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