Neudle.com: newborn screening

Differential
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abdominal protrusion

abortion, spontaneous

abscess, intracerebral

abscess, intracerebral, treatment of

abscess, intracranial

abscess, intracranial-neonatal

abscess, sphenoid sinus

achilles tendon, enlarged

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acrocyanosis

acromicria

ACTH

activated protein C resistance

acyclovir

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affective disorders

agitation

agraphia

Aicardi-Goutieres syndrome

airway obstruction

akinetic mute

alcohol

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

aluminum

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, visual variant

amniotic fluid, infection

amphetamines

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, treatment of

aneurysm, post traumatic

aneurysm, posterior communicating artery

aneurysm, ruptured

aneurysm, ruptured, without subarachnoid hemorrhage

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiofibroma, facial

angiography, cerebral

angiography, cerebral, indications

angiography, posterior fossa

anterior horn cell disease

antibiotic prophylaxis

antibiotics

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticholinergic drugs

anticoagulant, complications of

anticoagulant, restarting

anticoagulant, reversal of

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, selection of

anticonvulsants, untoward effects of

antiphospholipid antibodies

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apraxia, constructional

aqueduct of Sylvius, stenosis

arachnodactyly

areflexia

arm weakness

Arnold Chiari malformation

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arterial dissection, childhood

arterial dissection, intracranial

arterial dissection, precipitating events

arterial dissection, recurrent

arterial dissection, spontaneous

arterial dissection, vertebral

arteriopathy

arteriopathy, focal cerebral of childhood

arteriopathy, transient

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

arteritides

arthralgia

arthrogryposis multiplex

Asians

aspartate aminotransferase

aspartocyclase

aspiration

aspirin

asymmetric crying facies

asymptomatic

ataxia

ataxia telangiectasia

ataxic-dystonia syndromes

ataxin

ataxin-2

atherosclerosis, accelerated

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

atrioventricular septal defect

attention deficit disorder with hyperactivity

atypical

auditory and vestibular pathways

auditory evoked brainstem potentials

autism

autism, screening for

autistic behavior

autoimmune disease

automobile accidents

autonomic dysfunction

autonomic nervous system

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial endocarditis, neurologic manifestations of

bacterial infection

baldness

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

basilar artery stenosis

basilar impression

behavior, combative

behavioral disorder

behavioral disorder, acute

beractant

bicaudate index

bilirubin encephalopathy

biologic markers

biotinidase deficiency

blood dyscrasias, neurologic findings with

blood pressure

blood pressure, lowering

bone marrow transplantation

bone pain

bone scanning

border zone hypoperfusion

border zone infarct

border zone infarct, cortical

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, negative

brain biopsy, stereotaxic

brain damage

brain purpura

brainstem, atrophy

brainstem, dysfunction

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, injury in New Born

brainstem, lesion of

brainstem, vascular malformation of

Brazil

breech delivery

bronchopulmonary dysplasia

burst suppression pattern, electroencephalogram

cachexia

CAG repeats

calcification, gyral

calcification, intracranial

calf atrophy

calf hypertrophy

campylobacter infection

Canavan's disease

cancer, cerebrovascular accident complicating patients with

cardiac arrest and resuscitation

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiopulmonary bypass

cardiovascular disease

caribbean

carotid angiogram

carotid artery

carotid artery atherosclerosis

carotid artery disease

carotid artery disease, noninvasive evaluation of

carotid artery ligation

carotid artery narrowing

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery occlusion, neck-delayed CVA following

carotid artery occlusion, posttraumatic

carotid artery stenosis

carotid artery stenosis, bilateral

carotid artery stenosis, intracranial

carotid artery thrombus

carotid rete mirabile

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, cerebrovascular disease

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, delta sign, empty

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, fluid-blood level

CAT scan, head injury

CAT scan, indications for

CAT scan, isodense lesion with acute hemorrhage

CAT scan, mass effect on

CAT scan, ring sign

CAT scan, venography

CAT scan, xenon-enhanced

caudate nucleus, atrophy

caudate nucleus, hemorrhage of

caudate nucleus, infarction

caudate nucleus, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus, expansion

cavernous sinus, syndrome

cavernous sinus, thrombosis

cavernous sinus, thrombosis, septic

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral death, accomodation requests

