Neudle.com: neuronal migration disorder

Differential
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abdominal cramps

abducens nerve paralysis

abducens nerve paralysis, bilateral

abiotrophy

abortion, spontaneous

acanthocytosis

acetazolamide

acetylcholine receptor

acetylcholine receptor antibody

acetylcholine receptor antibody, ganglionic

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acoustic nerve

acral sensory symptoms

acute disseminated encephalomyelitis

adenylate kinase 5 autoantibodies

Adies pupil

adolescent medicine

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

afebrile

affect, flat

agalsidase alfa

agenesis of corpus callosum

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

AMPA receptor antibodies

AMPA receptors

amphiphysin antibodies

amygdala

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

angiitis, isolated of CNS

angina pectoris

angiokeratoma

angiotensin-converting enzyme

anterior horn cell disease

anterior tibial muscle weakness

anti basal ganglia antibodies

anti GQ1b IgG antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticholinesterase

anticoagulant, treatment

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antidepressant

anti-dopamine 2 receptor antibody

antiendomysial antibodies

antiganglioside antibodies

antimetabolite

antineutrophil cytoplasmic autoantibodies

antiphospholipid antibodies

antiphospholipid antibody syndrome

antiretinal antibodies

antiribosomal P antibody

antistreptolysin titer

antistriational muscle antibody

antithyroid antibodies

aphasia, progressive, primary

apnea

apnea, primary central

apraxia of eye movements

area postrema

area postrema syndrome

areflexia

arm swing, reduced

Arnold Chiari malformation

arrhythmia, cardiac

arteritis, temporal

arthralgia

arthrogryposis multiplex

arthropathy

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

atidarsagene autotemcel

atomic bomb

attention deficit disorder with hyperactivity

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

Barkhof MR criteria for MS

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavioral disorder, acute

Behcet's syndrome

Bell's phenomenon

benzodiazepine

Bickerstaff's brainstem encephalitis

bilateral periventricular nodular heterotopia

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain natriuretic peptide

brain transplantation

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, surface lesion of, hyperintense

bulbar palsy, childhood

bulbar palsy, progressive

burning feet

burning feet, differential diagnosis of

burning hands

burning paresthesia

burst suppression pattern, electroencephalogram

CA-125

CAG repeats

calcification, intracranial

calcium antagonist

calcium channel dysfunction

campylobacter infection

Canavan's disease

cancer associated myopathy

cancer, unknown origin

cane

CAR syndrome

carbon monoxide poisoning

carcinoma of pancreas

carcinoma of testis

carcinoma of unknown origin

carcinoma of uterus

cardiomyopathy

carotid artery atherosclerosis

carotid artery atherosclerosis, pathogenesis

carotid artery disease

CAT scan, emission, abnormal

CAT scan, false negative

cataracts, congenital

catatonia

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

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral dominance

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral folate deficiency syndrome

cerebral hemisphere left-right asymmetry

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

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

children

chloride channel dysfunction

chromosomal abnormality

chronic graft versus host disease

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic traumatic encephalopathy

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

collapsin response mediator protein 5 IgG

Collier's sign

coloboma

color vision

color vision, impaired

colpocephaly

coma

coma, episodic

coma, medically induced

common variable immunodeficiency

computers, neurologic diagnosis and

concentration, impaired

conduction block

confabulation

confusion

confusional state, acute

congenital birth defects

congenital malformation

congenital malformation, non CNS

congestive heart failure

conjugate gaze, forced

conjunctival biopsy

conjunctival injection

conjunctivitis

consanguinity

constipation

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

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytoarchitectonics, cerebral cortex

degenerative diseases of CNS

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

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatomyositis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digits, abnormal

