• Zika virus: neurologic complications
  • Anti-LGI1 encephalitis
  • Transient visual loss
  • Fatal familial insomnia
  • CNS germinoma
  • Vein of Galen malformations
  • Circumscribed astrocytic gliomas [Brief]
  • Glioneuronal and neuronal tumors [Brief]
  • Adult-type diffuse gliomas [Brief]
  • Pediatric-type diffuse high-grade gliomas [Brief]
  • Mesenchymal non-meningothelial tumors [Brief]
  • Alcohol withdrawal seizures
  • Gram-negative bacillary meningitis
  • Sleep and mental disorders
  • Ophthalmic electrophysiology
  • Hypermethioninemia
  • Multiple acyl-CoA dehydrogenase deficiency
  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Acupuncture
  • Epileptic lesions due to malformation of cortical development
  • Epileptic spasms
  • Hyperventilation syndrome
  • Nonketotic hyperglycinemia
  • Myositis and cancer
  • Neurologic disorders associated with behavioral symptoms
  • Cortical blindness
  • Infective endocarditis
  • Japanese encephalitis
  • Acute flaccid myelitis
  • Leukodystrophies
  • Mucopolysaccharidoses
  • Alexander disease
  • Migraine: pathogenesis and pathophysiology
  • Jacksonian seizures
  • New daily persistent headache
  • Headache associated with cervical spine dysfunction
  • Interventional options for cervicogenic headache
  • Heat stroke
  • Cardiac arrest: neurologic causes and complications
  • Cerebellar astrocytoma
  • Pain
  • Medical errors
  • ALS-like disorders of the Western Pacific
  • Illicit drug use: neurologic complications
  • Transient epileptic amnesia
  • Neurolymphomatosis
  • Norrie disease
  • Paraspinal neuromuscular syndromes
  • Dementia associated with amyotrophic lateral sclerosis
  • Klippel-Feil syndrome
  • Ophthalmic imaging
  • Coma due to supratentorial and cerebellar lesions
  • Argininosuccinic acidemia
  • Hydrocephalus
  • Bacterial meningitis
  • Alexia
  • Collagen VI-related dystrophies: Ullrich congenital muscular dystrophy, Bethlem muscular dystrophy, and intermediate COL6-RD
  • Generalized onset clonic seizures
  • Generalized onset tonic-clonic seizures
  • Migraine aura without headache
  • Epidemiology of headache
  • Rhinosinus-related headache
  • Migraine and epilepsy
  • Sleep, trauma, and anxiety
  • Sequelae of treatment of CNS tumors
  • Epidural hematoma
  • Sleepwalking
  • Palliative and end-of-life care for neuro-oncology patients
  • Sleep hyperkinetic (hypermotor) epilepsy
  • Transient global amnesia
  • Hemicrania continua
  • Spinal accessory neuropathy
  • Thallium neuropathy
  • Combined third, fourth, and sixth nerve palsies
  • Visual agnosias
  • Cerebellar infarction and cerebellar hemorrhage
  • Rehabilitation of spinal cord injury
  • Sleep and cerebral degenerative disorders
  • Brain abscess
  • Stereotactic radiosurgery
  • Primary CNS lymphoma
  • Paradoxical insomnia
  • Bell palsy
  • Acute autonomic neuropathies
  • Tibial nerve injuries
  • Hemiplegic migraine
  • Headache attributed to disorder of homeostasis
  • Neuroimaging of headache
  • Desmin body myofibrillar myopathy
  • Subcortical vascular cognitive impairment
  • Percutaneous treatment of cervical and lumbar disc herniations
  • Fever: neurologic causes and complications
  • Hemangioblastoma
  • Startle epilepsy
  • Cephaloceles
  • Central nervous system infection with Rickettsia species and related organisms
  • Pertussis encephalopathy
  • Progressive supranuclear palsy: cognitive and behavioral changes
  • Succinic semialdehyde dehydrogenase deficiency
  • Vascular disorders of the spinal cord
  • Nightmares
  • Acrocallosal syndrome
  • Neuroschistosomiasis
  • Optic neuritis
  • Disorders of articulation
  • Congenital toxoplasmosis
  • Leptomeningeal metastasis
  • Histoplasmosis of the nervous system
  • Mental status examination
  • Painful ophthalmoplegia
  • Yunis-Varon syndrome
  • Clinically isolated syndrome
  • Pseudobulbar affect
  • Neuromyelitis optica spectrum disorder
  • CDLK5-related developmental and epileptic encephalopathy
  • Colloid cysts
  • Leber hereditary optic neuropathy
  • Hippocampal atrophy in epilepsy
  • Scoliosis and kyphoscoliosis
  • Sturge-Weber syndrome
  • Vogt-Koyanagi-Harada syndrome
  • Retinal vascular disorders
  • Imaging of movement disorders
  • Mycoplasma pneumoniae infection: neurologic complications
  • Acute inflammatory demyelinating polyradiculoneuropathy
  • Septo-optic-pituitary dysplasia complex
  • Charcot-Marie-Tooth disease type 1A
  • Copper deficiency myeloneuropathy
  • Transverse myelitis
  • Rheumatoid arthritis: neurologic manifestations
  • Movement disorders in chromosomal aneuploidies
  • Hemiballism
  • Fragile X-associated tremor/ataxia syndrome
  • Functional (psychogenic) movement disorders
  • Movement disorders associated with autoimmune encephalitis
  • Neuro-ophthalmology of movement disorders
  • Tardive dyskinesia
  • Huntington disease
  • Spasmodic dysphonia
  • Motor control of movement disorders
  • Neuroleptic malignant syndrome
  • Akathisia
  • Progressive supranuclear palsy
  • Acute necrotizing hemorrhagic leukoencephalitis
  • Endovascular treatment of acute ischemic stroke
  • Spinal ependymoma
  • Systemic small-vessel vasculitis
  • Inadequate sleep hygiene
  • Sleep-related eating disorder
  • Cerebral toxoplasmosis
