMID 2710355 DOI: 10.1212/Wnl.39.5.648  0.589
1988 Wokke JH, Jennekens FG, van den Oord CJ, Veldman H, van Gijn J. Histological investigations of muscle atrophy and end plates in two critically ill patients with generalized weakness. Journal of the Neurological Sciences. 88: 95-106. PMID 3225632 DOI: 10.1016/0022-510X(88)90208-0  0.626
1988 Jennekens FG, Veldman H, Wokke JH, Smit LM, vd Oord CJ, Oen BS, Molenaar PC. Junctional plasticity in hereditary myasthenia. Monographs in Allergy. 25: 125-7. PMID 3173361  0.467
1988 Hoop RGvd, Neijt J, Jennekens F, Gispen W, Bär P, Wokke J, Jennekens F. Scientific meeting of the Amsterdamsche Neurologenvereeniging held in Amsterdam, 3rd December 1987 Clinical Neurology and Neurosurgery. 90: 183-184. DOI: 10.1016/S0303-8467(88)80047-7  0.586
1987 Jennekens FG, Wokke JH. Proximal weakness of the extremities as main feature of amyloid myopathy. Journal of Neurology, Neurosurgery, and Psychiatry. 50: 1353-8. PMID 3681315  0.53
1987 Wokke JH, de Koning J, Stanek G, Jennekens FG. Chronic muscle weakness caused by Borrelia burgdorferi meningoradiculitis. Annals of Neurology. 22: 389-92. PMID 3674804 DOI: 10.1002/ana.410220319  0.532
1987 Oosterhuis HJ, Newsom-Davis J, Wokke JH, Molenaar PC, Weerden TV, Oen BS, Jennekens FG, Veldman H, Vincent A, Wray DW. The slow channel syndrome. Two new cases. Brain : a Journal of Neurology. 110: 1061-79. PMID 3651795 DOI: 10.1093/Brain/110.4.1061  0.582
1987 Wokke JH, van Gijn J, Elderson A, Stanek G. Chronic forms of Borrelia burgdorferi infection of the nervous system. Neurology. 37: 1031-4. PMID 3587624 DOI: 10.1212/Wnl.37.6.1031  0.348
1987 Koudstaal PJ, Vermeulen M, Wokke JH. Argyll Robertson pupils in lymphocytic meningoradiculitis (Bannwarth's syndrome) Journal of Neurology, Neurosurgery, and Psychiatry. 50: 363-5. PMID 3559622 DOI: 10.1136/Jnnp.50.3.363  0.32
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