cerebral death, ancillary studies

cerebral death, apnea testing in

cerebral death, criteria

cerebral death, differential diagnosis

cerebral death, EEG in

cerebral death, infants and children

cerebral edema

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral palsy, work up

cerebral peduncle

cerebral perfusioin

cerebral vasculature

cerebral vasculature, calcification

cerebral veins

cerebral venous infarction

cerebral venous infarction in premature

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebritis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, childhood

cerebrospinal fluid, culture negative

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gamma amino butyric acid

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, newborn and infant

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, adolescent

cerebrovascular accident, bilateral

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, classification

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, complications with

cerebrovascular accident, cryptogenic

cerebrovascular accident, delayed onset

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, incidence of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, postpartum

cerebrovascular accident, posttraumatic

cerebrovascular accident, prehospital treatment

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, racial differences

cerebrovascular accident, recurrent

cerebrovascular accident, seizure with

cerebrovascular accident, severity

cerebrovascular accident, silent

cerebrovascular accident, surgical treatment of

cerebrovascular accident, three territory involvement

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, topographic pattern

cerebrovascular accident, vascular territory involved

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, infant and childhood

cerebrovascular disease, premature

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

cervical spine

cervical spine injury

cervical spine manipulation

cesarean section

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chickenpox

Chikungunya encephalomyeloradiculitis

chilbran skin lesions

child abuse

children

chiropractic manipulation

chiropractic manipulation, neurologic complications with

chloramphenicol

chloride channel dysfunction

choroid plexus, hemorrhage

choroid plexus, inflammation

chromosomal abnormality

chronic graft versus host disease

cigarette smoking

cingulate gyrus

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cocaine

cocaine, intrauterine exposure

collagen vascular disease

color vision

color vision, impaired

confusional state, acute

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

conjugate gaze, forced

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cortical ribbon sign

cortical vein thrombosis

cranial nerve palsies

cranial neuropathy

craniectomy, decompressive

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Cree leukoencephalopathy

Creutzfeldt-Jakob disease, genetic

cryopyrin-associated periodic syndrome

cryptorchidism

Cuba

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, arachnoid, infant

cyst, benign intracranial

cyst, cortical parenchyma

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cystinuria

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

Dandy Walker malformation

degenerative diseases of CNS

dehydration

Dejerine-Sottas syndrome

delay in diagnosis

delayed dentition

delivery, complicated

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

descending paralysis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diamond on quadriceps

diaphragmatic paralysis

diarrhea

dichlorphenamide

diet

differential diagnosis

difficulty climbing stairs

digits, abnormal

diplegia, spastic cerebral

disability rating scale, neurological

disability, neurological

disease modifying agents

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine beta hydroxylase

doppler

doppler, transcranial

down-beat nystagmus

downward deviation of eyes

downward gaze, paralysis of

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug addiction

drug induced neurologic disorders

drug induced neurologic disorders in children

drug interactions

drug overdose

duplex ultrasound

dural sinus thrombosis

dying

dysarthria

dysarthria-clumsy hand syndrome

dyskinesia, buccal lingual facial

dystonia, delayed onset

dystonia, etiology of

dystonia, focal

dystonia, painful

dystonia, treatment of

dystrophin

ear, abnormal

ears of the Lynx MR sign

ears, low set

eating disorder

echocardiogram

echocardiogram, transesophageal

ectatic carotid artery

eczema

efficacy

Ehlers-Danlos syndrome

Eisenmenger's syndrome

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electroencephalogram, inflammatory disease

electroencephalogram, interictal

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electrophoretic pattern, serum

