50 results on '"PARCHI, PIERO"'
Search Results
2. Diagnostic Value of the CSF α-Synuclein Real-Time Quaking-Induced Conversion Assay at the Prodromal MCI Stage of Dementia With Lewy Bodies
3. Gerstmann-Sträussler-Scheinker disease (PRNP p.D202N) presenting with atypical parkinsonism
4. Age at onset in genetic prion disease and the design of preventive clinical trials
5. Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey
6. Messenger RNA processing is altered in autosomal dominant leukodystrophy
7. Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)
8. Neuropathological and biochemical criteria to identify acquired Creutzfeldt‐Jakob disease among presumed sporadic cases
9. Messenger RNA processing is altered in autosomal dominant leukodystrophy†
10. Narcolepsy is a common phenotype in HSAN IE and ADCA-DN
11. Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
12. Gait Disorders in Fatal Familial Insomnia
13. Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex
14. PRION DISEASE: Diagnostic value of cerebrospinal fluid markers
15. The need to unify neuropathological assessments of vascular alterations in the ageing brain Multicentre survey by the BrainNet Europe consortium
16. Creutzfeldt-Jakob Disease: an under-Recognized Cause of Dementia
17. A Second Case of Gerstmann-Sträussler-Scheinker Disease Linked to the G131V Mutation in the Prion Protein Gene in a Dutch Patient
18. Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future
19. A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature
20. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
21. An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene
22. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
23. Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP
24. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification
25. Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study
26. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics
27. Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature
28. Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium
29. Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium
30. Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium
31. Staging of Neurofibrillary Pathology in Alzheimerʼs Disease: A Study of the BrainNet Europe Consortium
32. Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinsonʼs disease
33. Brain banks: Benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies
34. Inter-laboratory comparison of neuropathological assessments of β-amyloid protein: a study of the BrainNet Europe consortium
35. Management of a twenty-first century brain bank: experience in the BrainNet Europe consortium
36. Assessment of α-Synuclein Pathology: A Study of the BrainNet Europe Consortium
37. Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study
38. MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome
39. Brain Protein Preservation Largely Depends on the Postmortem Storage Temperature: Implications for Study of Proteins in Human Neurologic Diseases and Management of Brain Banks: A BrainNet Europe Study
40. Classification of sporadic Creutzfeldt–Jakob disease revisited
41. Interlaboratory Comparison of Assessments of Alzheimer Disease-Related Lesions: A Study of the BrainNet Europe Consortium
42. Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies
43. Expression of Excitatory Amino Acid Transporter-1 (EAAT-1) in Brain Macrophages and Microglia of Patients with Prion Diseases
44. Sporadic and familial CJD: classification and characterisation
45. Creutzfeldt-Jakob Disease in Unusually Young Patients Who Consumed Venison
46. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
47. Insomnia in Prion Diseases: Sporadic and Familial
48. Abnormal Diffusion-Weighted Magnetic Resonance Images in Creutzfeldt-Jakob Disease
49. Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia
50. Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
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