Neudle.com: cerebellar ataxia autoimmune

Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acute cerebellar ataxia

acute disseminated encephalomyelitis

Adies pupil

advances in neurology

adverse drug reaction

aggression

algorithm

altered states of consciousness

alternating rapid movement

AMPA receptor antibodies

amphiphysin antibodies

anemia

anemia, megaloblastic

antecedent illness

anti GQ1b IgG antibody

anti GT1aIgG antibody

anti mGluR1 encephalitis

antibodies to voltage-gated calcium channels

anticholinesterase

antiendomysial antibodies

antiganglioside antibodies

antineurofascin antibodies

antithyroid antibodies

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune GFAP astrocytopathy

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bickerstaff's brainstem encephalitis

brainstem, dysfunction

brainstem, lesion of

brucellosis, nervous system involvement with

calcium channel dysfunction

CAR syndrome

carbon monoxide poisoning

CAT scan, emission, abnormal

CAT scan, pelvis

celiac disease, adult

celiac disease, childhood

central core disease

central hypoventilation

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebral cortex

cerebral edema

cerebral folate deficiency syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

chairbound

chemical weapons

children

chloride channel dysfunction

chorea

choreoathetosis

choroid plexus

chromosomal abnormality

chronic fatigue syndrome

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cognition

collagen vascular disease

collapsin response mediator protein 5 IgG

coma

confusion

conjunctivitis

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

cortical ribbon sign

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

dementia, differential diagnosis of

dementia, rapidly progressive

dementia, treatment of

demyelinating disease

depression

dermatitis herpetiformis

differential diagnosis

diplopia

disorientation

distal muscle weakness

DPPX, antibodies, encephalitis

drowsiness

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dysmetria

dysphagia

dystonia

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, paraneoplastic

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, parainfectious

enteritis

Epstein-Barr virus

eye movement, disorders of

eye, pain in

face, numbness of

facial weakness

facial weakness, bilateral

falling

familial

familial hemiplegic migraine

fasciculation

fever

fine motor function, impaired

Fisher's syndrome

Fisher's syndrome, atypical

flaccid paralysis

flu-like illness

folic acid

folic acid deficiency

gait disorder

GALOP syndromes

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gangliosides

gastric biopsy

gastritis

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, vertical

genetic neurologic disorders

GFAP-IgG

gliadin antibodies

GluD2

glutamic acid decarboxylase, antibody

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

hemophagocytic lymphohistiocytosis, cerebromeningeal

heralding manifestation

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hypokalemic periodic paralysis

immune-mediated pathogenesis

immunodeficiency

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intracranial pressure, increased

intubation

iridoplegia

irritability

Jakob-Creutzfeldt disease

kelch-like protein 11 antibodies

leg weakness, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukopenia

level of consciousness, decreased

limbic encephalitis

lip biopsy

listeriosis, CNS

liver function enzymes

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

malabsorption

malignancy screen

malignancy, occult

malignant hyperpyrexia

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningoencephalitis

meningoencephalomyelitis

mental status, abnormal

mesial temporal lobe

mestinon

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, lumbosacral plexus

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, autoimmune

myelitis, longitudinal

myelopathy

myelopathy, chronic progressive

nerve root enhancement

nerve root hypertrophy

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronopathy, sensory

neuropathy, autoimmune

neuropathy, paraneoplastic

neuropathy, peripheral, treatment

nodopathy, autoimmune

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular flutter

ocular motility, disorders of

oculocephalic reflex

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

parasomnia

paresthesias

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland neoplasm

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis

peripheral nerve, lesion of

perivascular enhancement

pernicious anemia

personality change

plasmapheresis

pleocytosis of cerebrospinal fluid

POEMS syndrome

poison, organophosphate

polyneuropathy

pons, lesion of

positional head-hanging test

post infectious cerebellar ataxia

postinfectious

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

Purkinje cell

purkinje cell cytoplastic autoantibody

Purkinje cell surface antibody

pursuit eye movements, abnormal

pyramidal tract dysfunction

quadriparesis

quadriplegia

rapidly progressing neurologic illness

recurrent

Red flags

remote effect of cancer on the nervous system

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

retinopathy

retropulsion

reversible neurologic disorder

review article

rheumatoid arthritis factor(R.A.factor)

saccadic eye movements, abnormal

salivation, excessive

scannig speech

Schirmer test

screening

sedimentation rate, elevated

serologic testing, false negative

seronegative

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

sodium channel dysfunction

somnolence

speech disorder

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 6

splenomegaly

standing difficulty

staphylococcal protein A column therapy

startle reaction

status epilepticus

steroid

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

strabismus

striatal encephalitis

stuporous

superior cerebellar peduncle

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tauopathy

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

transglutaminase antibodies

treatment of neurologic disorder

triangle of Guillain and Mollaret

tuberculosis

uveitis

vaccination, neurologic complications with

walking, difficulty with

war

weakness

weakness, progressive

Showing articles 700 to 750 of 2532 << Previous Next >>

Complications of Intravenous Phenytoin for Acute Treatment of Seizures
JAMA 249:762-765, Earnest,M.P.,et al, 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Primary Position Vertical Nystagmus & Cerebellar Ataxia
Arch Neurol 40:310-314, Kattah,J.C.,et al, 1983

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

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Sensory Neuropathy from Pyridoxine Abuse
NEJM 309:445-448, Schaumburg,H.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Nervous System Complications of Relapsing Polychondritis
Neurol 33:513-515, Sundaram,M.B.M.,et al, 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Permanent Neurological Deficits Due to Lithium Toxicity
Ann Neurol 13:453-455, Apte,S.N.,et al, 1983

Sensory Ataxia, A Residual Disability of Guillain-Barre Syndrome
Arch Neurol 40:86-89, Sobue,G.,et al, 1983

Idiopathic Hemochromatosis (IHC) :Dementia & Ataxia as Presenting Signs
Neurol 33:1479-1483, Royden,H.,et al, 1983

Acute Cerebellar Ataxia & Hearing Loss as Initial Symptoms of Infectious Mononucleosis
Arch Neurol 40:760-762, Erzurum,S.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Cerebellar Dysfunction after Acute Carbon Tetrachloride Poisoning
Lancet 2:968, Forster,S.H.,et al, 1983

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Truncal Ataxia in Terminal Bronchial Carcinoma
Arch Neurol 39:787-788, Puvanendran,K., 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Peripheral Neuropathy & Starvation After Gastric Partitioning for Morbid Obesity
Ann Int Med 96:453-455, Feit,H.,et al, 1982

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Tick Paralysis With Persistent Weakness & Electromyographic Abnormalities
Arch Neurol 38:59-61, Donat,J.R., 1981

Neurologic Complications of Lymphomatoid Granulomatosis
Neurol 31:619-620, Hogan,P.J.,et al, 1981

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

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

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,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

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Central Nervous System Toxicity Associated With Metronidazole Therapy
Ann Int Med 93:59-60, Kusumi,R.K.,et al, 1980

Legionnaires'Disease With Profound Cerebellar Involvement
Arch Neurol 37:379-380, Shetty,K.R.,et al, 1980

Showing articles 700 to 750 of 2532 << Previous Next >>