User:CFR13/Books/Neurological Disorders
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- Neuroscience
- History of neuroscience
- Outline of neuroscience
- Neurology
- History of neurology
- Neuroanatomy
- Neurophysiology
- Neurotransmitter
- Psychoneuroimmunology
- Neuropsychiatry
- Neuroimaging
- Outline of the human nervous system
- Central nervous system
- Human brain
- Outline of the human brain
- List of regions in the human brain
- List of nerves of the human body
- Peripheral nervous system
- Autonomic nervous system
- Sympathetic nervous system
- Parasympathetic nervous system
- Motor system
- Sensory nervous system
- Dermatome (anatomy)
- Enteric nervous system
- Cerebellum
- Spinal cord
- Neurological examination
- Cranial nerve examination
- Upper limb neurological examination
- Neuropsychological assessment
- Mental status examination
- Mini–Mental State Examination
- Montreal Cognitive Assessment
- Addenbrooke's cognitive examination
- Glasgow Coma Scale
- Neurological disorder
- List of neurological conditions and disorders
- ICD-10 Chapter VI: Diseases of the nervous system
- Acquired brain injury
- Acute cerebellar ataxia of childhood
- Anencephaly
- Aqueductal stenosis
- Autosomal dominant porencephaly type I
- Basal ganglia disease
- Brain abscess
- Cerebellopontine angle syndrome
- Cerebral amyloid angiopathy
- Cerebral hypoxia
- Cerebral softening
- Cerebral vasospasm
- Cerebritis
- Cerebrospinal fluid leak
- Childhood acquired brain injury
- COACH Syndrome
- Cortical blindness
- Cortical visual impairment
- Encephalopathy
- Ethylmalonic encephalopathy
- Frontotemporal dementia and parkinsonism linked to chromosome 17
- Glial scar
- Gliosis
- Gomez and López-Hernández syndrome
- Halifax Consciousness Scanner
- Hashimoto's encephalopathy
- Hepatic encephalopathy
- Holmes rebound phenomenon
- Hypertensive leukoencephalopathy
- La Crosse encephalitis
- Leukoencephalopathy
- Leukoencephalopathy with neuroaxonal spheroids
- Medial medullary syndrome
- Meningioangiomatosis
- Micropolygyria
- Normal pressure hydrocephalus
- Olivopontocerebellar atrophy
- Pediatric acquired brain injury
- Pleomorphic xanthoastrocytoma
- Primary and secondary brain injury
- Progressive multifocal leukoencephalopathy
- Right hemisphere brain damage
- Sarnat staging
- Sports-related traumatic brain injury
- Temporal lobe necrosis
- Ventriculitis
- Visual extinction
- Central nervous system disease
- Frontal lobe disorder
- Cranial nerve disease
- Dysautonomia
- Movement disorders
- Epilepsy
- Accessory nerve disorder
- Alcoholic polyneuropathy
- Anesthesia dolorosa
- Anti-MAG peripheral neuropathy
- Autoimmune autonomic ganglionopathy
- Autonomic dysreflexia
- Autonomic neuropathy
- Axillary nerve dysfunction
- Axillary nerve palsy
- Charcot–Marie–Tooth disease
- Charcot–Marie–Tooth disease classifications
- Chemotherapy-induced peripheral neuropathy
- Chronic solvent-induced encephalopathy
- CMV polyradiculomyelopathy
- Congenital insensitivity to pain with anhidrosis
- Denervation
- Diabetic neuropathy
- Erythromelalgia
- Facial nerve paralysis
- Familial dysautonomia
- Guillain–Barré syndrome
- Hereditary sensory and autonomic neuropathy
- Hereditary sensory and autonomic neuropathy type I
- Horner's syndrome
- Multiple system atrophy
- Nerve compression syndrome
- Nerve injury
- Neurapraxia
- Neuritis
- Orthostatic hypotension
- Orthostatic intolerance
- Paroxysmal sympathetic hyperactivity
- Peripheral neuropathy
- Piriformis syndrome
- Plexopathy
- Polyneuropathy
- Postural orthostatic tachycardia syndrome
- Primary autonomic failure
- Pronator teres syndrome
- Proximal diabetic neuropathy
- Pudendal nerve entrapment
- Pure autonomic failure
- Quadrilateral space syndrome
- Radial nerve dysfunction
- Radial neuropathy
- Radiculopathy
- Sciatica
