Neudle.com: "neuropathy ataxic"

Differential
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abdominal distention

abdominal reflex, absent

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

acanthocytosis

acoustic nerve

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, medical precautions with

acral sensory symptoms

acute ataxia of childhood

acute ataxic sensory neuropathy

acute cerebellar ataxia

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

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

alcoholism

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

AMPA receptor antibodies

amphiphysin antibodies

amygdala

amyotrophic lateral sclerosis, differential diagnosis

ANA

anemia

anemia, megaloblastic

anesthesia, general

aneurysm

angiotensin-converting enzyme

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anti GT1aIgG antibody

antibiotics, neurologic complications with

anticholinesterase

antiendomysial antibodies

antiganglioside antibodies

antimetabolite

antineurofascin antibodies

antiviral agents

aphasia

apnea

apnea, primary central

apraxia of eye movements

areflexia

arm weakness

Arnold Chiari malformation

ataxia telangiectasia

attention deficit disorder with hyperactivity

atypical

atypical lymphocytes

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune GFAP astrocytopathy

automatism, postictal

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basilar impression

basophilic stippling of red blood cells

Bickerstaff's brainstem encephalitis

biologic markers

biological warfare

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

Borrelia burgdorferi infection

brachial plexus neuropathy

bradykinesia

brain atrophy

brain biopsy

brain biopsy, stereotaxic

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, syndrome

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

calcification, intracranial

calcitonin

carbamazepine

carcinoembryonic antigen

carcinoma of pancreas

carpal tunnel syndrome

CAT scan, contrast enhanced, subepend.

CAT scan, false negative

cataracts

cat-scratch disease

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

CD4 counts

celiac disease, adult

celiac disease, childhood

central artery of Percheron

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis

cerebellum

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, flow cytometry

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemical weapons

chemotherapy, CNS treatment and complications with

chest x-ray

chest x-ray, abnormal

chromosomal abnormality

chromosome 11

chromosome 9

chronic fatigue syndrome

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clonus

clubbing of fingers

clubfoot as related to neurologic disease

cognition

cogwheel rigidty

colchicine

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

coma

complications

compression fracture

concentration, impaired

confusional state, acute

congestive heart failure

conjunctivitis

consanguinity

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

cornea, abnormal

corneal reflex, abnormal

corneal reflex, depressed

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cough

CPAP

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial nerve palsies, unilateral

cranial nerves, toxins effecting

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cryopyrin-associated periodic syndrome

cryptococcal antigen

cryptococcal meningitis

Cuba

cultured skin fibroblasts

cyst, arachnoid

cyst, arachnoid, posterior fossa

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytokines

cytomegalovirus infection

degenerative diseases of CNS

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

dermatitis herpetiformis

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

diplegia, brachial

diplopia

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

doll's head maneuver

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drooling

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, parainfectious

encephalopathy, progressive

enteritis

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

ependymoma

epidemic

epidemiology of neurology

executive dysfunction

exercise intolerance

exome sequencing

exophthalmus

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

Fabry's disease

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial pain

facial pain, atypical

facial weakness

facial weakness, bilateral

fatal familial insomnia

fine motor function, impaired

finger nose finger test

fish poisoning

Fisher C.M.

Fisher's syndrome

Fisher's syndrome, atypical

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

fluorouracil

flush syndrome

folic acid

folic acid deficiency

foot ulcer, neuropathic

foot, swollen

foscarnet

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

frontal bossing

fundus, abnormality of

fungal infection

fungal infection, CNS

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gastrectomy, neurologic complications following

gastric partitioning

gastric surgery

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze deviation

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

general paresis of the insane

genetic counselling

genetic linkage

genetic neurologic disorders

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glossitis

glucagonoma

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen storage disease

glycosuria

gram negative rod

granulomatous disease

gray hair

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Gulf War syndrome

gumma

Hallervorden Spatz disease

hallucination

hallucination, visual

hand-foot-mouth disease

headache, intractable

headache, sudden onset of

hearing loss

hearing problems in children

heart block

heavy metal intoxication

heel-knee-shin test

hemianopia, homonymous

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus

herpes virus infection

herpes zoster

herpes zoster, disseminated

herpes zoster, ophthalmicus

herpes zoster, oticus

herpes, genital

hiccoughs

hiccoughs, intractable

high altitude sickness

high arched feet

hip flexor weakness

Hispanics

histamine-2 receptor blockers

histochemistry

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

hypertrophic intracranial pachymeningitis

hypogonadism, hypogonadotropic

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothermia

hypothyroidism

hypotonia

iatrogenic neurologic disorders

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

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

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incontinence, fecal

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

internuclear ophthalmoplegia, unilateral

intestinal biopsy

intestinal lymphangiectasia

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intravenous

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

Kernig's sign

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

labyrinth, disorder of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lateral medullary syndrome

