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Neurological disorders
- Neurological disorder
- List of neurological conditions and disorders
- Acquired non-inflammatory myopathy
- Acute disseminated encephalomyelitis
- Acute motor axonal neuropathy
- Adie syndrome
- Adiposogenital dystrophy
- Adult-onset basal ganglia disease
- Agrammatism
- Aicardi syndrome
- Alcohol withdrawal syndrome
- Alcoholic hallucinosis
- Alcoholic polyneuropathy
- Alice in Wonderland syndrome
- Alien hand syndrome
- Allochiria
- Altered level of consciousness
- Alternating hemiplegia
- Alternating hemiplegia of childhood
- Amaurosis
- Anaphia
- Angelman syndrome
- Angiolathyrism
- Anismus
- Anosmia
- Anosodiaphoria
- Anterior interosseous syndrome
- Antiphospholipid syndrome
- Anton–Babinski syndrome
- Apotemnophilia
- Aprosodia
- Arachnoid cyst
- Arachnoiditis
- Ashby House
- Asperger syndrome
- Asperger syndrome and neuroscience
- Astasis
- Atypical trigeminal neuralgia
- Auditory processing disorder
- Autism
- Autoimmune autonomic ganglionopathy
- Autosomal recessive cerebellar ataxia
- Avellis syndrome
- Balance disorder
- Bálint's syndrome
- Basilar invagination
- Behr syndrome
- Bell's palsy
- Benign fasciculation syndrome
- Bickerstaff's encephalitis
- Binswanger's disease
- Blocq's disease
- Bobble-head doll syndrome
- Borna disease
- Boston Diagnostic Aphasia Examination
- Bradyphrenia
- Bromism
- Brown-Séquard syndrome
- Brown–Vialetto–Van Laere syndrome
- Brudziński's sign
- Bruns ataxia
- Bulbar palsy
- Cheiralgia paresthetica
- Choreoathetosis
- Choroidal fissure cyst
- Chronic fatigue syndrome
- Chronic inflammatory demyelinating polyneuropathy
- Clinically isolated syndrome
- Cockayne syndrome
- Colloid cyst
- Compensatory hyperhidrosis
- Complex regional pain syndrome
- Congenital myasthenic syndrome
- Conjugate gaze palsy
- Constructional apraxia
- Cortical spreading depression
- Cramp fasciculation syndrome
- Critical illness polyneuropathy
- Crutch paralysis
- De Vivo disease
- Deep dyslexia
- Dejerine–Sottas disease
- Delirium tremens
- Demyelinating disease
- Dennie–Marfan syndrome
- Dentatorubral-pallidoluysian atrophy
- Developmental verbal dyspraxia
- Dialysis disequilibrium syndrome
- Diplegia
- Directed attention fatigue
- Disorders of consciousness
- Dissociated sensory loss
- Dizziness
- Dopamine dysregulation syndrome
- Dual consciousness (neuroscience)
- Dyskinesia
- Engel classification
- Enteric neuropathy
- Episodic ataxia
- Erb's palsy
- Ergotism
- Erythromelalgia
- Exploding head syndrome
- Fahr's syndrome
- Familial amyloid neuropathy
- Transthyretin-related hereditary amyloidosis
- Familial isolated vitamin E deficiency
- Fetal alcohol spectrum disorder
- Fetal alcohol syndrome
- Flynn–Aird syndrome
- Foix–Chavany–Marie syndrome
- Folderism
- Foot drop
- Forced normalization
- Foreign accent syndrome
- Foster–Kennedy syndrome
- FOUR score
- Functional neurological deficit
- Galloway Mowat syndrome
- General paresis of the insane
- Geniculate ganglionitis
- Geniospasm
- Giant axonal neuropathy
- Giant-cell arteritis
- Gray matter heterotopia
- Grinker myelinopathy
- Guillain–Barré syndrome
- Gulf War syndrome
- Hereditary cystatin C amyloid angiopathy
- Hereditary diffuse leukoencephalopathy with spheroids
- Hereditary hemorrhagic telangiectasia
- Hereditary motor and sensory neuropathy
- Hereditary neuralgic amyotrophy
- Hereditary neuropathy with liability to pressure palsy
- Holmes tremor
- Hopkins syndrome
- Hyperekplexia
- Hyperkinesia
- Hyperprosexia
- Hypokalemic sensory overstimulation
- Hypsarrhythmia
- Ideational apraxia
- Ideomotor apraxia
- Idiopathic inflammatory demyelinating diseases of the central nervous system
- Idiopathic intracranial hypertension
- Infantile convulsions and choreoathetosis
- Infantile neuroaxonal dystrophy
- Integrative agnosia
- Intention tremor
- Intracranial dolichoectasias
- Intracranial hypertension syndrome
- Jargon aphasia
- Joswig syndrome
- Joubert syndrome
- JUNQ and IPOD
- Karak syndrome
- Kernicterus
- Kindling model
- Konzo
- Korsakoff's syndrome
- Lafora disease
