Neudle.com: episodic ataxia

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Differential
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abdominal distention

abdominal migraine

abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acute cerebellar ataxia

acute disseminated encephalomyelitis

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agranulocytosis

alcohol intolerance

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

Alexanders disease

Alexanders disease, adult onset

alkalosis, respiratory

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

amaurosis fugax

aminoacidopathies

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

aneurysm, vertebral basilar system

Angelman syndrome

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, vertebral artery

angiotensin-converting enzyme

animal exposure

anti GQ1b IgG antibody

anti MAG antibodies

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

anticonvulsants, untoward effects of

antiendomysial antibodies

antithyroid antibodies

antiviral agents

apnea, primary central

arm swing, reduced

arteritis, temporal

arylsulfatase A

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune GFAP astrocytopathy

automobile accidents

autonomic dysfunction

B 12 deficiency

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign positional vertigo

Binswanger disease

biological warfare

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blindness, monocular

blindness, transient

blood dyscrasias, neurologic findings with

bone demineralization

bone marrow biopsy

bone marrow transplantation

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brain scan, abnormal

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

brucellosis, nervous system involvement with

burning paresthesia

calcification, intracranial

calcification, periventricular

calcium antagonist

calcium channel dysfunction

carbamazepine, toxicity

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, contrast enhanced, subepend.

cat-scratch disease

caudate nucleus, atrophy

celiac disease, adult

central core disease

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral folate deficiency syndrome

cerebral infarction

cerebral infarction, subcortical

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemical weapons

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chloride channel dysfunction

chorea, familial

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

ciguatera poisoning

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10 deficiency

cognitive delay

cogwheel rigidty

collagen vascular disease

color vision, impaired

concentration, impaired

congenital infection, CNS

congenital infection, viral

congenital malformation

conjunctival biopsy

contractures, joint

conversion reaction

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

cortical blindness

cortical ribbon sign

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

Cushing's syndrome

cyclic vomiting

cyclic vomiting syndrome

cyst, arachnoid

cyst, arachnoid, posterior fossa

cyst, porencephalic

cytomegalovirus infection

cytosine arabinoside

deafness, sudden

deafness, unilateral

decontamination

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, differential diagnosis of

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatoglyphics

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis dementia

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

digital subtraction angiography

disability, neurological

disease modifying agents

distal muscle atrophy

diurnal variation

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

Dravet syndrome

dropped head syndrome

drug induced neurologic disorders

drug induced neurologic disorders in children

drug withdrawal

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia, psychogenic

eating disorder

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalitis, viral-causes of

encephalomyopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extinction on double simultaneous stimulation

eye movement, disorders of

Fabry's disease

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

FARS2 deficiency

feeding disorder

fever, recurrent

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

fistula, perilymphatic

flu-like illness

fluorescene in situ hybridization

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

Friedreich's ataxia

frontal bossing

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastric partitioning

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

gaze palsy, vertical

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram negative rod

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

head circumference

head turning, neurologic complications with

headache, bifrontal

headache, elderly

headache, episodic

headache, occipital

headache, progressive

headache, recurrent

headache, severe

heavy metal intoxication

hemianopia, homonymous

hemimyoclonic jerks

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemosiderosis of CNS, superficial

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis, differential diagnosis of

herpes zoster, disseminated

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus, normal pressure

hydrocephalus, treatment of

hydroxyglutaric aciduria

hyperadrenalism

hyperhomocysteinemia

hyperinsulinism

hyperparathyroidism

hyperphosphatasia

hyperthyroidism

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hyperventilation

hypocalcemia, causes of

hypofibrinogenemia

hypoglycorrhachia

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immunocompetent

immunologic disease

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

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

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

industrial neurologic disorders

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial infection

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw claudication

judgement, impaired

Kearns-Sayre syndrome

keratoconjunctivitis

Korsakoff's psychosis

lactic acidemia

lacunar infarction

Lafora's disease

language disorders in children

laryngismus stridulus

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

lead and the nervous system

lead line, gingival

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

long bone lesion

lymphadenopathy

lymphocytic choriomeningitis

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

macular degeneration

malabsorption syndrome

malaria, cerebral

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

Marchiafava-Bignami disease

medulla oblongata, lesion of

melanoma, malignant

Melkersson's syndrome

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, elderly

meningitis, fungal

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, recurrent

meningitis, syphilitic

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

meralgia paresthetica

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acidemia

microangiopathy, brain

microglial nodules

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, equivalents

migraine, hemiplegic

migraine, visual symptoms in

Minamata disease

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy multiplex

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, angiography

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, curvilinear peppering enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, nodular enhancement

mucopolysaccharidoses

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenic syndrome

mycoplasma pneumoniae

myelopathy, chronic progressive

myeloradiculitis

myoclonic ataxia

myoclonic jerks

myoclonus, epilepsy

myopathy, genetic

myopathy, metabolic

myopathy, mitochondrial

myopathy, vacuolar

myositis, ocular

myotonia congenita

myxedema, neurologic manifestations of

N-acetylcysteine

nasal septum, perforation of

nausea and vomiting

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary of CNS

nephrotic syndrome

neuraminidase deficiency

neuroendocrinology

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromuscular disease, electrodiagnosis of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

