Jean M.B.V. de Jong

Affiliations: 
University of Amsterdam, Amsterdam, Netherlands 
Area:
Experimental neurology
Google:
"Jean Marie Baptiste Vianney de Jong"
Bio:

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

Mean distance: 17.76 (cluster 48)
 
SNBCP

Parents

Sign in to add mentor
Arie Biemond grad student 1967 Amsterdam
 (Over cervicale nystagmus en aanverwante verschijnselen)

Children

Sign in to add trainee
Dirk Troost grad student 1992 Amsterdam
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
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
Jansen GA, Wanders RJ, Jöbsis GJ, et al. (1996) Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 139: 91-4
See more...