- Small fiber peripheral neuropathy
- Thoracic outlet syndrome
- Ulnar neuropathy
- Vegetative-vascular dystonia
- Villaret’s syndrome
- Wartenberg's migratory sensory neuropathy
- Wartenberg's Syndrome
- Winged scapula
- Meningitis
- Encephalitis
- Myelitis
- Encephalomyelitis
- Arachnoiditis
- Tropical spastic paraparesis
- Huntington's disease
- Ataxia
- Cerebellar ataxia
- Ramsay Hunt syndrome
- Friedreich's ataxia
- Spinocerebellar ataxia
- Ataxia-telangiectasia
- Hereditary spastic paraplegia
- Spinal muscular atrophy
- Spinal muscular atrophies
- Fazio–Londe disease
- Motor neuron disease
- Amyotrophic lateral sclerosis
- Primary lateral sclerosis
- Progressive bulbar palsy
- Progressive muscular atrophy
- Atrophy
- Interstitial cystitis
- Limbic encephalitis
- Myxedema
- Parkinson's disease
- Parkinsonism
- Neuroleptic malignant syndrome
- Postencephalitic parkinsonism
- Degenerative disease
- Basal ganglia
- Pantothenate kinase-associated neurodegeneration
- Progressive supranuclear palsy
- Dystonia
- Tardive dyskinesia
- Spasmodic torticollis
- Meige's syndrome
- Dyskinesia
- Extrapyramidal system
- Tremor
- Myoclonus
- Chorea
- Tic
- Restless legs syndrome
- Alzheimer's disease
- Neurodegeneration
- Frontotemporal dementia
- Pick's disease
- Dementia with Lewy bodies
- Alpers' disease
- Leigh disease
- Subacute combined degeneration of spinal cord
- Multiple sclerosis
- Neuromyelitis optica
- Diffuse myelinoclastic sclerosis
- Marchiafava–Bignami disease
- Central pontine myelinolysis
- Transverse myelitis
- Demyelinating disease
- Balo concentric sclerosis
- Partial seizure
- Myoclonic epilepsy
- Absence seizure
- Generalised tonic-clonic seizure
- Epileptic spasms
- Lennox–Gastaut syndrome
- Epilepsia partialis continua
- Status epilepticus
- Migraine
- Aura (symptom)
- Headache
- Cluster headache
- Vascular headache
- Tension headache
- Transient ischemic attack
- Vertebrobasilar insufficiency
- Amaurosis fugax
- Transient global amnesia
- Cerebrovascular disease
- Middle cerebral artery syndrome
- Anterior cerebral artery syndrome
- Posterior cerebral artery syndrome
- Brainstem stroke syndrome
- Benedikt syndrome
- Claude's syndrome
- Foville's syndrome
- Millard–Gubler syndrome
- Lateral medullary syndrome
- Weber's syndrome
- Cerebellar stroke syndrome
- Lacunar stroke
- Trigeminal neuralgia
- Bell's palsy
- Geniculate ganglionitis
- Melkersson–Rosenthal syndrome
- Myokymia
- Brachial plexus injury
- Parsonage–Turner syndrome
- Phantom limb
- Carpal tunnel syndrome
- Ulnar nerve entrapment
- Sciatic nerve
- Meralgia paraesthetica
- Tarsal tunnel syndrome
- Hereditary motor and sensory neuropathy
- Dejerine–Sottas disease
- Roussy–Lévy syndrome
- Refsum disease
- Syringomyelia
- Myasthenia gravis
- Neuromuscular junction
- Neuromuscular disease
- Muscular dystrophy
- Emery–Dreifuss muscular dystrophy
- Distal muscular dystrophy
- Facioscapulohumeral muscular dystrophy
- Limb-girdle muscular dystrophy
- Oculopharyngeal muscular dystrophy
- Myotonia
- Myotonic dystrophy
- Myotonia congenita
- Neuromyotonia
- Paramyotonia congenita
- Central core disease
- Centronuclear myopathy
- Congenital fiber type disproportion
- Mitochondrial myopathy
- Myopathy
- Hyperkalemic periodic paralysis
- Muscle weakness
- Lambert–Eaton myasthenic syndrome
- Cerebral palsy
- Hemiparesis
- Spastic hemiplegia
- Paraplegia
- Tetraplegia
- Spastic quadriplegia
- Paralysis
- Monoplegia
- Diplegia
- Cauda equina syndrome
- Todd's paresis
- Hydrocephalus
- Toxic encephalopathy
- Choroid plexus cyst
- Cerebral edema
- Reye syndrome
- Syringobulbia
- Spinal cord compression
- Sleep disorder
- Back pain
- Neuropathic pain
- Autism
- Tourette syndrome
- Delirium
- Dizziness
- Vertigo
- Stupor
- Coma
- Head injury
- Stroke
- Neoplasm
- Prion
- Complex regional pain syndrome
- Neuroplasticity