  • Pharmacological treatment of epilepsy in infants
  • Intraoperative neurophysiological monitoring
  • Back pain in children
  • Breath-holding spells
  • Limbic-predominant age-related TDP-43 encephalopathy (LATE)
  • New-onset refractory status epilepticus (NORSE) and febrile infection-related epilepsy syndrome (FIRES)
  • Waardenburg syndrome
  • Insufficient sleep syndrome
  • Sleep terror
  • Multiple cranial neuropathies: anterior skull base
  • Juvenile myoclonic epilepsy
  • Placebo and nocebo effects in neurologic disorders
  • Alexia without agraphia
  • Coccidioidomycosis: neurologic manifestations
  • Sleeping sickness
  • Impact of sleep on epileptic manifestations
  • Epilepsy with myoclonic absences
  • Pituitary adenoma
  • Systemic sclerosis
  • MELAS
  • Disorders of lipid metabolism
  • Stroke associated with sickle cell disease
  • Hypertensive intracerebral hemorrhage
  • Stroke therapy
  • Fusiform and dolichoectatic aneurysms
  • Arteriovenous malformations of the brain
  • Subarachnoid hemorrhage
  • Depression after stroke
  • Stroke in young adults
  • Cerebral revascularization: surgical and endovascular approaches
  • TIAs (vertebrobasilar)
  • Hypercoagulable states and cerebrovascular disease
  • Horner syndrome
  • Cerebral palsy
  • Down syndrome
  • Multiple cranial neuropathies: Garcin syndrome
  • Multiple cranial neuropathies: intramedullary lesions
  • Multiple cranial neuropathies: overview
  • Tumefactive demyelinating lesions
  • Lafora disease
  • AIDS and HIV: neurologic manifestations and complications
  • Myotonic muscular dystrophy (neonatal)
  • Periventricular nodular heterotopia
  • Varicella-zoster virus infections of the nervous system
  • Sporadic schwannomas and neurofibromas
  • Mimickers of infantile epileptic spasms
  • Measles: neurologic complications
  • Anencephaly and other neural tube defects
  • Disorders of olfaction
  • Disorders of gustation
  • Electrical injuries: neurologic complications
  • Poliomyelitis
  • Paraneoplastic cerebellar degeneration
  • Neuropathy associated with anti-GD1b ganglioside antibodies
  • Lambert-Eaton myasthenic syndrome
  • Paraneoplastic opsoclonus myoclonus syndrome in adults
  • Pyruvate dehydrogenase complex deficiency
  • Hyperkinetic seizures
  • Brachial plexus palsy in neonates
  • Restless sleep disorder in children
  • Olfactory bulb agenesis, hypoplasias, and dysplasias
  • Insomnia
  • HIV-associated neurocognitive disorders
  • Alcohol abuse and its neurologic complications
  • West Nile virus
  • Methanol poisoning
  • Congenital syphilis
  • Congenital cytomegalovirus
  • Fabry disease
  • Neurologic disorders related to chemical warfare nerve agents
  • Neurologic disorders related to biological warfare agents and toxins
  • Vitamin B12 deficiency
  • Carbon monoxide poisoning
  • Meniere syndrome
  • Acromegaly and gigantism
  • Immunotherapy in neuromuscular disorders
  • Pain, headache, and oromandibular structures
  • Headache associated with neurologic deficits and CSF lymphocytosis
  • Headache associated with HIV and AIDS
  • Frontotemporal dementia
  • Headache associated with hormonal fluctuations
  • Multiple system atrophy
  • Vitamin D in neurologic disorders
  • Progressive myoclonic epilepsy type 1
  • Bilateral vestibulopathy
  • Superficial siderosis
  • Meningococcal meningitis
  • Benign adult familial myoclonic epilepsy
  • Achondroplasia
  • Nondominant hereditary ataxias
  • Lead poisoning in childhood
  • Cerebral vasculitis presenting with dementia
  • Anthrax meningoencephalitis
  • Mountain sickness: neurologic aspects
  • Drug-induced neurologic disorders
  • Ototoxicity
  • Myopathies associated with thyroid disease
  • Myopathies associated with parathyroid disorders
  • Sydenham chorea
  • Vertigo
  • Superior semicircular canal dehiscence syndrome
  • Psychophysiological dizziness
  • Pituitary apoplexy
  • Mushroom poisoning: overview
  • Sensorineural hearing loss
  • Postural orthostatic tachycardia syndrome
  • Falls and fall-related injuries
  • Ascomycota mushroom poisoning
  • Colpocephaly
  • Focal cortical dysplasias
  • Lipomas of the nervous system
  • Neonatal seizures
  • Susac syndrome
  • Noise-induced hearing loss
  • Lightning injuries: neurologic complications
  • Gaucher disease
  • 2-Hydroxyglutaric acidurias
  • Viral labyrinthitis and vestibular neuritis
  • Syncope
  • Microcephaly
  • Presbycusis
  • Menkes disease and other ATP7A-related disorders
  • Hypercalcemia
  • Herpes zoster oticus
  • Paraneoplastic limbic encephalitis
  • Autoimmune sensorineural hearing loss
  • Melkersson-Rosenthal syndrome
  • Hepatorenal tyrosinemia
  • Tick paralysis
  • Swallow syncope
  • Sudden deafness
  • Subjective tinnitus
  • Subclavian steal
  • Drug-induced disturbances of smell and taste
  • Posttraumatic movement disorders
  • Dizziness
  • Progressive subcortical gliosis
  • Presbyosmia
  • Polycythemia vera and its neurologic manifestations
  • PEHO
  • Brucellosis of the nervous system
  • Otalgia
  • Otic capsule dysplasia
  • Decompression sickness: neurologic manifestations
  • Nonhallucinogenic Basidiomycota mushroom poisoning
  • Motion sickness
  • Monoamine oxidase deficiency
  • Micturition syncope and defecation syncope
