Neudle.com: neuronal migration disorder

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abdominal cramps

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

acetylcholine receptor

acetylcholine receptor antibody

acetylcholine receptor antibody, ganglionic

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acute disseminated encephalomyelitis

adenylate kinase 5 autoantibodies

adolescent medicine

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agalsidase alfa

agenesis of corpus callosum

agnosia, visual

agranulocytosis

Aicardi's syndrome

alien hand syndrome

alpha glucosidase

alpha-fetoprotein

alpha-synuclein

altered states of consciousness

alternating rapid movement

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

aminoacidopathies

amnesia, anterograde

amnestic syndrome

AMPA receptor antibodies

amphiphysin antibodies

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anesthesia, general

anesthesia, local

angiitis, isolated of CNS

angina pectoris

angiotensin-converting enzyme

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti basal ganglia antibodies

anti GQ1b IgG antibody

anti Hu antibody

anti Jo1 antibody

anti Ku antibody

anti La antibody

anti MAG antibodies

anti Mi2 antibody

anti pan-neurofascin

anti Ri antibody

anti Ro antibody

anti signal recognition particle antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticholinesterase

anticoagulant, treatment

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

anti-dopamine 2 receptor antibody

antiendomysial antibodies

antiganglioside antibodies

antineutrophil cytoplasmic autoantibodies

antiphospholipid antibodies

antiphospholipid antibody syndrome

antiretinal antibodies

antiribosomal P antibody

antistreptolysin titer

antistriational muscle antibody

antithyroid antibodies

antiviral agents

aphasia, progressive

aphasia, progressive, primary

apnea, primary central

apolipoprotein E

apraxia of eye movements

area postrema syndrome

arm swing, reduced

Arnold Chiari malformation

arrhythmia, cardiac

arteritis, temporal

arthrogryposis multiplex

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

atidarsagene autotemcel

attention deficit disorder with hyperactivity

autoantibodies, SOX1

autoantibody prevalence in epilepsy score

autoimmune autonomic ganglionopathy

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autoimmune GFAP astrocytopathy

automatic behavior

automobile accidents

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

axonal degeneration

axonal spheroid

B 12 deficiency

bacterial infection

Balint's syndrome

ballismus, bilateral

Barkhof MR criteria for MS

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bell's phenomenon

Bickerstaff's brainstem encephalitis

bilateral periventricular nodular heterotopia

biologic markers

bladder dysfunction

blindness, sudden

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brachial neuritis

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain natriuretic peptide

brain transplantation

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, surface lesion of, hyperintense

bulbar dysfunction

bulbar palsy, childhood

bulbar palsy, progressive

burning feet, differential diagnosis of

burning paresthesia

burst suppression pattern, electroencephalogram

calcification, intracranial

calcium antagonist

calcium channel dysfunction

campylobacter infection

Canavan's disease

cancer associated myopathy

cancer, unknown origin

carbon monoxide poisoning

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of pancreas

carcinoma of testis

carcinoma of unknown origin

carcinoma of uterus

carotid artery atherosclerosis

carotid artery atherosclerosis, pathogenesis

carotid artery disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, adult

central core disease

central hypoventilation

central nervous system, infection of

central vein sign

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral dominance

cerebral edema, vasogenic

cerebral embolism

cerebral folate deficiency syndrome

cerebral hemisphere left-right asymmetry

cerebral infarction

cerebral ischemia

cerebral vasculature

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, childhood

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal bands, absent

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, intrauterine

cerebrovascular accident, mimics

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, pathophysiology

cerebrovascular accident, prevention of

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, time of presentation

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cesarean section

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

chloride channel dysfunction

chorea, autoimmune

chorea, causes of

chorea, familial

chorea, Sydenham's

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic graft versus host disease

