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Differential
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abdominal muscle paralysis

acetylcholine

acetylcholine in CNS

acetylcholine receptor

acetylcholine receptor antibody

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

alpha galactosidase A deficiency

aminoacylase 1 deficiency

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, guamian type of

angiotensin-converting enzyme

anorexia nervosa

anterior horn cell disease

anti IgLON5

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antidepressant

antiendomysial antibodies

apraxia

apraxia of eye movements

areflexia

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arrhythmia, CNS causes of

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biotinidase deficiency

blindness

blood dyscrasias, neurologic findings with

bone marrow transplantation

brainstem, dysfunction

brainstem, infarction of

burning feet, differential diagnosis of

burning hands

burning paresthesia

calcification, intracranial

calf hypertrophy

campylobacter infection

Canavan's disease

carbamazepine

carbamazepine, toxicity

carbamyl phosphate synthetase-I deficiency

carbidopa

carbonic anhydrase II deficiency

cardiomegaly

cardiomyopathy

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid siphon

carotid-siphon occlusion

CAT scan

CAT scan, abnormal

CAT scan, false negative

catalepsy

cataplexy

cataracts

caudate nucleus, lesion of

celiac disease, adult

celiac disease, childhood

central hypoventilation

central nervous system, infection 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, gammaglobulin of

cerebrospinal fluid, glycine

cerebrospinal fluid, oligoclonal IgG in

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, pathophysiology

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Chediak-Higashi syndrome

cherry red spot

cherry red spot-myoclonus syndrome

children

cholesterol

choline acetyltransferase

choline chloride

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

cranial nerve enlargement

cranial nerve palsies

craniopharyngioma

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyclosporine

cystinuria

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis herpetiformis

dermatomyositis

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

diarrhea

diet

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine

drooling

dropped head syndrome

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dystonic reaction, acute

echolalia

efficacy

electrocardiogram, abnormal

electrocardiogram, loop

electromyogram

electron microscopy

emergencies, neurologic

encephalitis, autoimmune

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

enteritis

enzyme treatment

enzyme, defect

enzyme, muscle disease

eosinophilia-myalgia syndrome

epidemiology of neurology

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

fatty acid, elevated plasma content

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

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gangliosidosis GM2-AB variant

gastrointestinal disease, neurologic complications

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

Gilles de la Tourette syndrome

gliadin antibodies

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glycogen debranching enzyme deficiency

glycogen storage disease

glycoprotein

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

hallucination, hypnagogic

hallucination, visual

headache, progressive

headache, thunderclap

headbanging

hearing loss

heart murmur

hematopoietic tissue, extramedullary

hemianopia, homonymous

heralding manifestation

herniated disc, thoracic

hexosaminidase-A

hexosaminidase-A and B

histochemistry

histochemistry of muscle

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hypersensitivity reaction

hypersomnia

hypersomnia, idiopathic

hypertension

hypertonia

hypocretin

hypogammaglobulinemia

hypothalamus, disturbance of

hypothermia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

imbalance

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

ischemic exercise test

jaundice

jaw jerk, abnormal

Jewish

juvenile myoclonus epilepsy

Kearns-Sayre syndrome

keratitis

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lacunar infarction

L-dopa

Leber's hereditary optic neuropathy

left-right orientation

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

leukocyte alkaline phosphotase

leukocyte enzyme abnormality

lipid storage disorder of CNS

lipoprotein receptor-related protein 4

livedo reticularis

liver disease

Lyme disease

lymphadenopathy, hilar

lysosomal storage disease

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

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

methotrexate

microspherophakia

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

modafinil

molecular genetics

monoclonal antibodies

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya

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, muscle

MRI, negative

MRI, paramagnetic effect

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, conjugal

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, familial

multiple sclerosis, pathogenesis

multiple sclerosis, risk factors for

multiple sclerosis, treatment of

multiple sclerosis, with CSF bands

multiple sclerosis, without CSF bands

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle spasm, face

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

MuSK antibodies

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, diagnosis

myasthenia gravis, familial incidence of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenia gravis, variants

myasthenic crisis

myelitis

myelitis, transverse

myelitis, transverse, recurrent

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

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuronal ceroid-lipofuscinosis

