Neudle.com: autoimmune cerebellar ataxia

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 50 to 100 of 2532 << Previous Next >>

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Autoantibodies in Postinfectious Acute Cerebellar Ataxia
Neurol 65:1114-1116, Uchibori,A.,et al, 2005

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
Medicine 82:216-223, Rojas-Marcos,I.,et al, 2003

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 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

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
Neurol 44:1184-1185, Counsell,C.E.,et al, 1994

Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
Neurol 44:1521-1522, Casado,J.L.,et al, 1994

Paraneoplastic Opsoclonus-Myoclonus Associated with Anti-Hu Antibody
Neurol 44:1754-1755, Hersh,B.,et al, 1994

Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
Neurol 44:1506-1507, Ito,H.,et al, 1994

Treatable Gait Disorder & Polyneuropathy Assoc with High Titer Serum IgM Binding to Atg that Copurify with MAG
Muscle & Nerve 17:1293-1300994., Pestronk,A.,et al, 1994

Anti-Ri-Associated Paraneoplastic Neurologic Disorder without Opsoclonus in a Patient with Breast Cancer
Neurol 43:1605-1606, Escudero,D.,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

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

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

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

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

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Gait Analysis in Neurologic Disorders, Methodology, Applications and Clinical Considerations
Neurol 105:e214154, Ali,F.,et al, 2025

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

Niemann-Pick Disease Type C
Gene Reviews www.genereview.org, Bremova-Ertl,T. & Patterson, M., 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Showing articles 50 to 100 of 2532 << Previous Next >>