Neudle.com: acute ataxia of childhood

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Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

advances in neurology

adverse drug reaction

alcohol intolerance

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

AMPA receptor antibodies

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, posterior fossa

angiotensin-converting enzyme

animal exposure

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

antithyroid antibodies

arterial dissection

arterial dissection, carotid

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, ruptured

arterial dissection, vertebral

ascending paralysis

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autonomic dysfunction

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basilar artery occlusion

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

behavioral disorder, acute

biotinidase deficiency

blindness, monocular

blindness, transient

brain biopsy, stereotaxic

brain scan, abnormal

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

calcium antagonist

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

carotid artery disease

CAT scan, abnormal

CAT scan, angiography

CAT scan, dense artery sign

CAT scan, pelvis

cat-scratch disease

cauda equina, enhancement

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar infarction

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, mechanical extraction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, genetic

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, rehabilitation of

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

congenital infection, CNS

congenital infection, viral

conjunctival biopsy

contractures, joint

cranial nerve palsies

cranial nerves, toxins effecting

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

dementia, reversible

dementia, treatment of

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei, lesion of

developmental disability

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

doll's head maneuver

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

electroencephalogram, abnormalities of

electron microscopy

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyopathy

encephalopathy, acute

encephalopathy, Hashimoto's

endovascular therapy

enterovirus infection of CNS

epileptic encephalopathy

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial nerve palsy

failure to thrive

FARS2 deficiency

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fisher's syndrome

flaccid paralysis

fornix, lesion of

fracture, long bone

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

genetic counselling

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gram negative rod

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hand-foot-mouth disease

headache, bifrontal

headache, occipital

headache, recurrent

headache, severe

headache, sudden onset of

headache, throbbing

heavy metal intoxication

heel-knee-shin test

hepatic failure

herniated disc, thoracic

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hyperintense vessel sign

hyperosmolality

hypertension, cerebrovascular disease with

hypoglycorrhachia

hypothalamus, disturbance of

iatrogenic neurologic disorders

immunodeficiency

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

industrial neurologic disorders

intellectual deficit

intellectual deterioration

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Kearns-Sayre syndrome

lactic acidemia

laughing, pathologic

lead and the nervous system

lead line, gingival

Leber's hereditary optic neuropathy

left handedness

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

limbic encephalitis

liver function enzymes

locked-in syndrome

lymphadenopathy

lymphoma involving CNS

marche a petits pas

melanoma, malignant

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, lymphomatous

meningitis, recurrent

meningoencephalitis

meningovascular syphilis

mental status, abnormal

mesial temporal lobe

metabolic acidosis

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, visual symptoms in

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, hyperkinetic

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle weakness

mycoplasma pneumoniae

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

nausea and vomiting

neonatal screening, genetic neurologic disorders

nephrotic syndrome

nerve conduction studies

neurologic complications

neurologic complications of, systemic cancer

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination, focal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuropathy, acute

neuropathy, painful

neuropathy, recurrent

neuropathy, sensory

neurotoxicity, acute

NMDA antagonists

nystagmus, monocular

nystagmus, rotary

nystagmus, spontaneous

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

optic neuropathy, toxic

oral ulcerations

orthostatic hypotension

osmotic demyelination syndrome

ovary, enlarged

pain, abdominal

palmomental response

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

patent foramen ovale

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Penumbra System

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

polymerase chain reaction

polyneuropathy, chronic relapsing

pons, infarction of

pons, lesion of

posterior leukoencephalopathy syndrome

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary edema

pulmonary infection

pulmonary infiltrates

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal tubular acidosis

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

riboflavin transporter deficiency

root lesion, nerve

rubella encephalitis, progressive

rubella syndrome

sarcoidosis, CNS

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

shunt procedure, ventricular

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

spastic diplegia

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 7

startle myoclonus

status epilepticus

steroid therapy, CNS treatment and complications with

striatal encephalitis

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, recurrent

substantia nigra

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

teratoma, ovarian

tissue plasminogen activator, intravenous

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

tuberculosis, miliary

upgaze, paralysis of

urinary incontinence

urinary retention

vasospasm, cerebral

vertebral-basilar insufficiency

violent behavior

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

visual loss, transient

visual obscurations, transient

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness, generalized

weakness, progressive

white matter disease

wide based gait

Wolfram syndrome

Showing articles 150 to 200 of 8069 << Previous Next >>

Association of Pediatric Acute-Onset Neuropsychiatric Syndrome with Microstructural Differences in Brain Regions Detected via Diffusion-Weighted Magnetic Resonance Imaging
JAMA Network Open 3:doi:10.1001/JAMANETWORKOPEN.2020.4063, Zheng, J.,et al, 2020

Large-Vessel Stroke as a Presenting Feature of Covid-19 in the Young
NEJM 382:e61-e63, Oxley, T.J., et al, 2020

New Onset Weakness in the Face and Arm
BMJ 368:L7077, Brites, L.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Stenting for Acute Carotid Artery Dissection
Stroke 51:e3-e6, Brown, S.C.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

Postraumatic Stress Disorder and Risk for Stroke in Young and Middle-Aged Adults
Stroke 50:2996-2003, Rosman, L.,et al, 2019

Reversible Cerebral Vasoconstriciton Syndrome
www.UptoDate.com, June, Singhal, A., 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

May-Thurner Syndrome as a Cause of Embolic Stroke of Undetermined Source in a Young Patient
Neurol 92:e2507-e2509, De Leon-Benedetti, A.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Delayed Complications of Cranial Irradiation
www.UptoDate.com, May, Dietrich, J.,et al, 2019

Clinical Characteristics and Outcomes of Methamphetamine-Associated Intracerebral Hemorrhage
Neurol 93:e1-e7, Swor, D.E.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Lyme Myelopathy:Case Report and Literature Review of a Rare But Treatable Disorder
Mult Scler Relat Disord 29:1-6, Kaiser,E.A.,et, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Early Prediction of Malignant Brain Edema after Ischemic Stroke
Stroke 49:2918-2927, Wu, S.,et al, 2018

Mystery Myelitis in Children
JAMA 320:2069, Kuehn, B., 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

The Dangers of Playing Squash
BMJ 362:K3062, Marrinan,E.,et al, 2018

Patent Foramen Ovale Closure, Antiplatelet Therapy or Anticoagulation Therapy Alone for Management of Cryptogenic Stroke?
BMJ 362:k2515, Kuijpers, T.,et al, 2018

Brachial Plexus Ultrasound and MRI in Children with Brachial Plexus Birth Injury
AJNR 39:1745-1750, Gunes, A.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Showing articles 150 to 200 of 8069 << Previous Next >>