Neudle.com: abnormal leukocyte enzyme

Differential
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abdominal muscle paralysis

acetylcholine

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

alopecia

alpha galactosidase A deficiency

aminoacylase 1 deficiency

angiotensin-converting enzyme

anorexia nervosa

anterior horn cell disease

anticonvulsants

anticonvulsants, untoward effects of

apraxia

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arthropathy

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

biotin deficiency

biotinidase deficiency

blindness

blood dyscrasias, neurologic findings with

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

burning feet

burning feet, differential diagnosis of

burning hands

burning paresthesia

calcification, intracranial

calf hypertrophy

Canavan's disease

carbamyl phosphate synthetase-I deficiency

carbidopa

carbonic anhydrase II deficiency

CAT scan, false negative

cataracts

caudate nucleus, lesion of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cherry red spot

cherry red spot-myoclonus syndrome

children

cholesterol

choline acetyltransferase

choline chloride

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

coma

compression fracture

confusion

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

cranial nerve enlargement

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cry, abnormal

crying

cultured skin fibroblasts

cystinuria

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

dementia

dementia, presenile

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

diet

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine

drooling

dropped head syndrome

dystonic reaction, acute

echolalia

efficacy

electrocardiogram, abnormal

electromyogram

electron microscopy

emergencies, neurologic

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

exercise

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

fatty acid, elevated plasma content

feeding disorder

fever

floppy infant

flow study, carotid artery

fornix, lesion of

fracture, pathologic

frontal bossing

frontal lobe, behavior with disease of

frontal lobe, lesion of

fucosidosis

fundus, abnormality of

gangliosidosis GM2-AB variant

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glutaric acidemia

glutaric aciduria

glycine

glycogen debranching enzyme deficiency

glycogen storage disease

glycoprotein

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

headache, progressive

headache, thunderclap

headbanging

hearing loss

heart murmur

hematopoietic tissue, extramedullary

hemianopia, homonymous

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

hexosaminidase-A

hexosaminidase-A and B

histochemistry

histochemistry of muscle

homocystinuria

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hypogammaglobulinemia

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intrauterine

iron, brain

irritability

ischemic exercise test

jaundice

Jewish

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lacunar infarction

L-dopa

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

leukocyte enzyme abnormality

leukodystrophy

life expectancy

lipid storage disorder of CNS

livedo reticularis

liver disease

lysosomal storage disease

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

microspherophakia

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucopolysaccharidoses

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

myopathy, distal, vacuolar

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

neonatal screening, genetic neurologic disorders

nerve biopsy

nerve conduction studies

neuraminidase deficiency

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuropathology

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

ornithine transcarbamylase deficiency

paraspinal muscle weakness

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

Pompe's disease of glycogen storage

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

putamen, lesion of

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

rash

recurrent

renal failure

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

retinopathy

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

scoliosis, neurologic association with

screaming

screening

second wind phenomena

seizure

seizure, children

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

short stature

skin, biopsy

skin, lesions in neurologic disorders

small vessel disease

sodium valproate

sodium valproate, toxicity

somnolence

spasticity

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

substantia nigra

suck, poor

symmetric brain lesions

systemic illness

Tay-Sachs disease

temporal lobe, lesion

term infant

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

tinnitus

tone, muscle, increased

tongue, enlarged

tongue, weakness

transketolase

treatment of neurologic disorder

tyrosine

tyrosine hydroxylase deficiency

tyrosinemia

umbilical-cord blood transplantation

urea

urea-cycle enzymopathies

uremia

urinary incontinence

urine test for metabolic disorders

urine, dark

vasculitides

vasculopathy

vertebral-basilar insufficiency

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

wheelchair

white matter disease

winging of scapula

Showing articles 1350 to 1400 of 13591 << Previous Next >>

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Intrasellar Herniation
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A 22-year-old Man Presenting with Headache and Right Leg Jerks
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Clinicopathologic Conference, Lyme Meningoradiculitis
NEJM 379:1862-1868, Case 34-2018, 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

MR Neurography of the Lumbosacral Plexus for Lower Extremity Radiculopathy: Frequency of Findings, Characteristics of Abnormal Intraneural Signal, and Correlation with Electromyography
AJNR 39:2154-2160, Chazen, J.L.,et al, 2018

Spinal Coccidioidomycosis: MR Imaging Findings in 41 Patients
AJNR 39:2148-2153, Crete, R.N.,et al, 2018

Neuroimaging Findings of Zika Virus-Associated Neurologic Complications in Adults
AJNR 39:1967-1974, Hygino da Cruz, L.C.,et al, 2018

Surviving Cerebral Malaria
Neurol 91:978-979, Wijdicks, E.F.M. & Park, J.G., 2018

Japanese Encephalitis
Neurol 91:e2031-e2032, Zhang, B.,et al, 2018

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

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

The Heart Sign in a Patient with Apparent Locked-In Syndrome
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Clinicopathologic Conference, Susacs Syndrome
NEJM 379:2152-2159, Case 37-2018, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

Hemimeningitis Mimicking Acute Ischemic Stroke
Neurol 91:e2280-e2281, Castillo-Torres, S.A. & Martinez, H.R., 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

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Delayed-Onset MRI Findings in Acute Chorea Related to Anoxic Brain Injury
Clin Imaging 48:22-25, Ghasemi, M.,et al, 2018

Thalamic Strokes that Severely Impair Arousal Extend Into the Brainstem
Ann Neurol 84:926-930, Hindman, J.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
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Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Intravenous Thrombolysis in Unwitnessed Stroke Onset: MR WITNESS Trial Results
Ann Neurol 83:980-993, Schwamm, L.H.,et al, 2018

Rolling Stones Sign as Hard and Fast Evidence of Calcified Cerebral Emboli
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Presentation of Diffuse Large B-Cell Lymphoma with Bilateral Sequential Oculomotor Neuropathy
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A 41-year-old man with Thunderclap Headache
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Autoimmune Pancerebellitis Associated with Pembrolizumab Therapy
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Cerebrovascular Manifestations of Neurosarcoidosis: An Underrecognized Aspect of the Imaging Spectrum
AJNR 39:1194-1200, Bathla, G.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
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Drug Reaction with Eosinophilia and Systemic Symptoms after Daclizamub Therapy
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Alexander Disease with Features of Both Frontal and Bulbospinal Involvement
Neurol 91:e396-e397, Nam,T-S.,et al, 2018

A Patient With Multiple Cranial Nerve Palsies and Areflexic Paraparesis
Neurol 91:e392-e395, Garg,R.K.,et al, 2018

Andexxa-An Antidote for Apixaban and Rivaroxaban
JAMA 320:399-400, , 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
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Coxa Saltans Misdiagnosed as Functional Gait Disorder
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An Infant with Episodic Facial Flushing
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Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

Showing articles 1350 to 1400 of 13591 << Previous Next >>