Church Music and the Council of Trent

Autor: Fellerer, K. G., Hadas, Moses

Publikováno v: The Musical Quarterly, 1953 Oct 01. 39(4), 576-594.

Externí odkaz: https://www.jstor.org/stable/739857

Zum Wandel der abendländischen Musikauffassung

Autor: Fellerer, K. G.

Publikováno v: Studia Musicologica Academiae Scientiarum Hungaricae, 1969 Jan 01. 11(1/4), 159-167.

Externí odkaz: https://www.jstor.org/stable/901276

Early increase of CSF sTREM2 in Alzheimer's disease is associated with tau related-neurodegeneration but not with amyloid- pathology

Autor: Suarez-Calvet, M, Morenas-Rodriguez, E, Kleinberger, G, Schlepckow, K, Caballero, MAA, Franzmeier, N, Capell, A, Fellerer, K, Nuscher, B, Eren, E, Levin, J, Deming, Y, Piccio, L, Karch, CM, Cruchaga, C, Shaw, LM, Trojanowski, JQ, Weiner, M, Ewers, M, Haass, C, Alzheimers Dis Neuroimaging

Publikováno v: Molecular Neurodegeneration
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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BackgroundTREM2 is a transmembrane receptor that is predominantly expressed by microglia in the central nervous system. Rare variants in the TREM2 gene increase the risk for late-onset Alzheimer's disease (AD). Soluble TREM2 (sTREM2) resulting from s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::8cad209e182c55aad6c082f454920ca6
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3048

P454: Loss-of progranulin leads to a cell-autonomouslysosomal phenotype

Autor: Werner, G, Fellerer, K., Lang, C. M., Haass, Christian, Capel, A.

Publikováno v: Journal of neurochemistry 138(Supplement 1), 419 (2016).

Heterozygous loss-of-function mutations in the progranulin(GRN) gene result in GRN haploinsufficiency, which is, besidesthe C9orf72 repeat expansions, the major cause of familialfrontotemporal lobar degeneration (FTLD) with TAR DNA-bindingprotein (T

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10678::d6ba0371592a852a64564d881df96101

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