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic traumatic encephalopathy

Churg-Strauss syndrome

cigarette smoking

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

cogwheel rigidty

cold hands sign

cold intolerance

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

coma, medically induced

common variable immunodeficiency

compression fracture

computers, neurologic diagnosis and

concentration, impaired

conduction block

confusional state, acute

congenital birth defects

congenital malformation

congenital malformation, non CNS

congestive heart failure

conjugate gaze, forced

conjunctival biopsy

conjunctival injection

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

Coombs test, positive

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corneal reflex, abnormal

corneal ulceration

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical dysplasia, focal

cortical ribbon sign

cortical-basal ganglionic degeneration

cost effectiveness

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

creatinine, elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

cyclophosphamide

cyst, porencephalic

cytoarchitectonics, cerebral cortex

cytochrome c oxidase

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, autoimmune

dementia, cerebrovascular disease causing

dementia, childhood

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, subcortical

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dichlorphenamide

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digits, abnormal

diplopia, transient

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

dopamine receptor, D2

dopaminergic dysfunction

double-cortex syndrome

down-beat nystagmus

DPPX, antibodies

DPPX, antibodies, encephalitis

dropped head syndrome

drug induced neurologic disorders

drug interactions

dura, thickened

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dysostosis multiplex

dysplasia of C.N.S.

dysthyroid ocularmyopathy

dystonia, children

dystonia, focal

dystonic lipidosis

efgartigimod alfa

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, activation procedures

electroencephalogram, triphasic delta waves

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

electronystagmography

electroretinograph

emergencies, neurologic

emotional lability

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, episodic

encephalitis, etiology

encephalitis, focal

encephalitis, Japanese

encephalitis, lobar

encephalitis, paraneoplastic

encephalitis, Rasmussen's

encephalitis, recurrent

encephalitis, unknown etiology

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, autoimmune

encephalomyelitis, parainfectious

encephalomyelitis, paraneoplastic

encephalomyelitis, postinfectious

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, post traumatic

encephalopathy, progressive

endocarditis, marantic

enzyme treatment

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

esophageal manometry

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exercise-related muscle strength increase

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

Fabry's disease

face, contractions

face, numbness of

facial anomalies

facial appearance, abnormal

facial asymmetry

facial nerve palsy

facial nerve, lesion of

facial weakness, bilateral

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

Farber's disease

Fazio-Londe's disease

feeding disorder

fetal alcohol syndrome

fever of unknown origin

fibrinolytic agents

fine motor function, impaired

finger flexor weakness

finger weakness

fingerprint bodies

Fisher's syndrome

flail arm syndrome

flu-like illness

folic acid deficiency

football neurologic injuries

fourth ventricle, floor

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

fundus, abnormality of

GALOP syndromes

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal disease, neurologic complications

Gaucher's disease

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

glare, light-induced

gliadin antibodies

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1 deficiency syndrome

glutamic acid decarboxylase

glutamic acid decarboxylase, antibody

glutaric acidemia

gluten sensitivity

gluten-free diet

glycine receptor antibodies

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

gonadotropin-releasing hormone

granular osmiphilic material

granulomatosis with polyangiitis

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, recurrent

Guillain Barre syndrome, variant forms of

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, olfactory

hallucination, visual

head circumference

head injury, repetitive

headache, episodic

health insurance

hearing loss, bilateral

heat intolerance

heavy metal intoxication

heel-knee-shin test

hemifacial spasm

hemihypertrophy, congenital

hemimyoclonic jerks

hemispherectomy

hemorrhagic diathesis

Henoch-Schonlein purpura

heparin, low-molecular-weight

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, recurrent

herpes simplex virus

hexosaminidase-A

hexosaminidase-A and B

high arched feet

highly active antiretroviral therapy

hippocampal atrophy

hippocampus, hyperintense

HMGcoA reductase inhibitors

hockey stick sign

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

H-reflex testing

H-sign, spinal cord

human immunodeficiency virus type 1

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's chorea, genetic counselling

