Neudle.com: cerebellar ataxia children

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acetazolamide

aciduria

acute ataxia of childhood

acute cerebellar ataxia

advances in neurology

aggression

alcohol intolerance

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, vertebral basilar system

Angelman syndrome

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

aniridia

ankle reflex, absent

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

anxiety

apraxia of eye movements

areflexia

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign

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

blindness

blood dyscrasias, neurologic findings with

brachycephaly

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

CAG repeats

calcification, intracranial

carcinoembryonic antigen

CAT scan, emission, abnormal

CAT scan, pelvis

cataplexy

cataracts

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

cerebellitis, autoimmune

cerebellum, neoplasms of

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral palsy

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

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonus

coenzyme Q10

coenzyme Q10 deficiency

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

degenerative diseases of CNS

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

drug induced neurologic disorders in children

electroencephalogram, abnormalities of

electromyogram

electron microscopy

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

finger nose finger test

fingerprint bodies

fish

Fisher's syndrome

fluorescene in situ hybridization

folic acid

folic acid deficiency

foot deformity

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gait disorder

gait, spastic

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

glutamic acid

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

granulomatous disease

growth hormone

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

headache, sudden onset of

hearing loss

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

huntingtin

Huntington's chorea

hydroxyglutaric aciduria

hypertension, cerebrovascular disease with

hypopigmentation of skin

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunodeficiency

immunosuppression

immunotherapy

inborn errors of metabolism

inclusion bodies

incoordination

infection

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrathecal medication

iris, abnormal

irritability

Jakob-Creutzfeldt disease

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia

leukodystrophy

limbic encephalitis

lipid storage disorder of CNS

lymphoma

lysosomal storage disease

Marinesco-Sjogren syndrome

masked facies

mediastinum, mass of

memory, impairment of

meningismus

meningitis

meningitis, carcinomatous

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, children

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal antibodies

mortality

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, negative

MRI, serial

multiple sclerosis

multiple system atrophy

mycoplasma pneumoniae

myelinolysis, extrapontine

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

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

optical coherence tomography

oral ulcerations

oscillopsia

osmotic demyelination syndrome

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

past pointing

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

personality change

piperazine

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

Poretti-Boltshauser syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

progeria

prognathism

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

recurrent

Refsum's disease

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

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

seronegative

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

smiling

sodium channel dysfunction

spastic ataxia

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

startle myoclonus

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

tongue, protrusion of

topiramate

torticollis

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

vertebral-basilar insufficiency

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

Von Hippel Lindau

walking, difficulty with

X-linked bulbospinal neuronopathy

Showing articles 350 to 400 of 4245 << Previous Next >>

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Clinicopath Conf
Q Fever, Acute (with Cerebellar and Meningeal Involvement) , Case 38-1996, NEJM 335:1829-1834., , 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 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

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Tumoral Multiple Sclerosis of the Cerebellum in a Child
AJNR 16:1164-1166, Rusin,J.A.,et al, 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

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

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

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Roller-coaster-induced vertebral artery dissection
Lancet 346:767, Biousse, V.,et al, 1995

The Syndrome of'Cerebellar'Mutism and Subsequent Dysarthria
Neurol 44:2040-2046, vanDongen,H.R.,et al, 1994

Neuropathologic Correlated of Persistent Neurologic Deficit in Lithium Intoxication
Ann Neurol 36:928-931, Schneider,J.A.&Mirra,S.S., 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
Neurol 44:1506-1507, Ito,H.,et al, 1994

Spectrum of Lateral Medullary Syndrome:Correlation Between Clinical Findings and Magnetic Resonance Imaging in 33 Subjects
Stroke 25:1405-1410, Kim,J.S.,et al, 1994

Ataxia-Telangiectasia:MR and CT Findings
J Comput Assist Tomogr 18:724-727, Farina,L.,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

Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
Neurol 44:1184-1185, Counsell,C.E.,et al, 1994

Neurologic Manifestations of Cocaine Exposure in Childhood
Pediatrics 93:557-560, Mott,S.H.,et al, 1994

Small Primary Intracerebral Hemorrhage:Clinical Presentation of 28 Cases
Stroke 25:1500-1506, Kim,J.S.,et al, 1994

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

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Pathogenesis of Superficial Siderosis of the Central Nervous System
Ann Neurol 34:646-653, 635-6361993., Koeppen,A.H.,et al, 1993

MRI in Lightning Encephalopathy
Neurol 43:1437-1438, Cherington,M.,et al, 1993

The Prevalence of CT Abnor of the Cerebrum in 100 Consecutive Children Symptomatic with the HIV
Ann Neurol 34:198-205, DeCarli,C.,et al, 1993

Posterior Cranial Fossa Tumours in Childhood
Neuroradiology 35:274-278, Chang,T.,et al, 1993

MRI of Gangliocytoma of Cerebellum and Spinal Cord
J Comput Assist Tomogr 17:488-491, Furie,D.M.,et al, 1993

Wallenberg's Lateral Medullary Syndrome
Arch Neurol 50:609-614, Sacco,R.L.,et al, 1993

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

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

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

Showing articles 350 to 400 of 4245 << Previous Next >>