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abducens nerve paralysis, bilateral

acetazolamide

aciduria

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

alkalosis, respiratory

alopecia

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

aminoacidurias

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, posterior fossa

angiotensin-converting enzyme

anti GQ1b IgG antibody

antibodies to measles

anticonvulsants

anticonvulsants, effectiveness

antithyroid antibodies

apraxia of eye movements

areflexia

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basilar artery occlusion

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency

biotinidase deficiency

blindness

blindness, monocular

blindness, transient

blood dyscrasias, neurologic findings with

bone marrow biopsy

brachycephaly

brain biopsy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

bruxism

CAG repeats

calcification, intracranial

calcium antagonist

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

CAT scan, angiography

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

cat-scratch disease

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, prognosis in

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

channelopathy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

corpus callosum, thinning

cortical ribbon sign

cough

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying

cultured skin fibroblasts

degenerative diseases of CNS

dementia, treatment of

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

digital subtraction angiography

dilantin

diplopia

disability, neurological

disease modifying agents

drug induced neurologic disorders

drug induced neurologic disorders in children

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

electron microscopy

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

endovascular therapy

enterovirus

enterovirus infection of CNS

epidemiology of neurology

epinephrine

episodic disorders

episodic neurologic deficits

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

finger nose finger test

fluorescene in situ hybridization

folic acid

folic acid deficiency

foot deformity

fornix, lesion of

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gait disorder

gait, apraxic

gait, spastic

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

GluD2

glutamic acid

glutamic acid decarboxylase, antibody

granulomatous disease

gray matter

growth hormone

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, variant forms of

hallucination

hallucination, visual

hammertoes

hand flapping

hand-foot-mouth disease

headache, sudden onset of

hearing loss

hearing problems in children

heart block

heavy metal intoxication

heel-knee-shin test

hemiparesis

hemiplegia

hemosiderosis of CNS, superficial

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

huntingtin

Huntington's chorea

hydroxyglutaric aciduria

hyperactivity

hyperintense vessel sign

hyperosmolality

hyperreflexia

hypertension

hypertension, cerebrovascular disease with

hyperventilation

hypocalcemia

hypocalcemia, causes of

hypopigmentation of skin

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunodeficiency

immunosuppression

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incoordination

industrial neurologic disorders

infection

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal medication

iris, abnormal

irritability

Jakob-Creutzfeldt disease

jaundice

Kearns-Sayre syndrome

lactic acidemia

language disorders in children

laryngismus stridulus

laughing, pathologic

lead and the nervous system

lead line, gingival

lead poisoning

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

liver disease

liver function enzymes

lysosomal storage disease

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

miglustat

migraine

migraine, children

migraine, visual symptoms in

mimics

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

monoparesis

mortality

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, high signal foci on

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

mycoplasma pneumoniae

myelinolysis, extrapontine

myopathy, mitochondrial

neonatal screening, genetic neurologic disorders

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination, focal

neurologic symptoms

neuromyotonia

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

nystagmus, hereditary

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

opsoclonus

opsoclonus-myoclonus syndrome

optic neuritis, children

optic neuropathy

optical coherence tomography

oral ulcerations

oscillopsia

osmotic demyelination syndrome

paralysis, acute areflexic

paranoia

paraparesis

paraparesis, familial spastic

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

past pointing

patent foramen ovale

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Penumbra System

personality change

pica

pigmentary retinopathy

piperazine

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polymerase chain reaction

Poretti-Boltshauser syndrome

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary episodic ataxia

progeria

prognathism

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

Purkinje cell

Purkinje cell surface antibody

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

respirations in CNS disease

respiratory failure

respiratory tract infection

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rubella encephalitis, progressive

rubeola virus

safety

salivation, excessive

seizure, differential diagnosis of

seizure, drug-induced

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serologic testing

serologic testing, false negative

seronegative

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slurred speech

smiling

sodium channel dysfunction

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuporous

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, recurrent

suck, poor

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

telangiectases

temporal lobe, lesion

tetany, normocalcemic

tongue, protrusion of

tonic spasms

topiramate

torticollis

toxins, nervous system

transient ischemic attack

transient neurologic deficit

trauma

treatment of neurologic disorder

trinucleotide repeats

urine test for metabolic disorders

urine test in toxic screen

urticaria

vaccination, neurologic complications with

vaccine

vasculopathy

vasospasm, cerebral

vertebral-basilar insufficiency

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

visual loss, transient

visual obscurations, transient

visuospatial disturbance

von Bonsdorff's sign

Von Hippel Lindau

walking, difficulty with

weakness

weakness, generalized

X-linked bulbospinal neuronopathy

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Niemann-Pick Type C Disease
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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Neuroimaging Features of Biotinidase Deficiency
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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An 8-Year-Old with Acute Onset Ataxia
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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Complex Ataxia
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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
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When MRI is a Clue in Episodic Ataxia
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A 27-year-old man with Acute-Onset Ataxia
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Extraintestinal Manifestations of Coeliac Disease
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lead
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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Heterogeneity of Coenzyme Q10 Deficiency
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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Mitochondrial DNA Polymerase-y and Human Disease
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Cerebellar Ataxia and Coenzyme Q10 Deficiency
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Showing articles 0 to 50 of 4289 Next >>