lead and the nervous system

lead line, gingival

lead poisoning

Leber's hereditary optic neuropathy

leg atrophy

leg numbness

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

Lhermitte's sign

light-near dissociation, causes of

limbic encephalitis

limbic system

lip, biting

lipid storage disorder of CNS

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

listeria monocytogenes

listeriosis, CNS

lithium

low back pain

lumbosacral radiculopathy

Lyme disease

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

malabsorption syndrome

malignancy screen

malignancy, occult

manganese intoxication

mania

marche a petits pas

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

masked facies

mastoiditis

mediastinum, mass of

medulla oblongata, infarction of

medulla oblongata, lesion of

melanoma, malignant

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal enhancement, nodular

meningeal gliomatosis

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, elderly

meningitis, fungal

meningitis, lymphomatous

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, recurrent

meningitis, syphilitic

meningitis-encephalitis PCR panel

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

meralgia paresthetica

MERRF syndrome

mestinon

metabolic acidosis

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

metronidazole

microcephaly

microglial nodules

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

Minamata disease

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, negative

MRI, nodular enhancement

MRI, ring sign

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple myeloma

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

muscle atrophy, progressive

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, autoimmune

myelitis, longitudinal

myelopathy, chronic progressive

myelopathy, tract-specific

myopathy, mitochondrial

myxedema, neurologic manifestations of

nasal septum, perforation of

nemaline rod myopathy

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve agents

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, immune

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

nodopathy, autoimmune

numbness, generalized

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, spontaneous

nystagmus, upbeating on upgaze

ocular motility, disorders of

old age, neurology of

onconeural antibodies

one and a half syndrome

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic ataxia

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic atrophy, unilateral

optic disc edema

optic nerve

optic neuritis

optic neuritis, children

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, toxic

optical coherence tomography

oral ulcerations

organ transplantation

orthostatic hypotension

oscillopsia

osteoporosis

otitis, neurologic complications with

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraplegia

paraproteinemia

parasitic infection, CNS

parenteral alimentation

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease, dystonia with

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

past pointing

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

perivascular enhancement

photosensitivity, skin

phytanic acid

pica

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

pneumonia

poison, mercury

poison, neurologic problems with

poison, organophosphate

POLG1 gene

poliosis

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuritis

polyneuritis, acute sensory

polyneuropathy

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyradiculoneuropathy

position sensation, abnormal

positional head-hanging test

posterior column disease

posterior inferior cerebellar artery syndrome

postinfectious

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

pretectal syndrome

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception

proprioception, abnormal

proton pump inhibitors

pseudoathetosis

pseudobulbar palsy

pseudochorea

pseudointernuclear ophthalmoplegia

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

pyridoxine

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

rash, hand

reading disorder, acquired

real-time quaking-induced conversion

relapsing polychondritis

release phenomena

remote effect of cancer on the nervous system

renal cell carcinoma

renal tubular acidosis

respiratory depression

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

reversible neurologic disorder

review article

RFC1 gene

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhinorrhea

riboflavin transporter deficiency

rubella encephalitis, progressive

rubella virus

Russia

Sabin-Feldman dye test

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, crossed pattern

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory nerve action potentials

sensory polyneuropathy

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum glutamic oxaloacetic transaminase

shooting pain

short stature

shunt procedure, ventricular

Shy-Drager syndrome

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slurred speech

small vessel disease

small vessel disease, cerebral

somatosensory evoked potentials

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

splenomegaly

splinter hemorrhages

spongy degeneration of brain

standing difficulty

stare

startle myoclonus

starvation, therapeutic

status epilepticus

steatorrhea

steroid

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

stridor

strokelike episodes

stuporous

subarachnoid hemorrhage

superior orbital fissure syndrome

suspended sensory loss

swayback

sweating, abnormality of

symmetric brain lesions

syncope

synovitis

synucleinopathy

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

syringomyelia

systemic illness

systemic lupus erythematosus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

thiamine deficiency

third nerve palsy

third nerve palsy, bilateral

tongue, fasciculations of

tonsillar herniation of cerebellum

torticollis

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

triphenyltin intoxication

tripping

trochlear nerve palsy

tuberculoma

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

vaccination, neurologic complications with

vaccine

varicella zoster virus

varicella zoster virus, encephalitis

vasculitides

Venereal Disease Research Laboratory test

ventriculitis

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

vitamin supplementation

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

walking, difficulty with in dark

war

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Wernicke's encephalopathy

Western immunoblot test

wheelchair

white hair

white matter disease

white matter disease, subcortical

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Neurol 104:e213713, Rawat,R.,et al, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
NEJM 393:176-184, Case 19-2025, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,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

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

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