35 results on '"Kretzschmar, H A"'
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2. Clinical predictors of survival in patients with progressive supranuclear palsy: 324
3. Co-pathology and clinical correlation in progressive supranuclear palsy: 302
4. The oligomer modulator anle138b is effective in the prodromal phase of a transgenic mouse model of Parkinson’s disease: EP1256
5. Influence of the blood-CSF-barrier function on S100B in neurodegenerative diseases
6. Recruitment of neural precursor cells from circumventricular organs of patients with cerebral ischaemia
7. Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium
8. Cerebral angiitis in four patients with chronic GVHD
9. Definite multiple system atrophy in a German family
10. Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options
11. MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement study
12. How a neuropsychiatric brain bank should be run: a consensus paper of Brainnet Europe II
13. Creutzfeldt–Jakob disease in Germany: a prospective 12-year surveillance
14. Detection of chorein in postmortem brain tissue of chorea-acanthocytosis patients and nonaffected controls by Western blot: 25
15. Significant association of a M129V independent polymorphism in the 5′ UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study
16. Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimerʼs disease
17. NEUROPATHOLOGY AND PROTEOME: W1.B
18. A New family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects
19. Follow-up investigations in cerebrospinal fluid of patients with dementia with Lewy bodies and Alzheimerʼs disease
20. Immunoglobulins and virus-specific antibodies in patients with Creutzfeldt–Jakob disease
21. Loss of glycosylation associated with the T183A mutation in human prion disease
22. Predictors of survival in sporadic Creutzfeldt–Jakob disease and other human transmissible spongiform encephalopathies
23. Bcl-2 expression inversely correlates with tumour cell differentiation in medulloblastoma
24. Phospho-tau/total tau ratio in cerebrospinal fluid discriminates Creutzfeldt-Jakob disease from other dementias
25. Patients with Alzheimerʼs disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease
26. Disease latency in Creutzfeldt–Jakob disease via dural grafting: A case report
27. Creutzfeldt-Jakob disease and oxidative stress
28. Isoform Pattern of 14-3-3 Proteins in the Cerebrospinal Fluid of Patients with Creutzfeldt–Jakob Disease
29. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2
30. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
31. Prion (PrP sup Sc)-specific epitope defined by a monoclonal antibody
32. Diffusion of Randon in Porous Media Saturated with Gels and Emulsions
33. Typing prion isoforms
34. Fatal spongiform encephalopathy in a patient who had handled animal feed
35. 91 AN ELISA AND TRANSBLOT STUDY OF GFAP IN HEPATIC ENCEPHALOPATHY
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