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Differential
(Click to cross reference)
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 700 to 750 of 1944 << Previous Next >>

Toxoplasmosis Manifesting as Hydroephalus on Computed Tomography
Infect Dis Clin Practice 9:390-392, Finelli,P.F. &Uphoff,D.F., 2000

Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
Radiology 214:209-216, Brunereau,L.,et al, 2000

A Locus for Paroxysmal Kinesigenic Dyskinesia Maps to Human Chromosome 16
Neurol 54:125-130, Bennett,L.B.,et al, 2000

Remission of HIV Myelopathy After Highly Active Antiretroviral Therapy
Neurol 54:267-268, Staudinger,R.&Henry,K., 2000

The Brain Code in Health and Disease
Arch Neurol 57:50-51, Rosenberg,R.N., 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

St Louis Encephalitis,A Review of 11 Cases in a 1995 Dallas, Tex, Epidemic
Arch Neurol 57:114-118, Wasay,M.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Role of Brain Biopsy in the Management of Focal Brain Lesions in HIV-Infected Patients
Neurol 54:993-997, Antinori,A.,et al, 2000

Screening CT of the Brain Determined by CD4 Count in HIV-Positive Patients Presenting with Headache
AJNR 21:451-454,441, Graham III,C.B.,et al, 2000

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

Reduced Prevalence of AD in Users of NSAIDs and H2 Receptor Antagonists
Neurol 54:2066-2071, Anthony,J.C.,et al, 2000

Remedies for HIV-Associated Peripheral Neuropathy
Neurol 54:2037-2038, Berger,J.R.&Nath,A., 2000

Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
NEJM 342:1560-1567, Lucking,C.B.,et al, 2000

Hypersexuality in Patients with Dementia: Possible Response to Cimetidine
Neurol 54:2024, Wiseman,S.V.,et al, 2000

Decreasing Incidence of CNS AIDS-Defining Events Associated with Antiretroviral Therapy
Neurol 54:1856-1859, d'Arminion Monforte,A.,et al, 2000

National Institutes of Health Consensus Conference: Tuberous Sclerosis Complex
Arch Neurol 57:662-665, Hyman,M.H.&Whittemore,V.H., 2000

Therapeutic Dilemma
Neurol 54:1404-1407, Romanelli,F.,et al, 2000

Hereditary Spastic Paraparesis: A Review of New Developments
JNNP 69:150-160, McDermott,C.J. et al, 2000

Human Immunodeficiency Virus-Associated Pure motor Lumbosacral Polyradiculopathy
Arch Neurol 57:1034-1039, Benatar,M.G. & Eastman,R.W., 2000

Epstein-Barr Virus Infection
NEJM 343:481-492, Cohen,J.I., 2000

Long-term Effect of Bone-marrow Transplantation for Childhood-onset Cerebral X-linked Adrenoleukodystrophy
Lancet 356:713-718, Shapiro,E. et al, 2000

Central Nervous System Aspergillosis in Patients with Human Immunodeficiency Virus Infection
Medicine 79:269-280, Mylonakis,E. et al, 2000

Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Cerebral Infarction in Adult AIDS Patients
Stroke 31:2117-2126, Connor,M.D. et al, 2000

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

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000

New-Onset Seizures Associated with HIV Infection
Neurol 55:1558-1560, Modi,G.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Remedies for HIV-associated Peripheral Neuropathy
Neurol 54:2037-2038, Berger,J.R. &Nath,A., 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

West Nile Viral Encephalitis in an HIV-Positive Woman in New York
NEJM 342:59-60, Szilak,I.&Minamoto,G.Y., 2000

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Brain Biopsy in Patients with Acquired Immunodeficiency Syndrome, Diagnostic Value, Clinical Performance, and Survival Time
Arch Int Med 159:2590-2596, Hornef,M.W.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Cerebral Tumor-Like American Trypanosomiasis in Acquired Immunodeficiency Syndrome
Ann Neurol 45:403-406, Pagano,M.A.,et al, 1999

HAART Improves Prognosis in HIV-Associated Progressive Multifocal Leukoencephalopathy
Neurol 52:623-625,440, Clifford,D.B.,et al, 1999

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Progressive Multifocal Leukoencephalopathy and Human Immunodeficiency Virus-associated White Matter Lesions in AIDS:Magnetization Transfer MR Imaging
Radiology 210:539-543, Ernst,T.,et al,, 1999

Isolated,Chronic,Epilepsia Partialis Continua in an HIV-Infected Patient
Arch Neurol 56:111-114, Bartolomei,F.,et al, 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Value of Combined Approach with Thallium-201 Single-Proton Emission Computed Tomography and Epstein-Barr Virus DNA Polymerase Chain Reaction in CSF for the Diagnosis of AIDS-Related Primary CNS Lympho
J Clin Oncol 17:554-560, Antinori,A.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999



Showing articles 700 to 750 of 1944 << Previous Next >>