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Differential
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abscess, intracerebral

acetylcholinesterase

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

anesthesia, general

Angelman syndrome

angiofibroma, facial

angiography, spinal

anterior horn cell disease

anticonvulsants

anticonvulsants, absorption

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, pulmonary

arylsulfatase B

aspartate aminotransferase

ataxia, hereditary

ataxia, paroxysmal

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

basal ganglia, calcification of

behavior, combative

behavioral disorder

bleeding disorder

bone marrow transplantation

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

cafe au lait spots

calcification, intracranial

calf hypertrophy

Canavan's disease

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

CAT scan, abnormal

CAT scan, chest

CAT scan, indications for

cataracts, congenital

Central America

central nervous system, infection of

cerebellar ataxia, children

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy, risk factors

cerebral palsy, work up

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, recurrent

cerebrovascular disease

ceruloplasmin, serum

cesarean section

Charcot-Marie-Tooth

chilbran skin lesions

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

chronic graft versus host disease

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

Cockayne's syndrome

cold temperature

confidentiality

congenital birth defects

congenital heart disease

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

congestive heart failure

contractures, joint

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum, atrophy of

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, porencephalic

degenerative diseases of CNS

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental retardation

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

digits, abnormal

dilantin, toxicity

disability, neurological

dissociated sensory loss

distal muscle weakness

diurnal variation

dopamine agonist

drug interactions

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dysostosis multiplex

dystonia, children

eating disorder

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electron microscopy

embolism, paradoxical

encephalopathy, neonatal

endovascular therapy

enzyme treatment

enzyme, induction

epidemiology of neurology

epileptic encephalopathy

epistaxis, recurrent

epoxide hydrolase

esophageal varices

ethics in neurology

extracorporeal membrane oxygenation

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

fatty acid, elevated plasma content

feeding disorder

fibroma, ungual

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flow study, carotid artery

fragile-X syndrome

fragile-X syndrome, carrier

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

Gaucher's disease

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen storage disease

granular osmiphilic material

growth hormone deficiency

growth retardation

Guillain Barre syndrome

health insurance

hemiplegia, congenital

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

hereditary hemorrhagic telangiectasia(HHT)

hexosaminidase-A

high arched palate

hormone replacement

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperpyrexia, CNS disorder causing

hypoalbuminemia

hypopigmentation of skin

hypothyroidism, congenital

hypothyroxinemia

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

immunohistochemistry

in situ hybridization

inborn errors of metabolism

inborn errors of metabolism, screening

infant, evaluation of

infection, recurrent

intellectual deficit

intellectual deterioration

intelligence quotient

intelligence testing in children

interferon alpha

intracranial hemorrhage

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

Kayser-Fleischer ring

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

learning disability

learning disability, in children

leg weakness, bilateral

lens, dislocation of

leukoencephalopathy

lipid storage disorder of CNS

liver function enzymes

long bone lesion

low birth weight

lymphangiomyomatosis

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malformation, vascular, cerebral

medical-legal aspects of neurology

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

Miller-Dieker syndrome

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

motor dysfunction

motor neuron disease

movement disorder

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, indications for

MRI, intrauterine

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myelomeningocele

myelopathy, chronic progressive

myopathy, distal

myopathy, metabolic

myopathy, vacuolar

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

nasal bridge, wide

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, primary of CNS

nerve conduction studies

nerve growth factor

neural tube defect

neuroendocrinology

neurofibromatosis 1

neurofibromatosis 2

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic practice

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathy, hereditary peripheral

neuropathy, peripheral

newborn, evaluation of

Niemann-Pick disease

nystagmus, hereditary

nystagmus, periodic

obstetric neurologic injuries

oculopharyngeal muscular dystrophy

oral contraceptives

ornithine transcarbamylase deficiency

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

percussion induced muscle contraction

periventricular leukomalacia

peroxisomal disease

personality change

phenylketonuria

pheochromocytoma

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

post hemorrhagic hydrocephalus

postoperative neurologic complications

postpartum coma

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pyramidal tract dysfunction

recombinant DNA

Refsum's disease

respiratory failure

restless leg syndrome

retinal degeneration

retinal hamartoma

reversible neurologic disorder

rhabdomyoma, cardiac

rubella syndrome

scoliosis, neurologic association with

seizure, complications following

seizure, diagnosis of

seizure, etiology of

seizure, familial

seizure, intractable

seizure, neonatal

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

seizure, workup of

self-mutilation

skin, darkening of

skin, lesions in neurologic disorders

slit lamp examination

Southern immunoblot test

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord, compression of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spongy degeneration of brain

