Neudle.com: sensory ataxia

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Differential
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abducens nerve paralysis

acral sensory symptoms

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

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 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

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

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, 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

night blindness

nitrogen mustard

NMDA antagonists

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

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, 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 900 to 950 of 1775 << Previous Next >>

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
Neurol 47:10-17, Dyck,P.J.,et al, 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Spinal Cord Infarction:Etiology and Outcome
Neurol 47:321-330, Cheshire,W.P.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Ataxic Hemiparesis and Hemiageusia from an Isolated Post-Traumatic Midbrain Lesion
Neurol 47:1348-1349, Johnson,T.M., 1996

Radiologic-Clinical Correlation:One-and-a-Half Syndrome Associated with Cheirooral Syndrome
AJNR 17:1482-1484, Shintani,S.,et al, 1996

Neurotoxicity Related to the Use of Topical Tretinoin (Retin-A)
Ann Int Med 124:227-228, Bernstein,A.L.&Leventhal-Rochon,J.L., 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Prevalence of Parkinsonian Signs and Associated Mortality in a Community Population of Older People
NEJM 334:71-76, Bennett,D.A.,et al, 1996

Peripheral Neurotoxicity Induced by Docetaxel
Neurol 46:104-108, 21996., Hilkens,P.H.E.,et al, 1996

Oral and Genital Pain Syndromes in Parkinson's Disease
Movement Disorders 11:421-426, Ford,B.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Takayasu's Arteritis
Stroke Syndromes, Eds Bogousslavsky & Caplan, Cambridge Univ Press, Chp 48, p 439-442, Naritomi,H., 1995

Cutaneous Nerve Lesions of the Shoulder and Arm After Arthroscopic Shoulder Surgery
J Shoulder Elbow Surg 4:254-258, Segmuller,H.E.,et al, 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Acute Anterior Interosseous Neuropathy in Pt with Hereditary Neuropathy with Liability to Press Palsies:Clin & EMG Study
Muscle & Nerve 18:1329-1331995., Felice,K.J., 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995

Hemiplegia Vegetativa Alterna (Ipsilateral Horner's Synd & Contralat Hemihyperhidrosis) Post Cerebral Art Occl
Stroke 26:702-704, Bassetti,C.&Staikov,I.N., 1995

Thalamic Hemorrhage:A Prospective Study of 100 Patients
Stroke 26:964-970, Kumral,E.,et al, 1995

Massive Infarcts Involving the Territory of the Anterior Choroidal Artery and Cardioembolism
Stroke 26:609-613, Levy,R.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Reversible Downbeat Nystagmus and Ataxia in Felbamate Intoxication
Neurol 45:845, Hwang,T.L.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Showing articles 900 to 950 of 1775 << Previous Next >>