  • Mal de debarquement
  • Hallucinogenic mushroom intoxication and poisoning
  • Locked-in syndrome
  • Labyrinthine infarction
  • Hypoparathyroidism
  • GLUT1DS-related developmental and epileptic encephalopathy
  • Globoid cell leukodystrophy
  • Galactosemia
  • Folate deficiency
  • Ethylmalonic encephalopathy and SCAD deficiency
  • Choroid plexus tumors of childhood
  • Complex II deficiency
  • Chediak-Higashi syndrome
  • Cerebral gas embolism
  • Cognitive aspects of central auditory disorders
  • Auditory hallucinations due to central nervous system lesions
  • Alpha-ketoglutarate dehydrogenase deficiency
  • Peripheral nerve hyperexcitability syndromes
  • Parkinson disease
  • Nerve plexus metastases
  • Prader-Willi syndrome
  • Typical absences
  • Mucolipidosis II alpha/beta and mucolipidosis III alpha/beta/gamma
  • Hypopituitarism
  • Spinal subdural empyema
  • Osmotic demyelination syndromes
  • Korsakoff syndrome
  • Cerebrotendinous xanthomatosis
  • Spinal epidural abscess
  • Diagnosis of CNS infections
  • Visual hallucinations in blindness
  • Central deafness
  • Ciguatera
  • Sialidosis
  • Shellfish poisoning
  • Sex hormones and the nervous system
  • Reflex syncope (neurally-mediated syncope)
  • Pyridoxine deficiency and toxicity
  • Mannosidosis
  • Glutathione synthetase deficiency
  • Fucosidosis
  • Radiation: CNS complications
  • Congenital cocaine syndrome
  • Multiple sclerosis: biological differences in children and adults
  • Foix-Chavany-Marie syndrome
  • Cerebral folate deficiency
  • Neurologic complications of vaccination
  • Pathologic yawning
  • Objective tinnitus
  • Lesch-Nyhan disease
  • Isovaleric acidemia
  • Inner ear concussion
  • Hyposmia in neurodegenerative disorders
  • Disequilibrium
  • High-pressure neurologic syndrome
  • Fumarase deficiency
  • Farber disease
  • Drop attacks
  • Drug-induced aseptic meningitis
  • Dopamine beta-hydroxylase deficiency
  • Alcoholic myopathy
  • Cough syncope
  • Adenylosuccinate lyase deficiency
  • Pure-tone audiometry (audiogram)
  • Generalized tonic-clonic status epilepticus
  • Batten disease
  • Acalculia
  • Cerebellar mutism syndrome
  • Developmental language disorder
  • Lyme disease: controversial issues
  • Normal pressure hydrocephalus
  • Maple syrup urine disease
  • Neurodegeneration with brain iron accumulation
  • Infantile neuroaxonal dystrophy
  • Sjögren-Larsson syndrome
  • Chiari malformation
  • Angelman syndrome
  • Congenital muscle fiber-type disproportion
  • Pharmacological treatment of insomnia
  • Sleep disorders
  • Hospital-based neurologic care
  • Pure autonomic failure
  • Cardiovascular intervention: neurologic complications
  • Behcet disease
  • Paraneoplastic sensory neuronopathy
  • Recurrent painful ophthalmoplegic neuropathy
  • Driving and epilepsy
  • Hippocampal and parahippocampal seizures
  • Congenital myasthenic syndromes
  • Metabolic encephalopathy and metabolic coma
  • Diphtheritic neuropathy
  • Dysembryoplastic neuroepithelial tumor
  • Oligodendroglioma
  • Central neurocytoma
  • Academic underachievement
  • Ketogenic diet in the treatment of epilepsy
  • Sleep and intellectual disability
  • Intellectual disability
  • Dravet syndrome
  • Neuromyotonia and myokymia
  • Viral and retroviral myositis
  • Walker-Warburg syndrome
  • Disorders of peroxisome assembly and function
  • Canavan disease
  • Sleep-related bruxism
  • Sacral agenesis
  • Hashimoto encephalopathy
  • Acute disseminated encephalomyelitis
  • Pituitary aplasia, dysplasia, and ectopic neurohypophysis
  • Recurrent meningitis
  • Bipolar disorder
  • Functional neurologic disorders and related disorders
  • Porencephaly
  • EEG in epilepsy
  • Benign sleep myoclonus of infancy
  • Cerebral concussion in childhood
  • Migrainous infarction
  • Abdominal migraine
  • Headache associated with illicit drug use
  • Epilepsy surgery in children
  • Epilepsy: treatment in low and middle income countries
  • Vagus nerve stimulation
  • Chronic autonomic neuropathies
  • Acquired sensory neuronopathies
  • Abnormalities of tetrahydrobiopterin metabolism
  • Carbon disulfide neuropathy
  • Dementia with Lewy bodies
  • Infant botulism
  • Nonlysosomal muscle glycogenoses
  • Epileptic encephalopathy with spike-wave activation during sleep
  • Pediatric and adult histone altered tumors
  • Childhood absence epilepsy
  • Haemophilus influenzae meningitis
  • Organophosphate neuropathy
  • Acrylamide neuropathy
  • Hexacarbon neuropathy
  • Toxic peripheral neuropathies
  • Neonatal intraventricular hemorrhage
  • Migraine with brainstem aura
  • Headache associated with intracranial infection
  • Becker muscular dystrophy
  • Congenital heart disease: neurologic complications
  • Guillain-Barre syndrome in children
  • Abusive head trauma
  • Cerebral venous thrombosis in infants and children
  • Fragile X syndrome
  • Congenital lymphocytic choriomeningitis virus infection
  • Hemimegalencephaly
  • Parenteral nutrition in infants and children
  • Primary stabbing headache
  • Screening of newborns for neurogenetic abnormalities
  • Hearing loss in infants and children
  • Lyme disease
  • Acquired hepatocerebral degeneration
  • Leptospirosis
  • Neurosyphilis
  • Cat-scratch disease
