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Differential
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abdominal distention

abdominal protrusion

abducens nerve paralysis, bilateral

abscess, brainstem

abscess, intracerebral

acute ataxia of childhood

acute cerebellar ataxia

adult polyglucosan body disease

advances in neurology

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, abdominal aortic

aneurysm, aortic arch

angiography, cerebral

angiography, posterior fossa

animal exposure

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

aorta, abdominal

aorta, abnormal

arterial dissection

arterial dissection, carotid

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, ruptured

arterial dissection, vertebral

ascending paralysis

ataxia, acute onset

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

axonal degeneration

bacterial infection

bacterial infection, CNS

basal ganglia, lesion of

basilar artery migraine

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

bladder dysfunction

blindness, monocular

blindness, transient

bone marrow biopsy

brachial plexus neuropathy

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy, progressive

carcinoma of bladder

carotid artery disease

CAT scan, abdomen

CAT scan, abnormal

cat-scratch disease

cauda equina, enhancement

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, genetic

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

choreoathetosis

chorioretinitis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

conduction block

contractures, joint

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

degenerative diseases of CNS

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

disability, neurological

disease modifying agents

distal muscle atrophy

doll's head maneuver

Dravet syndrome

drug induced neurologic disorders in children

dysdiadochokinesia

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

enterovirus infection of CNS

epileptic encephalopathy

Epstein-Barr virus

executive dysfunction

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, recurrent

failure to thrive

FARS2 deficiency

fine motor function, impaired

Fisher's syndrome

flaccid paralysis

food-borne infection

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

glutamic acid decarboxylase, antibody

glycogen storage disease

gram negative rod

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

hand-foot-mouth disease

Hartnup's disease

headache, occipital

headache, severe

headache, sudden onset of

headache, throbbing

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

herpes, genital

heterophile antibody test

histochemistry of muscle

Hodgkin's disease

hyperosmolality

hypertension, cerebrovascular disease with

hyperthyroidism

hypokalemic periodic paralysis

hypotension, systemic

iatrogenic neurologic disorders

immunization, neurologic complications with

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

lactic acidemia

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

lymphadenopathy

lymphadenopathy, paraaortic

lysosomal storage disease

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

mental status, abnormal

migraine, children

migraine, visual symptoms in

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, brachial plexus

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, spinal cord

MRI, susceptibility weighted

multiple sclerosis

muscle atrophy, progressive

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

mycobacterial infection

mycobacterium bovis

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myeloneuropathy

myelopathy, chronic progressive

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, vacuolar

myositis, ocular

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

nerve conduction studies, motor

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuromuscular disease, electrodiagnosis of

neuronal intranuclear inclusion disease

neuropathy, acute

neuropathy, motor

neuropathy, motor, multifocal

Niemann-Pick disease

NMDA antagonists

nystagmus, monocular

nystagmus, rotary

old age, neurology of

ophelia syndrome

ophthalmoplegia

oral ulcerations

osmotic demyelination syndrome

otitis, neurologic complications with

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis

periodic paralysis, thyrotoxic

pleocytosis of cerebrospinal fluid

poison, mercury

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

post infectious cerebellar ataxia

potassium channel antibodies

practice guidelines

precipitating factors

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

psychotic behavior

ptosis, bilateral

pulmonary nodules

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

quadriplegia, transient

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

Refsum's disease

regional enteritis

renal tubular acidosis

respiratory failure

respiratory tract infection

retina, abnormal

riboflavin transporter deficiency

salivation, excessive

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory loss, band distribution

serologic testing

serologic testing, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

sodium channel dysfunction

solitary scerlosis

spastic diplegia

speech, loss of

spinal cord, cervical

standing difficulty

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

suspended sensory loss

systemic illness

tandem gait, ataxic

temporal lobe, atrophy

tongue, fasciculations of

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

ulcerative colitis

urinary incontinence

urinary retention

vertebral-basilar insufficiency

viral infection

viral infection, CNS

visual acuity, decreased

visual impairment

visual loss, sudden-unilateral

visual loss, transient

walking, difficulty with

weakness, acute

weakness, episodic

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease

whole genome sequencing

wide based gait

Showing articles 500 to 550 of 8215 << Previous Next >>

Vagus Nerve Stimulation for Medication-Resistant Generalized Epilepsy
Neurol 52:1510-1512, Labar,D.,et al, 1999

