Neudle.com: primary episodic ataxia

Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acute cerebellar ataxia

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

advances in neurology

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

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

alcoholism

algorithm

alkalosis

alkalosis, respiratory

alkylating agents

alopecia

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

anemia

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiokeratoma

angiotensin-converting enzyme

animal exposure

anorexia

anosmia

anti GQ1b IgG antibody

anti IgLON5

antibiotics

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

antimetabolite

antithyroid antibodies

anxiety

aphasia

apnea

apnea, primary central

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

Babinski sign

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

biotin deficiency, juvenile form

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blindness

blindness, monocular

blood dyscrasias, neurologic findings with

brain biopsy, stereotaxic

brucellosis, nervous system involvement with

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

carcinoma

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

caudate nucleus, atrophy

central core disease

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cephalosporins

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 vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, young adult

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

chest x-ray, abnormal

children

chloride channel dysfunction

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clonus

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

concentration, impaired

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

corpus callosum, atrophy of

corpus callosum, lesion of

cortical blindness

cortical ribbon sign

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cultured skin fibroblasts

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis

dermatoglyphics

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

differential diagnosis

dilantin

diplopia

disease modifying agents

disorientation

distal muscle atrophy

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

drooling

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia, psychogenic

eating disorder

efficacy

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalomyopathy

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

enzyme, defect

epinephrine

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

erethism

evoked potentials

executive dysfunction

extinction on double simultaneous stimulation

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

fingerprint bodies

fish

fluorescene in situ hybridization

fluorouracil

flush syndrome

folic acid

folic acid deficiency

foot drop

Friedreich's ataxia

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gargoylism

gastric partitioning

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glycosuria

gout

gram negative rod

granular osmiphilic material

granulomatous disease

gray hair

growth hormone deficiency

Guillain Barre syndrome

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

hand flapping

Hand-Schuller-Christian disease

headache

headache, elderly

headache, progressive

hearing loss

heart block

hemianopia, homonymous

hemiparesis

hemiplegia

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemosiderosis of CNS, superficial

herpes simplex encephalitis, differential diagnosis of

herpes virus

herpes zoster

herpes zoster, disseminated

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocystinuria

hung reflex

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydroxyglutaric aciduria

hypocalcemia, causes of

hypokalemic periodic paralysis

hypopigmentation of skin

hyporeflexia

hyposmia

hypothalamus

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

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

inappropriate behavior

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Kearns-Sayre syndrome

keratoconjunctivitis

keratoconus

Korsakoff's psychosis

kyphosis

lactic acidemia

laryngismus stridulus

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability, in children

Leber's hereditary optic neuropathy

Legionnaires'disease

Leigh's disease

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

level of consciousness, decreased

life expectancy

limbic encephalitis

limbic system

lipid storage disorder of CNS

liver disease

lymphadenopathy

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

macrognathia

macular degeneration

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

mania

maple syrup urine disease

marche a petits pas

Marchiafava-Bignami disease

melanoma, malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, elderly

meningitis, fungal

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, recurrent

meningitis, TB

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methotrexate

methylhydrazine derivatives

methylmalonic acidemia

metronidazole

microcephaly

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, negative

MRI, serial

mucopolysaccharidoses

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

mycoplasma pneumoniae

myelitis

myelogram

myelopathy

myelopathy, chronic progressive

myopathy, mitochondrial

myxedema, neurologic manifestations of

nausea and vomiting

neck pain

negative

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary of CNS

nephrotic syndrome

neuraminidase deficiency

neuritis

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromyotonia

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, painful

neuropathy, peripheral

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

obesity

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic neuropathy, ischemic

optokinetic nystagmus, abnormal

organ transplantation

organomegaly

orthostatic hypotension

paramyotonia congenita

paranoia

paraparesis

paraparesis, familial spastic

Parkinson disease, arteriosclerotic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

penicillin

pericarditis

periodic paralysis

perivascular enhancement

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleurisy

pneumoencephalogram(PEG)

polymerase chain reaction

pontocerebellar atrophy

post transplant lymphoproliferative disease

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

primary aldosteronism

primary episodic ataxia

procarbazine

prognathism

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

progressive supranuclear palsy

proteinuria

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

rectal biopsy

recurrent

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal transplantation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

safety

salivation, excessive

sedimentation rate, elevated

seizure

seizure, children

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

short stature

shunt procedure, ventricular

simultanagnosia

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

slurred speech

smiling

sodium channel dysfunction

speech disorder, childhood

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 6

splenium of corpus callosum

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

strabismus

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

symmetric brain lesions

temporal lobe, lesion

tensilon test

tetany

tetany, latent

tetany, normocalcemic

tongue, protrusion of

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

trinucleotide repeats

tuberculosis, miliary

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

uveitis

varicella zoster virus

varicella zoster virus, encephalitis

vasculopathy

venous thrombosis, non-cerebral

vertigo

vertigo, episodic

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

Vogt-Koyanagi-Harada syndrome

von Bonsdorff's sign

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Wernicke's encephalopathy

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolfram syndrome

wrist drop

Showing articles 250 to 300 of 8394 << Previous Next >>

A 77-year-old man presenting with episodic expressive aphasia
Neurol 90:e1822-e1826, Shanklin, A.,et al, 2018

A 60-year-old woman with ataxia
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Encephalitis with mGluR5 antibodies
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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An 18-year-old man with progressive headache and visual loss
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Recurrent Glioblastoma Treated with Recombinant Poliovirus
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Clinicopathological Conference, Insulinoma
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Isolated Gait Dysfunction Due to Intracranial Hypotension
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Recurrent Dysarthria and Ataxia in a Young Girl
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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Paraneoplastic and Autoimmune Encephalitis
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An 82-year-old man with Worsening Gait
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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A Demure Teenager and Her Dystonic Foot
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Investigations in GABA? Receptor Antibody-Associated Encephalitis
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Primary Angiitis of the Central Nervous System
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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Clinicopathologic Conference, Primary Adrenal Insufficiency (Addisons Disease)
NEJM 376:1159-1167, Case 9-2017, 2017

A Woman in her 40s with Headache and New-Onset Seizures
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Pure Sensory Ganglionopathy as the First Sign of Relapse in Non-Hodgkin Lymphoma
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Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
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A 27-year-old man with Acute-Onset Ataxia
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
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Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q
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Tumor-Like Presentation of Primary Angiitis of the Central Nervous System
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A Case of Subacute Cognitive Decline in a 76-year-old Man
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Neurological Management of Von Hippel-Lindau Disease
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Clinicopathologic Conference, Neurosarcoidosis
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Metastatic Spinal Cord Compression: Diagnosis and Management
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Human Neurexin-3a Antibodies Associate with Encephalitis and Alter Synapse Development
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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Showing articles 250 to 300 of 8394 << Previous Next >>