  • Autonomic dysfunction in sleep disorders
  • Urinary dysfunction in neurologic disorders
  • NF2-related schwannomatosis
  • Carnitine palmitoyltransferase II deficiency
  • Ambiguous paroxysmal events
  • Cavum septi pellucidi and cavum Vergae
  • Aicardi-Goutieres syndrome
  • 22q11.2 deletion syndrome
  • Oral-facial-digital syndromes
  • Cockayne syndrome
  • Status migrainosus
  • Retinal migraine
  • Primary exercise headache
  • Atypical teratoid/rhabdoid tumors
  • Rostral brainstem and thalamic infarctions
  • Irregular sleep-wake rhythm disorder
  • Epilepsia partialis continua of Kozhevnikov
  • Nonconvulsive status
  • Delayed sleep-wake phase disorder
  • Neuropathies associated with cytomegalovirus infection
  • Basal ganglia: functional anatomy and neuropharmacology
  • Dysphagia
  • Peripheral neuropathies: supportive measures and rehabilitation
  • Methylmalonic acidemia
  • Neurovascular injuries
  • Arboviral encephalitis
  • Rett syndrome
  • Sleep-related rhythmic movement disorder
  • Takayasu arteritis
  • Spinal muscular atrophy
  • Myelomeningocele
  • Focal to bilateral tonic-clonic seizures
  • Sjogren syndrome: neurologic complications
  • Tardive dystonia
  • Lennox-Gastaut syndrome
  • Stereotypies
  • Theory of mind
  • Schizophrenia
  • Focal sensory seizures with elementary symptoms
  • Drug-induced parasomnias, sleep apnea, and restless legs syndrome
  • Protocadherin19 clustering epilepsy
  • Botulinum toxin treatment of neurologic disorders
  • Spinocerebellar ataxia type 3
  • Acute drug-induced movement disorders
  • Cervical dystonia
  • Drug-induced parkinsonism
  • Corticobasal degeneration
  • Stiff-person syndrome
  • Focal unaware status epilepticus
  • Focal seizures with experiential symptoms
  • Hyperammonemia not caused by liver failure
  • Neonatal herpes encephalitis
  • Mesial temporal lobe epilepsy with hippocampal sclerosis
  • Mitochondrial disorders
  • Encephalitis lethargica
  • Neuropathies associated with cryoglobulinemia
  • Neurologic complications of coronavirus infections
  • Astrocytoma IDH mutant, WHO grade 2
  • Non-24-hour sleep-wake disorder
  • Oromandibular dystonia
  • Blepharospasm
  • Gait disorders
  • Tourette syndrome
  • Central alveolar hypoventilation
  • GAD antibody-spectrum disorders
  • Hyperekplexia
  • Inclusion body myositis
  • Dermatomyositis
  • Polymyositis, necrotizing autoimmune myositis, overlap-myositis, and myofasciitis
  • Shift work disorder
  • Aortic diseases: neurologic complications
  • Intracranial epidural abscess
  • HHH syndrome
  • Citrullinemias types 1 and 2
  • Hyperargininemia
  • Carbamoyl phosphate synthetase 1 deficiency
  • N-acetylglutamate synthase deficiency
  • Ornithine transcarbamylase deficiency
  • Sarcoidosis neuropathy
  • Neuromuscular pathology: overview
  • Autonomic neuropathy: treatment
  • Primary headache associated with sexual activity
  • Migraine: psychiatric comorbidities
  • Cluster headache
  • CADASIL
  • Basilar artery stroke
  • Pregnancy and stroke
  • Neoplastic and infectious aneurysms
  • Basal ganglia hemorrhage
  • Stroke associated with myocardial infarction
  • TIAs (carotid)
  • Rasmussen syndrome
  • Back pain
  • Cardiac catheterization: neurologic complications
  • Reducing body myopathy
  • Developmental and epileptic encephalopathies
  • Neonatal meningitis
  • Meckel-Gruber syndrome
  • Myoadenylate deaminase deficiency
  • Spinal meningioma
  • Unruptured cerebral aneurysms
  • DNA- and RNA-directed gene therapies
  • Headache associated with acute substance use or exposure
  • Eosinophilic granulomatosis with polyangiitis
  • Niemann-Pick disease type C
  • Nonparaneoplastic autoimmune cerebellar ataxias
  • Memory loss
  • Nonparalytic horizontal strabismus
  • Attention deficit hyperactivity disorder
  • Alien hand syndrome
  • Sexual dysfunction in neurologic disorders
  • Dermoid and epidermoid tumors
  • Absence status epilepticus
  • Sleep and alcohol use and abuse
  • Sleep-related laryngospasm
  • Sudden unexplained nocturnal death syndrome
  • Creutzfeldt-Jakob disease
  • Aicardi syndrome
  • Multiple sclerosis: neuroimmunology
  • Ethical issues in neurology
  • Fibromyalgia
  • Prion diseases
  • Candidiasis of the nervous system
  • Intracranial subdural empyema
  • Eyelid myoclonia with and without absences
  • Leukemia: neurologic complications
  • Arsenic neuropathy
  • Anti-IgLON5 disease
  • Botulism
  • Erythromelalgia
  • Motor and multifocal motor neuropathies
  • Pharmacological treatment of epilepsy in neonates
  • Perinatal hypoxic-ischemic encephalopathy
  • Congenital rubella
  • Asymmetric tonic seizures
  • Femoral neuropathy
  • Neurosurgical management of chronic pain
  • Kearns-Sayre syndrome
  • Diabetic amyotrophy
  • Hypertensive encephalopathy
  • Neuropathic pain: treatment
  • Environmental and behavioral sleep disorders
  • Systemic lupus erythematosus
  • Hereditary amyloid polyneuropathy
  • Self-limited (familial) infantile epilepsy
  • Renal failure: neurologic complications
  • Transplantation: neurologic complications
  • Myoclonic status epilepticus
  • Febrile seizures
  • Pontocerebellar hypoplasia
  • Myofascial pain syndrome
  • Visual-sensitive epilepsies
  • Sleep and chronic pulmonary disorders