Left Vagal nerve Stimulation in Children with Medically Refractory epilepsy
J Pediatr 134:563-566, 532, Murphy,J.V.&Pediatric VNS Study Group, 1999

Vagal Nerve Stimulation in epileptic Encephalopathies
Pediatrics 103:778-782, 821, Parker,A.P.J.,et al, 1999

Intractable Epilepsy
Lancet 353:1238, Shuper,A.,et al, 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Diffusion-Weighted MRI Characterized the Ischemic Lesion in Transient Global Amnesia
Neurol 51:901-903, Ay,H.,et al, 1998

Headache Characteristics in Subarachnoid Haemorrhage and Benign Thunderclap headache
JNNP 65:791-793, Linn,F.H.H.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Childhood Onset of Benign Positional Vertigo
Neurol 50:1494-1495, Baloh,R.W.&Honrubia,V., 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,et al, 1998

Brain Tumors in the Elderly
Arch Neurol 55:922-928, Lowry,J.K.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

A Comparison of Rectal Diazepam Gell and Placebo for Acute Repetitive Seizures
NEJM 338:1869-1875, 19161998., Dreifuss,F.E.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

I. V. t-PA for Acute Ischemic Stroke, Feasibility, Safety & Efficacy in the First Year of Clinical Practice
Stroke 29:18-22, Chiu,D.,et al, 1998

Factors Determining the Therapeutic Window for Stroke
Neurol 50:599-603, Zivin,J.A., 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Incidence of Status Epilepticus in Rochester, Minnesota, 1965-1984
Neurol 50:735-741, Hesdorffer,D.C.,et al, 1998

Delayed Hospital Arrival for Acute Stroke:The Minnesota Stroke Survey
Ann Int Med 129:190-196, Smith,M.A.,et al, 1998

Critical Factors Determining Access to Acute Stroke Care
Neurol 51:427-432, Menon,S.C.,et al, 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

If First AED Fails to Control Child's Epilepsy, What Are the Chances of Success with Next Drug
J Pediatr 131:821-824, 7941997., Camfield,P.R.,et al, 1997

Epilepsy in Childhood
BMJ 315:924-930, Neville,B.G.R., 1997

Total Quality Improvement Method for Reduct of Delays Between ER Dept Adm & Trtm of Acute Ischemic Stroke
Arch Neurol 54:1466-1474, Tilley,B.C.,et al, 1997

Predictors of Intracranial Path Findings in Pts Who Seek ER Care Because of Headache
Arch Neurol 54:1506-1509, Ramirez-Lassepas,M.,et al, 1997

Why Would You Remove Half a Brain? Outcome of 58 Children after Hemispherectomy-Johns Hopkins 1968-96
Pediatrics 100:163-171, Vining,E.P.G.,et al, 1997

Risk Factors for Status Epilepticus in Children with Symptomatic Epilepsy
Neurol 49:533-537, Novak,G.,et al, 1997

Intracranial Aneurysm Rupture Presenting as Delayed Stroke Secondary to Cerebral Vasospasm
Stroke 28:2078-2080, Nussbaum,E.S.,et al, 1997

A Blinding Headache
Lancet 350:182, Embil,J.J.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Stroke Patients'Knowledge of Stroke
Stroke 28:912-915, Williams,L.S.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Variables Associated with Hospital Arrival Time After Stroke
Stroke 28:537-542, Azzimondi,G.,et al, 1997

Seizures and Epilepsy in the Elderly
Arch Int Med 157:605-617, Thomas,R.J., 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Showing articles 500 to 550 of 8215 << Previous Next >>