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Neurology Specific Literature Search

Differential
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abortion, spontaneous

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acute necrotizing encephalitis

adenine arabinoside

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Alexanders disease

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

anemia, hemolytic

anesthesia, general

angiitis, isolated of CNS

anterior tibial muscle weakness

anti double-stranded DNA

anticardiolipin antibodies

anticoagulant, treatment in CVD

antiphospholipid antibodies

antiviral agents

apolipoprotein E

apraxia of eye movements

arrhythmia, cardiac

arthrogryposis multiplex

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

ataxic-dystonia syndromes

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavioral disorder

benign familial neonatal convulsions

bladder dysfunction

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain biopsy, indication

brain scan, abnormal

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

bulbar palsy, progressive

cafe au lait spots

calcification, intracranial

candida albicans

carcinoembryonic antigen

carcinoma of lung

carcinoma of pancreas

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

cavernous hemangioma

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral embolism

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy, etiology

cerebral palsy, work up

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, anti DNA

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, complement of

cerebrospinal fluid, cytology

cerebrospinal fluid, DNA in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, young adult

ceruloplasmin, serum

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choreoathetosis

choreoathetosis, paroxysmal

chorioretinitis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

Cockayne's syndrome

cogwheel rigidty

compression neuropathy

compression neuropathy, recurrent

congenital myasthenic syndromes

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cost effectiveness

cranial nerve enhancement

creatine phosphokinase(CPK)elevated

creatinine, elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cyst, neoplastic cerebellum

cyst, porencephalic

cytomegalic inclusion disease

cytomegalovirus infection

cytosine arabinoside

degenerative diseases of CNS

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

depression, psychotic

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

difficulty going down stairs

distal muscle atrophy

distal muscle weakness

double-cortex syndrome

drug induced neurologic disorders

dystonia musculorum deformens

dystonia, paroxysmal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalitis, brainstem

encephalitis, focal

encephalitis, Rasmussen's

encephalitis, viral

encephalomyelitis, postinfectious

enzyme, muscle disease

epidemiology of neurology

Epstein-Barr virus

ethics in neurology

exome sequencing

eye movement, disorders of

face, elongated

facial appearance, abnormal

facial nerve palsy

facial weakness

fatal familial insomnia

flow study, cerebral

fourth ventricle, compression

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

fungal infection

fungal infection, CNS

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of, bilateral

gonadotropin-releasing hormone

gram positive cocci

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hallucination, auditory

hallucination, olfactory

hallucination, visual

headache, awakening with

headache, positional

headache, progressive

helminthic infection of CNS

hemangioblastoma

hemiparesis, transient

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

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, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

herpes virus infection

herpes zoster, myelitis

herpes, genital

high arched feet

high arched palate

human immunodeficiency virus type 1

Hunter's syndrome

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, presymptomatic detection of

Huntington's disease, children

hydrocephalus, non-communicating(obstructive)

hyperbilirubinemia

hyperhomocysteinemia

hyperkalemic periodic paralysis

hypoglycorrhachia

hypogonadism, hypogonadotropic

hypotonia, causes of

hypotonia, infants

iatrogenic neurologic disorders

immunodeficiency

immunofluorescence

immunofluorescent exam of CSF cells

immunohistochemistry

immunoperoxidase staining

immunosuppression

in situ hybridization

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

infectious mononucleosis

intellectual deficit

interferon inducer

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection, viral

intrauterine infection, viral of CNS

intravenous drug abuse

intraventricular chemotherapy

intrinsic hand muscles, wasting of

iododeoxyuridine

Jakob-Creutzfeldt disease

joint hypermobility

Kallmann's syndrome

Kearns-Sayre syndrome

Krabbe's disease

Kugelberg-Welander syndrome

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

life expectancy

limbic encephalitis

liver function enzymes

lung-brain syndromes

lupus anticoagulant

lupus erythematosis, discoid

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malignant hyperpyrexia

manic-depressive

McArdle's disease

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, aseptic

meningitis, basilar

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, leukemic

meningitis, neutrophilic

meningitis, recurrent

meningitis, relapse

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

methylmalonic acidemia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamines, brain

mononeuropathy, recurrent

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, blooming effect

MRI, contrast enhanced

MRI, diffusion weighted

MRI, mass effect on

MRI, nodular enhancement

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle phosphorylase deficiency

muscle stiffness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myelin basic protein gene