  • Central sleep apnea due to high-altitude periodic breathing
  • Adult Refsum disease
  • Ataxia-telangiectasia
  • Thoracic disc prolapse
  • Nutrition-related peripheral neuropathies
  • Pregnancy: CNS complications
  • Dandy-Walker syndrome
  • Joubert syndrome
  • Isolated hypogonadotropic hypogonadism
  • Neonatal white matter injury
  • Aura continua
  • Radiologic abnormalities in patients with neuropathy
  • Autoantibodies: mechanism and testing
  • Familial dysautonomia
  • Ependymal and choroid plexus cysts
  • Quality-of-life scales for neurologic diseases
  • Epilepsy in infancy with migrating focal seizures
  • Neuralgic amyotrophy
  • Paroxysmal hemicrania
  • Critical illness myopathy and polyneuropathy
  • Polyneuropathy associated with anti-MAG IgM antibodies
  • Lead neuropathy
  • Neurofibromatosis 1
  • Local anesthesia: neurologic complications
  • Prognosis after cardiac arrest
  • Use of focused ultrasound in neurologic disorders
  • Neurosurgical shunts and their complications
  • Visual snow
  • IgG4-related disease: neurologic manifestations
  • Psychophysiological insomnia
  • Chemotherapy-induced neuropathies
  • Vasculitic neuropathies
  • Uremic neuropathy
  • Acupuncture in headache treatment
  • Positional vertigo
  • Primary carnitine transporter deficiency
  • Primary spinal cord tumors
  • Post-polio syndrome
  • Radial neuropathy
  • Indomethacin-responsive headache syndromes
  • British anti-Lewisite
  • Brain death/death by neurologic criteria
  • Nucleoside analogue neuropathies
  • Median neuropathy
  • Interventional neuroradiology for neurologic disorders
  • Lathyrism, konzo, and tropical ataxic neuropathy
  • Neurologic aspects of burn injuries
  • Fibular neuropathy
  • Myoclonic absences
  • Hemiclonic seizures
  • Generalized onset tonic seizures
  • Inhibitory motor seizures
  • Focal onset generalized absence seizures
  • Focal clonic seizures
  • Epilepsy with generalized tonic-clonic seizures alone
  • Hemophilia and other coagulation disorders: neurologic aspects
  • Thrombotic thrombocytopenic purpura: neurologic complications
  • Ankylosing spondylitis
  • Lumbar disc disease
  • Neurogenic bladder
  • SUNCT syndrome
  • Sleeptalking
  • Herpes simplex encephalitis
  • Cryptococcal meningitis
  • Neurologic manifestations of celiac disease and gluten sensitivity
  • Duchenne muscular dystrophy
  • Glioblastoma, IDH wildtype
  • Mitochondrial epilepsy
  • Carnitine palmitoyltransferase 1A deficiency
  • Movement disorders in childhood
  • Overview of electromyography and nerve conduction studies
  • Progressive myoclonus epilepsies
  • Sleep-related movement disorders
  • Overview of neuropathology updates for infiltrating gliomas
  • Gold neurotoxicity
  • Perhexiline maleate neuropathy
  • Posttraumatic epilepsy
  • Hemispheric low-grade gliomas and neuronal and glioneuronal tumors of childhood
  • Visual pathway gliomas
  • Amiodarone neuropathy
  • Hereditary spastic paraplegia
  • Aminoacylase 1 deficiency
  • Brainstem gliomas in childhood
  • Ependymoma
  • Medulloblastoma
  • Lobar hemorrhage
  • Nontraumatic intracerebral hemorrhage
  • Chronic subdural hematoma
  • Clinical trials in multiple sclerosis
  • Traumatic intracerebral hemorrhage
  • Carotid bruit
  • Cerebral arteriopathies
  • Secondary stroke prevention
  • Primary prevention of stroke
  • Traumatic intracranial aneurysms
  • Convulsive syncope
  • Thyrotoxicosis
  • Porphyria
  • Hypoglycemia
  • Seizures associated with eclampsia
  • Tuberculosis of the CNS
  • Ataxia
  • Tremors
  • Idiopathic basal ganglia calcification
  • Paroxysmal dyskinesias
  • Neuropathy associated with leprosy
  • Peripheral nerve complications of HIV-1 infection
  • Juvenile Huntington disease
  • HMG-CoA lyase deficiency
  • Incontinentia pigmenti
  • Opsoclonus-myoclonus
  • Chiropractic manipulation: neurologic complications
  • Diplopia
  • Congenital muscular dystrophy: merosin deficient form
  • Congenital muscular dystrophies
  • Drug-induced neuropathies
  • Antibiotic-induced neuropathy
  • Kennedy disease
  • Small fiber neuropathies
  • Sleep and multiple sclerosis
  • Arachnoid cyst
  • Epilepsy
  • X-linked myotubular myopathy
  • Sleep and parkinsonism
  • Headache associated with ischemic cerebrovascular disease
  • Cognition and epilepsy
  • Psychological factors and headache
  • Kawasaki disease
  • Lissencephalies
  • Tonic status epilepticus
  • Non-progressive aphasia
  • Obstructive sleep apnea
  • Sleep and dementia
  • Disorders of consciousness
  • Brain metastases: considerations for surgical and radiosurgical treatment
  • Hypnic headache
  • Hypomelanosis of Ito
  • X-linked hydrocephalus (L1 syndrome)
  • Childhood occipital visual epilepsy
  • Chronic fatigue syndrome
  • Atonic seizures
  • Neglect
  • Charcot-Marie-Tooth disease type 1B and other CMT neuropathies associated with MPZ mutations
  • Adrenoleukodystrophy
  • Disulfiram neuropathy
  • Polyneuropathy associated with antisulfatide antibodies
  • CLIPPERS
  • Personal approach to multiple sclerosis treatment
  • Antibody-mediated epilepsies
  • Acute motor axonal neuropathy
  • Acquired human cytomegalovirus
  • Autonomic seizures
  • Tumors of the skull base
  • Reflex seizures
