Neudle.com: sensory ataxia

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Differential
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abducens nerve paralysis

acral sensory symptoms

acute ataxic sensory neuropathy

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

alcohol intolerance

alien hand syndrome

alkylating agents

altered states of consciousness

alternating rapid movement

amaurosis fugax

amphiphysin antibodies

anemia, megaloblastic

aneurysm, intracranial

angiography, spinal

antecedent illness

anterior choroidal artery

anti GQ1b IgG antibody

anti Hu antibody

anti Ri antibody

anti Yo antibody

antiamphiphysin

antibiotics, neurologic complications with

antiganglioside antibodies

arrhythmia, cardiac

arterial dissection, vertebral

ascending paralysis

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic hemiparesis

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

axonopathy, distal

B 12 deficiency

basal ganglia, lesion of

Bassen-Kornzweig syndrome

behavioral disorder

Bell's phenomenon

bladder dysfunction

blood dyscrasias, neurologic findings with

bovine spongiform encephalopathy

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, syndrome

burning paresthesia

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of uterus

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, false negative

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

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

collagen vascular disease

collapsin response mediator protein 5 IgG

concentration, impaired

conduction block

congestive heart failure

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

contactin associated protein like 2 antibodies

conus medullaris, lesion of

convergence, impaired

conversion reaction

copper deficiency

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deafness, unilateral

deep gray nuclei

delay in diagnosis

demyelinating disease

dermatomyositis

dexterity, impaired

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disability, neurological

dissociated sensory loss

distal muscle weakness

down-beat nystagmus

drug induced neurologic disorders

dural arteriovenous malformation

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystrophic calcification

ejection fraction, abnormal

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electronystagmography

electroretinograph

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalomyelitis, paraneoplastic

enzyme, muscle disease

epidemiology of neurology

erythema migrans

evoked potentials

exercise-induced leg numbness

exercise-induced vascular symptoms

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

family planning

fine motor function, impaired

Fisher's syndrome

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

food-borne infection

Friedreich's ataxia

Friedreich's ataxia, late onset

fundus, abnormality of

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gasserian ganglia

gastrectomy, neurologic complications following

gastric partitioning

gastroenteritis

gaze palsy, horizontal

genetic counselling

genetic linkage

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, visual

headache, severe

headache, sudden onset of

heel-knee-shin test

hemianopia, homonymous

hemisensory loss

hemisensory syndrome

hemorrhage, thalamic

herpes simplex virus

herpes virus infection

herpes, genital

Hodgkin's disease

homocysteine, serum

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

hyperhomocysteinemia

hypersegmented polys

hypophosphatemia

iatrogenic neurologic disorders

immune checkpoint inhibitors

immunologic disease

immunology and the nervous system

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

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

inclusion bodies

incontinence, fecal

intellectual deficit

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracerebral hemorrhage

intracerebral hemorrhage, small

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lateral medullary syndrome

Laurence-Moon-Bardet-Biedl syndrome

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

Lhermitte's sign

limbic encephalitis

listeria monocytogenes

listeriosis, CNS

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

macular degeneration

malformation, vascular

malignancy screen

malignancy, occult

medial medullary syndrome

mediastinum, mass of

medulla oblongata, infarction of

memory, impairment of

meningitis, aseptic

meningitis, chronic

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Minamata disease

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy multiplex

motor dysfunction

movement disorder

movement disorder, psychogenic

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, disappearing lesion on

MRI, flow void, blood

MRI, mass effect on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis, longitudinal

myeloneuropathy

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, tract-specific

myopathy, mitochondrial

myopathy, proximal

nasal septum, perforation of

nausea and vomiting

nerve conduction studies

nerve conduction studies, sensory

nerve growth factor

nerve root enhancement

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, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, immune