electroretinograph

embolic stroke of unknown source

embolism

embolism, fat

embolism, paradoxical

embolism, septic

emergencies, neurologic

emergency room

Emery-Dreifuss muscular dystrophy

encephalitis, bacterial

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, viral

encephalocele

encephalomalacia

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, acute

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, post traumatic

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endocarditis, marantic

endocarditis, prophylaxis

endolymphatic sac tumors

enzyme, muscle disease

ependymoma

epicanthal folds

epidemic

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

evidence-based research

evoked potentials

executive dysfunction

exercise

exercise intolerance

exome sequencing

extracorporeal membrane oxygenation

extracranial-intracranial arterial bypass

eye movement, disorders of

Fabry's disease

face, elongated

facial anomalies

facial appearance, abnormal

facial weakness, bilateral

facioscapulohumeral syndrome

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

ferritin, elevated

ferritinemia

fetal alcohol syndrome

fetal distress

fetal monitor, intrapartum

fibrinolytic agents, complications

fibrinolytic agents, contraindications

fibrinolytic agents, intra-arterial local infusion

fibrinolytic therapy, intraventricular

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

finger nose finger test

finger tapping

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, pulmonary

fourth ventricle, floor

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

fresh frozen plasma

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal balding

frontal bossing

frontotemporal dementia, behavioral variant

fundus, abnormality of

fungal infection

fungal infection, CNS

fungal infection, CNS, treatment of

gamma amino butyric acid

gastrointestinal bleeding

Gaucher's disease

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

gestational age, estimation of

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glucose level, serum

glucose tolerance test, abnormal

glycogen storage disease

gout

Gowers maneuver

gram positive rod

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hallucination, visual

head injury, pediatric

headache, sudden onset of

health insurance

hearing loss

hearing loss, bilateral

hearing loss, sudden, unilateral

heart block

heart murmur

heart rate

heart valve, prosthetic

hemangioblastoma

hematoma, epidural-cranial

hematoma, intracerebral

hemianopia

hemianopia, homonymous

hemianopia, transient

hemichorea

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, congenital

hemoglobin abnormality, neurologic complications of

hemolytic-uremic syndrome

hemophagocytic lymphohistiocytosis

hemophilia

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhage, putamenal

hemorrhage, thalamic

hemorrhagic shock encephalopathy syndrome

hemosiderosis of CNS, superficial

heparin

heparin, low-molecular-weight

hepatic encephalopathy

hepatic failure

hepatic failure, acute

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc, thoracic

herniation syndromes, intracranial

herpes encephalitis

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, atypical

herpes simplex encephalitis, chronic

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, extra temporal

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, pathogenesis of

herpes simplex, neurocutaneous lesions in

herpes virus infection

hot, red, angry babies

human genome

human immunodeficiency virus type 1

human parechovirus

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydrocephalus

hydrocephalus, acute

hydrocephalus, classification of

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hydroxyurea

hyperactivity

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypercapnia

hypercoagulable state

hyperglycemia

hyperglycemia, neurologic dysfunction associated with

hyperglycemia, nonketotic

hyperhomocysteinemia

hyperkalemic periodic paralysis

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertelorism

hypertension

hypertension, children and adolescents

hyperthermia

hypertonia

hypertrophic intracranial pachymeningitis

hyperviscosity

hyperviscosity, neonatal

hypocalcemia

hypodontia

hypogammaglobulinemia

hypoglycemia

hypoglycemia, newborn and infant

hypoglycemic coma

hypoglycorrhachia

hypogonadism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

hypoplastic left heart syndrome

hyporeflexia

hyposmia

hypotelorism

hypotension, neurologic causes of

hypotension, systemic

hypoxia, intrauterine

hypoxia, newborn

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

hypsarrhythmia

iatrogenic neurologic disorders

implantable cardioverter defibrillator

impulsivity

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidence

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

incoordination

Indian Ocean islands

indomethacin

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

infantile hemiplegia

infantile hemiplegia, causes of

infantile spasm

infection

infertility

inflexibility, mental

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internal carotid artery

internal cerebral vein

internet

interstitial pulmonary fibrosis

intracerebral hemorrhage

intracerebral hemorrhage, bilateral

intracerebral hemorrhage, causes of

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, familial

intracerebral hemorrhage, incidence of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, location of

intracerebral hemorrhage, multiple

intracerebral hemorrhage, pathophysiology

intracerebral hemorrhage, progression of

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, treatment of

intracerebral hemorrhage, volume

intracerebral hemorrhage, work up

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial pressure monitoring

intracranial pressure, increased

intranasal medication

intrathecal treatment of meningitis

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intravenous drug abuse

intraventricular antibiotic administration

intraventricular chemotherapy

intraventricular hemorrhage

intraventricular hemorrhage, clot evacuation

intraventricular hemorrhage, primary

intraventricular hemorrhage, treatment

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jugular foramen syndrome

klippel feil syndrome

Krabbe's disease

KRIT1 gene

kyphoscoliosis, neurologic causes of

labor, complicated

laboratory values, normal

lactate

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

Lafora body

Lafora's disease

lateral sinus thrombosis

learning disability, in children

Leber's hereditary optic neuropathy

left handedness

leg spasms

leg spasms, painful

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leucine-rich repeat kinase 2 gene