diplopia

diplopia, transient

disability rating scale, neurological

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

DNA probes

donepezil

dopa responsive dystonia

dopamine

dopamine agonist

dopamine receptor, D2

dopaminergic dysfunction

double-cortex syndrome

DPPX, antibodies, encephalitis

drooling

dropped head syndrome

drowsiness

drug abuse

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dysthyroid ocularmyopathy

electroencephalogram, abnormalities of

electroencephalogram, activation procedures

electroencephalogram, triphasic delta waves

electromyogram

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

electronystagmography

electroretinograph

ELISA

embolism

emergencies, neurologic

emotional lability

employment

encephalitis

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

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, post traumatic

encephalopathy, progressive

endocarditis, marantic

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

episodic unconsciousness

executive dysfunction

exercise intolerance

exome sequencing

extralimbic encephalitis

eye closure

eye movement, disorders of

eye movement, painful

facial appearance, abnormal

facial asymmetry

facial nerve palsy

facial nerve, lesion of

facial weakness, bilateral

faciobrachial dystonic seizure

familial hemiplegic migraine

Farber's disease

fasciculation

fatigue

Fazio-Londe's disease

fear

feeding disorder

fetal alcohol syndrome

fetal tissue

fever

fever of unknown origin

fibrillations

fibrinolytic agents

fine motor function, impaired

finger flexor weakness

folic acid deficiency

foot deformity

foot drop

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

fucosidosis

fundus, abnormality of

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

GFAP-IgG

Gilles de la Tourette syndrome

glabellar sign

glare, light-induced

gliadin antibodies

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

GluD2

GLUT1 deficiency syndrome

glutamic acid

glutamic acid decarboxylase

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycogen storage disease

glycoprotein

GM1 ganglioside

GM1 ganglioside antibodies

gonadotropin-releasing hormone

granular osmiphilic material

granulomatosis with polyangiitis

grasp reflex

Graves ophthalmopathy

grimacing

growth hormone

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

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, olfactory

hallucination, visual

head injury, repetitive

hearing loss, bilateral

heat intolerance

heavy metal intoxication

hemihypertrophy, congenital

hemimyoclonic jerks

hemiparesis

hemispherectomy

hemorrhagic diathesis

Henoch-Schonlein purpura

heparin

heparin, low-molecular-weight

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, recurrent

herpes simplex virus

heterotopia

hexosaminidase-A

hexosaminidase-A and B

hiccoughs

high arched feet

highly active antiretroviral therapy

hippocampal atrophy

hippocampus

hippocampus, hyperintense

histochemistry

histopathology

HLA

HMGcoA reductase inhibitors

hoarseness

hockey stick sign

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

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

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

Hurler's syndrome

hydrocephalus

hydrocephalus, acute

hydrocephalus, non-communicating(obstructive)

hypercapnia

hyperekplexia

hyperesthesia

hypergammaglobulinemia

hyperglycemia

hyperhidrosis

hyperkalemic periodic paralysis

hypokalemic periodic paralysis

hypomelanosis of Ito

hypomyelination

hyponatremia

hyponatremia with cerebral disorders

hypophonia

hypopigmentation of skin

hyporeflexia

hyposmia

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, lesion of

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic

idiopathic inflammatory myopathy

imbalance

imbalance, postural

immune checkpoint inhibitors

immune reconstitution inflammatory syndrome

immune-related adverse events

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

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

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incoordination

infantile bilateral striatal necrosis

intellectual deterioration

intelligence quotient

internet

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

interstitial pulmonary fibrosis

intestinal biopsy

intracerebral hemorrhage

intrathecal medication

intrauterine

intrauterine growth retardation

intrauterine infection

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

juvenile idiopathic inflammatory myopathy

Kallmann's syndrome

karyotyping

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

klippel feil syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kuru

kyphoscoliosis, neurologic causes of

language disorder in adults

lateropulsion

laughing

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

L-dopa, drug interactions with and side effects of

lead poisoning

learning disability, in children

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

Lesch-Nyhan syndrome

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness

level of consciousness, decreased

Lewy body disease, diffuse

libido, decreased

lid abnormalities

lid closure, weakness of

lid lag

lid twitch

life expectancy

life support, withdrawal of

lipid storage disorder of CNS

lipoprotein receptor-related protein 4

lissencephaly

livedo reticularis

liver disease

liver function enzymes

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lymphoma

lymphoma involving CNS

lysosomal storage disease

magnetic susceptibility

malabsorption

malformation, CNS, congenital

malformation, vascular

malignancy screen

malignancy, occult

malignant hyperpyrexia

mania

maple syrup urine disease

marche a petits pas

Marcus Gunn pupil

Marinesco-Sjogren syndrome

Mary Walker phenomenon

masked facies

masseter muscle wasting

medial longitudinal fasciculus(MLF)

mediastinum, mass of

mediastinum, widening

medulla oblongata

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningoencephalomyelitis

mental retardation

mental retardation, familial

mental status, abnormal

MERRF syndrome

mesial temporal lobe

mesial temporal sclerosis

mestinon

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

microangiopathy, brain

microangiopathy, spinal cord

microcephaly

micrognathia

microhemorrhage, intracerebral

micropthalmia

microscopic polyangiitis

midbrain

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

modafinil

molecular genetics

mongolism

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

Montreal cognitive assessment

mood change

mortality

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, FLAIR

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, muscle

MRI, negative

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, T1 weighted high signal foci

