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Biology
Neurobiology/Neuroscience
Neurology
1. Introduction to Neurology
2. Foundations of Clinical Neuroscience
3. The Neurological Examination
4. Diagnostic Procedures in Neurology
5. Cerebrovascular Diseases
6. Epilepsy and Seizure Disorders
7. Neurodegenerative Disorders
8. Demyelinating and Inflammatory Diseases
9. Headache Disorders
10. Infections of the Nervous System
11. Neuro-oncology
12. Disorders of the Peripheral Nervous System
13. Neuromuscular Junction Disorders
14. Muscle Diseases
15. Spinal Cord Disorders
16. Trauma to the Nervous System
17. Disorders of Consciousness
18. Sleep Disorders
19. Neurological Therapeutics
20. Special Topics in Neurology
Neurodegenerative Disorders
General Principles
Definition and Classification
Common Pathological Mechanisms
Protein Aggregation
Oxidative Stress
Mitochondrial Dysfunction
Neuroinflammation
Excitotoxicity
Genetic Factors
Environmental Factors
Biomarkers
Dementias
Alzheimer's Disease
Epidemiology
Risk Factors
Age
Genetics
Cardiovascular Risk Factors
Education
Lifestyle Factors
Pathophysiology
Amyloid Plaques
Neurofibrillary Tangles
Neuronal Loss
Synaptic Dysfunction
Clinical Features
Cognitive Symptoms
Memory Impairment
Executive Dysfunction
Language Problems
Visuospatial Deficits
Behavioral Symptoms
Apathy
Depression
Agitation
Psychosis
Functional Decline
Diagnosis
Clinical Criteria
Neuropsychological Testing
Biomarkers
CSF Biomarkers
PET Imaging
Blood Biomarkers
Differential Diagnosis
Management
Pharmacological Treatment
Cholinesterase Inhibitors
NMDA Receptor Antagonists
Aducanumab
Non-Pharmacological Interventions
Behavioral Management
Caregiver Support
Lewy Body Dementia
Dementia with Lewy Bodies
Clinical Features
Cognitive Fluctuations
Visual Hallucinations
Parkinsonism
REM Sleep Behavior Disorder
Pathophysiology
Diagnosis
Management
Parkinson's Disease Dementia
Clinical Features
Pathophysiology
Diagnosis
Management
Frontotemporal Dementia
Behavioral Variant FTD
Clinical Features
Pathophysiology
Diagnosis
Management
Primary Progressive Aphasia
Semantic Variant
Non-Fluent Variant
Logopenic Variant
FTD with Motor Neuron Disease
Vascular Dementia
Multi-Infarct Dementia
Strategic Infarct Dementia
Subcortical Vascular Dementia
Mixed Dementia
Clinical Features
Diagnosis
Management
Other Dementias
Normal Pressure Hydrocephalus
Creutzfeldt-Jakob Disease
Huntington's Disease
Progressive Supranuclear Palsy
Corticobasal Degeneration
Movement Disorders
Parkinson's Disease
Epidemiology
Risk Factors
Age
Genetics
Environmental Factors
Pathophysiology
Alpha-Synuclein Aggregation
Dopaminergic Cell Loss
Lewy Bodies
Non-Motor Pathology
Clinical Features
Motor Symptoms
Bradykinesia
Rigidity
Tremor
Postural Instability
Non-Motor Symptoms
Autonomic Dysfunction
Sleep Disorders
Cognitive Impairment
Psychiatric Symptoms
Sensory Symptoms
Diagnosis
Clinical Criteria
DaTscan
Response to Levodopa
Differential Diagnosis
Management
Pharmacological Treatment
Levodopa
Dopamine Agonists
MAO-B Inhibitors
COMT Inhibitors
Anticholinergics
Amantadine
Surgical Treatment
Deep Brain Stimulation
Lesional Surgery
Non-Pharmacological Treatment
Physical Therapy
Speech Therapy
Occupational Therapy
Complications Management
Motor Fluctuations
