Neudle.com: sensory ataxia

Differential
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abducens nerve paralysis

acanthocytosis

acoustic nerve

acral sensory symptoms

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

altered states of consciousness

alternating rapid movement

amaurosis fugax

amphiphysin antibodies

amygdala

ANA

anemia

anemia, megaloblastic

anterior choroidal artery

anti GQ1b IgG antibody

antibiotics, neurologic complications with

antiganglioside antibodies

antimetabolite

areflexia

arrhythmia, cardiac

arterial dissection, vertebral

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

Bassen-Kornzweig syndrome

blood dyscrasias, neurologic findings with

bovine spongiform encephalopathy

bradykinesia

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

carpal tunnel syndrome

CAT scan, false negative

cataracts

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebral cortical atrophy

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, vascular territory involved

cervical myelopathy

Charcot-Marie-Tooth

Cheiro-oral syndrome

chemotherapy, CNS treatment and complications with

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

cognition

collagen vascular disease

collapsin response mediator protein 5 IgG

concentration, impaired

conduction block

confusion

congestive heart failure

constipation

contactin associated protein like 2 antibodies

conus medullaris, lesion of

convergence, impaired

conversion reaction

copper deficiency

cortical-basal ganglionic degeneration

cough

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

demyelinating disease

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

dissociated sensory loss

distal muscle weakness

drug induced neurologic disorders

dural arteriovenous malformation

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystrophic calcification

ejection fraction, abnormal

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electronystagmography

electroretinograph

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

enzyme, muscle disease

epidemiology of neurology

exercise-induced leg numbness

exercise-induced vascular symptoms

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

fine motor function, impaired

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

Friedreich's ataxia, late onset

fundus, abnormality of

gait disorder

gait, spastic

gammaglobulin therapy, intravenous

ganglionitis

gangliosides

gasserian ganglia

gastrectomy, neurologic complications following

gastric partitioning

gastroenteritis

gaze palsy

gaze palsy, horizontal

genetic neurologic disorders

genetic testing

girdle sensation

gluten sensitivity

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination

hallucination, visual

headache, sudden onset of

hearing loss

heel-knee-shin test

hemianopia, homonymous

herpes virus infection

human immunodeficiency virus type 1

iatrogenic neurologic disorders

idiopathic

imbalance

immune checkpoint inhibitors

immunologic disease

immunology and the nervous system

immunosuppressive agents

immunotherapy

impotence

inappropriate antidiuretic(A.D.H.)hormone

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

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracerebral hemorrhage

intracerebral hemorrhage, small

iridoplegia

irritability

isoniazid

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaundice

jaw pain

Jewish

Kearns-Sayre syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

kyphosis

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lateral medullary syndrome

lateropulsion

Laurence-Moon-Bardet-Biedl syndrome

leg numbness

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

listeria monocytogenes

lymphadenopathy, hilar

malformation, vascular

malignancy screen

malignancy, occult

mastoiditis

medial medullary syndrome

mediastinum, mass of

medulla oblongata, infarction of

memory, impairment of

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

methotrexate

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

metronidazole

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mortality

motor dysfunction

movement disorder

movement disorder, psychogenic

MRI

MRI, abnormal

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, disappearing lesion on

MRI, flow void, blood

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRS

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle weakness, proximal

muscular dystrophy

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, ascending

myelopathy, chronic progressive

myoclonus

myopathy, mitochondrial

myopathy, proximal

myopia

nasal septum, perforation of

nasal speech

nausea and vomiting

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

nerve growth factor

nerve root enhancement

neuritis

neurofibromatosis 1

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, motor, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

