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Differential
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acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
adrenoleukodystrophy
advances in neurology
adverse drug reaction
algorithm
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
anticonvulsants
anticonvulsants, effectiveness
antiviral agents
apolipoprotein E
APP
APP gene
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
ataxin
ataxin-2
audiogram
auditory evoked brainstem potentials
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
brain biopsy
brain purpura
brainstem, infarction of
cafe au lait spots
CAG repeats
calcification, intracranial
CAT scan, abnormal
cataracts
CD4 counts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral infarction, hemorrhagic
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 1
chromosome 12
chromosome 14
chromosome 17
chromosome 19
chromosome 2
chromosome 20
chromosome 21
chromosome 22
chromosome 3
chromosome 4
Cockayne's syndrome
cognition
confidentiality
consanguinity
cranial nerve tumor
Cuba
deafness
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dementia
developmental retardation
diabetes mellitus
DNA probes
Dravet syndrome
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, paroxysmal
dystonia, symptomatic
dystonia, treatment of
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electronystagmography
electroretinograph
enzyme, defect
ependymoma
epidemiology of neurology
equinovarus
eye movement, disorders of
familial
fever
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
gyrate atrophy of choroid and retina
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hamartoma
hearing loss
hepatosplenomegaly
highly active antiretroviral therapy
hot cross bun sign
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hyperornithinemia
hyperreflexia
hypogammaglobulinemia
hyposmia
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
intellectual deficit
intellectual deterioration
iron, brain
Kearns-Sayre syndrome
lacunar infarction
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
lenticular nucleus, lesion of, bilateral
leucine-rich repeat kinase 2 gene
livedo reticularis
long bone lesion
macular degeneration
meningioma
mental retardation
merlin
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, spine
MRI, susceptibility weighted
mucopolysaccharidoses
multiple system atrophy
muscle cramp
muscle stiffness
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, Duchenne
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy, mitochondrial
myopia
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neoplasm, intracranial
neoplasm, intracranial, multiple
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-multiple
nerve growth factor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neurodegeneration with brain iron accumulation
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuronopathy
neuropathy
neuropathy, hereditary peripheral
night blindness
optic atrophy
optic glioma
optic nerve
optic neuropathy
orbit, tomograms of
palilalia
PANK2 mutation
Parkinson disease
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
patient information and support
peroxisomal disease
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
postural abnormality
practice guidelines
pregnancy, neurologic complications in
presenilin-1 gene
presenilin-2 gene
prognosis
progressive neurologic disorder
proximal myotonic myopathy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
recombinant DNA
recurrent
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
root lesion, nerve
saccadic eye movements, abnormal
schwannoma
SCN1A gene
sea-blue histiocytes
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
sinemet
skin, biopsy
skin, lesions in neurologic disorders
sodium channel dysfunction
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
status epilepticus
steroid
stimulation, deep brain
substantia nigra
symmetric brain lesions
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
tinnitus
topiramate
treatment of neurologic disorder
tremor
trinucleotide repeats
tubular aggregates, muscle
type 2 muscle fiber
Usher's syndrome
vasculitides
vasculopathy
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual loss
wheelchair
Wood's light
workup
Showing articles 750 to 800 of 1917 << Previous Next >>

Incidence of Dilated Cardiomyopathy and Detection of HIV in Myocardial Cells of HIV-Positive Patients
NEJM 339:1093-1099,1153, Barbaro,G.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Chorea as a Form of Presentation of Human Immunodeficiency Virus-Associated Dementia Complex
Neurol 50:568-569, Pardo,J.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Evaluation and Management of Intracranial Mass Lesions in AIDS
Rpt of Quality Stnds Subcomm of the AAN, Neurol 50:21-261998., , 1998

Human Herpesvirus 8 DNA in CNS Lymphomas from Patients With and Without AIDS
Neurol 50:335-340, 3221998., Corboy,J.R.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

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

Variable Progression of HIV-Associated Dementia
Neurol 50:1814-1820, Bouwman,F.H.,et al, 1998

HIV-Protease Inhibitors
NEJM 338:1281-1292, Flexner,C., 1998

Optic Neuritis Heralding Varicella Zoster Virus Retinitis in a Patient with Acquired Immunodeficiency Syndrome
Ann Neurol 43:534-536, Meenken,C.,et al, 1998

Neuropathy in Diffuse Infiltrative Lymphocytosis Syndrome
Neurol 50:1041-1044, 8551998., Gherardi,R.K.,et al, 1998

Cerebral Aneurysmal Arteriopathy in Childhood AIDS
Neurol 51:560-565, Dubrovsky,T.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,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

Failure of Cytarabine in Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
NEJM 338:1345-1351, 13781998., , 1998

Herpes Zoster Ophthalmicus in Patients with Human Immunodeficiency Virus Infection
Am J Ophthalmol 125:285-291, Margolis,T.P.,et al, 1998

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

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Epilepsies in Twins:Genetics of the Major Epilepsy Syndromes
Ann Neurol 43:435-445, Berovic,S.F.,et al, 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

Predictive Factors for Prolonged Survival in AIDS-Associated PML
Ann Neurol 44:341-349, Berger,J.R.,et al, 1998

Chromosome 20 Ring:A Chromosomal Disorder Associated with a Particular Electroclinical Pattern
Epilepsia 39:942-951, Canevini,M.P.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

Numb Chin Syndrome as the Initial Manifestation of HIV Infection
Neurol 50:511-512, Benito-Leon,J.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

AIDS-Related MR Hyperintensity of the Basal Ganglia
AJNR 19:83-89, Meltzer,C.C.,et al, 1998

Regress of HIV Enceph & Basal Ganglia Signal Intensity Abnor MRI in AIDS after Protease Inhibitor
Neuroradiology 206:491-498, Filippi,C.G.,et al, 1998

Adenoidal Width and HIV Factors
AJNR 18:1721-1725, Yousem,D.M.,et al, 1997

A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
Neurol 49:1231-1238, 11931997., Gardner,K.,et al, 1997

Progressive Multifocal Leukoencephalopathy in AIDS:Initial and Follow-up CT and MRI
Neuroradiology 39:611-618, Thurnher,M.M.,et al, 1997

Comparison of T2-Weighted & Fluid-Attenuated Inversion-Recovery Fast Spin-Echo MR Seq in Intracerebral AIDS-Assoc Dis
AJNR 18:1601-1609, 16111997., Thurnher,M.W.,et al, 1997

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



Showing articles 750 to 800 of 1917 << Previous Next >>