Questions
Summaries
Videos
Audios
What is the main function of the autonomic nervous system (ANS)?
Where is the ANS regulated mainly in the brain?
Which vitamin deficiencies can play a role in the development of dementia?
Which are risk factors for vascular dementia?
Which biomarker is associated with Alzheimer’s disease?
What factors contribute to Alzheimer’s disease?
What is dementia?
Can ALS be cured?
Is Babinski sign positive in amyotrophic lateral sclerosis (ALS)?
Here are four descriptions related to neurological status, including one that represents typical findings in a patient with amyotrophic lateral sclerosis (ALS):
Which of the following clinical cases would include the ALS in the differential diagnosis?
What pathophysiological processes in the nervous system lead to the symptoms seen in amyotrophic lateral sclerosis (ALS)?
Is amyotrophic lateral sclerosis (ALS) associated with genetic factors?
Which of the following characteristics is associated with amyotrophic lateral sclerosis (ALS)?
Which symptoms are characteristic of an absence (petit mal) seizure?
Which symptoms are characteristic of a grand mal seizure?
What are the possible causes of epilepsy?
What is epilepsy?
A 60-year-old man presents to the emergency department with sudden-onset right-sided weakness and difficulty speaking. His symptoms began approximately 2 hours ago. On examination, you note right hemiparesis and expressive aphasia. His blood pressure is within normal limits, and there are no signs of trauma. A non-contrast CT scan of the head shows no acute abnormalities. What is the most likely diagnosis?
What does it indicate when, during the Latent Paresis test (Mingazzini Strumpel test), the patient’s left arm and leg exhibit weakness and descend (like shown on the picture)?
Neurotransmission
Parkinson’s Disease Differential Diagnosis Questionnaire
Role of the Direct and Indirect Pathways in the Extrapyramidal System: Balancing Motor Control
The Unified Parkinson’s Disease Rating Scale (UPDRS)
Lewy Body Dementia with Parkinsonism versus Parkinson’s Disease
Aging as a Risk Factor for Parkinson’s Disease
The Role of Genetics in Parkinson’s Disease
Protective Factors for Parkinson’s Disease: Physical Activity, Smoking, and Caffeine
Alpha-Synuclein vs. Tau Protein: A Comparative Overview
Tau Protein
Alpha-Synuclein and α-Synucleinopathies
Genetics and Multiple Sclerosis
Etiology of Multiple Sclerosis
Differential Diagnosis for Parkinson’s Disease
Cauda Equina Syndrome (CES)
Brachial Plexus
Treatment Options for Multiple Sclerosis
Diet Recommendations for Patients with Multiple Sclerosis
Wallenberg Syndrome (Lateral Medullary Syndrome)
Circle of Willis
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Q 2.35. Emergencies in Neurology
Q 2.34. Dementia
Q 2.33. Headache
Q 2.32. Wilson’s Disease
Q 2.31. Chorea
Q 2.30. Progressive Muscular Dystrophy
Q 2.29. Spinal Muscular Atrophy
Q 2.28. Amyotrophic Lateral Sclerosis
Q 2.27. Parkinson’s Disease
Q 2.26. Status Epilepticus
Q 2.25. Epilepsy
Q 2.24. Traumatic Brain Injury
Q 2.23. Spinal Cord Tumors
Q 2.22. Cerebral Tumors
Q 2.21. Cerebral Vein and Dural Thrombosis
Q 2.20. Subarachnoid Haemorrhage
Q 2.19. Parenchymal Brain Haemorrhage
Q 2.18. Part 2 Cerebral Infarction – Diagnosis and Differential Diagnosis
Q 2.18. Part 1 Cerebral Infarction – Types and Warning Signs
Q 2.17. Asymptomatic Cerebrovascular Disease. Transient Ischemic Attacks.