Development of a Monitoring Set-up and Algorithm Using Functional MRI (fMRI) and EEG for Prediction of Response to Repetitive Deep Transcranial Magnetic Stimulation (rDTMS) for Patients With Parkinson's Disease

Inclusion Criteria: 1. Idiopathic PD patients aged 40-75 years; 2. Hoehn and Yahr stages II to IV 3. Patients on stable antiparkinsonian therapy for 1 month 4. Right hand dominance with right afflicted side. Exclusion Criteria: 1. Participation in current clinical study or clinical study within 30 days prior to this study. 2. Subject has an atypical parkinsonian syndrome or secondary parkinsonism (e.g., due to drugs, metabolic neurogenetic disorders, encephalitis, cerebrovascular disease or other degenerative disease) 3. Patients with significant psychiatric symptoms or history. 4. Patients with psychotic symptoms or active depressive symptoms 5. Treatment with neuroleptics. 6. Beck depression inventory (BDI) score \<14 7. Mini Mental status examination (MMSE) score \<25 8. History of migraine or frequent or severe headaches. 9. Significant sensory deficits, e.g., deafness or blindness History of head injury or neurosurgical interventions. 10. Subjects who have concomitant epilepsy, a history of seizure/s, heat convulsions or history of epilepsy in first degree relative. 11. History of any metal in the head (outside the mouth). 12. The presence of cochlear implants 13. Known history of any metallic particles in the eye, implanted cardiac pacemaker, implanted neurostimulators, surgical clips (above the shoulder line) or any medical pumps. 14. Subjects with an unstable medical disorder. 15. Current drug abuse (including Cannabis) or alcoholism. 16. Pregnancy or not using a reliable method of birth control. 17. Patients with severe tremor or dyskinesia