Neudle.com: "leukocytes"

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 0 to 50 of 159 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
Neurol 102:e209190, Cheng,Y. & Zachariah,J., 2024

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 960, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans
NEJM 364:1134-1143, McCormack,M.,et al, 2011

HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans
NEJM 364:1126-1133, Chen,P.,et al, 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data
Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009

Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
Lancet 371:2201-2212, Feldman,B.M.,et al., 2008

Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007

Narcolepsy With Cataplexy
Lancet 369:499-511, Dauvilliers,Y.,et al, 2007

Neurological Findings in Aminoacylase 1 Deficiency
Neurol 68:2151-2153, Sass,J.O.,et al, 2007

Behcets Disease Presented with Isolated Peduncular Hallucinosis: A Case Report
Internet J Neurol 9, Celik, Y.,et al, 2007

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Multiple Sclerosis with and without CSF Bands:Clinically Indistinguishable but Immunogenetically Distinct
Neurol 67:1062-1064, Imrell,K.,et al, 2006

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis?
Neurol 67:1519, Koppel,S.,et al, 2006

Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
Eur J Radiol Extra 54: 5-9, Teksam,M.,et al., 2005

Aromatic L-Amino Acid Decarboxylase Deficiency
Neurol 62:1058-1065, Pons,R.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

Cardiac Arrhythmias in Focal Epilepsy: A Prospective Long-Term Study
Lancet 364:2212-2219,2157, Rugg,F.J.,et al, 2004

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

Solving the Mysteries of Narcolepsy
Neurol 56:1616-1618, Silber,M.H. &Rye,D.B., 2001

Coma in a Young Anorexic Woman
Lancet 357:1944, Blans,M.J.,et al, 2001

Interaction Between HLA-DR2 and Abnormal Brain MRI in Optic neuritis and Early MS
Neurol 54:1859-1861, Hauser,S.L.,et al, 2000

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Behcet's Disease
NEJM 341:1284-1291, Sakane,T.,et al, 1999

Showing articles 0 to 50 of 159 Next >>