Jean M.B.V. de Jong

University of Amsterdam, Amsterdam, Netherlands 
Experimental neurology
"Jean Marie Baptiste Vianney de Jong"

Prof. dr. J.M.B.V. de Jong at the Album Academicum of the University of Amsterdam

Mean distance: 17.76 (cluster 48)


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Arie Biemond grad student 1967 Amsterdam
 (Over cervicale nystagmus en aanverwante verschijnselen)
Bernard Cohen post-doc 1970-1970 Mt Sinai


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Dirk Troost grad student 1992 Amsterdam
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Seelen M, Visser AE, Overste DJ, et al. (2014) No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy. Neurobiology of Aging. 35: 1956.e9-1956.e11
Sta M, Sylva-Steenland RM, Casula M, et al. (2011) Innate and adaptive immunity in amyotrophic lateral sclerosis: evidence of complement activation. Neurobiology of Disease. 42: 211-20
Brugman F, Veldink JH, Franssen H, et al. (2009) Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes. Archives of Neurology. 66: 509-14
van der Graaff MM, de Jong JM, Baas F, et al. (2009) Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging review. Neuromuscular Disorders : Nmd. 19: 53-8
Van Vught PW, Van Wijk J, Bradley TE, et al. (2007) Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis. Neuromuscular Disorders : Nmd. 17: 964-7
Van Vught PW, Sutedja NA, Veldink JH, et al. (2005) Lack of association between VEGF polymorphisms and ALS in a Dutch population. Neurology. 65: 1643-5
Spliet WG, Aronica E, Ramkema M, et al. (2004) Immunohistochemical localization of vascular endothelial growth factor receptors-1, -2 and -3 in human spinal cord: altered expression in amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology. 30: 351-9
Visser J, Mans E, de Visser M, et al. (2003) 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
Veldink JH, van den Berg LH, Cobben JM, et al. (2001) Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 56: 749-52
Vyth A, Timmer JG, Bossuyt PM, et al. (1996) Survival in patients with amyotrophic lateral sclerosis, treated with an array of antioxidants. Journal of the Neurological Sciences. 139: 99-103
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