myeloneuropathy

myopathy, mitochondrial

myopathy, proximal

myotonia dystrophica

nausea and vomiting

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

neoplasm, intracranial, multiple

neoplasm, metastatic to CNS

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-multiple

nerve growth factor

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neurotransmitter

newborn, evaluation of

next-generation sequencing

night blindness

ocular motility, disorders of

oculopharyngeal muscular dystrophy

Ommaya reservoir

ophthalmoplegia

optic atrophy, hereditary

optic neuropathy

optic neuropathy, hereditary

ovarian dysgenesis

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal neurologic deficits

patient information and support

peptides, brain

periodic paralysis

peroxisomal disease

Perrault syndrome

personality change

pheochromocytoma

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polycystic kidneys

polyglucosan body disease

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polyneuropathy, familial

pons, lesion of

posterior fossa, lesion of

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal myotonic myopathy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

recombinant DNA

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory tract infection

retinal artery occlusion

retinal degeneration

retinal hemangioma

retinitis pigmentosa

risus sardonicus

Rosenthal fibers

salivation, excessive

seizure, familial

seizure, intractable, treatment of

seizure, neonatal

seizure, psychomotor-temporal lobe

sensorineural hearing loss

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

Southern immunoblot test

spastic paraplegia, type 7

spinal cord, infarction of

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

startle reaction

steroid therapy, CNS treatment and complications with

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

subarachnoid hemorrhage

subtemporal decompression

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

testicular enlargement

thalamus, lesion of

thrombocytopenia

thrombophlebitis

tomaculous neuropathy

transient ischemic attack

transplacental virus infections

treatment of neurologic disorder

tremor, intention

trigeminal neuralgia

trinucleotide repeats

urinary urgency

Usher's syndrome

varicella zoster virus

ventricular garlands

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral infection, CNS, treatment of

vision loss, sequential

vision, blurred

visual acuity, decreased

visual field defect

visual loss, transient

visual obscurations, transient

visuospatial disturbance

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, delayed

walking, difficulty with

weakness, fatiguable

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Western immunoblot test

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

X-linked neuropathy

Showing articles 100 to 150 of 175 << Previous Next >>

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

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

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

Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989

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

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

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

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988

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

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
Wertelecki. W. , et al, NEJM 319:276-2838., , 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

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

Alzheimer's Disease
Down's Syndrome, & Chromosome 21, Editorial, Lancet 1:1011-1012., , 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987

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

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Vidarabine Versus Acyclovir Therapy in Herpes Simplex Encephalitis
NEJM 314:144-149, Whitley,R.J.,et al, 1986

Huntington's Disease, Pathogenesis & Management
NEJM 315:1267-1276, Martin,J.B.&Gusella,J.F., 1986

Genetic Prediction & Family Structure in Huntington's Chorea
BMJ 290:1929-1931, Harper,P.S.,et al, 1985

Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985

Central Nervous System Toxicity with High-Dose Ara-C
Neurol 35:1475-1479, Hwang,T.,et al, 1985

A DNA Polymorphism for Huntington's Disease Marks the Future
Arch Neurol 42:20-24, Wexler,N.S.,et al, 1985

Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984

Vidarabine Encephalopathy
JNNP 47:1351-1354, Cullis,P.A.,et al, 1984

Acyclovir Versus Vidarabine in Herpes Simplex Encephalitis
Lancet 2:707-711, Skoldenberg,B.,et al, 1984

Clin Path. Conference
Necrotizing Encephalomyelopath, Secondary to Irradiation & Intrathecal Methotrexate, Case Record 36-, 983, 311:653-662,1984., 1984

Molecular Genetics, Recombinant DNA Techniques, & Genetic Neurological Disease
Ann Neurol 15:511-520, Rosenberg,R.N., 1984

Treatment of Herpes Virus Infections
NEJM 309:963-970, 1034-10391983., Hirsch,M.S.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Recombinant DNA & Neurologic Disease:The Coming of a New Age
Neurol 33:622-625, Rosenberg,R.N., 1983

Myelopathy after Herpes Zoster
Arch Neurol 40:445-446, Muder,R.R.,et al, 1983

Paraparesis Following Intrathecal Chemotherapy
Neurol 33:1032-1038, Hahn,A.F.,et al, 1983

A Genetic Marker for Huntington's Chorea
BMJ 287:1567-1568, Harper,P.S., 1983

Showing articles 100 to 150 of 175 << Previous Next >>