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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 500 to 550 of 1944 << Previous Next >>

Frequent Hemorrhagic Lesions in Cerebral Toxoplasmosis in AIDS Patients
J Neuroimaging 19:169-173, Bhagavati, S. & Choe, J., 2009

Reversible Posterior Leukoencephalopathy Syndrome in 2 HIV-Infected Patients Receiving Antiretroviral Therapy
CID 49:e19-e22, Ridolfo, A.L.,et al, 2008

Decoding Cryptogenic Cardioembolism
Ann Neurol 64:364-365, Meschia,J.F., 2008

Update on Blepharospasm: Report from the BEBRF International Workshop
Neurol 71:1275-1282, Hallett,M.,et al, 2008

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Familiality in Brain Tumors
Neurol 71:1015-1020, Blumenthal,D.T.&Cannon-Albright,L.A., 2008

Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
Neurol 71:1035-1037, V�lker,W.,et al, 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Human Immunodeficiency Virus Associated Intracranial Aneurysms: Report of Three Adult Patients With an Overview of the Literature
JNNP 79:44-46, Modi,G.,et al, 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

a-Synuclein Gene Duplication Is Present in Sporadic Parkinson Disease
Neurol 70:43-49,7, Ahn,T.-B.,et al, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Tuberous Sclerosis Complex: A Tale of Two Genes
Neurol 70:904-905, Nass,R. &Crino,P.B., 2008

Nearly Completely Reversible Brain Abnormalities in a Patient With Incontinentia Pigmenti
AJNR 29:431-433, Lou,H.,et al, 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Changes in the Incidence and Predictors of Human Immunodeficiency Virus-Associated Dementia in the Era of Highly Active Antiretroviral Therapy
Ann Neurol 63:213-221, Bhaskaran,K.,et al, 2008

T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
Neurol 70:1614-1619, McNeill,A.,et al, 2008

Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3
Neurol 70:2357-2363, Mineharu,Y.,et al, 2008

Controlled Trial of High-Concentration Capsaicin Patch for Treatment of Painful HIV Neuropathy
Neurol 70:2305-2313, Simpson,D.M.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Neurofibromatosis
JAMA 300:352, Torpy,J.M.,et al., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

SLC01B1 Variants and Statin-Induced Myopathy -- A Genomewide Study
NEJM 359:789-799, The SEARCH Collaborative Group, 2008

JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008

Primary Central Nervous System Plasmablastic Lymphoma in AIDS
Neuropath Appl Neurobiol 34:245-247, Shuangshoti, S.,et al, 2008

HIV Infection Presenting with Motor Axonal Variant of Guillain-Barre Syndrome
J Clin Neuromusc Dis 9:303-305, Wagner, J.C. and Bromberg, M.B., 2007

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007

Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007

Corticosteroids for Acute Bacterial Meningitis
NEJM 357:2507-2509, Greenwood,B.M., 2007

Phenylketonuria
eMedicine (December), Arnold,G.L., 2007

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Adult-Onset Vanishing White Matter Leukoencephalopathy Presenting as Psychosis
Neurol 68:1538-1539, Denier,C.,et al, 2007

Inclusion Body Mositis With Human Immunodeficiency Virus Infection: Four Cases with Clonal Expansion of Viral-Specific T Cells
Ann Neurol 61:466-475, Dalakas,M.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Prothombotic Mutations as Risk Factors for Cryptogenic Ischemic Cerebrovascular Events in Young Subjects With Patent Foramen Ovale
Stroke 38:2070-2073, Botto,N.,et al, 2007

Inflammatory Progressive Multifocal Leukoencephalopathy in Human Immunodeficiency Virus-Negative Patients
Ann Neurol 62:34-39, Huang,D.R.,et al, 2007

A Genetic Risk Factor for Periodic Limb Movements in Sleep
NEJM 357:639-647, Stefansson,H.,et al, 2007

Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
Neurol 69:1366-1373, Schiff,D.,et al, 2007

Parental Transmission of MS in a Population-Based Canadian Cohort
Neurol 69:1208-1212,1202, Herrera,B.M.,et al, 2007

Angelman Syndrome Revisited
Neurologist 13:305-312, Paprocka,J.,et al, 2007

Daclizumab Phase II Trial in Relapsing and Remitting Multiple Sclerosis
Neurol 69:785-789, Rose,J.W.,et al, 2007

Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
Neurol 69:2093-2104, Klein,C. &Schlossmacher,M.G., 2007

Stroke in Patients with Human Immunodeficiency Virus Infection
JNNP 78:1320-1324,1291, Tipping,B.,et al, 2007



Showing articles 500 to 550 of 1944 << Previous Next >>