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abdominal contractions

abdominal distention

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acquired immunodeficiency syndrome, infants and children

ACTH, ectopic syndrome of

adverse drug reaction

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alpha-fetoprotein

alternating rapid movement

amphiphysin antibodies

amyloid plaques

aneurysm, intracranial

angiography, cerebral

anti Hu antibody

anti mGluR1 encephalitis

anti Ri antibody

anti Tr antibodies

anti Yo antibody

antibodies to voltage-gated calcium channels

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

apraxia of eye movements

Arnold Chiari malformation

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

auditory evoked brainstem potentials

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

axonal spheroid

basal ganglia, calcification of

behavioral disorder

Bergmann's gliosis

bone marrow biopsy

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

calcification, intracranial

calcium channel dysfunction

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carcinoma of ovary

CAT scan, abdomen

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral vasculature

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, prevention of

chemotherapy, CNS treatment and complications with

chorea, familial

choreoathetosis

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

Cockayne's syndrome

coenzyme Q10 deficiency

collapsin response mediator protein 5 IgG

compression neuropathy

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytosine arabinoside

degenerative diseases of CNS

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

dermatomyositis

developmental abnormality of brain

developmental retardation

dexterity, impaired

diabetes mellitus

differential diagnosis

dilantin, factors influencing metabolism of

dilantin, serum level

dilantin, toxicity

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

ectatic basilar artery

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

epidemiology of neurology

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial nerve palsy

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fourth ventricle, enlargement of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, horizontal

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

gliadin antibodies

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

heel-knee-shin test

hemianopia, transient

hemifacial spasm

hepatic encephalopathy

heralding manifestation

highly active antiretroviral therapy

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

human immunodeficiency virus type 1

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

hydroxytryptophan L-5(L-5 HTP)

hyperpigmentation of skin

hypogonadism, hypogonadotropic

hypokalemic alkalosis

hypomyelination

hypothalamus, damage to

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

immunosuppression

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

Jakob-Creutzfeldt disease

Korsakoff's psychosis

lactic acidemia

laughing, pathologic

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukodystrophy, 4H

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

lymphadenopathy

lymphoma involving CNS

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mediastinum, mass of

memory, defect of recent

memory, impairment of

mental retardation

mental status, abnormal

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

monoclonal antibodies

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, spinal cord

multiple sclerosis

multiple system atrophy

muscle weakness

muscle weakness, proximal

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelopathy, carcinomatous

myelopathy, necrotizing

myoclonic jerks

myoclonus, abdominal

myoclonus, epilepsy

myoclonus, segmental

myopathy, alcoholic

myopathy, mitochondrial

Native Americans

nausea and vomiting

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

nephrotic syndrome

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathy, motor

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

Niemann-Pick disease

NMDA antagonists

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occipital lobe, infarction

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

old age, neurology of

onconeural antibodies

ophthalmoplegia

opsoclonus-myoclonus syndrome

optic neuropathy

optic neuropathy, nutritional

orbit, tomograms of

pain, abdominal

palatal myoclonus

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, spastic

parietal lobe, lesion of

Parkinson disease

Parkinsonism syndrome

parotid gland neoplasm

peripheral nerve, lesion of

photosensitivity, skin

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, infarction of

pons, lesion of

positional head-hanging test

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

pyramidal tract dysfunction

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

reading disorder, acquired

reflex, brainstem

remote effect of cancer on the nervous system

respiratory depression

reticulum cell sarcoma

retina, abnormal

reversible splenial lesion syndrome

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, children

seizure, withdrawal

sensorineural hearing loss

serologic testing

serum tumor markers

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

speech disorder

speech disorder, non aphasic

spinal cord, injury of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenium of corpus callosum

staphylococcal protein A column therapy

startle myoclonus

status epilepticus

stiff man syndrome

subarachnoid hemorrhage

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

testicular germinoma

testicular teratoma

thalamus, lesion of

thalamus, lesion of-bilateral

transglutaminase antibodies

transient ischemic attack

treatment of neurologic disorder

tremor, intention

tremor, writing

trichopoliodystrophy

trigeminal neuralgia

trinucleotide repeats

urinary gonadotropin

vertebral-basilar insufficiency

vertigo, positional

vibratory sensation

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral infection, CNS, treatment of

vision, failure of in childhood

visual evoked response

visual impairment

voice, abnormality of

walking, difficulty with

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Wernicke's encephalopathy

Western immunoblot test

Whipple's disease

white matter disease

wide based gait

Showing articles 250 to 300 of 3682 << Previous Next >>

Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994

MR Findings in Seven Patients with Organic Mercury Poisoning (Minamata Disease)
AJNR 15:1575-1578, Korogi,Y.,et al, 1994

MR of Sarcoidosis in the Head and Spine:Spectrum of Manifestations and Radiographic Response to Steroid Therapy
AJNR 15:973-982, Lexa,F.J.&Grossman,R.I., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Spectrum of Complications During Bacterial Meningitis in Adults
Arch Neurol 50:575-581, Pfister,H-W.,et al, 1993

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

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Cerebellar and Cerebral Abnormalities in Rett Syndrome:A Quantitative MR Analysis
AJR 159:177-183, Murakami,J.W.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

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

MR Imaging Features of Medulloblastoma
AJR 158:859-865, Meyers,S.P.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Babinski-Nageotte Syndrome on Magnetic Resonance Imaging
Stroke 22:272-275, Nakane,H.,et al, 1991

Neuroanatomy of Fragile X Syndrome:The Posterior Fossa
Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991

Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
Neuroradiology 33:239-242, Sugita,K.,et al, 1991

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,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

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

The Significance of MRI Abnormalities in Children with Neurofibromatosis
Neurol 39:373-378, Duffner,P.K.,et al, 1989

A New Sign of Neurofibromatosis on Magnetic Resonance Imaging of Children
Arch Neurol 46:1222-1224, Goldstein,S.M.,et al, 1989

Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism
NEJM 318:1349-1354, 13901988., Courchesne,E.,et al, 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Magnetic Resonance Imaging of Cerebral Lesions in Pts with the Sjogren Syndrome
Ann Int Med 108:815-823, Alexander,E.L.,et al, 1988

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

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Acute Cerebellar Hemorrhage & CT Evidence of Tight Posterior Fossa
Neurol 36:858-860, Weisberg,L.A., 1986

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

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

Intracranial Hemorrhage in the Term Newborn
Arch Neurol 41:30-34, Fenichel,G.M.,et al, 1984

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Unilateral Cerebellar Hypoplasia
J Comput Assist Tomogr 7:1077-1078, Mendelsohn,D.B.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Neuro-Ophthalmologic Signs in the Angiitic Form of Neurosarcoidosis
Neurol 33:1130-1135, Caplan,L.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Cerebellar Strokes:Mortality, Surgical Indications, & Results Of Ventricular Drainage
Lancet 2:429-432, Shenkin,H.A.,et al, 1982

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

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

Showing articles 250 to 300 of 3682 << Previous Next >>