Kretzschmar, Hans A.
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Kretzschmar, Hans A. 1953-2014
Hans A. Kretzschmar
Hans A. Kretzschmar deutscher Mediziner
Kretzschmar, H. A. (Hans A.)
VIAF ID: 29708094 (Personal)
Permalink: http://viaf.org/viaf/29708094
Preferred Forms
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Hans A. Kretzschmar
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Hans A. Kretzschmar
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deutscher Mediziner
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Kretzschmar
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Hans A.
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Kretzschmar, H. A.
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(Hans A.)
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100 1 _ ‡a Kretzschmar, Hans A.
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100 1 _ ‡a Kretzschmar, Hans A. (sparse)
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100 1 _
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Kretzschmar, Hans A.
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100 1 _ ‡a Kretzschmar, Hans A.
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Kretzschmar, Hans A.
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1953-2014
4xx's: Alternate Name Forms (18)
5xx's: Related Names (6)
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Georg-August-Universität Göttingen
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https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
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Göttingen
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https://d-nb.info/standards/elementset/gnd#placeOfActivity
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Institut für Neuropathologie
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Göttingen
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https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
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Ludwig-Maximilians-Universität München
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Zentrum für Neuropathologie und Prionforschung
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https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
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München
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https://d-nb.info/standards/elementset/gnd#placeOfBirth
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München
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https://d-nb.info/standards/elementset/gnd#placeOfActivity
Works
| Title | Sources |
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| Amyloid precursor protein intracellular domain modulates cellular calcium homeostasis and ATP content. |
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| Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions |
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| Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease |
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| Archives of virology. Supplementum. 16 |
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| Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins |
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| Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions |
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| Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA |
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| CSF amyloid-β peptides in neuropathologically diagnosed dementia with Lewy bodies and Alzheimer's disease. |
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| Different CSF β-amyloid processing in Alzheimer’s and Creutzfeldt–Jakob disease |
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| Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD. |
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| Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study |
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| Einfluss der Kupferbindung an der Aminosäureposition 95 im Prionprotein auf den Krankheitsverlauf nach Prioninfektion |
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| Gamma-secretase inhibition reduces spine density in vivo via an amyloid precursor protein-dependent pathway. |
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| Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis |
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| Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy |
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| Heart fatty acid binding protein as a potential diagnostic marker for neurodegenerative diseases. |
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| hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations |
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| Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification |
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| Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype |
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| Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease |
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| Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids |
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| Prion diseases diagnosis and pathogenesis |
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| Prionen und Prionkrankheiten |
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| Prions in humans and animals |
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| Proteomic Analysis of the Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease |
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| Quantitative immunhistochemische Untersuchungen zur Histogenese der malignen fibrösen Hystiozytome |
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| R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia |
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| A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule |
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| Serum heart-type fatty acid-binding protein and cerebrospinal fluid tau: marker candidates for dementia with Lewy bodies |
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| Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium |
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| Untersuchung der Spaltung des zellulären Prionproteins bei zerebralem Trauma und ischämischem Insult im Mausmodell |
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| Untersuchung zur Bedeutung des Transkriptionsfaktors FoxM1 beim humanen Medulloblastom |
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