Hans A. Kretzschmar

Affiliations: 
Neuropathology Georg-August-Universität Göttingen, Göttingen, Niedersachsen, Germany 
Area:
neurodegeneration, prions, neuropathology
Google:
"Hans Kretzschmar"
Bio:

MD

UNIVERSITY MUNICH
NEUROPATHOLOGY DEPT
FEODOR-LYNEN STR 23
MUNICH, 81377
Germany

Mean distance: 17.87 (cluster 17)
 
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Publications

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Cali CP, Patino M, Tai YK, et al. (2019) C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy. Acta Neuropathologica
Rutherford NJ, Heckman MG, Dejesus-Hernandez M, et al. (2012) Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype. Neurobiology of Aging. 33: 2950.e5-7
Notari S, Strammiello R, Capellari S, et al. (2008) Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 283: 30557-65
Krebs B, Bader B, Klehmet J, et al. (2007) A novel subtype of Creutzfeldt-Jakob disease characterized by a small 6 kDa PrP fragment. Acta Neuropathologica. 114: 195-9
Pfeifer A, Eigenbrod S, Al-Khadra S, et al. (2007) Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice. The Journal of Clinical Investigation. 116: 3204-10
de Silva R, Lashley T, Strand C, et al. (2006) An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathologica. 111: 329-40
Roeber S, Krebs B, Neumann M, et al. (2005) Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment. Acta Neuropathologica. 109: 443-8
Giese A, Kretzschmar HA. (2001) Prion-induced neuronal damage--the mechanisms of neuronal destruction in the subacute spongiform encephalopathies. Current Topics in Microbiology and Immunology. 253: 203-17
Herms JW, Tings T, Dunker S, et al. (2001) Prion protein affects Ca2+-activated K+ currents in cerebellar purkinje cells. Neurobiology of Disease. 8: 324-30
Dürig J, Giese A, Schmücker U, et al. (2001) Decreased prion protein expression in human peripheral blood leucocytes from patients with paroxysmal nocturnal haemoglobinuria. British Journal of Haematology. 112: 658-62
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