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic neuritis

optic neuritis, recurrent

optic neuropathy

optic neuropathy, bilateral

oral ulcerations

ornithine transcarbamylase deficiency

paraspinal muscle weakness

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

peduncular hallucinosis

phosphorylase b kinase deficiency

photophobia

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polycythemia, primary

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic relapsing

polysomnogram

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

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

renal tubular acidosis

respirations in CNS disease

respiratory failure

respiratory tract infection

retinal degeneration

retinopathy

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

salivation, excessive

scoliosis, neurologic association with

screaming

screening

second wind phenomena

seizure

seizure, cardiac arrhythmia resulting from

seizure, children

seizure, complications following

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

serologic testing

serologic testing of cerebrospinal fluid

short stature

skin, biopsy

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

small vessel disease

sodium valproate

sodium valproate, toxicity

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

steroid

steroid therapy, CNS treatment and complications with

Stevens-Johnson syndrome

stuttering following CVA

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

symmetric brain lesions

systemic illness

systemic lupus erythematosus

temporal lobe, lesion

term infant

tetrahydrobiopterin

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

third ventricle, mass of

tone, muscle, increased

tongue, enlarged

tongue, ulcer

tongue, weakness

toxic epidermal necrolysis

transketolase

treatment of neurologic disorder

tyrosine hydroxylase deficiency

tyrosinemia

umbilical-cord blood transplantation

undiagnosed

upgaze

urea

urea-cycle enzymopathies

uremia

urinary incontinence

urine test for metabolic disorders

urine, dark

uveitis

vaccination, neurologic complications with

vasculitides

vasculopathy

vertebral-basilar insufficiency

weakness, generalized

weakness, progressive

weakness, proximal

weight gain

weight loss

Wernicke's encephalopathy

wheelchair

white matter disease

winging of scapula

Showing articles 50 to 100 of 159 << Previous Next >>

Diagnostic Aspects of Narcolepsy
Neurol 50:S2-S7, Aldrich,M.S., 1998

Optic Neuritis, Prognosis for Multiple Sclerosis from MRI, CSF, and HLA Findings
Neurol 50:708-714, Soderstrom,M.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

HLA Typing in Acute Optic Neuritis, Relation to MS & Magnetic Resonance Imaging Findings
Arch Neurol 54:76-80, Frederiksen,J.L.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
Multiple Sclerosis 1:170-172, Constantinescu,C.S.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Myasthenia Gravis and Sarcoidosis:Report of 2 Cases
Eur Neurol 36:326-327, DeBleecker,J.,et al, 1996

Fisher Syndrome after Campylobacter Jejuni Enteritis:Human Leukocyte Antigen and the Bacterial Serotype
J Pediatr 126:55-57, Yuki,N.,et al, 1995

Bilateral Simultaneous Optic Neuropathy in Adults:Clinical, Imaging, Serological, and Genetic Studies
JNNP 58:70-74, Morrissey,S.P.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Inborn Errors of Urea Synthesis
Ann Neurol 35:133-141, Batshaw,M.L., 1994

Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994

Human Leukocyte Antigens in Fisher's Syndrome
Ann Neurol 33:655-657, Yuki,N.,et al, 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Idiopathic Childhoos Stroke is Associated with Human Leukocyte Antigen (HLA) -B51
Ann Neurol 31:675-677, Mintz,M.,et al, 1992

Polymorphonuclear Leukocytes and Monocytes/Macrophages in the Pathogenesis of Cerebral Ischemia and Stroke
Stroke 23:1367-1379, Kochanek,P.M.&Hallenbeck,J.M., 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Recurrent Transverse Myelitis, Myasthenia Gravis, and Autoantibodies
Ann Neurol 32:407-409, Lindsey,J.W.,et al, 1992

Conjugal Multiple Sclerosis:Immunogenetic Characterization and Analysis of T-and B-Cell Reactivity to Myelin Proteins
Neurol 42:577-582, Frederickson,S.,et al, 1992

Central-Nervous-System Demyelination after Immunisation with Recombinant Hepatitis B Vaccine
Lancet 338:1174-1175, Herroelen,L.,et al, 1991

Central Nervous System Abnormalities in Lyme Neuroborreliosis
Neurol 41:1571-1582, Halperin,J.J.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
Lancet 337:1071-1074, Kaufman,L.D.,et al, 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 1990

A Long-Term Prospective Study of Optic Neuritis:Evaluation of Risk Factors
Ann Neurol 27:386-393, Sandberg-Wollheim,M.,et al, 1990

Risk Factors for Multiple Sclerosis:Race or Place? Editorial
JNNP 53:821-823, 903, 906990., Compston,A., 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

Characteristics of Narcolepsy in Preteenaged Children
Pediatrics 85:205-209, Kotalgal,S.,et al, 1990

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Narcolepsy Associated with Lesions of the Diencephalon
Neurol 39:1505-1508, Aldrich,M.S.&Naylor,M.W., 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Showing articles 50 to 100 of 159 << Previous Next >>