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acute ataxia of childhood

acute cerebellar ataxia

advances in neurology

alcohol intolerance

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, children

aneurysm, fusiform

aneurysm, vertebral basilar system

Angelman syndrome

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

ankle reflex, absent

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

apraxia of eye movements

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

blood dyscrasias, neurologic findings with

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, neoplasms of

cerebral cortical atrophy

cerebral folate deficiency syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, prognosis in

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognitive delay

conjunctival biopsy

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, parenchymal

cyst, subcortical

deep gray nuclei

degenerative diseases of CNS

delayed dentition

dementia, childhood

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

Dravet syndrome

drug induced neurologic disorders in children

dysdiadochokinesia

electroencephalogram, abnormalities of

electron microscopy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalomyopathy

epicanthal folds

Epstein-Barr virus

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

feeding disorder

finger nose finger test

fingerprint bodies

Fisher's syndrome

fluorescene in situ hybridization

folic acid deficiency

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

Hartnup's disease

headache, severe

headache, sudden onset of

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Huntington's chorea

hydroxyglutaric aciduria

hyperosmolality

hypertension, cerebrovascular disease with

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunosuppression

inborn errors of metabolism

inclusion bodies

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrathecal medication

Jakob-Creutzfeldt disease

lactic acidemia

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

limbic encephalitis

lipid storage disorder of CNS

lysosomal storage disease

macular degeneration

marche a petits pas

Marinesco-Sjogren syndrome

mediastinum, mass of

memory, impairment of

meningitis, carcinomatous

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

multiple sclerosis

multiple system atrophy

muscle weakness

mycoplasma pneumoniae

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

myotonia dystrophica

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

nephrotic syndrome

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuronal ceroid-lipofuscinosis

neuropathy, acute

neurotransmitter

Niemann-Pick disease

NMDA antagonists

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

optical coherence tomography

oral ulcerations

osmotic demyelination syndrome

ovary, enlarged

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

personality change

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

pons, lesion of

Poretti-Boltshauser syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

puberty, delayed

pulmonary infection

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Refsum's disease

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinitis pigmentosa

sarcoidosis, CNS

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

sodium channel dysfunction

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

startle myoclonus

status epilepticus

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

teratoma, ovarian

tongue, protrusion of

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

upgaze, paralysis of

urinary incontinence

urinary retention

vertebral-basilar insufficiency

vertigo, episodic

viral infection

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

Von Hippel Lindau

walking, difficulty with

white matter disease

wide based gait

Wolfram syndrome

X-linked bulbospinal neuronopathy

Showing articles 500 to 550 of 4245 << Previous Next >>

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Acute Cerebellar Ataxia & Hearing Loss as Initial Symptoms of Infectious Mononucleosis
Arch Neurol 40:760-762, Erzurum,S.,et al, 1983

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

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Cerebellar Dysfunction after Acute Carbon Tetrachloride Poisoning
Lancet 2:968, Forster,S.H.,et al, 1983

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

Primary Position Vertical Nystagmus & Cerebellar Ataxia
Arch Neurol 40:310-314, Kattah,J.C.,et al, 1983

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

Permanent Neurological Deficits Due to Lithium Toxicity
Ann Neurol 13:453-455, Apte,S.N.,et al, 1983

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

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

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

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

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

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

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

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

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

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

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

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

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 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

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Neurological Manifestations & Mycoplasma Pneumoniae Infection
BMJ 2:832-833, Hodges,G.R.,et al, 1979

Acute Transitory Cerebellar Dysfunction Associated with Piperazine Adipate
Arch Neurol 36:180-181, Berger,J.R.,et al, 1979

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Beneficial Effect of Propranolol in Familial Ataxia
Ann Neurol 5:207, Braham,J.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978

Varicella & Acute Cerebellar Ataxia
Arch Neurol 35:769-771, Peters,A.C.B.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

The Benign Lateral Medullary Syndrome
Arch Neurol 35:112, Bernat,J.L.,et al, 1978

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

Showing articles 500 to 550 of 4245 << Previous Next >>