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 800 to 850 of 1775 << Previous Next >>

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

Reversible Periph Neuropathy Induced by Single Admin of High-Dose Paclitaxel
Neurol 51:868-870, Iniquez,C.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Clinicopath Conf
Sarcoidosis, Involving the Spinal Cord & Mediastinal Lymph Nodes, Case 8-1998, NEJM 338:747-754., , 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,Y.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Acupuncture and Amitriptyline for Pain Due to HIV-Related Peripheral Neuropathy
JAMA 280:1590-1595, Shlay,J.C.,et al, 1998

Distal Sensory Axonopathy after Sarin Intoxication
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Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Utility of Anti-Hu Antibodies in the Diagnosis of Paraneoplastic Sensory Neuropathy
Ann Neurol 44:976-980, Molinuevo,J.L.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

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

Vasculitis and Relate Disorders
In Textbook of Rheumatology, W.B. Saunders Co, 5th Ed, Chp 68, 1088, Valente,R.M.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Gradenigo Syndrome in a Human Immunodeficiency Virus-Positive Patient
Arch Int Med 157:2149, Morales,C.&Tachauer,A., 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Olfactory Dysfunction in Parkinson's Disease
JNNP 62:436-446, Hawkes,C.H.,et al, 1997

Clinical Features of Perineuritis
Muscle & Nerve 20:1153-1157997., Sorenson,E.J.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

Clinicopath Conf
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Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

HIV Infection of Dorsal Root Ganglion Neurons Detected by PCR in Situ Hybridization
Ann Neurol 42:368-372, Brannagan,T.H.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Clinicopath Conf
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Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Showing articles 800 to 850 of 1775 << Previous Next >>