Dyskinesias
Non-Motor Complications
Atypical Parkinsonism
Progressive Supranuclear Palsy
Clinical Features
Pathophysiology
Diagnosis
Management
Multiple System Atrophy
MSA-P (Parkinsonian Type)
MSA-C (Cerebellar Type)
Clinical Features
Pathophysiology
Diagnosis
Management
Corticobasal Degeneration
Clinical Features
Pathophysiology
Diagnosis
Management
Dementia with Lewy Bodies
Huntington's Disease
Genetics
CAG Repeat Expansion
Anticipation
Genetic Testing
Pathophysiology
Huntingtin Protein
Striatal Degeneration
Cortical Changes
Clinical Features
Motor Symptoms
Chorea
Dystonia
Bradykinesia
Cognitive Symptoms
Psychiatric Symptoms
Diagnosis
Genetic Testing
Clinical Criteria
Imaging
Management
Symptomatic Treatment
Genetic Counseling
Supportive Care
Dystonia
Classification
Primary Dystonia
Secondary Dystonia
Dystonia-Plus Syndromes
Clinical Types
Focal Dystonia
Cervical Dystonia
Blepharospasm
Writer's Cramp
Laryngeal Dystonia
Segmental Dystonia
Generalized Dystonia
Pathophysiology
Diagnosis
Management
Botulinum Toxin
Oral Medications
Deep Brain Stimulation
Physical Therapy
Essential Tremor
Clinical Features
Action Tremor
Postural Tremor
Associated Features
Pathophysiology
Diagnosis
Clinical Criteria
Differential Diagnosis
Management
Pharmacological Treatment
Surgical Treatment
Lifestyle Modifications
Tourette's Syndrome
Clinical Features
Motor Tics
Vocal Tics
Associated Conditions
Pathophysiology
Diagnosis
Management
Behavioral Interventions
Pharmacological Treatment
Deep Brain Stimulation
Motor Neuron Diseases
Amyotrophic Lateral Sclerosis
Epidemiology
Risk Factors
Genetic Factors
Environmental Factors
Pathophysiology
Motor Neuron Degeneration
Protein Aggregation
Oxidative Stress
Neuroinflammation
Clinical Features
Upper Motor Neuron Signs
Lower Motor Neuron Signs
Bulbar Symptoms
Respiratory Symptoms
Cognitive Changes
Diagnosis
El Escorial Criteria
Electrophysiology
Imaging
Biomarkers
Differential Diagnosis
Management
Disease-Modifying Treatment
Riluzole
Edaravone
Symptomatic Treatment
Respiratory Support
Nutritional Support
Multidisciplinary Care
Primary Lateral Sclerosis
Clinical Features
Diagnosis
Management
Progressive Muscular Atrophy
Clinical Features
Diagnosis
Management
Spinal Muscular Atrophy
Genetics
SMN1 Gene
SMN2 Gene
Classification
Type 1 (Werdnig-Hoffmann)
Type 2 (Intermediate)
Type 3 (Kugelberg-Welander)
Type 4 (Adult Onset)
Clinical Features
Diagnosis
Management
Gene Therapy
Antisense Oligonucleotides
Small Molecule Therapy
Supportive Care
Ataxias
Classification
Hereditary Ataxias
Acquired Ataxias
Friedreich's Ataxia
Genetics
Frataxin Gene
GAA Repeat Expansion
Pathophysiology
Mitochondrial Dysfunction
Iron Accumulation
Clinical Features
Progressive Ataxia
Cardiomyopathy
Diabetes
Scoliosis
Diagnosis
Genetic Testing
Clinical Criteria
Management
Symptomatic Treatment
Experimental Therapies
Spinocerebellar Ataxias
SCA1
SCA2
SCA3 (Machado-Joseph Disease)
SCA6
SCA7
Other SCAs
Clinical Features
Genetics
Diagnosis
Management
Episodic Ataxias
EA1
EA2
Clinical Features
Genetics
Management
Acquired Ataxias
Alcohol-Related Ataxia
Vitamin Deficiencies
Paraneoplastic Ataxia
Immune-Mediated Ataxias
Toxic Ataxias
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8. Demyelinating and Inflammatory Diseases