neurotoxicity, acute

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

NMDA antagonists

nutritional deficiency

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

ocular motility, disorders of

ocular myopathy

oculodentodigital dysplasia

oculomasticatory myorhythmia

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic neuritis, children

optic neuropathy

optic neuropathy, ischemic

optokinetic nystagmus, abnormal

organ transplantation

orthostatic hypotension

otitis, neurologic complications with

pain, abdominal

pain, testicular

palatal myoclonus

paralysis, acute areflexic

paramyotonia congenita

paraparesis, familial spastic

paraparesis, spastic

parasitic infection

parathyroid adenoma

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

PAS positive material in the brain

pathologic reflex

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

perivascular enhancement

perivascular inflammation

peroxisomal disease

Persistent postural-perceptual dizziness

personality change

personality disorder

phenylketonuria

pheochromocytoma

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poison, organophosphate

polymerase chain reaction

polyneuropathy, chronic relapsing

pons, lesion of

pontocerebellar atrophy

post transplant lymphoproliferative disease

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary episodic ataxia

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive supranuclear palsy

protozoan infection

pseudobulbar palsy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pupil, abnormality in neurologic disorders

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia, transient

radiation therapy, CNS treatment and complications with

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

regional enteritis

relapsing polychondritis

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal transplantation

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal degeneration

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

root lesion, nerve

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, differential diagnosis of

seizure, drug-induced

seizure, familial

seizure, febrile

seizure, hysterical

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serotonin norepinephrine reuptake inhibitors

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

sodium channel dysfunction

spastic diplegia

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 6

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

spongy degeneration of brain

status epilepticus

status tetanicus

stereotyped behavior

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

subdural hematoma

substantia nigra

superior cerebellar artery infarction

superior cerebellar peduncle

supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, wide-spaced

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular biopsy

tetany, normocalcemic

thalamus, lesion of

thiamine deficiency

third nerve palsy

thrombocytopenia

thrombophlebitis

tongue, enlarged

tongue, protrusion of

toxic encephalopathy

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, psychogenic

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

triphenyltin intoxication

Trousseau's sign

tuberculosis, miliary

ulcerative colitis

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

upgaze, sustained

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

Usher's syndrome

vaccination, neurologic complications with

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

vasospasm, cerebral

Venereal Disease Research Laboratory test

venous thrombosis, non-cerebral

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, treatment of

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

Virchow-Robin spaces, dilated

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-unilateral

visual loss, transient

visuospatial disturbance

vitamin D deficiency

vitamin deficiency

vitamin E deficiency

vitreous opacities

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

von Bonsdorff's sign

walking, difficulty with

weakness, acute

weakness, episodic

weakness, functional

weakness, generalized

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

Whipple's disease

white matter disease

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolfram syndrome

Showing articles 2700 to 2750 of 4569 << Previous Next >>

Risk of Intracranial Hemorrhage & Adverse Outcomes-Cocaine Expose in 323 Very Low Birth Wt Infants
J Pediatr 122:438-445, Dusick,A.M.,et al, 1993

Cardiac Anomalies in Ataxia-Telangiectasia
Am J Dis Child 147:20-21, Bastianon,V.,et al, 1993

Human Walking and Higher-Level Gait Disorders, Particularly in the Elderly
Neurol 43:268-279, Nutt,J.G.,et al, 1993

Acute Renal Failure Resulting from Intravenous Immunoglobulin Therapy
Arch Neurol 50:137-139, 1351993., Tan,E.,et al, 1993

Clinicopath Conf
Subacute Bacterial Endocarditis with Multiple Cerebral Emboli and Mycotic Aneurysm, Case 10-1993, NE, M 8:717-725,1993., 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
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Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
Lancet 341:595-596, Spitzer,E.D.,et al, 1993

Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993

Rasmussen's Chronic Encephalitis in Adults
Arch Neurol 50:269-274, McLachlan,R.S.,et al, 1993

Reversible Neurologic Toxicity with Fludarabine Phosphate for Mycosis Fungiodes & Chronic Lymphocytic Leukemia
Ann Int Med 118:114-116, Cohen,R.B.,et al, 1993

Antineuronal (anti-Ri) Antibodies in a Pt with Steroid-Responsive Opsoclonus-Myoclonus
Neurol 43:207-211, Dropcho,E.J.,et al, 1993

Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
Neurol 43:36-41, Silver,K.&Andermann,F., 1993

Neuroradiological Manifestations of Focal Polymorphic Delta Activity in Children
Arch Neurol 50:181-184, Maytal,J.,et al, 1993

Magnetic Resonance Imaging
NEJM 328:708-716, 785-7911993., Edelman,R.R.&Warach,S., 1993

Electrographic Seizures in Preterm & Full-Term Neonates:Clin Corr Brain Lesions, Risk for Sequelae
Pediatrics 91:128-134, Scher,M.S.,et al, 1993

