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Differential
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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

Adies pupil

adverse drug reaction

agitation

alcohol

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic polyneuropathy

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

alcoholism

alpha-fetoprotein

alternating rapid movement

amenorrhea

amnesia

amphiphysin antibodies

amyloid plaques

anatomy of

anemia

aneurysm, intracranial

angiography, cerebral

anti mGluR1 encephalitis

antibodies to voltage-gated calcium channels

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia

apraxia of eye movements

areflexia

Arnold Chiari malformation

arthralgia

ataxia

ataxia telangiectasia

auditory evoked brainstem potentials

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

axonal spheroid

basal ganglia, calcification of

brainstem, infarction of

calcification, intracranial

calcium channel dysfunction

CAR syndrome

carcinoembryonic antigen

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

catalepsy

cataracts

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

cerebellitis, autoimmune

cerebellum

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

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

collapsin response mediator protein 5 IgG

coma

compression neuropathy

confusion

consanguinity

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, lesion of

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytosine arabinoside

deafness

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

depression

dermatomyositis

developmental abnormality of brain

developmental retardation

differential diagnosis

dilantin

dilantin, factors influencing metabolism of

dilantin, serum level

dilantin, toxicity

diplopia

disease modifying agents

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

drooling

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

dystonia

echolalia

ectatic basilar artery

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

enzyme, defect

eosinophilia

epidemiology of neurology

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

familial hemiplegic migraine

familial periodic ataxia

fatigue

fetal alcohol syndrome

fever

fine motor function, impaired

finger nose finger test

foam cells

foot deformity

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

gadolinium

gait disorder

gammaglobulin therapy, intravenous

ganglionitis

gangliosidosis GM2

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

gene

gene mutation

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

gliadin antibodies

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

Hallervorden Spatz disease

hearing loss, bilateral

heatstroke

heel-knee-shin test

hemianopia

hemianopia, transient

hemifacial spasm

hemiparesis

hemiplegia

hepatic encephalopathy

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

histochemistry

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)

hydrocephalus

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hypercalcemia

hyperesthesia

hyperpigmentation of skin

hypogonadism, hypogonadotropic

hypokalemia

hypokalemic alkalosis

hypometric saccades

hypomyelination

hyponatremia

hypothalamus, damage to

hypothyroidism

hypotonia

imbalance

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

intellectual deterioration

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

irritability

isoniazid

Jakob-Creutzfeldt disease

jaundice

JC virus

Korsakoff's psychosis

lactic acidemia

laughing, pathologic

leg numbness

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

lymphadenopathy

lymphoma

lymphoma involving CNS

lysosomal storage disease

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mediastinum, mass of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningitis

mental retardation

mental status, abnormal

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

multiple system atrophy

muscle biopsy

muscle pain

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, paraneoplastic

myelopathy, carcinomatous

myelopathy, necrotizing

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy

myopathy, alcoholic

myopathy, mitochondrial

myopia

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

neuronopathy, sensory

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

Niemann-Pick disease

NMDA antagonists

NMDA receptors

nutritional deficiency

nystagmus

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 flutter

ocular motility, disorders of

old age, neurology of

onconeural antibodies

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

optic neuropathy, nutritional

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

parietal lobe, lesion of

Parkinson disease

Parkinsonism syndrome

parotid gland neoplasm

pathology

pellagra

pelvic mass

peripheral nerve, lesion of

pes cavus

photosensitivity, skin

pigmentary retinopathy

pitfalls

pituitary, lesion of

plasmapheresis

pleocytosis of cerebrospinal fluid

POLG1 gene

polymerase chain reaction

polymyositis

polyneuropathy, chronic inflammatory demyelinating

pons, atrophy

pons, infarction of

pons, lesion of

positional head-hanging test

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

pursuit eye movements, abnormal

pyramidal tract dysfunction

quadriplegia

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

rash

reading disorder, acquired

Red flags

reflex, brainstem

remission

remote effect of cancer on the nervous system

renal failure

respiratory depression

reticulum cell sarcoma

reversible splenial lesion syndrome

saccadic eye movements, abnormal

salivation, excessive

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, withdrawal

sensorineural hearing loss

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

solvent

spasticity

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

splenomegaly

staphylococcal protein A column therapy

subarachnoid hemorrhage

syphilis, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

thiamine

thyroiditis

titubation

transglutaminase antibodies

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

ubiquitination

urinary gonadotropin

vertebral-basilar insufficiency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral infection, CNS, treatment of

vision, failure of in childhood

visual evoked response

visual impairment

visual loss

vitiligo

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Wernicke's encephalopathy

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

whole genome sequencing

Showing articles 250 to 300 of 4121 << Previous Next >>

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

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

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 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

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

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

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

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

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

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

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 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

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

Neurosurgical Management of Cerebellar Haematoma and Infarct
JNNP 59:287-292, Mathew,P.,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

MR Findings in Adult-Onset Adrenoleukodystrophy
AJNR 16:1227-1237, Kumar,A.J.,et al, 1995

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

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

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

Guidelines for the Management of Aneurysmal Subarachnoid Hemorrhage
Stroke 25:2315-2328, Mayberg,M.R.,et al, 1994

Acute Bilateral Cerebellar Infarction in the Territory of the Medial Branches of Posterior Inferior Cerebellar Arteries
Stroke 25:686-688, Yoshimasa,T.,et al, 1994

Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
Neurol 44:1064-1068, Roh,J.K.,et al, 1994

The Brain in Infantile Autism:Posterior Fossa Structures are Abnormal
Neurol 44:214-223, Courchesne,E.,et al, 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

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

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

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

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

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

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

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

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Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991

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

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

Showing articles 250 to 300 of 4121 << Previous Next >>