Search

Your search keyword '"Hanagasi, H"' showing total 157 results

Search Constraints

Start Over You searched for: Author "Hanagasi, H" Remove constraint Author: "Hanagasi, H"
157 results on '"Hanagasi, H"'

Search Results

2. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

3. Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.

4. Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort

6. Electrophysiological characteristics of autosomal-recessive spastic ataxia of Charlevoix-Saguenay in a Turkish family

7. Using global team science to identify genetic parkinson's disease worldwide

11. Clinico-Genetic, Imaging and Molecular Delineation of COQ8A-Ataxia: A Multicenter Study of 59 Patients

20. Using global team science to identify genetic Parkinson's disease worldwide

21. Using global team science to identify genetic parkinson's disease worldwide

24. Theta burst repetitive transcranial magnetic stimulation in a case with cortical-basal ganglionic degeneration

25. TREM2 variants in Alzheimer's disease

26. The Effects Of Rasagiline On Cognitive Deficits in Parkinson's Disease Patients Without Dementia: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study

28. Botulinum toxin injections for the facial region

35. Differences between essential tremor developing Parkinson's disease and essential tremor.

36. Clinical and electrophysiological investigations of changes in muscle activation patterns before and after botulinum toxin injections for idiopathic cervical dystonia.

37. The Arg194 Trp polymorphism in DNA repair gene XRCC1 and the risk for sporadic late-onset Alzheimer's disease.

38. Unrecognized depression in community-dwelling elderly persons in Istanbul.

40. GRN c.708+1_+4del TGAG deletion in a large family diagnosed with fronto-temporal dementia

41. The distinct genetic pattern of ALS in Turkey

43. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

44. Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.

45. The distinct genetic pattern of ALS in Turkey and novel mutations

46. Quantitative Gait and Balance Outcomes for Ataxia Trials: Consensus Recommendations by the Ataxia Global Initiative Working Group on Digital-Motor Biomarkers.

47. Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.

48. Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.

49. TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients.

50. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.

Catalog

Books, media, physical & digital resources