MRS

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 biopsy

muscle cramp

muscle diseases, characteristics of

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

mutism

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

myelitis, autoimmune

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, idiopathic

myelitis, transverse, recurrent

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, paraneoplastic

myocardial infarction

myoclonus, orthostatic

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

myositis specific autoantibody

N-acetyl-L-aspartic acid

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

neuroblastoma

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

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

neuromyotonia

neuronal cell death

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathic pain scale

neuropathology

neuropathology, brain

neuropathy

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

next-generation sequencing

Niemann-Pick disease

night blindness

night sweats

nigrostriatal pathway

nimodipine

nivolumab

NMDA antagonist, late onset

NMDA antagonists

NMDA receptors

noncommunicative

non-dominant hemisphere

norepinephrine

normal

NOTCH2NLC

novel cell-membrane antigens

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obsessive-compulsive disorder

obstetric complications

occipital lobe

ocular dipping

ocular flutter

ocular motility, disorders of

oculocephalic reflex

oculogyric crisis

ofatumumab

old age, neurology of

olfactory bulb

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

oopherectomy

operculum syndrome

operculum syndrome, bilateral

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic chiasm

optic chiasm, lesion of

optic disc edema

optic nerve

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis

optic neuritis, alternating

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

optokinetic nystagmus, abnormal

organ transplantation

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteopetrosis

ovarian tumor

overlap syndrome

owl's eye sign of spinal cord

pachygyria

pachymeningitis, cranial

paralysis, acute areflexic

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

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

PAS positive material in the brain

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric neurology

peek sign

penguin silhouette sign

penicillamine

peptides, brain

periaqueductal lesion

peripheral blood smear

peripheral nerve, lesion of

perivascular enhancement

peroxisomal disease

perseveration

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

pes cavus

photophobia

photosensitivity, eye

photosensitivity, skin

physician assisted suicide

Pick bodies

Pick's disease

pigmentary retinopathy

pitfalls

plasmapheresis

platelet inhibiting drugs

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

pneumonia

POEMS syndrome

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

potassium channel antibodies

potassium channel dysfunction

Potter syndrome

practice guidelines

pramipexole

precipitating factors

preclinical

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary lateral sclerosis

prion disease

PRKN gene

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, unilateral

prosopagnosia

proteinuria

proximal muscle atrophy

pruritus

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

psoriasis

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, light reflex of

pupil, light reflex, abnormal

pupil, light reflex, reversed

pupil, tonic

pure autonomic failure

Purkinje cell

purkinje cell cytoplastic autoantibody

Purkinje cell surface antibody

purpura

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

radiation therapy, total body

radiation, ionizing

radiation, ionizing, intrauterine

radiculopathy

radioimmunoassay

ragged-red fibers

rapidly progressing neurologic illness

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal tubular acidosis

renal vein thrombosis

repetitive nerve stimulation

research

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal arteriole attenuation

reversal of sleep wake cycle

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rippling muscle disease

risk factors

rituximab

Romberg's sign

saccadic eye movements

saccadic eye movements, abnormal

safety

salivation, excessive

scoliosis, neurologic association with

scotoma

scotoma, central

scotoma, paracentral-homonymous

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure

seizure, adult onset

seizure, children

seizure, diagnosis of

seizure, drug resistance

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

sensorineural hearing loss

sensory level

sensory loss

sensory loss, asymmetric

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

seropositive

serum alanine aminotransferase

serum tumor markers

sex reassignment surgery

sexual behavior, disorder of

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, dry

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

sleep apnea, obstructive

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

slit lamp examination

slurred speech

small vessel disease

small vessel vasculitis

smell

SMN1 gene

soccer

sodium channel dysfunction

sodium-glucoe cotransporter-2 inhibitors

speech disorder, childhood

speech, delayed development of

speech, loss of

sphingomyelin

spinal cord

