31 results on '"Caracciolo, Manuela"'
Search Results
2. Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study
3. In vivo evidence for decreased scyllo-inositol levels in the supplementary motor area of patients with Progressive Supranuclear Palsy: A proton MR spectroscopy study
4. A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease
5. Increased glutamate + glutamine levels in the thalamus of patients with essential tremor: A preliminary proton MR spectroscopic study
6. Thalamic neurometabolic alterations in tremulous Parkinson's disease: A preliminary proton MR spectroscopy study
7. Breadsticks Flavoured with Olives and Onions: One-Year Shelf Life
8. The movement time analyser task investigated with functional near infrared spectroscopy: an ecologic approach for measuring hemodynamic response in the motor system
9. Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer’s disease
10. Effects of Shortening Replacement with Extra Virgin Olive Oil on the Physical–Chemical–Sensory Properties of Italian Cantuccini Biscuits
11. Refining initial diagnosis of Parkinson's disease after follow‐up: A 4‐year prospective clinical and magnetic resonance imaging study
12. A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3
13. Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy
14. Increased cerebellar gray matter volume in head chefs
15. MR parkinsonism index predicts vertical supranuclear gaze palsy in patients with PSP–parkinsonism
16. The movement time analyser task investigated with functional near infrared spectroscopy: an ecologic approach for measuring hemodynamic response in the motor system
17. The neuroanatomical correlates of anxiety in a healthy population: differences between the State‐Trait Anxiety Inventory and the Hamilton Anxiety Rating Scale
18. Leber’s hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man
19. P1-427: Depressive mood in patients with Alzheimer's disease
20. DJ‐1 mutations and parkinsonism‐dementia‐amyotrophic lateral sclerosis complex
21. Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?
22. FRAXE intermediate alleles are associated with Parkinson’s disease
23. No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case–control sample
24. Further evidence thatSPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
25. Body Weight Influences Pharmacokinetics of Levodopa in Parkinson's Disease
26. The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease
27. Apolipoprotein E polymorphisms and Parkinson's disease
28. A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
29. Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia.
30. Further evidence that <TOGGLE>SPG3A</TOGGLE> gene mutations cause autosomal dominant hereditary spastic paraplegia
31. Further evidence that SPG3Agene mutations cause autosomal dominant hereditary spastic paraplegia
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