startle reaction

stem cell transplantation

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

sudden infant death syndrome

Tay-Sachs disease

temper tantrums

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratogenic drugs

testicular atrophy

testicular enlargement

thrombocytopenia

tissue plasminogen activator, intravenous

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxoplasmosis, CNS

toxoplasmosis, congenital

treatment of neurologic disorder

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

umbilical-cord blood transplantation

urea-cycle enzymopathies

urine test for metabolic disorders

vertigo, episodic

very long chain fatty acids

viral infection

viral infection, CNS

vitamin supplementation

walking, difficulty with

weakness, congenital

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Western immunoblot test

white matter disease

wide based gait

x-linked hydrocephalus

x-linked mental retardation

Zika virus infection

Showing articles 1000 to 1050 of 2198 << Previous Next >>

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Pregnancy Outcome Following First Trimester Exposure to Sumatriptan
Neurol 51:581-583, Shuhaiber,S.,et al, 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

Postpartum Coma
Lancet 351:1700, McCormack,G.,et al, 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Effects of Prenatal & Postnatal Methylmercury Exposure from Fish Consump on Neurodevelop; Outcomes at 66 Months
JAMA 280:701-707, 7371998., Davidson,P.W.,et al, 1998

Familial Idiopathic Intracranial Hypertension with Spinal and Radicular Pain
Arch Neurol 55:854-856, Santinelli,R.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
JAMA 278:1237-1241, 12821997., Pericak-Vance,M.A.,et al, 1997

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
JAMA 278:51-57, Gutmann,D.H.,et al, 1997

Endolymphatic Sac Tumors, A Source of Morbid Hearing Loss in von Hippel-Lindau Disease
JAMA 277:1461-1466, Manski,T.J.,et al, 1997

Maternal Infection and Cerebral Palsy in Infants of Normal Birth Weight
JAMA 278:207-211, 2471997., Grether,J.K.&Nelson,K.B., 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Predictors of Recurrent Febrile Seizures
Arch Pediatr Adolesc Med 151:371-378, Berg,A.T.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

von Hippel-Lindau Disease
Medicine 76:381-391, Maher,E.R.&Kaelin,W.G., 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

Chromosome 19 Single-Locus & Multilocus Haplotype Assoc with MS, Evid of New Suscept Locus in Caucasian & Chinese Pts
JAMA 278:1256-1262, 12821997., Barcellos,L.F.,et al, 1997

Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997

Practice Guidelines for the Use of Imaging in Transient Ischemic Attacks and Acute Stroke
Stroke 28:1480-1497, Culebras,A.,et al, 1997

CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
Ann Neurol 41:689-692, Penney,J.B.,et al, 1997

Offspring Recurrence Rates and Clinical Characteristics of Conjugal Multiple Sclerosis
Lancet 349:1587-1590, Robertson,N.P.,et al, 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Apolipoprotein E e4 Associated with Chronic Traumatic Brain Injury in Boxing
JAMA 278:136-140, Jordan,B.D.,et al, 1997

Comparison of First Degree Relatives and Spouses of Poeple with Chronic Tension Headache
BMJ 314:1092-1093, Ostergaard,S.,et al, 1997

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
Arch Neurol 54:888-894, Rudnik-Schoneborn,S.,et al, 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Treatment of Acquired Myasthenia Gravis
Neurol 48 (Suppl 5) :S46-S51997., Massey,J.M., 1997

Acute Intermittent Porphyria:Clinicopathologic Correlation
Neurol 48:1678-1683, Suarez,J.I.,et al, 1997

Showing articles 1000 to 1050 of 2198 << Previous Next >>