Neudle.com: spastic ataxia

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal reflex, absent

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alternating rapid movement

Alzheimer's disease

amyloid plaques

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, spinal

ankle reflex, absent

anterior horn cell disease

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

B 12 deficiency

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

bladder dysfunction

bone marrow biopsy

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

burning paresthesia

calcification, intracranial

carcinoma of pancreas

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

caudate nucleus, atrophy

caudate nucleus, lesion of, bilateral

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

cerebral folate deficiency syndrome

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chorea, causes of

chorea, familial

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

cold hands sign

color vision, impaired

concentration, impaired

congenital infection, CNS

controversies in neurology

conversion reaction

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cyst, epidermoid of CNS

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

diplegia, spastic cerebral

disability, neurological

distal muscle atrophy

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis, viral

encephalomyelitis

endovascular therapy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

evoked potentials

exome sequencing

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, recurrent

failure to thrive

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

Friedreich's ataxia

Friedreich's ataxia, late onset

fundus, abnormality of

gammaglobulin therapy, intravenous

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hearing problems in children

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

Hodgkin's disease

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's disease, children

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

lactic acidemia

laughing, pathologic

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

life expectancy

locked-in syndrome

lymphoma involving CNS

marche a petits pas

Marinesco-Sjogren syndrome

medulla oblongata, lesion of

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylglutaconic aciduria

methylmalonic acidemia

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, contrast enhanced

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, spinal cord

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

myeloneuropathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, vacuolar

myoclonic jerks

myoclonus, epilepsy

myopathy, vacuolar

myositis, ocular

myxedema, neurologic manifestations of

Native Americans

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuropathology, brain

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

numb clumsy hands syndrome

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optical coherence tomography

orthostatic hypotension

pain, abdominal

palatal myoclonus

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Pelizaeus Merzbacher

pernicious anemia

personality change

photosensitivity, skin

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

portal caval shunt

posterior column disease

postural abnormality

precipitating factors

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

regional enteritis

release phenomena

remote effect of cancer on the nervous system

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sarcoidosis, CNS

scalp tenderness

sclerae, hyperpigmented

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, tonic-clonic

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

solitary scerlosis

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

startle reaction

status epilepticus

stereotyped behavior

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, abnormal

teeth, number of in infants

tendon, enlarged

thalamus, lesion of

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tonsillar herniation of cerebellum

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

ulcerative colitis

ulcers, fingertip

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary urgency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

vitamin deficiency

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness, progressive

weakness, proximal

Western immunoblot test

white matter disease

wide based gait

xanthoma, tendon

xeroderma pigmentosa

Showing articles 50 to 100 of 1499 << Previous Next >>

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 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

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

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

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

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

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

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

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

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

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Neurologic Sequelae of Chronic Solvent Vapor Abuse
Neurol 36:698-702, Hormes,J.T.,et al, 1986

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

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

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

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

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

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Showing articles 50 to 100 of 1499 << Previous Next >>