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Differential
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abortion, spontaneous

absence

acanthocytosis

acetazolamide

acetylcholine

acetylcholine receptor

acetylcholine receptor antibody

acetylcholinesterase

acetylcholinesterase deficiency

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

adolescent medicine

adoption

advances in neurology

adverse drug reaction

Alzheimer's disease, familial

amantadine

amnesia

amyloid angiopathy, cerebral

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

anterior horn cell disease

antibiotics

antibiotics, neurologic complications with

anticholinergic drugs

anticonvulsants, cognitive function with

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

apraxia of eyelid opening

arthrogryposis multiplex

arylsulfatase A

aspartate aminotransferase

asthma

asthma, poliomyelitis-like syndrome with

atidarsagene autotemcel

atlanto axial dislocation, congenital

atypical lymphocytes

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

automobile accidents

autonomic dysfunction

axonal spheroid

azathioprine

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

blacks

body mass index

bone marrow transplantation

brain transplantation

bulbar palsy, juvenile

bulbar palsy, progressive

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous sinus, syndrome

central nervous system, infection of

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral glucose metabolism

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gamma amino butyric acid

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

comorbidities

complications

congenital birth defects

congenital infection, CNS

congenital malformation

congenital myasthenic syndromes

congenital paresis

conjunctivitis

consanguinity

controversies in neurology

corpus callosum, lesion of

cortical muscular atrophy

cough

crawl regression

cryopyrin-associated periodic syndrome

D-dimer

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delivery, complicated

dementia

dementia, childhood

dementia, frontotemporal

dementia, presenile

dementia, subcortical

dentatorubral-pallidoluysian atrophy

depression

dermatitis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplopia

distal muscle atrophy

distal muscle weakness

DNA probes

donepezil

dopa responsive dystonia

dropped head syndrome

drug abuse

drug abuse, adolescent

drug addiction

drug induced neurologic disorders

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, painful

dystonia, treatment of

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

encephalopathy, neonatal

ephedrine

epidemiology of neurology

episodic neurologic deficits

exercise-induced neurologic dysfunction

extrapyramidal

extremity, cold

eye movement, disorders of

facial weakness

facial weakness, bilateral

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

gait disorder

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gilles de la Tourette syndrome

Hallervorden Spatz disease

headache, drug induced

headache, icepick

headache, severe

headache, treatment of

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

Huntington's chorea, age at onset

Huntington's chorea, akinetic-rigid form

Huntington's chorea, differential diagnosis

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, membrane abnormality

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydroxyindole acetic acid 5(5HIAA)

hypoxic encephalopathy

imbalance

immunologic disease

immunosuppression

immunosuppressive agents

inclusion bodies, intranuclear

India

indomethacin

infantile tremor syndrome

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

internet

intracranial hypertension, benign

intranasal medication

intrauterine infection

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

irritability

isoniazid

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juvenile idiopathic inflammatory myopathy

juvenile myoclonus epilepsy

juvenile paresis

keratoconjunctivitis

Kluver-Bucy syndrome

Kugelberg-Welander syndrome

leg weakness, unilateral

leukocytosis

leukodystrophy

leukoencephalopathy

Lewy body disease, diffuse

Lhermitte's sign

lipoma of CNS

liver disease

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lymphocyte capping, diminished

lysosomal storage disease

magnesium sulfate

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

manic-depressive

Mary Walker phenomenon

masked facies

medical-legal aspects of neurology

memory, impairment of

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

migraine

migraine, children

migraine, seizures in

migraine, treatment of

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, juvenile form

motor signs

movement disorder

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, sunburst pattern

MRI, volumetry

MRS

multiple sclerosis

multiple system atrophy

muscimol

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, passive transfer of

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, receptor site in

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myoclonus, stimulus sensitive

myopathy

myopathy inflammatory, classification

myopathy, inflammatory

myopathy, inflammatory, classification

myositis

myositis specific autoantibody

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neuroleptic

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic history

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal intranuclear inclusion disease

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, peripheral

neurosyphilis

neurotoxin

neurotransmitter

newborn, evaluation of

next-generation sequencing

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

optic atrophy

optic atrophy, bilateral

parechovirus encephalitis

paresthesias

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, treatment of

Parkinsonism syndrome

peptides, brain

periodic paralysis

periodic paralysis, thyrotoxic

persistent vegetative state

photosensitivity, skin

Pick's disease

piracetam

plasmapheresis

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

pneumonia

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

pregnancy, neurologic complications in

prevention of neurologic disorders

PRKN gene

procyclidine

prognosis

progressive neurologic disorder

progressive supranuclear palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

putamen, lesion of, bilateral

repetitive nerve stimulation

respiratory depression

respiratory failure

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubella encephalitis, progressive