  • Progressive multifocal leukoencephalopathy
  • Eye-related headache
  • Tension-type headache
  • Trigeminal neuralgia
  • Headache in children: overview and treatment approaches
  • Acute traumatic spinal cord injury
  • Epidural anesthesia
  • Complex regional pain syndrome
  • Isolated beta-methylcrotonyl-CoA carboxylase deficiency
  • Biotin holocarboxylase synthetase deficiency
  • Biotinidase deficiency
  • Propionyl-CoA carboxylase deficiency
  • Pyruvate carboxylase deficiency
  • Sotos syndrome
  • Pathogenesis and pathology of tauopathies
  • Cerebrovascular complications of cancer
  • Isolated sixth nerve palsy
  • Movement disorder emergencies
  • Myoclonus
  • Rating scales of movement disorders
  • Deep brain stimulation in movement disorders
  • Isolated dystonia
  • Parasomnia overlap disorder and status dissociatus
  • Sleep and depression
  • Primary CNS angiitis
  • Cardiovascular procedures: neurologic complications
  • Stroke associated with atrial fibrillation
  • Immunoglobulin light chain amyloidosis: neurologic complications
  • CNS listeriosis
  • Juvenile absence epilepsy
  • Headache in transplant patients
  • Headache associated with spontaneous spinal CSF leak
  • Toxic and nutritional deficiency optic neuropathies
  • Neuroimaging of sleep disorders
  • Sleep paralysis
  • Alzheimer disease
  • Outpatient rehabilitation of chronic neurologic conditions
  • Neuromodulation
  • Lumbar spinal stenosis
  • Malaria
  • Epstein-Barr virus infections of the nervous system
  • Cyclic alternating pattern
  • Coma due to drug intoxication
  • Hereditary neuropathy with predisposition to pressure palsy
  • Rabies
  • Suprascapular neuropathy
  • Early infantile epileptic encephalopathies
  • Vascular cognitive impairment
  • Hepatitis viruses: neurologic complications
  • Thoracic outlet syndromes
  • Papilledema
  • Myoclonus epilepsy with ragged-red fibers
  • Holoprosencephaly
  • Nodding syndrome
  • Subcortical laminar heterotopia
  • Atypical absence seizures
  • Pre-mild cognitive impairment
  • Schizencephaly
  • Self-limited familial neonatal infantile seizures
  • Medical complications of stroke
  • Reversible cerebral vasoconstriction syndromes
  • Spontaneous carotid and vertebral artery dissection
  • Moyamoya disease
  • Spasticity
  • Autoantibodies: disease markers
  • Neurosarcoidosis
  • Multiple sclerosis: treatment of its symptoms
  • Metal neurotoxicity
  • Stereotactic neurosurgery
  • Serotonin syndrome
  • Brachial plexus injuries
  • Monoclonal gammopathy of neurologic significance
  • Turcot syndrome
  • Metastatic epidural spinal cord compression
  • Chordoma
  • Mevalonate kinase deficiency
  • Long-chain fatty acid oxidation defects
  • Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
  • Craniopharyngioma
  • Intracranial nongerminomatous germ cell tumors
  • Paraneoplastic syndromes
  • Radiation plexopathy
  • Radiation myelopathy
  • Vestibular schwannoma
  • Acute pandysautonomia
  • Rhombencephalosynapsis
  • X linked Charcot-Marie-Tooth disease type 1
  • Cervical spondylotic myelopathy
  • Carpal tunnel syndrome
  • Periodic limb movements
  • Anti-GQ1b antibody syndrome
  • Catatonia
  • Alternating hemiplegia of childhood
  • Management of chronic neuromuscular disease in children
  • Neurocysticercosis
  • Pregnancy: neuromuscular complications
  • Rhabdomyolysis (myoglobinuria)
  • Acute hemiplegia in childhood
  • Core myopathies
  • Automatic-voluntary dissociation
  • NonREM parasomnias
  • Myotonic dystrophy
  • Isolated fourth nerve palsy
  • Cerebellar hypoplasia, dysplasia, and enlargement
  • Principles of rehabilitation of patients with neurologic disorders
  • Management of multiple sclerosis in COVID-19 pandemic
  • Hypothyroidism
  • Chronic progressive external ophthalmoplegia
  • Aphasic seizures
  • Stimulant-dependent sleep disorder
  • Whiplash injuries
  • 3-alpha-methylcrotonylglycinuria
  • Carnitine-acylcarnitine translocase deficiency
  • Multiple sclerosis: neurobehavioral aspects
  • Pneumococcal meningitis
  • HSD10 disease
  • Malformations of the brain
  • Chronic idiopathic axonal polyneuropathy
  • Neuropsychologic correlates in pediatric sleep apnea
  • Sleep and cardiac disorders
  • Mobius syndrome
  • Asymptomatic hyperCKemia
  • Familial Alzheimer disease
  • Sports activities: neurologic complications
  • Photosensitive occipital lobe epilepsy
  • Central sleep apnea
  • Ganglioglioma
  • Neonatal status epilepticus
  • Charcot-Marie-Tooth disease: CMT2, CMT4, and others
  • Genetic epilepsy with febrile seizures plus
  • Sleep and epilepsy
  • Fetal anticonvulsant syndrome
  • Aqueductal stenosis
  • Extracorporeal life support
  • Migraine treatment
  • Cyclic vomiting syndrome
  • Tuberous sclerosis complex
  • Autism spectrum disorder
  • Advanced sleep-wake phase disorder
  • Fetal alcohol syndrome
  • Leigh syndrome
  • Posttraumatic sleep disturbance
  • Distal myopathies
  • Idiopathic insomnia
  • Self-limited (familial) neonatal epilepsy
  • Peripheral nerve injuries
  • Hot water epilepsy
  • Medication overuse headache
  • Headache associated with intracranial neoplasms
  • Wilson disease
  • Wolman disease
  • Apraxia
  • Sleep disorders in women
  • Vestibular migraine
  • GABA-transaminase deficiency