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

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, nonconvulsive

stem cell transplantation

steroid

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

stiff man syndrome, variant

storage disease of CNS

strabismus

streptococcal infection

streptococcus pyogens

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

stroke disability scale

stroke, progression of

strokelike episodes

Sturge-Weber syndrome

stuttering

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

subarachnoid hemorrhage

sudden infant death syndrome

suicide

sulcal effacement

superior cerebellar peduncle

survival motor neuron gene

sweating

sweating, abnormality of

sweet taste

symmetric brain lesions

syphilis, neurologic complications with

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tangential

tapetoretinal degeneration

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporal lobe, status

temporal lobectomy

tensilon

tensilon test

tensilon test, false negative

tensilon test, false positive

tensilon test, paradoxical

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thymectomy

thymic hyperplasia

thymoma

thymus and neuromuscular function

thyroglobulin antibodies

thyroid function tests

thyroid peroxidase antibodies

tissue plasminogen activator, intravenous

titubation

toe walking

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

trauma

treatment delay

treatment of neurologic disorder

triangle of Guillain and Mollaret

trichopoliodystrophy

tricresylphosphate

trinucleotide repeats

ultrasonography, head, fetus-neonate

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

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

varicella zoster virus

vasculitides

vasculopathy

ventricular enlargement

vertebral anomalies

vertebral-basilar insufficiency

vertigo

vestibular function, tests of

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

voice, abnormality of

vomiting, intractable

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

water channel antibodies

weakness

weakness, end of day

weakness, fatiguable

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

West Nile fever

Western immunoblot test

white matter disease, periventricular

white matter disease, subcortical

word-finding difficulty

X-linked bulbospinal neuronopathy

X-linked lissencephaly

x-linked mental retardation

Showing articles 600 to 650 of 17414 << Previous Next >>

An Antineuronal Autoantibody in Paraneoplastic Opsoclonus
Ann Neurol 23:528-531, Budde-Steffen,C.,et al, 1988

Autoantibody Activity in Lambert-Eaton Myasthenic Syndrome
Editorial, Lancet 1:9201988., , 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Posterior Cortical Atrophy
Arch Neurol 45:789-793, Benson,D.F.,et al, 1988

Treatment of Patients with Neuropathy and Anti-MAG IgM M-Proteins
Ann Neurol 24:93-97, Nobile-Orazio,E.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Association Between Lupus Psychosis & Anti-Ribosomal P Protein Antibodies
NEJM 317:265-271, 3091987., Bonfa,E.,et al, 1987

Pituitary Growth Hormone from Human Cadavers:Neurologic Disease in Ten Recipients
Neurol 37:1211-1213, Rappaport,E.B.&Graham,D.J., 1987

MR Imaging of Heterotopic Gray Matter
J Comput Assist Tomogr 11:878-879, Hayden,S.A.,et al, 1987

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Enzyme Replacement in Nervous Tissue After Allogeneic Bone-Marrow Transplantation for Fucosidoisis in Dogs
Lancet 2:772-774, Taylor,R.M.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

Hypomelanosis of Ito, Wood's Light & Magnetic Resonance Imaging as Diagnostic Measures
Arch Neurol 43:848-850, Ardinger,H.H.&Bell,W.E., 1986

The Pathophysiology of Penicillamine-Induced Myasthenia Gravis
Ann Neurol 20:740-744, Kuncl,R.W.,et al, 1986

Developmental Dyslexia:Four Consecutive Patients with Cortical Anomalies
Ann Neurol 18:222-233, Galaburda,A.M.,et al, 1985

Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:I
Arch Neurol 42:428-459, 4271985., Geschwind,N.&Galaburda,A.M., 1985

The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases
Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985

Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging
Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985

Persistent Vegetative State, Extension of the Syndrome to Include Chronic Disorders
Arch Neurol 42:1045-1047, Walshe,T.M.&Leonard,C., 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984

A Progressive Neurologic Disorder with Supranuclear Vertical Gaze Paresis & Distinctive Bone Marrow Cells
Mayo Clin Proc 59:404-410, Yan-go,F.L.,et al, 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Familial Occurrences of Adult-Type Neuronal Ceroid Lipofuscinosis
Arch Neurol 41:1091-1094, Tobo,M.,et al, 1984

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Infantile Osteopetrosis & Neuronal Storage Disease
Neurol 33:437-441, Ambler,M.W.,et al, 1983

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
Neurol 32:1295-1299, Longstreth,W.T.Jr.,et al, 1982

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Brain Peptides
(part I & II) NEJM 304:876-885, 944-951., Krieger,D.T.&Martin,J.G., 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Cytoarchitectonic Abnormalities in Developmental Dyslexia:A Case Study
Ann Neurol 6:94-100, Galaburda,A.M.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Showing articles 600 to 650 of 17414 << Previous Next >>