non-dominant hemisphere

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, upbeating on upgaze

nystagmus, vertical

old age, neurology of

onconeural antibodies

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic nerve

optic neuropathy

orthostatic hypotension

otitis, neurologic complications with

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

parenteral alimentation

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

pathologic reflex

penicillin

periarteritis nodosa

perineum, numbness of

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

poison, mercury

POLG1 gene

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polyneuritis

polyneuritis, acute sensory

polyneuropathy

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, chronic relapsing

polyradiculoneuropathy

position sensation, abnormal

positional head-hanging test

posterior column disease

posterior inferior cerebellar artery syndrome

postoperative neurologic complications

prion disease

procarbazine

prognosis

progressive neurologic disorder

proprioception

proprioception, abnormal

pruritus

pseudoathetosis

pseudochorea

psychiatric problems in neurologic disorders

psychological testing

psychosis

ptosis

ptosis, bilateral

pulmonary infiltrates

pupil

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, light reflex, abnormal

pure motor hemiplegia

pyramidal tract dysfunction

reading disorder, acquired

real-time quaking-induced conversion

rectal sphincter tone, decreased

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

restiform body

retinal artery occlusion

reversible neurologic disorder

review article

RFC1 gene

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

saccadic eye movements, abnormal

sarcoidosis

sarcoidosis, CNS

scleroderma

scleroderma, neurologic involvement with

scoliosis

scotoma

screening

sedimentation rate, elevated

seizure

seizure, hysterical

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory level

sensory loss

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, cortical

sensory loss, crossed pattern

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

small vessel disease

somatosensory evoked potentials

spastic ataxia

spasticity

speech disorder

speech disorder, non aphasic

spinal cord

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, enlargement

spinal cord, lesion of

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

starvation, therapeutic

steroid

steroid therapy, CNS treatment and complications with

superior cerebellar artery syndrome

suspended sensory loss

swayback

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

tachycardia

tandem gait, ataxic

tapetoretinal degeneration

tauopathy

testicular biopsy

thalamic ataxia syndrome

thalamic syndrome

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, thalamic

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

vertebral artery occlusion

vertebral artery stenosis

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

vision, blurred

visual cortex

visual evoked response

visual field defect

visual fields, constricted

voice, abnormality of

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, functional

weakness, generalized

weakness, progressive

Showing articles 1550 to 1600 of 1775 << Previous Next >>

Computed Tomography in Patients Presenting with Lacunar Syndromes
Stroke 11:256-261, Nelson,R.F.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

The Use of Choline Chloride in Ataxic Disorders
JNNP 43:452-454, Lawrence,C.M.,et al, 1980

The Chronic Pain Syndrome:Misconceptions & Management
Ann Int Med 93:588-596, Reuler,J.B.,et al, 1980

Trigeminal Sensory Neuropathy & Bilateral Carpal Tunnel Syndrome:The Initial Manifest of Mixed Connective Tissue Disease
JNNP 43:458-460, Vincent,F.M.,et al, 1980

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

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Progressive & Treatable Cerebellar Ataxia in Macroglobulinemia
Neurol 30:536-538, Spencer,S.S.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Clinical Pathological Conference
Foramen Magnum Meningioma, Case Record 29-1979, NEJM 301:147-154979., , 1979

Spinal Cord Injury as a Complication of an Acupunture
Neurol 29:1180-1182, Shiraishi,S.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Neurological Manifestations & Mycoplasma Pneumoniae Infection
BMJ 2:832-833, Hodges,G.R.,et al, 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Peripheral Neuropathy in Arsenic Smelter Workers
Neurol 29:939-944, Feldman,R.G.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Tarsal Tunnel Syndrome:Electrophysiological Study
Ann Neurol 5:327-330, Oh,S.J.,et al, 1979

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Jaw Reflex in Friedreich Ataxia
Neurol 29:1049-1050, Salisachs,P., 1979

Beneficial Effect of Propranolol in Familial Ataxia
Ann Neurol 5:207, Braham,J.,et al, 1979

Age-related Changes in Peripheral & Central Nerve Conduction in Man
Neurol 29:38-44, Dorfman,L.J.,et al, 1979

Optic Neuropathy & Ophthalmoplegia in Herpes Zoster Oticus
Neurol 29:726-729, Carroll,W.M.,et al, 1979

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Position & Vibration Sensations:Fuctions of the Dorsal Spinocerebellar Tracts
Ann Neurol 5:171-176, Ross,E.D.,et al, 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Paraneoplastic Vasculitis of Nerve:A Remote Effect of Cancer
Ann Neurol 5:437-444, Johnson,P.C.,et al, 1979

Acute Transitory Cerebellar Dysfunction Associated with Piperazine Adipate
Arch Neurol 36:180-181, Berger,J.R.,et al, 1979

Adult Polysaccharidosis
Arch Neurol 36:840-845, Peress,N.S.,et al, 1979

Risks Of The Neurologist's Pin
NEJM 301:1288, Noseworthy,J.H., 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

Trichlorethylene
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 457, Feldman,R.G., 1979

Hysterical Gaits
In the Neurologic Examination, Ed. Russell N. DeJong, 4th Edition, Harper & Row, Publ, Hagerstown, p, 426, 1979

Meningiomas & Aneurysms of the Cavernous Sinus, Neuro-ophthalmolicic Features
Arch Ophthalmol 96:457-467, Trobe,J.D.,et al, 1978

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Showing articles 1550 to 1600 of 1775 << Previous Next >>