- Laminopathy
- Leigh's disease
- LENA Foundation
- Lennox–Gastaut syndrome
- Leukodystrophy
- Lhermitte–Duclos disease
- Longitudinal callosal fascicle
- Low pressure hydrocephalus
- Lytico-bodig disease
- Macropsia
- Mad hatter disease
- Management of multiple sclerosis
- Manganism
- Marche a petit pas
- McDonald criteria
- Meckel syndrome
- Meige's syndrome
- Ménière's disease
- Mental confusion
- Meralgia paraesthetica
- Mevalonate kinase deficiency
- Micropsia
- Migraine-associated vertigo
- Minimally conscious state
- Möbius syndrome
- Motion sickness
- Motor disorder
- Motor speech disorders
- Movement disorder
- Muenke syndrome
- Multifocal motor neuropathy
- Multiple sclerosis signs and symptoms
- Multisystem proteinopathy
- Muscle fatigue
- Muscle weakness
- Myelitis
- Myelomalacia
- National Institutes of Health Stroke Scale
- Neuralgia
- Neurapraxia
- Neurasthenia
- Neurodegeneration
- Neurodevelopmental disorder
- Neurofibromatosis type I
- Neurofibromatosis type II
- Neurogenic shock
- Neuroglycopenia
- Neurological deficit
- Portal:Pervasive developmental disorders
- Neuroma
- Neuromodulation (medicine)
- Neuronal migration disorder
- Neurosarcoidosis
- Neurotoxicity
- NIH Toolbox
- Norman–Roberts syndrome
- Notalgia paresthetica
- Occipital neuralgia
- Oculogyric crisis
- Ohtahara syndrome
- Ondine's curse
- Oneirophrenia
- Opsoclonus myoclonus syndrome
- Optic papillitis
- Organophosphate-induced delayed neuropathy
- Ortner's syndrome
- PANDAS
- Paradoxical embolism
- Paresthesia
- Parkinson plus syndrome
- Paroxysmal attack
- Paroxysmal exercise-induced dystonia
- Paroxysmal extreme pain disorder
- Paroxysmal kinesigenic choreoathetosis
- Paroxysmal nonkinesigenic dyskinesia
- Pathophysiology of chronic fatigue syndrome
- Pediatric acute-onset neuropsychiatric syndrome (PANS)
- Peduncular hallucinosis
- Perineodynia
- Phantom eye syndrome
- Phantom limb
- Phantosmia
- Phonagnosia
- Phonological dyslexia
- Photophobia
- Pleurothotonus
- Pneumocephalus
- POEMS syndrome
- Poser criteria
- Post-chemotherapy cognitive impairment
- Posterior cortical atrophy
- Posterior rami syndrome
- Posterior reversible encephalopathy syndrome
- Postherpetic neuralgia
- Postperfusion syndrome
- Presyncope
- Progressive inflammatory neuropathy
- Protein aggregation
- Proteopathy
- PRRT2
- Pseudobulbar affect
- Psychoorganic syndrome
- Quadrigia
- Rabbit syndrome
- Rabies
- Rage syndrome
- Ramsay Hunt syndrome
- Ramsay Hunt syndrome type I
- Ramsay Hunt syndrome type II
- RASopathy
- Reflex neurovascular dystrophy
- Regressive autism
- Retinal migraine
- Rett syndrome
- Revesz syndrome
- Rhythmic movement disorder
- Rich focus
- Scanning speech
- Schumacher criteria
- Scintillating scotoma
- Sensory Integration Dysfunction
- Sensory processing disorder
- Sensory Processing Disorder Foundation
- Shapiro syndrome
- Simulated presence therapy
- Sluggish cognitive tempo
- Small fiber peripheral neuropathy
- Social-Emotional Agnosia
- Sopite syndrome
- Spasmodic torticollis
- Spastic diplegia
- Spastic quadriplegia
- Spinal muscular atrophies
- Spinocerebellar ataxia type 6
- Spinocerebellar ataxia type-13
- Spontaneous cerebrospinal fluid leak
- Sports-related traumatic brain injury
- Stereotypic movement disorder
- Strephosymbolia
- Subacute myelo-optic neuropathy
- Subarachnoid hemorrhage
- Subclavian steal syndrome
- Subclinical seizure
- Subdural effusion
- Subdural hygroma
- Subgaleal hemorrhage
- Suboccipital puncture
- Superficial siderosis
- Supernumerary phantom limb
- Susac's syndrome
- Sydenham's chorea
- Synaptopathy
- Synkinesis
- Synucleinopathies
- Taenia solium
- Tardive dyskinesia
- Tardive dysmentia
- Tarlov cyst
- Tick paralysis
- Timothy syndrome
- Tolosa–Hunt syndrome
- Transverse myelitis
- Triparesis
- Triplegia
- Upper motor neuron lesion
- Vertebral artery dissection
- Vertigo
- Viliuisk encephalomyelitis
- Wartenberg's migratory sensory neuropathy
- Wartenberg's sign
- Wartenberg's Syndrome
- Weakness
- Wernicke's encephalopathy
- Wernicke–Korsakoff syndrome
- Wilson's disease
- Yoga foot drop
- Zenker's paralysis