Hurler's syndrome

hydrocephalus, acute

hydrocephalus, non-communicating(obstructive)

hypergammaglobulinemia

hyperkalemic periodic paralysis

hyperthyroidism

hypoglycorrhachia

hypokalemic periodic paralysis

hypomelanosis of Ito

hypomyelination

hyponatremia with cerebral disorders

hypopigmentation of skin

hypotension, systemic

hypothalamus, damage to

hypothalamus, lesion of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic inflammatory myopathy

imbalance, postural

immune checkpoint inhibitors

immune reconstitution inflammatory syndrome

immune-related adverse events

immunodeficiency

immunofluorescence

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infantile bilateral striatal necrosis

infantile spasm

infection, recurrent

initiative, lack of

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

interstitial pulmonary fibrosis

intestinal biopsy

intracerebral hemorrhage

intrathecal medication

intrauterine growth retardation

intrauterine infection

intrinsic hand muscles, wasting of

Isaacs syndrome

ischemic penumbra

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw claudication

juvenile idiopathic inflammatory myopathy

Kallmann's syndrome

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

klippel feil syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

labor, complicated

lactic acidemia

Lafora's disease

language disorder in adults

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa, drug interactions with and side effects of

learning disability, in children

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

Lesch-Nyhan syndrome

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness

level of consciousness, decreased

Lewy body disease, diffuse

libido, decreased

lid abnormalities

lid closure, weakness of

life expectancy

life support, withdrawal of

limb-girdle weakness

limbic encephalitis

lipid storage disorder of CNS

lipoprotein receptor-related protein 4

livedo reticularis

liver function enzymes

loss of sympathy

lupus anticoagulant

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnesium sulfate

magnetic susceptibility

malformation, CNS, congenital

malformation, vascular

malignancy screen

malignancy, occult

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

Marcus Gunn pupil

Marinesco-Sjogren syndrome

Mary Walker phenomenon

masseter muscle wasting

medial longitudinal fasciculus(MLF)

mediastinum, mass of

mediastinum, widening

medulla oblongata

medulla oblongata, lesion of

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, chronic

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental retardation, familial

mental status, abnormal

mesial temporal lobe

mesial temporal sclerosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

mGlu R5 antibodies

microangiopathy, brain

microangiopathy, spinal cord

microhemorrhage, intracerebral

microscopic polyangiitis

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

Montreal cognitive assessment

Morvan's fibrillary chorea

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, psychogenic

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, contrast enhanced, cloud-like

MRI, cortical enhancement

MRI, cranial nerves

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, optic nerve

MRI, paramagnetic effect

MRI, ring sign, open

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple organ failure

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple sclerosis, tumefactive

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle diseases, characteristics of

muscle spasm, face

muscle stiffness

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Duchenne

MuSK antibodies

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, cold test for

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, drug induced

myasthenia gravis, drug resistant

myasthenia gravis, etiology of

myasthenia gravis, exacerbation

myasthenia gravis, late-onset

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, paraneoplastic

myasthenia gravis, passive transfer of

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, receptor site in

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenia gravis, unmasked

myasthenia gravis, variants

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, etiology

myelination of nervous system

myelitis, autoimmune

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, idiopathic

myelitis, transverse, recurrent

myeloneuropathy

myelopathy, ischemic

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, paraneoplastic

myocardial infarction

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, orthostatic

myoclonus, segmental

myokymia, facial

myopathy inflammatory, classification

myopathy, autoimmune

myopathy, carcinomatous

myopathy, drug-induced

myopathy, inclusion body

myopathy, inflammatory

myopathy, inflammatory, classification

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, quadriceps

myopathy, vacuolar

myositis specific autoantibody

myositis, juvenile

myotonia congenita

myotonia dystrophica

N-acetyl-L-aspartic acid

N-acetyl-L-leucine

nasal bridge, wide

Native Americans

nausea and vomiting

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neural tube defect

neuraminidase deficiency

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neuroinfectious diseases

neurolipidosis IV

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, multiple

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic history

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica (Devic's disease), screening