  • Hormonal contraception and stroke
  • Ischemic stroke
  • Antiphospholipid antibody syndrome
  • Ischemic stroke syndromes and their anatomic localization
  • Atrial myxoma
  • Pediatric-type diffuse high-grade gliomas (excluding diffuse midline gliomas)
  • Trichinosis
  • Agenesis of the corpus callosum
  • Acute cerebellar ataxia in children
  • Migraine in childhood
  • Traumatic cranial neuropathy
  • Severe closed head injury
  • Clinical evaluation of peripheral neuropathies
  • Self-limited epilepsy with autonomic seizures
  • Cervical disc disease
  • Viral meningitis
  • Mercury neuropathy
  • REM sleep-related parasomnias
  • Polymicrogyria
  • Primary cough headache
  • Vagal nerve stimulation for headaches
  • Migraine: clinical aspects
  • Medications and substances causing headache
  • Acute headache: diagnosis
  • Benign paroxysmal vertigo
  • Dementia in Parkinson disease
  • Self-limited epilepsy with centrotemporal spikes
  • POEMS syndrome
  • Technical aspects of EEG
  • Neuroimaging of epilepsy
  • Brain stimulation for epilepsy
  • Multiple sclerosis: presentation and course
  • Familial mesial temporal lobe epilepsy
  • Crohn disease: neurologic manifestations
  • Aromatic L-amino acid decarboxylase deficiency
  • Neurologic disorders associated with MOG antibodies
  • Cerebral edema in childhood
  • Sleep and aging
  • Neurotechnology: brain-computer and brain-machine interfaces
  • Neonatal opioid withdrawal syndrome
  • Natalizumab and PML in MS
  • EEG monitoring in the intensive care unit
  • EEG in encephalopathic conditions
  • Pharmacological treatment of epilepsy in adolescents and adults
  • Hemorrhagic transformation of ischemic stroke
  • Thalamic hemorrhage
  • Stroke associated with drug abuse
  • Patent foramen ovale
  • White matter abnormalities in the brain
  • Intracerebral hemorrhage due to thrombolytic therapy
  • Anterior cerebral artery stroke syndromes
  • Fatigue in multiple sclerosis
  • Nemaline myopathy
  • Dopa-responsive dystonia
  • Hemifacial spasm
  • Restless legs syndrome
  • Neurologic disorders associated with obesity
  • Viral hemorrhagic fevers: neurologic complications
  • Periodic paralysis and the nondystrophic myotonias (skeletal muscle channelopathies)
  • Telehealth and cognitive behavioral therapy for insomnia (CBT-I0)
  • Optical coherence tomography in multiple sclerosis and neurologic disorders
  • Developmental delay in children: evaluation and management
  • Whipple disease
  • Amyotrophic lateral sclerosis
  • Hemorrhagic shock and encephalopathy syndrome
  • Sleep-related leg cramps
  • Electroconvulsive therapy (ECT)
  • Neurocutaneous syndromes
  • Cerebral amyloid angiopathy
  • Carotid-cavernous fistulas
  • Amaurosis fugax
  • Paget disease of bone: neurologic complications
  • Executive dysfunction
  • Third nerve palsy
  • Andermann syndrome
  • Sleep, stroke, and vascular dementia
  • Amebic meningoencephalitis
  • Epilepsy with reading-induced seizures
  • Sciatic neuropathy
  • Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy
  • Eating disorders: neurologic manifestations
  • Chemotherapy: neurologic complications
  • Sleep and headaches
  • Treatment of neurologic disorders with marijuana
  • Autosomal dominant hereditary ataxias
  • HTLV-1 associated myelopathy/Tropical spastic paraparesis
  • Narcolepsy
  • Lumbosacral plexus injuries
  • Ulnar neuropathy at the elbow
  • First unprovoked seizure: workup and management
  • Nystagmus
  • Orbital disease in neuro-ophthalmology
  • Pupillary abnormalities
  • Sleep and neuromuscular and spinal cord disorders
  • Chronic inflammatory demyelinating polyradiculoneuropathy
  • Limb dystonia
  • Progressive encephalomyelitis with rigidity and myoclonus and glycine receptor antibodies
  • Peripheral dystonia
  • Chorea
  • Anti-NMDA receptor encephalitis
  • Temporal arteritis
  • Ischemic optic neuropathy
  • Phenylketonuria
  • Central hypotonia in infancy and childhood
  • Epidermal nevus syndromes: neurologic phenotypes
  • Multiple sclerosis and fertility
  • Headache attributed to head trauma
  • Ulnar neuropathies
  • Right hemisphere language disorders
  • POLG-related disorders
  • Benign paroxysmal positional vertigo
  • Hypersomnolence
  • Malignant hyperthermia
  • Amyloid myopathy
  • Facioscapulohumeral muscular dystrophy
  • Depressive disorders in epilepsy
  • Thiamine deficiency
  • Seizures presenting in childhood
  • Idiopathic hypersomnia
  • Jet lag disorder
  • Confusional arousal
  • Basilar impression
  • Smith-Lemli-Opitz syndrome
  • Meningiomas
  • Homocystinuria due to cystathionine beta-synthase deficiency
  • Hyperornithinemia
  • Chronic traumatic encephalopathy
  • Approach to headache patient
  • Seizures of the posterior neocortex
  • Infantile epileptic spasms syndrome
  • PART (Primary age-related tauopathy)
  • Neuroimaging in acute stroke
  • Syringomyelia
  • Idiopathic intracranial hypertension
  • Rare brain embryonal tumors in infancy and early childhood
  • Drug-induced myasthenic syndromes
  • Sudden unexpected death in epilepsy
  • Neocortical temporal lobe seizures
  • Diabetic neuropathies
  • Pyridoxine/P5P-dependent developmental epileptic encephalopathy
  • Horizontal gaze palsy
  • Vertical gaze palsy