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

night blindness

nitrogen mustard

NMDA antagonists

nodopathy, autoimmune

non-dominant hemisphere

numbness, ascending

numbness, extremity

numbness, generalized

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-myoclonus syndrome

optic neuropathy

orthostatic hypotension

otitis, neurologic complications with

overlap syndrome

pain, abdominal

pain, neuropathic

pain, testicular

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paraparesis, spastic

parenteral alimentation

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

pathologic reflex

periarteritis nodosa

perineum, numbness of

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pernicious anemia

peroxisomal disease

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polyneuritis, acute sensory

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

pons, infarction of

pons, lesion of

pontine hemorrhage

position sensation

position sensation, abnormal

positional head-hanging test

posterior column disease

posterior inferior cerebellar artery syndrome

postoperative neurologic complications

progressive neurologic disorder

proprioception, abnormal

pseudoathetosis

psychiatric problems in neurologic disorders

psychological testing

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, light reflex, abnormal

pure motor hemiplegia

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

rapidly progressing neurologic illness

Raynaud's phenomenon

reading disorder, acquired

real-time quaking-induced conversion

rectal sphincter tone, decreased

reflex, cutaneous

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retinal artery occlusion

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

Riley-Day syndrome

saccadic eye movements, abnormal

sarcoidosis, CNS

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure, hysterical

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

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

sensory symptoms

serologic testing

shell fish poisoning

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

small vessel disease

somatosensory evoked potentials

speech disorder

speech disorder, non aphasic

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 therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

superior cerebellar artery syndrome

suspended sensory loss

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

testicular biopsy

thalamic ataxia syndrome

thalamic syndrome

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

tongue, numbness of

tongue, swelling

tongue, weakness

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, resting

tremor, thalamic

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

ulcers, fingertip

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

Usher's syndrome

vertebral artery occlusion

vertebral artery stenosis

vestibular areflexia

vibratory sensation

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

vision, blurred

visual evoked response

visual field defect

visual fields, constricted

vitamin deficiency

vitamin E deficiency

vitamin, multiple

vocal cord paralysis

voice, abnormality of

walking, difficulty with

walking, difficulty with in dark

weakness, functional

weakness, generalized

weakness, progressive

white matter disease

wide based gait

Showing articles 1250 to 1300 of 1802 << Previous Next >>

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

The Olfactory and Cognitive Deficits of Parkinson's Disease:Evidence for Independence
Ann Neurol 25:166-171, Doty,R.L.,et al, 1989

Diabetic Truncal Neuropathy:Topography of the Sensory Deficit
Ann Neurol 25:233-238, Stewart,J.D., 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989

Peripheral Neuropathy in Primary Sjogren's Syndrome
Neurol 39:390-394, Mellgren,S.I.,et al, 1989

Opsoclonus-Myoclonus Syndrome:Correlation of Radiographic and Pathological Observations
Neuroradiology 31:250-252, Turchman,R.F.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Pure Sensory Stroke Due to a Pontine Lacune
Stroke 20:406-408, Hommel,M.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

The Radiologic Assessment of Trigeminal Neuropathy
AJR 153:1275-1282, Hutchins,L.G.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Cheiro-Oral Syndrome: Does It Have a Specific Localizing Value?
Eur Neurol 28:326-330, Holter,J.T. &Tijssen,C., 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Risk Factors for Falls Among Elderly Persons Living in the Community
NEJM 319:1701-1707, Tinetti,M.E.,et al, 1988

A Sensory Level on the Trunk in Lower Lateral Brainstem Lesions
Neurol 38:1515-1519, Matsumoto,S.,et al, 1988

Clinicopath Conf
Paraneoplastic Encephalitis (Limbic and Brain-Stem Encephalitis) , Case Record 39-1988, NEJM 319:849, 860,, 1988

Pontine Lesion in Opsoclonus-Myoclonus Syndrome Shown by MRI
JNNP 51:1572-1575, Hattori,T.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Predominantly Sensory Neuropathy in Pts with AIDS & AIDS-Related Complex
Neurol 38:794-796, Cornblath,D.R.&McArthur,J.C., 1988

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Thalamic Astasia:Inability to Stand After Unilateral Thalamic Lesions
Ann Neurol 23:596-603, Masdeu,J.C.&Gorelick,P.B., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Cognitive Impairment and Sensory Loss Associated with Chronic Low-Level Ethylene Oxide Exposure
Neurol 38:567-569, Crystal,H.A.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
Medicine 67:100-109, Anderson,N.E.,et al, 1988

Olfactory Dysfunction in Parkinsonism:A General Deficit Unrelated to Neurologic Signs, Disease Stage, or Duration
Neurol 38:1237-1244, Doty,R.L.,et al, 1988

Injuries Caused by Handcuffs
BMJ 297:111-112, Richmond,P.W.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Regional Pain is Rarely Hysterical
Arch Neurol 45:915-918, Merskey,H., 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Showing articles 1250 to 1300 of 1802 << Previous Next >>