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, hereditary diffuse

level of consciousness

level of consciousness, decreased

lid

lid abnormalities

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

limb-girdle weakness

linear lesion

lipid storage disorder of CNS

lipoproteins

listeria monocytogenes

listeriosis, CNS

livedo reticularis

liver disease

liver function enzymes

lumbar puncture, indications for

lupus anticoagulant

lymphangiomyomatosis

lysosomal storage disease

macrocephaly

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, Vein of Galen

malignant hyperpyrexia

malpractice

mania

manic-depressive

maple syrup urine disease

masseter muscle weakness

mastoiditis

McLeod syndrome

meconium staining

medical-legal aspects of neurology

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

medulla oblongata, neoplasm of

medullary streaks

medullary veins

melanoma, malignant

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningismus

meningitis

meningitis, acquired drug resistance in

meningitis, adults

meningitis, antibacterial treatment in

meningitis, aseptic

meningitis, bacterial

meningitis, bacteriologic etiology of

meningitis, basilar

meningitis, candida

meningitis, carcinomatous

meningitis, children

meningitis, chronic

meningitis, citrobacter

meningitis, CSF cell count-normal

meningitis, CSF findings in

meningitis, escherichia coli

meningitis, fungal

meningitis, gram negative

meningitis, gram negative-treatment of

meningitis, iatrogenic

meningitis, leptospira

meningitis, leukemic

meningitis, listeria monocytogenes

meningitis, lymphomatous

meningitis, neurologic aspects and complications of

meningitis, newborn

meningitis, pneumococcal

meningitis, postoperative neurosurgical

meningitis, predisposing factors in

meningitis, recurrent

meningitis, spinal fluid smear and culture-negative

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

mental retardation, familial

mental status, abnormal

mental status, abnormal, acute

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methylmalonic acidemia

Mexican

mexiletine

microabscesses, cerebral

microangiopathy, brain

microcephaly

microdontia

micrognathia

microhemorrhage, intracerebral

micropthalmia

microspherophakia

microvascular anastomosis, intracranial

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery

middle cerebral artery territory infarction

middle cerebral artery territory infarction, malignant

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine, seizures in

migratory lesion pattern

mimics

mineralization

mineralizing angiopathy

minimally invasive surgery

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

mitral valve vegetation

mitral valve, Lambl excrescences

molecular genetics

molybdenum cofactor deficiency

mongolism

monoclonal antibodies

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, contrast enhanced

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, disappearing lesion on

MRI, early changes in CVA

MRI, eye of tiger sign

MRI, false negative

MRI, fetal

MRI, field strength, high

MRI, FLAIR

MRI, FLAIR, hyperintense vessels

MRI, flow void, blood

MRI, functional

MRI, gradient-echo

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, spinal cord, increased intramedullary cord signal

MRI, sulcal hyperintensity

MRI, sunburst pattern

MRI, susceptibility weighted

MRI, venography

MRI, vessel wall

MRI, vessel wall enhancement

MRI, volumetry

MRS

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle spasm

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myelin protein zero gene

myelination of nervous system

myelopathy, chronic progressive

myeloproliferative disorder

myocardial infarction

myocardial infarction, acute

myoclonus, stimulus sensitive

myopathy, drug-induced

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, metabolic

myopathy, mitochondrial

myotonia dystrophica, classification

myotonia dystrophica, type 2

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

neoplasm, intracranial, children

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, metastatic causing intracranial hemorrhage

