145 results on '"Revesz, T."'
Search Results
2. Argyrophilic grain disease type 1 tau filament
3. Limbic-predominant neuronal inclusion body 4R tauopathy type 2 tau filament
4. Globular glial tauopathy type 2 tau filament
5. Globular glial tauopathy type 1 tau filament
6. Limbic-predominant neuronal inclusion body 4R tauopathy type 1b tau filament
7. Limbic-predominant neuronal inclusion body 4R tauopathy type 1a tau filament
8. Progressive supranuclear palsy tau filament
9. Argyrophilic grain disease type 2 tau filament
10. Globular glial tauopathy type 3 tau filament
11. Spinocerebellar ataxia type 11
12. Pathology of familial Alzheimer’s disease with Lewy bodies
13. Foix–Chavany–Marie syndrome due to type E TDP43 pathology
14. Risk factors for symptomatic venous thromboembolism during therapy for childhood acute lymphoblastic leukemia
15. Frontotemporal lobar degenerations: from basic science to clinical manifestations
16. Lipid imaging to detect myelin breakdown in multiple sclerosis
17. Treatment of Childhood Acute Nonlymphocytic Leukemia: Cooperative Austrian-Hungarian Study AML-IGCI-84
18. Evolving concepts of chronic traumatic encephalopathy as a neuropathological entity
19. Frontotemporal lobar degeneration-TDP with ‘multiple system atrophy phenocopy syndrome’
20. 9.4 T MR microscopy of the substantia nigra with pathological validation in controls and disease
21. Xenograft-directed personalized therapy for a patient with post-transplant relapse of ALL
22. Input-Output Model for Analyzing National Economics of Varying Energy Intensities
23. Aclacinomycin-A in the Induction Treatment of Childhood Acute Myelogenous Leukemia
24. IMMUNOLOGICAL APPROACHES TO THE IDENTIFICATION OF LEUKAEMIC CELLS
25. Analysis of Human Leukaemic Cells Using Cell Surface Binding Probes and the Fluorescence Activated Cell Sorter
26. The optimal use of PEG-Asparaginase in relapsed ALL—lessons from the ALLR3 Clinical Trial
27. Neuropathological features of multiple system atrophy with cognitive impairment
28. Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant
29. C9orf72 expansion in atypical parkinsonism
30. C9ORF72 expansions, parkinsonism, and Parkinson disease: A clinicopathologic study
31. The midbrain to pons ratio: A simple and specific MRI sign of progressive supranuclear palsy
32. Pantothenate kinase-associated neurodegeneration is not a synucleinopathy
33. Review: Genetics and neuropathology of primary pure dystonia
34. Authors response to scientific correspondence
35. Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
36. High resolution MR anatomy of the subthalamic nucleus: Imaging at 9.4T with histological validation
37. The neuropathology, pathophysiology and genetics of multiple system atrophy
38. 1.133 INVESTIGATING THE ROLE OF OLIGODENDROCYTE PRECURSOR CELLS IN MULTIPLE SYSTEM ATROPHY AND RELATED DISORDERS
39. LRRK2 expression in idiopathic and G2019S positive Parkinson's disease subjects: a morphological and quantitative study
40. Testing an aetiological model of visual hallucinations in Parkinson's disease
41. Does levodopa accelerate the pathologic process in Parkinson disease brain?
42. Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
43. A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies
44. Open biopsy in patients with acute progressive neurologic decline and absence of mass lesion
45. Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?
46. Increased T regulatory cells and decreased Th1 pro-inflammatory cytokines correlate with culture-positive infection in febrile neutropenia childhood oncology patients
47. PATU2 Novel truncation mutation of PRNP causes chronic diarrhoea, sensory neuropathy and autonomic failure associated with prion protein deposition in the cerebral blood vessels and small bowel
48. POMD01 Blinded analysis of conventional MRI in a cohort of pathologically confirmed parkinsonian illnesses
49. The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration
50. Does corticobasal degeneration exist? A clinicopathological re-evaluation
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.