saccadic eye movements

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, classification of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, treatment of

septicemia

serologic testing

serologic testing, false negative

single photon emission computed tomography

skin, lesions in neurologic disorders

speech disorder, childhood

spina bifida

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

sports medicine, neurology of

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stiff joints

stillbirth

striatum, lesion of

striatum, lesion of, bilateral

stridor

stuttering

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

symmetric brain lesions

syphilis, congenital

syphilis, neurologic complications with

systemic illness

systemic juvenile idiopathic arthritis

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

tensilon test, false negative

term infant

tetrabenazine

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytosis

thymectomy

thymus and neuromuscular function

tongue, fasciculations of

transplacental virus infections

trauma

treatment of neurologic disorder

tremor

tremor, postural

trigeminal autonomic cephalgia

trinucleotide repeats

varicella zoster virus

varicella zoster virus, encephalitis

viral infection

viral infection, CNS

viral isolation

visual evoked response

visual loss

visual loss, progressive

visuospatial disturbance

vocal cord paralysis

walking

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weaning from respirator, failure to

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 237 << Previous Next >>

Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
JAMA 270:2321-2325, Babul,R.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Putamen Volume Reduction on Magnetic Resonance Imaging Exceeds Caudate Changes in Mild Huntington's Disease
Ann Neurol 31:69-75, Harris,G.J.,et al, 1992

Postural Stability in Patients with Huntington's Disease
Neurol 42:1232-1238, Tian,J.,et al, 1992

Presymptomatic Testing for Huntington's Disease in the United Kingdom
BMJ 304:1593-1596, Tyler,A.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

A Follow-Up Study of Isolated Cases of Suspected Huntington's Disease
Ann Neurol 31:293-298, Bateman,D.,et al, 1992

Ideomotor Apraxia in Huntington's Disease
Arch Neurol 48:35-41, Shelton,P.A.&Knopman,D.S., 1991

Myoclonus in Adult Huntington's Disease
Ann Neurol 29:213-215, Vogel,C.M.,et al, 1991

Neonatal Lupus Erythematosus Simulating Transient Myasthenia Gravis at Presentation
J Pediatr 118:417-419, Rider,L.G.,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

Myasthenia Gravis in Mothers and Their Newborns
Clin Obstet Gynecol 34:82-99, Plauche,W.C., 1991

Chronic Acetazolamide Monotherapy in the Treatment of Juvenile Myoclonic Epilepsy
Neurol 40:1677-1681, Resor,S.R.&Resor,L.D., 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
NEJM 322:1293-1298, Albin,R.L.,et al, 1990

Epileptic Seizures and Syndromes
Lancet 336:161-163, Gram,L., 1990

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Predictive Testing for Huntington's Disease with Linked DNA Markers
Lancet 2:463-466, Brock,D.J.H.,et al, 1989

Problems in Genetic Prediction for Huntington's Disease
Lancet 2:601-603, Morris,M.J.,et al, 1989

Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
Neurol 39:796-801, Bamford,K.A.,et al, 1989

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Adoption and Genetic Prediction for Huntington's Disease
Lancet 2:1069-1070, Morris,M.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Autonomic Nervous Function in Huntington's Disease
Arch Neurol 45:309-312, DenHeijer,J.C.,et al, 1988

Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Neonatal Myasthenia Gravis:A New Clinical & Immunologic Appraisal on 30 Cases
Neurol 38:138-142, Morel,E.,et al, 1988

Huntington's Disease Mortality in the United States
Neurol 38:769-772, Lanska,D.J.,et al, 1988

Presymptomatic Neuropsychological Impairment in Huntington's Disease
Arch Neurol 45:769-773, Jason,G.W.,et al, 1988

Maternal-Fetal Transmission of Myasthenia Gravis with Acetylcholine-Receptor Antibody
NEJM 318:996, Melber,D., 1988

Huntington's Disease:Deterioration in Clinical State During Treatment with ACE Inhibitor
BMJ 294:1659-1660, Goldblatt,J.&Bryer,A., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes
et al Lancet 1:1284-1285, Hayden,M.R., 1987

Plasmapheresis for Myasthenic Crisis in a Young Child
J Pediatr 110:740-742, Snead,O.C.III.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Juvenile Parkinsonism:Clinical & Metabolic Characteristics
JNNP 50:345-348, Lima,B.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

PET Scan Investigations of Huntington's Disease:Cerebral Metabolic Corr. of Neuro & Funct Decline
Ann Neurol 20:296-303, Young,A.B.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Neuropeptides in Neurological Disease
Ann Neurol 20:547-565, Beal,M.F.&Martin,J.B., 1986

Subcortical Dementia
BMJ 292:1035-1036, Foster,J.B., 1986

Showing articles 100 to 150 of 237 << Previous Next >>