Neudle.com: ataxia intermittent

Neurology Specific Literature Search

Differential
(Click to cross reference)

abducens nerve paralysis

adverse drug reaction

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

amaurosis fugax

aminoacidopathies

amyloid angiopathy, cerebral

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, vertebral artery

antibodies to voltage-gated calcium channels

arteritis, temporal

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune disease

autonomic dysfunction

behavioral disorder

bladder dysfunction

brainstem, infarction of

brainstem, lesion of

calcium antagonist

calcium channel dysfunction

CAT scan, abnormal

CAT scan, angiography

central core disease

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral infarction

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chloride channel dysfunction

chromosomal abnormality

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

conversion reaction

cornea, abnormal

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dementia, subcortical

dentate nuclei, lesion of

developmental retardation

diabetes insipidus

diagnostic criteria

differential diagnosis

digital subtraction angiography

diurnal variation

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drug induced neurologic disorders

dystonia, psychogenic

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalopathy, acute

episodic disorders

episodic neurologic deficits

episodic unconsciousness

exercise intolerance

eye movement, disorders of

face, numbness of

facial nerve palsy

facial weakness

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

Friedreich's ataxia

fundus, abnormality of

genetic neurologic disorders

genetic testing

globus pallidus, lesion of, bilateral

Guillain Barre syndrome

hallucination, visual

head turning, neurologic complications with

headache, bifrontal

headache, elderly

headache, occipital

headache, recurrent

headache, severe

hemianopia, homonymous

hemimyoclonic jerks

hyperparathyroidism

hyperthyroidism

hypokalemic periodic paralysis

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

jaw claudication

lactic acidemia

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

limbic encephalitis

lysosomal storage disease

malignant hyperpyrexia

maple syrup urine disease

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, elderly

mental status, abnormal

metabolic disorder, primary

microhemorrhage, intracerebral

migraine, hemiplegic

molecular genetics

mononeuropathy multiplex

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, angiography

MRI, diffusion weighted

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

muscle weakness

muscle weakness, proximal

myasthenic syndrome

myoclonic jerks

myotonia congenita

nasal septum, perforation of

nausea and vomiting

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

neurotoxicity, acute

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, periodic

nystagmus, vertical

old age, neurology of

ophthalmoplegia

optic neuropathy, ischemic

otitis, neurologic complications with

pain, abdominal

pain, testicular

palatal myoclonus

paralysis, acute areflexic

paramyotonia congenita

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peroxisomal disease

personality disorder

pleocytosis of cerebrospinal fluid

posterior leukoencephalopathy syndrome

potassium channel antibodies

potassium channel dysfunction

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis, acute

pulmonary infiltrates

pupil, abnormality in neurologic disorders

quadriplegia, transient

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

REM sleep behavior disorder

retinal artery occlusion

reversible cerebral vasoconstrictive syndromes

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

sedimentation rate, elevated

seizure, differential diagnosis of

sensorineural hearing loss

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

spinal cord, compression of

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia

spinocerebellar ataxia type 6

status epilepticus

steroid therapy, CNS treatment and complications with

stress, emotional

strokelike episodes

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

symmetric brain lesions

tandem gait, ataxic

temporal lobe, lesion, bilateral

testicular biopsy

third nerve palsy

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, psychogenic

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, sustained

urea-cycle enzymopathies

urinary frequency

urinary incontinence

vaccination, neurologic complications with

vasospasm, cerebral

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

Virchow-Robin spaces, dilated

vision, blurred

visual field defect

vitamin E deficiency

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

white matter disease

wide based gait

Showing articles 1400 to 1450 of 1634 << Previous Next >>

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Ataxic Hemiparesis from a Midbrain Mass
Ann Neurol 9:405-407, Bendheim,P.E.,et al, 1981

Ataxic Hemiparesis with Trigeminal Weakness
Neurol 31:635-636, Sakai,T.,et al, 1981

Epstein-Barr-virus-carrying Lymphoma in a Patient with Ataxia-telangiectasia
BMJ 282:425-427, Saemundsen,A.K.,et al, 1981

Lecithin Treatment in Friedreich's Ataxia
BMJ 282:1197-1198, Pentland,B.,et al, 1981

Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Tick Paralysis With Persistent Weakness & Electromyographic Abnormalities
Arch Neurol 38:59-61, Donat,J.R., 1981

Neurologic Complications of Lymphomatoid Granulomatosis
Neurol 31:619-620, Hogan,P.J.,et al, 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Remission of Cerebellar Dysfunction After Pneumonectomy For Bronchogenic Carcinoma
NEJM 302:156, Paone,J.F.,et al, 1980

The Acute Sensory Neuronopathy Syndrome:A Distinct Clinical Entity
Ann Neurol 7:354-358, Sterman,A.B.,et al, 1980

Cerebellar Degeneration Due to Chronic Phenytoin Therapy
Ann Neurol 7:18-23, McLain,L.W.,et al, 1980

Homolateral Ataxia & Crural Paresis:Case Report
Neurol 30:1013-1015, Perman,G.P.,et al, 1980

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Phenytoin Plasma Concentrations in Paroxysmal Kinesigenic Choreoathetosis
Neurol 30:673-676, Homan,R.W.,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

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

Central Nervous System Toxicity Associated With Metronidazole Therapy
Ann Int Med 93:59-60, Kusumi,R.K.,et al, 1980

Legionnaires'Disease With Profound Cerebellar Involvement
Arch Neurol 37:379-380, Shetty,K.R.,et al, 1980

Acute Ataxia Associated with Ciguatera-type (Grouper) Tropical Fish Poisoning, Letter
Ann Neurol 7:491, Jones,H.R.Jr., 1980

Carpal Tunnel Syndrome in Porphyria
Lancet 2:808, Massey,E.W., 1980

Alcoholic Downbeat Nystagmus
Ann Ophthalmol 1127-1131, October 1980., Costin,J.A.,et al, 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

Neck-tongue Syndrome on Sudden Turning of the Head
JNNP 43:97-101, Lance,J.W.,et al, 1980

Showing articles 1400 to 1450 of 1634 << Previous Next >>