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal cell death

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathic pain scale

neuropathology, brain

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, chronic

neuropathy, cryoglobulinemic

neuropathy, demyelinating

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, work up for

neuroprotective agents

neurotransmitter

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

NMDA antagonist, late onset

NMDA antagonists

noncommunicative

non-dominant hemisphere

novel cell-membrane antigens

numbness, ascending

numbness, extremity

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obsessive-compulsive disorder

obstetric complications

ocular motility, disorders of

oculocephalic reflex

oculogyric crisis

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

operculum syndrome

operculum syndrome, bilateral

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic chiasm, lesion of

optic disc edema

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis, alternating

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

optokinetic nystagmus, abnormal

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

pachymeningitis, cranial

pain, abdominal

pain, neuropathic

pain, sensation

palatal myoclonus

palliative care

palmomental response

paralysis, acute

paralysis, acute areflexic

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraproteinemia

paraspinal muscle

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, postencephalitic

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland neoplasm

parotid gland swelling

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

PAS positive material in the brain

pathologic reflex

patient in waiting

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric neurology

penguin silhouette sign

peptides, brain

periaqueductal lesion

perineural invasion

perineuritis, optic

periodic paralysis

perioral numbness

peripheral blood smear

peripheral nerve, lesion of

perivascular enhancement

peroxisomal disease

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

photosensitivity, eye

photosensitivity, skin

physician assisted suicide

pigmentary retinopathy

platelet inhibiting drugs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

Pompe's disease of glycogen storage

Pompe's disease, infantile

pons, lesion of

pontocerebellar atrophy

positional head-hanging test

post herpes simplex encephalitis immune-mediated relapse

post infectious polyneuropathy

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

potassium channel dysfunction

Potter syndrome

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary lateral sclerosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis, unilateral

proximal muscle atrophy

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis, acute

psychosis, childhood

psychotic behavior

ptosis, asymmetric

ptosis, bilateral

ptosis, unilateral

pulmonary infection

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, light reflex of

pupil, light reflex, abnormal

pupil, light reflex, reversed

pure autonomic failure

purkinje cell cytoplastic autoantibody

Purkinje cell surface antibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriceps weakness

quality of life

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

radiation therapy, total body

radiation, ionizing

radiation, ionizing, intrauterine

radioimmunoassay

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

refractive errors

Refsum's disease

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal tubular acidosis

renal vein thrombosis

repetitive nerve stimulation

respirations in CNS disease

respiratory failure

respiratory tract infection

retina, abnormal

retinal arteriole attenuation

retinal degeneration

retinitis pigmentosa

reversal of sleep wake cycle

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

rigidity, axial

rippling muscle disease

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

Sandhoff's disease

sarcoidosis, CNS

scalp tenderness

Schmidt syndrome

scoliosis, neurologic association with

scotoma, central

scotoma, paracentral-homonymous

sea-blue histiocytes

sedimentation rate, elevated

seizure, adult onset

seizure, children

seizure, diagnosis of

seizure, drug resistance

seizure, dystonic

seizure, equivalents

seizure, etiology of

seizure, familial

seizure, intractable

seizure, intractable, treatment of

seizure, laughing as manifestation

seizure, medication failure

seizure, neonatal

seizure, paradoxical

seizure, precipitating factors

seizure, prevalence of

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, surgical treatment of

seizure, treatment of

seizure, unknown origin

seizure, workup of

semantic dementia

sensorineural hearing loss

sensory loss, asymmetric

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

serum tumor markers

sex reassignment surgery

sexual behavior, disorder of

sick sinus syndrome

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea, obstructive

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel vasculitis

sodium channel dysfunction

sodium-glucoe cotransporter-2 inhibitors

spastic diplegia

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar degeneration

splenium of corpus callosum

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

status epilepticus

status epilepticus, intractable

status epilepticus, nonconvulsive

stem cell transplantation

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stiff man syndrome, variant

stimulant drugs

storage disease of CNS

streptococcal infection

streptococcus pyogens

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stroke disability scale

stroke, progression of

strokelike episodes

Sturge-Weber syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subthalamic nucleus