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS, hemorrhagic

neoplasm, metastatic to CNS-hemorrhage into

neoplasm, metastatic to CNS-origin of

neoplasm, metastatic to CNS-treatment of

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-hemorrhage in

neoplasm, primary of CNS-intraventricular

nephritis

nerve biopsy

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neural tube defect

neuroaxonal leukodystrophy

neuroblastoma

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurofibromatosis 2, presymptomatic

neurofibromin

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurological intensive care

neuromuscular junction

neuromyotonia

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, classification of

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, work up for

neuroprotective agents

newborn, evaluation of

next-generation sequencing

non-dominant hemisphere

Notch3 gene, false negative

numbness, extremity

nusinersen

nystagmus

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, vertical

obesity

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

oculodentodigital dysplasia

oculopharyngeal muscular dystrophy

odontoid process

odontoid process, aplasia

old age, neurology of

omeprazole

Ommaya reservoir

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic ataxia

optic atrophy

optic atrophy, bilateral

optic chiasm, enlarged

optic disc edema

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic tract, lesion of

optical coherence tomography

orbit, cellulitis of

organ donor

organ transplantation

organomegaly

ornithine transcarbamylase deficiency

orthopnea

orthostatic hypotension

osteogenesis imperfecta

osteomyelitis

osteomyelitis, skull

osteoporosis

otitis, neurologic complications with

otosclerosis

outcome research

ovarian dysgenesis

ovarian insufficiency

oxidative stress

pacemaker, cardiac-transvenous

pain, increased response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection, CNS

paraspinal muscle

parechovirus encephalitis

paresthesias

paresthesias, feet

paresthesias, lower extremity

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, juvenile

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

partruition

PAS positive

PAS positive material in the brain

past pointing

patent ductus arteriosus

patent foramen ovale

pathology

patient in waiting

patient information and support

percussion induced muscle contraction

periodic paralysis

peripheral blood smear

peripheral nerve, lesion of

periventricular leukomalacia

peroxisomal disease

peroxisomes

Perrault syndrome

persistent vegetative state

placenta, infection of

placenta, thrombosis of

platelet inhibiting drugs

PLEDs

pleocytosis of cerebrospinal fluid

pneumocystis carinii

poison, neurologic problems with

POLG1 gene

POLR3B

polycythemia, neonatal

polycythemia, primary

polycythemia, secondary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymicrogyria

