18 results on '"Hauser, Ann Kathrin"'
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2. CSF Protein Level of Neurotransmitter Secretion, Synaptic Plasticity, and Autophagy in PD and DLB
3. A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease
4. The longevity gene Klotho and its cerebrospinal fluid protein profiles as a modifier for Parkinson´s disease
5. The Mutation Matters: CSF Profiles of GCase , Sphingolipids, α‐Synuclein inPD GBA
6. HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype
7. Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha‐Synuclein Profiles
8. Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha‐synuclein profile
9. HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype
10. Polygenic load: Earlier disease onset but similar longitudinal progression in Parkinson's disease
11. Cognitive impairment in Glucocerebrosidase (GBA)-associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profiles
12. SNCA: major genetic modifier of age at onset of Parkinson's disease
13. Mutations in CIZ1 are not a major cause for dystonia in Germany
14. GBA ‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study
15. SNCA: Major genetic modifier of age at onset of Parkinson's disease
16. Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvement
17. Cerebrospinal fluid fatty acids in glucocerebrosidase-associated Parkinson's disease
18. Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers
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