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Molecular imaging of neuroinflammation in patients after mild traumatic brain injury: a longitudinal ¹²³I‐CLINDE single photon emission computed tomography study.

Autor: Ebert, S. E., Jensen, P., Ozenne, B., Armand, S., Svarer, C., Stenbaek, D. S., Moeller, K., Dyssegaard, A., Thomsen, G., Steinmetz, J., Forchhammer, B. H., Knudsen, G. M., Pinborg, L. H.

Publikováno v: European Journal of Neurology; Dec2019, Vol. 26 Issue 12, p1426-1432, 7p, 1 Color Photograph, 2 Charts

Robust increase of the translocator protein 18 kDa (TSPO), demonstrated with radiotracer [123I]CLINDE, in an adult rat model of Traumatic Brain Injury

Autor: Donat, C. K., Gaber, K., Meixensberger, J., Brust, P., Pinborg, L. H., Mikkelsen, J. D.

Publikováno v: 60th Annual Meeting of the German Society for Neuropathology and Neuroanatomy, 26.-28.08.2015, Berlin, Deutschland

Question Traumatic brain injury (TBI) can result in long-term disability, but the mechanisms are not fully elucidated. Neuroinflammation is part of these secondary injury mechanisms, and is therefore regarded as a potential target for treatment and d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4577::17adeeac027a0243949f82b7c390dc07
https://www.hzdr.de/publications/Publ-21909-1

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

Autor: Lindquist, S. G., Duno, M., Batbayli, M., Puschmann, A., Braendgaard, H., Mardosiene, S., Svenstrup, K., Pinborg, L. H., Vestergaard, Karsten, Hjermind, L. E., Stokholm, J., Andersen, B. B., Johannsen, P., Nielsen, J. E.

Publikováno v: Lindquist, S G, Duno, M, Batbayli, M, Puschmann, A, Braendgaard, H, Mardosiene, S, Svenstrup, K, Pinborg, L H, Vestergaard, K, Hjermind, L E, Stokholm, J, Andersen, B B, Johannsen, P & Nielsen, J E 2013, ' Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease ', Clinical Genetics, vol. 83, no. 3, pp. 279-283 . https://doi.org/10.1111/j.1399-0004.2012.01903.x
Lindquist, S G, Dunø, M, Batbayli, M, Puschmann, A, Braendgaard, H, Mardosiene, S, Svenstrup, K, Pinborg, L H, Vestergaard, K, Hjermind, L E, Stokholm, J, Andersen, B B, Johannsen, P & Nielsen, J E 2013, ' Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease ', Clinical Genetics, vol. 83, no. 3, pp. 279-83 . https://doi.org/10.1111/j.1399-0004.2012.01903.x

Recently, a hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72 was reported as the cause of chromosome 9p21-linked frontotemporal dementia-amyotrophic lateral sclerosis (FTD-ALS). We here report the prevalence of the expansion in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3b07273650dffb06dca1107d188a5b02
https://vbn.aau.dk/da/publications/8ac68839-2bae-46b1-983f-3107e64d7cc7