sudden infant death syndrome

sulcal effacement

superior cerebellar peduncle

survival motor neuron gene

sweating, abnormality of

symmetric brain lesions

synucleinopathy

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporal lobe, status

temporal lobectomy

tensilon test, false negative

tensilon test, false positive

tensilon test, paradoxical

teratogenic drugs

teratoma, ovarian

testicular germinoma

testicular teratoma

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thymic hyperplasia

thymus and neuromuscular function

thyroglobulin antibodies

thyroid function tests

thyroid peroxidase antibodies

thyrotropin receptor

tissue plasminogen activator, intravenous

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

tonic foot response

toxic encephalopathy

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

treatment delay

treatment of neurologic disorder

treatment, empirical

tremor, cerebellar

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

trichopoliodystrophy

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

tumefactive lesion

twitching, face

ulnar neuropathy

ultrasonography

ultrasonography, head, fetus-neonate

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

upright-tilt test

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary retention

urinary sulfatidase excretion

urine test for metabolic disorders

Usher's syndrome

varicella zoster virus

ventricular enlargement

vertebral anomalies

vertebral-basilar insufficiency

vestibular function, tests of

violent behavior

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visual symptoms

vocal cord paralysis

voice, abnormality of

vomiting, intractable

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

water channel antibodies

weakness, end of day

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

West Nile fever

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole body imaging

wide based gait

Wolfram syndrome

word-finding difficulty

X-linked bulbospinal neuronopathy

X-linked lissencephaly

x-linked mental retardation

Showing articles 550 to 600 of 17414 << Previous Next >>

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Late Onset Globoid Cell Leukodystrophy
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Myasthenia Gravis in Mothers and Their Newborns
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NEurologic Complications of Nonneuronopathic Gaucher's Disease
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Wegener's Granulomatosis Mimicking Temporal Arteritis
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The Bioloigcal Basis for the Treatment of Acute Stroke
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Tissue Plasminogen Activator Plus Glutamate Antagonist Improves Outcome after Embolic Stroke
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Neurodegenerative Diseases of Childhood:MR and CT Evaluation
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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Autoantibodies and Rheumatic Disorders in a Neurology Inpatient Population:A Prospective Study
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Thyroid-Associated Eye Disease:Clinical Management
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The Spectrum of Lissencephaly:Report of Ten Patients Analyzed by Magnetic Resonance Imaging
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N-Methyl-D-Aspartate Antagonists in the Treatment of Parkinson's Disease
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Immunosuppressive Treatment in Multifocal Motor Neuropathy
Ann Neurol 30:397-401, Feldman,E.L.,et al, 1991

MRI in the Diagnosis of Heterotopic Gray Matter, Report of Three Cases First Discovered in Adulthood
Neuroradiology 33:527-528, Zisch,R.&Artmann,W., 1991

Focal Neuronal Migration Disorders and Intractable partial Epilepsy:A Study of 30 Patients
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Focal Neuronal Migration Disorders and Intractable Partial Epilepsy:Results of Surgical Treatment
Ann Neurol 30:750-757, Palmini,A.,et al, 1991

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Diagnostic Value of Anti-Neuronal Antibodies for Paraneoplastic Disorders of the Nervous System
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The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Epilepsy and Disorders of Neuronal Migration
Editorial, Lancet 336:10351990., , 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

High-Intensity Basal Ganglia Lesions on T1-Weighted MR Images in Neurofibromatosis
AJR 154:369-373, Mirowitz,S.A.,et al, 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
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Progress in Tuberous Sclerosis
Editorial, Lancet 336:598-5991990., , 1990

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
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Autoantibodies to Gaba-Ergic Neurons & Pancreatic Beta Cells in Stiff-Man Syndrome
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The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Autoantibody Synthesis in the Central Nervous System of Patients with Paraneoplastic Syndromes
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Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
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Magnetic Resonance Imaging and Neurobehavioral Correlates in Schizencephaly
Arch Neurol 47:911-916, Aniskiewicz,A.S.,et al, 1990

Antineural Autoantibodies in Patients with Paraneoplastic Cerebellar Degeneration
Arch Neurol 46:1225-1229, Tsukamoto,T.,et al, 1989

Anticerebellar Antibodies in Neurologically Normal Patients with Ovarian Neoplasm
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The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
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Sleep Abnormalities in Progressive Supranuclear Palsy
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Neurologic Complications in Long-Standing Nephropathic Cystinosis
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Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
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Bilateral Opercular Polymicrogyria
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Bilateral Central Macrogyria:Epilepsy, Pseudobulbar Palsy, and Mental Retardation-A Migration Disorder
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Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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Nervous System Involvement in Fabry's Disease:Clinicopath & Biochemical Correlation
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Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Showing articles 550 to 600 of 17414 << Previous Next >>