Withdrawal of Antiepileptic Medication in Children-Effects of Congit Funct Multicenter Holmfrid Study
Aldenkamp. A. P. , et al, neurol 43:41-50., , 1993

Which Child Will Have a Febrile Seizure?
Am J Dis Child 147:35-39, 141993., Bethune,P.,et al, 1993

Tonic Clonic Status Epilepticus
JNNP 56:125-134, Shorvon,S., 1993

Epilepsy Mistaken for Panic Attacks in an Adolescent Girl
BMJ 306:709-710, Laidlaw,J.D.D.&Maung-Zaw,K., 1993

Epilepsy as a Risk Factor for Submersion Injury in Children
Pediatrics 91:612-616, Biekema,D.S.,et al, 1993

Random Trial AEDs in Reducing Risk of Relapse After First Unprovoked Tonic-Clonic Seizure
First Seizure Trial Gr, Neurol 43:478-4831993., , 1993

New-Onset Seizures in an Elderly Hospitalized Population
Neurol 43:489-492, Ettinger,A.B.&Shinnar,S., 1993

Efficacy of Felbamate in Childhood Epileptic Encephalopathy (Lennox-Gestaut Syndrome)
Felbamate Study Group in Lennox-Gestaut Synd, NEJM 328:29-331993., , 1993

Epileptic Seizures after Subarachnoid Hemorrhage
Ann Neurol 33:286-291, Hasan,D.,et al, 1993

Unilateral Amnesic Stroke:Six New Cases and a Review of the Literature
Stroke 24:1033-1042, Ott,B.R.&Saver,J.L., 1993

Brief Report:Treatment of Vasospastic Amaurosis Fugax with Calcium-Channel Blockers
NEJM 329:396-398, 4261993., Winterkorn,J.M.S.,et al, 1993

Reflex Anoxic Seizures
BMJ 307:214-215, Appleton,R.E., 1993

Transient Neurologic and Ocular Manifestations in Primary Thrombocythemia
Neurol 43:1107-1110, Michiels,J.J.,et al, 1993

Idiopathic Granulomatous Angiitis of the Central Nervous System
Arch Neurol 50:925-930, Vollmer,T.L.,et al, 1993

Hemiplegic Migraine and Moyamoya Disease
Am J Dis Child 147:718-719, Bernstein,A.L., 1993

Low Incidence of Seizures in Patients with Chronic Subdural Haematoma
JNNP 56:1231-1233, Ohno,K.,et al, 1993

Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
Neurol 43:1911-1917, Chiba, A.,et al, 1993

Infantile Panthalamic Infarct with a Striking Sonographic Finding:The"Bright Thalamus"
Neuroradiology 35:92-96, Wang,H.S.&Huang,S.C., 1992

Cerebral Venous Thrombosis
Bousser, M-G & Barnett, H. J. M. , in Stroke, Pathophysiol, Diag & Manage, 2nd Ed, Churchhill Living, tone, NY, Ch 19,, 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

National General Practice Study of epilepsy (NGPSE) :Partial Seizure Patterns in a General Population
Neurol 42:1911-1917, Manford,M.,et al, 1992

Accuracy and Interobserver Reliability of Scalp Ictal EEG
Neurol 42:2279-2285, Walczak,t.S.,et al, 1992

Convulsions at Christmas
BMJ 305:1580, Kirker,S., 1992

Effect of Add-on Amantadine Therapy for Refractory Absence epilepsy
J Pediatr 121:819-821, Shahar,E.M.&Brand,N., 1992

Typical Absence Seizures in Adults:Clinical, EEG, Video-EEG Findings & Diagnostic/Syndr Consider
JNNP 55:1002-1008, Panayiotopoulos,C.P.,et al, 1992

Safety and Efficacy of Valproate and Carbamazepine in the Treatment of Complex Partial Seizures
J Epilepsy 5:149-152, So,E.L.,et al, 1992

The Best Medicine for Febrile Seizures
NEJM 327:1161-1163, Freeman,J.M., 1992

A Longitudinal Assessment of Seizure Outcome and Overall Benefit From 100 Cortectomies for Epilepsy
JNNP 55:762-767, Rougier,a.,et al, 1992

A prospective Study of Recurrent Febrile Seizures
NEJM 327:1122-1127, 11611992., Berg,A.T.,et al, 1992

Epilepsy in the First 10 Years of Life:Findings of the Child Health & Education Study
BMJ 305:857-861, Verity,C.M.,et al, 1992

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992

Central Nervous System Involvement in the Eosinophilia-Myalagia Syndrome
Arch Neurol 49:1082-1085, Lynn,J.,et al, 1992

Paraneoplastic Cerebellar Degener I A Clinical Analysis of 55 Anti-Yo Antibody-Positive Pts
Neurol 42:1931-1937, Peterson,K.,et al, 1992

The Ocular Manifestations of Multiple Sclerosis, 2, Abnormalities of Eye Movements
JNNP 55:863-868, Barnes,D.&McDonald,W.I., 1992

Risk FActors for Central Nervous System Manifest of Gastroenteritis-Associated Hemolytic-Uremic Syndrome
Pediatrics 90:616-621, Cimolai,N.,et al, 1992

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