197 results on '"Olszewska, Diana A"'
Search Results
2. PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson’s disease in Ireland
3. The First Report of Myoclonus and Putaminal Cysts in Salla Disease—The Phenotype Expanded (P6-4.001)
4. Teaching Video NeuroImage: Unilateral Myorhythmia in a Patient With a Midbrain-Diencephalic Junction Cavernous Malformation
5. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
6. Autosomal Dominant Gene Negative Frontotemporal Dementia-Think of SCA17
7. The benefits of a Neurogenetics clinic in an adult Academic Teaching Hospital
8. Genotype–phenotype relations for episodic ataxia genes: MDSGene systematic review
9. Parkinson’s Disease
10. A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene
11. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
12. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
13. Genetics of Frontotemporal Dementia
14. Initiating dopamine agonists rather than levodopa in early Parkinson's disease does not delay the need for deep brain stimulation
15. Chapter 1 - The definition of precision medicine in neurodegenerative disorders and the one disease-many diseases tension
16. PO100 Familial parkinson’s disease in ireland
17. PO098 A lesson from the dat scan
18. PO099 Autosomal dominant gene negative frontotemporal dementia-think sca17
19. Endoplasmic Reticulum Proteostasis/Protein Trafficking Enhancement: A Novel Synergistic Approach to Tackling α‐Synuclein
20. Cathepsin B p.Gly284Val Variant in Parkinson’s Disease Pathogenesis
21. Periodic Limb Movements while Awake (PLMA) as a Manifestation of Wearing‐Off in Parkinson's Disease: A Case Series and Review of the Literature
22. A rapid, ultra-sensitive, RT-QuIC assay, with novel protocol, for MSA and PD using a single site skin biopsy and serum neurofilament light chain. (P1-1.Virtual)
23. The Role of Insular Cortex in Gut‐Inflammation Memory: What Does It Mean for Parkinson's Disease?
24. Oculogyric crisis phenotype of levodopa‐induced ocular dyskinesia
25. Neuroimaging Pearls from the MDS Congress Video Challenge. Part 2: Acquired Disorders
26. Combining Skin α‐Synuclein Real‐Time Quaking‐Induced Conversion and Circulating Neurofilament Light Chain to Distinguish Multiple System Atrophy and Parkinson's Disease
27. Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders
28. Closing the tau loop: the missing tau mutation
29. Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants
30. Dancing Feet Dyskinesia in a Patient with GBA-PD
31. Severe amnestic syndrome due to theophylline toxicity
32. Exacerbation of Stiff Person Syndrome by Selective Serotonin Reuptake Inhibitors
33. PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson’s disease in Ireland
34. Dystonia as complication of thalamic neurosurgery
35. Lack of Accredited Clinical Training in Movement Disorders in Europe, Egypt, and Tunisia
36. “Opening” New Insights Into LRRK2 Conformation and the Microtubule
37. Reply to STUB1 ‐Related Ataxias: A Challenging Diagnosis
38. Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland
39. Reply to Comment on: A 57‐Year‐Old Woman With Progressive Left Hand Clumsiness and Falls
40. The second case of dystonia associated with an autosomal recessive spinocerebellar ataxia type 16-the phenotype expanded. (948)
41. Qualitative and quantitative measurement of skin surface fatty acids in Parkinson’s disease-the results of the first case-control study in any neurological condition. (2581)
42. Extending the Phenotypic Spectrum Associated with STUB1 Mutations: A Case of Dystonia
43. Reversible Corticobasal Syndrome due to Coeliac Disease
44. Lysosomal Storage Disorders and Parkinson's Disease: New Susceptibility Loci Identified
45. A 57‐Year‐Old Woman With Progressive Left Hand Clumsiness and Falls
46. Association between glucocerebrosidase mutations and Parkinson’s disease in Ireland (S53.003)
47. The second clinical-pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene. (P3.8-028)
48. Reversible Corticobasal Syndrome due to Coeliac Disease
49. Lysosomal Storage Disorders and Parkinson's Disease: New Susceptibility Loci Identified
50. Psychiatric symptoms in preclinical behavioural-variant frontotemporal dementia in MAPT mutation carriers
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