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

pons, infarction of

pons, lesion of

pontine hemorrhage

pontine tegmental cap dysplasia

port wine nevus

portal caval shunt

post hemorrhagic hydrocephalus

posterior cerebral artery territory infarction

posterior cortical atrophy

posterior fossa, lesion of

postoperative neurologic complications

postpartum

posttraumatic

postural abnormality

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

preclinical

pre-eclampsia

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

pretectal syndrome

prethrombic state, screening for

prethrombotic state

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

primary thrombocythemia

primitive neuroectodermal tumors

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein C deficiency

protein S deficiency

proteinuria

proton pump inhibitors

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pulmonary hypertension

pulmonary stenosis

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, light reflex, abnormal

pupil, normal

pure motor hemiplegia

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyridoxine

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadrantanopsia, homonymous

quadriparesis

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

rash, hand

reaction time

real-time quaking-induced conversion

recanalization, arterial

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

revascularization, surgical

reversible neurologic disorder

review article

Reye's syndrome, prognosis of

RFC1 gene

RFLPs

rhabdomyolysis

rhabdomyosarcoma of heart

risk-benefit assessment

saccadic eye movements

saccadic eye movements, abnormal

safety

salivation, excessive

scoliosis, neurologic association with

sedimentation rate, elevated

seizure

seizure, age of onset

seizure, children

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, drug resistance

seizure, etiology of

seizure, focal

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, prognosis in childhood

seizure, pyridoxine dependent

seizure, stimulus sensitive

seizure, teenager

seizure, treatment of

seizure, workup of

selective vulnerability

self-mutilation

sensorimotor stroke

sensorineural hearing loss

serum alanine aminotransferase

setting sun phenomena

shoulder-girdle wasting

shunt procedure, ventricular

shunt procedure, ventricular-complications of

single photon emission computed tomography

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

slit lamp examination

small for dates infant, problems in

small vessel disease

small vessel disease, cerebral

SMN1 gene

SNCA duplication

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

solitaire device

somatostatin

somnolence

Southern immunoblot test

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spasticity

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

sphenoiditis

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, classification

spinal reflexes

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

spondylolysis

spongy degeneration of brain

spontaneous remission

sports medicine, neurology of

stem cell transplantation

steppage gait

stereotyped behavior

steroid

steroid therapy, CNS treatment and complications with

streptococcus viridans

streptokinase

stress, emotional

striatocapsular infarction

striatum, lesion of

stridor

string sign

striopallidodentate calcifications, familial idiopathic

stroke, completed

stroke, progression of

strokelike episodes

stuporous

Sturge-Weber syndrome

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, nonaneurysmal

subaxial subluxation

subcortical hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, chronic

subdural hematoma, neonates and infants

subdural hematoma, posterior fossa

sudden infant death syndrome

suicide

superficial temporal artery

superficial temporal artery - synangiosis

superior ophthalmic vein, dilated

superior sagittal sinus thrombosis

surfactant

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, childhood CNS

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

telangiectases

telangiectases, retinal

temper tantrums

temporal lobe, atrophy

temporal lobe, infarction

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thrombolysis, mechanical

thrombophlebitis

thrombosis, cerebral

tinnitus

tissue plasminogen activator, intravenous

tongue, fasciculations of

tongue, protrusion of

toxoplasmosis, congenital

transient ischemic attack

transient ischemic attack, evaluation

transient ischemic attack, young adult

transient neurologic deficit

transplacental virus infections

transposition of the great vessels

transverse smile

trauma

travel, foreign

treatment of neurologic disorder

trinucleotide repeats

tuberous sclerosis, screening for

tumefactive lesion

tumor suppressor gene

twins

tyrosine

tyrosine hydroxylase deficiency

tyrosinemia

ulcerative colitis

ultrasonography

ultrasonography, carotid artery

ultrasonography, head

ultrasonography, head, fetus-neonate

ultrasonography, nerve

umbilical-cord phlebitis

unconsciousness

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

ureaplasma urealyticum

uric acid, low

urinary frequency

urinary incontinence

urinary lactate:creatinine ratio

urine test for metabolic disorders

urine test in toxic screen

varicella zoster virus

varicella zoster virus, vasculopathy

vascular malformation, children, intracranial

vasculitides

vasculopathy

vasospasm, cerebral

vasospasm, internal carotid artery

vegetarianism

vein of Galen

venous thrombosis, non-cerebral

ventricular garlands

ventriculitis

ventriculostomy

ventriculostomy, endoscopic

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo

very long chain fatty acids

vestibular areflexia

vestibular migraine

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visuospatial disturbance

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

web sites

weight loss

Werdnig-Hoffman disease

Wernicke's encephalopathy

Western immunoblot test

wheelchair

whistle, inability to

white matter disease

white matter disease, periventricular

white matter disease, subcortical

white matter disease, unilateral

whites

whole genome sequencing

wide based gait

Williams syndrome

winging of scapula

Wolff-Parkinson-White syndrome

Wood's light

word-finding difficulty

workup

writing

xanthoma, tendon

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

x-linked mental retardation

x-ray, cervical spine

Zika virus infection

Showing articles 400 to 450 of 788 << Previous Next >>

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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Practice Parameter:Genetic Testing Alert
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Cerebrovascular Complications of HIV in Children
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Routine Indomethacin Prophylaxis:Has the Time Come
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Basal Ganglia and Thalamic Infarction in Children
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Intracranial Abnor in Infants Treated with Extracorporeal Membrane Oxygenation:Update on Sonographic & CT Findings
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Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
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Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
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Motor Changes in Presymptomatic Huntington Disease Gene Carriers
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
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Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Perinatal Brain Injury in Premature Infants Born to Mothers Using Alcohol in Pregnancy
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Expanded Spectrum of Herpes Simplex Encephalitis in Childhood
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Postvaricella Basal Ganglia Infarction in Children
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Postoperative Neurologic Complications after Open Heart Surgery on Young Infants
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
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Epidemiologic Association Between maternal Smoking During Pregnancy and Intracranial Hemorrhage in Preterm Infants
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Predictors of Neonatal Encephalopathy in Full Term Infants
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Rapid Antibody Test for Fragile X Syndrome
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Validity of Brain Death Criteria in Infants
Pediatrics 96:513-518, Fishman,M.A., 1995

Ischemic Stroke and Intracranial Multifocal Cerebral Arteriopathy in Williams Syndrome
J Pediatr 126:945-958, Soper,R.,et al, 1995

Cerebral Artery Stenosis in Williams Syndrome Causes Strokes in Childhood
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Showing articles 400 to 450 of 788 << Previous Next >>