Neudle.com: ataxia acute onset

Differential
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abdominal distention

abdominal protrusion

abducens nerve paralysis, bilateral

abscess, brainstem

abscess, intracerebral

abscess, lung

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

arterial dissection, carotid

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, ruptured

arterial dissection, vertebral

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

axonal degeneration

Babinski sign

bacterial infection

bacterial infection, CNS

basal ganglia, lesion of

basilar artery migraine

Bassen-Kornzweig syndrome

brachial plexus neuropathy

bradykinesia

brain atrophy

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy

bulbar palsy, progressive

carotid artery disease

cauda equina, enhancement

CD4 counts

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

cerebellitis

cerebral cortex

cerebral cortical atrophy

cerebral palsy

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

chromosomal abnormality

chromosome 2

Clinical Pathologic Conference(C.P.C.)

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cyanide poison

deafness

degenerative diseases of CNS

delirium

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

dilantin

disability, neurological

disease modifying agents

distal muscle atrophy

doll's head maneuver

Dravet syndrome

drug induced neurologic disorders in children

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

enterovirus

enterovirus infection of CNS

epidemic

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

fine motor function, impaired

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gait disorder

gait, spastic

gait, waddling

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

GFAP gene

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

gynecomastia

hand deformity

hand-foot-mouth disease

headache, sudden onset of

heralding manifestation

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

heterophile antibody test

hiccoughs

histochemistry of muscle

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycemia

hypokalemia

hypokalemic periodic paralysis

hyponatremia

hyporeflexia

hypotension, systemic

hypotonia

hypoxia

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

incoordination

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

learning disability, in children

leg numbness

leg weakness, bilateral

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

lipid storage disorder of CNS

listeria monocytogenes

lymphadenopathy, paraaortic

lysosomal storage disease

macrocephaly

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

mental status, abnormal

migraine, visual symptoms in

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, brachial plexus

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, negative

MRI, spinal cord

MRI, susceptibility weighted

multiple sclerosis

mumps virus

muscle atrophy, progressive

muscle weakness, proximal

myasthenia gravis

mycobacterial infection

mycobacterium bovis

mycoplasma

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myoclonus, stimulus sensitive

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

neuropathy, acute

neuropathy, motor

neuropathy, motor, multifocal

old age, neurology of

osmotic demyelination syndrome

otitis, neurologic complications with

paralysis, acute areflexic

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

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

polymyositis

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

post infectious cerebellar ataxia

postinfectious

potassium

potassium channel antibodies

practice guidelines

precipitating factors

prion disease

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia, transient

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

recurrent

Refsum's disease

regional enteritis

renal tubular acidosis

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

review article

riboflavin transporter deficiency

risk factors

rituximab

Romberg's sign

salivation, excessive

schizophrenia

SCN1A gene

screening

sedimentation rate, elevated

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

seronegative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

slurred speech

sodium channel dysfunction

spinal cord, cervical

splenomegaly

standing difficulty

status epilepticus

stem cell transplantation

steroid

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

topiramate

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

vertebral-basilar insufficiency

vertigo

viral infection

viral infection, CNS

visual acuity, decreased

visual impairment

visual loss

visual loss, sudden-unilateral

visual loss, transient

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

wheelchair

white matter disease

whole genome sequencing

wide based gait

workup

wrist drop

Showing articles 650 to 700 of 8215 << Previous Next >>

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

Identification and Treatment of Cerebral Aneurysms After Sentinal HEadache
Neurol 42:1118-1119, Hughes,R.L., 1992

Urgent Therapy for Stroke Part I, Pilot Study of Tissue Plasminogen Activator Administered within 90 Minutes
Stroke 23:632-640, Brott,T.G.,et al, 1992

Temporal Lobectomy for Intractable Epilepsy in Patients Over Age 45 Years
Neurol 42:662-665, McLachlan,R.S.,et al, 1992

'De Novo'Absence Status of Late Onset:Report of 11 Cases
Neurol 42:104-110, Thomas,P.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

Clinical Features of Vascular Thrombosis Following Varicella
Am J Dis Child 146:100-102, Bodensteiner,J.B.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

Multifocal Inflammatory Leukoencephalopathy with 5-Fluorouracil and Levamisole
Ann Neurol 31:262-267, Hook,C.C.,et al, 1992

Paraneoplastic Syndrome Manifesting as Chronic Cerebellar Ataxia in a Child with Hodgkin Disease
J Pediatr 120:275-277, Topeu,M.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Subarachnoid Haemorrhage
Lancet 339:653-655, Van Gijn,J., 1992

Effects of Public and Professional Education on Reducing the Delay in Presentation and Referral of Stroke Patients
Stroke 23:352-356, Alberts,M.J.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

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

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

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Ataxia in epidural Spinal Cord Compression
Neurol 42:2193-2195, Hainline,B.,et al, 1992

Paraneoplastic Cerebellar Degener II, Clin & Immunologic Find in 21 Pts with Hodgkin's Disease
Neurol 42:1938-1943, Hammack,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

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Dental Chair Apoplexy
South Med J 84:907-909, Cawley,C.M.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

The Bioloigcal Basis for the Treatment of Acute Stroke
Neurol 41:1867-1873, Scheinberg,P., 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Corpus Callosotomy for Intractable Seizures in the Pediatric Age Group
Arch Neurol 48:364-372, Nordgren,R.E.,et al, 1991

Surgery for Focal Epilepsy in the Older Patients
Neurol 41:1415-1417, Cascino,G.D.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Medical Assessment and Treatment of Chronic Epilepsy
BMJ 302:363-366, Shorvon,S.D., 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

When Sex is a Headache, Not Funny but Usually not Serious
BMJ 303:202-203, Lance,J.W., 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Anti-Ri:An Antibody Associated with Paraneoplastic Opsoclonus and Breast Cancer
Ann Neurol 29:241-251, Luque,F.A.,et al, 1991

Cortical Resection for Children with Epilepsy
Am J Dis Child 145:314-320, Wyllie,E., 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Does Ageing Aggravate Parkinsonisn Disability?
JNNP 54:780-782, Blin,J.,et al, 1991

Clinicopath Conf
Case 50-1991, Renal Cell Carcinoma & Inflammatory Polyneuropathy (? paraneoplastic) , NEJM 325:1723-, 735, 199, 1991

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Central Nervous System Complications of Infective Endocarditis
Stroke 22:1461-1463, Salgado,A.V., 1991

An Analysis of Time of Presentation After Stroke
JAMA 263:65-68, Alberts,M.J.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Clinicopath Conf
Sarcoidosis of CNS and Mediastinal Lymph Nodes, Case Record 6-1990, NEJM 322:388-397990., , 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Showing articles 650 to 700 of 8215 << Previous Next >>