  • Diagnosis of childhood immune-mediated CNS vasculitides
  • Myasthenia gravis
  • Frontal lobe seizures
  • Myoclonic seizures
  • Hemiconvulsion-hemiplegia-epilepsy syndrome
  • Myoclonic-atonic seizures
  • Myoclonic epilepsy in infancy
  • Brain metastases
  • Dysplastic gangliocytoma of the cerebellum
  • Pleomorphic xanthoastrocytoma
  • Tetanus
  • Emery-Dreifuss muscular dystrophy
  • Drug-induced seizures
  • Functional, dissociative, or psychogenic nonepileptic seizures
  • Paraneoplastic retinopathy
  • GM1 gangliosidosis
  • GM2 gangliosidoses
  • Single enzyme defects of peroxisomal beta-oxidation
  • Techniques of lumbar puncture and intrathecal and epidural injections
  • Stroke: supportive care
  • Congenital disorders of glycosylation
  • Reflex anoxic seizures
  • Chondrodysplasia punctata
  • Corticosteroid myopathies
  • Radiologically isolated syndrome
  • Limb-girdle muscular dystrophies
  • Sleep and medical disorders
  • Von Hippel-Lindau disease
  • Aprosodia
  • Morvan syndrome and related disorders associated with CASPR2 antibodies
  • Genital herpes: neurologic complications
  • Fingerprint body myopathy
  • PANDAS
  • Intramedullary spinal cord metastatic tumors
  • SIADH
  • Recurrent hypersomnia
  • Tyrosine hydroxylase deficiency
  • Gelastic seizures with hypothalamic hamartoma
  • Perspectives: Dr. Christopher Walsh and genetic mechanisms underlying the developing and aging brain
  • Presurgical embolization of tumors of the brain, head and neck, and spinal cord
  • Lacunar infarction
  • Minor closed head injury
  • Rapid eye movement sleep behavior disorder
  • Pelizaeus-Merzbacher disease
  • Amblyopia
  • Glutaric aciduria
  • Failed back surgery syndrome
  • Acid sphingomyelinase deficiency (Niemann-Pick disease types A and B)
  • Perspectives: Life and Work of Dr. Stanley Fahn
  • Epilepsy with myoclonic-atonic seizures
  • Late-life migrainous accompaniments
  • Familial focal epilepsy with variable foci
  • Epilepsy with auditory features
  • Cerebral embolism
  • Brain tumor-related epilepsy
  • Focal emotional seizures with laughing
  • Perspectives: Dr. Josep Dalmau and autoimmune encephalitis
  • Perspectives: Dr. Carlos Schenck discusses REM-sleep behavior disorder
  • Sudden infant death syndrome
  • Cerebral venous thrombosis
  • Brainstem hemorrhage
  • Cavernous malformations
  • Sneddon syndrome
  • Stroke associated with cerebral angiography
  • Fibromuscular dysplasia
  • Bowel dysfunction in neurologic disorders
  • Chorea in childhood
  • Unusual retinopathies
  • Neurofibromatosis 1 and intracranial neoplasms of childhood
  • Balo concentric sclerosis
  • Perspectives: Dr. Jerry Mendell discusses Duchenne muscular dystrophy and gene therapy
  • Aortic atherosclerosis and stroke
  • Neurostimulation in sleep medicine
  • Pregnancy and epilepsy
  • Epilepsy and psychoses
  • Neuroacanthocytosis
  • Triptans
  • SSRIs
  • Neurogastroenterology
  • Nutrition and the brain
  • Ion channels and neurologic disorders
  • Vitamin E in neurologic disorders
  • Drug-induced cerebrovascular disease
  • Drug-induced delirium
  • Cerebral vasospasm: treatment
  • Ziconotide
  • Tizanidine
  • Riluzole
  • Selegiline
  • Rasagiline
  • Perampanel
  • Ropinirole
  • Modafinil
  • Fluoxetine
  • Glatiramer acetate
  • Dimethyl fumarate
  • Pregabalin
  • Eteplirsen
  • Vigabatrin
  • Valproic acid
  • Tolcapone
  • Phenytoin
  • Lamotrigine
  • Donepezil
  • Propofol
  • Lacosamide
  • Interferon beta 1b
  • Gabapentin
  • Carbamazepine
  • Tapentadol
  • Tiagabine
  • Pramipexole
  • Entacapone
  • Coenzyme Q10
  • Atomoxetine
  • Sodium oxybate
  • Ponesimod
  • Rotigotine
  • Fingolimod
  • Landau-Kleffner syndrome
  • Oxcarbazepine
  • Nimodipine
  • Citalopram
  • Hyperhomocysteinemia
  • Drug-induced insomnia and excessive daytime sleepiness
  • Clopidogrel
  • Alternative therapies
  • Topiramate
  • Hepatic encephalopathy
  • Methylphenidate
  • Aducanumab
  • Memantine
  • Antipsychotics
  • Anticholinergics
  • Alemtuzumab
  • Staphylococcal infections: neurologic manifestations
  • Onasemnogene abeparvovec
  • Edaravone
  • Azathioprine
  • Infliximab
  • Headache guidelines
  • Levodopa
  • Zonisamide
  • Rivastigmine
  • Duloxetine
  • Chelation therapy [Archived]
  • Anti-CGRP monoclonal antibodies for prevention of migraine
  • Nusinersen
  • Galantamine
  • Ocrelizumab
  • Mitoxantrone
  • Mycophenolate
  • Pyridostigmine
  • Benzodiazepines
  • Prednisone
  • Sumatriptan
  • Intravenous immune globulin
  • Interferon beta 1a
  • Fosphenytoin
  • Dalfampridine
  • Dihydroergotamine
  • Primidone
  • Risperidone
  • Tissue plasminogen activator
  • Intrathecal baclofen
  • Levetiracetam
  • Natalizumab
  • Split cord malformation
  • Extracerebral fluid collections in infants
  • Megalencephaly
  • Tethered spinal cord
  • Chemical and drug poisoning in children
  • Barth syndrome
  • Sleep enuresis
  • Atlantoaxial dislocation
  • Cerebro-oculo-facio-skeletal syndrome
  • Childhood ataxia with central nervous system hypomyelination
  • Intracranial atherosclerosis
  • Neurogenetics and genetic and genomic testing
  • Craniosynostosis
  • Congenital HIV-1 infection
  • Intermittent explosive disorder
  • Child maltreatment
  • Epilepsy surgery in adults