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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 1550 to 1600 of 1944 << Previous Next >>

Expression of Human Immunodeficiency Virus in Cerebrospinal Fluid of Children with Progressive Encephalopathy
Ann Neurol 21:397-401, Epstein,L.G.,et al, 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

False Negative Results in Patients with fra (X) (q) Mental Retardation Taking Oral Vitamin Supplements
NEJM 316:1093, Froster-Iskenius,U.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987

Von Hippel-Lindau Disease in an Adolescent
Pediatrics 79:632-637, Seitz,M.L.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

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

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

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

Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
Arch Int Med 147:1317-1320, Sloan,J.B.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

ABC of AIDS, Neurological Manifestations
BMJ 294:1399-1401, Carne,C.A., 1987

Neurologic Manifestations of Infection with Human Immunodeficiency Virus, Clinical Features & Pathogenesis
Ann Int Med 107:383-391, Gabuzda,D.H.,et al, 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Neurologic Abnormalities & Recovery of Human Immunodeficiency Virus from Cerebrospinal Fluid
Ann Int Med 106:692-695, Hollander,H.&Levy,J.A., 1987

Human Immunodeficiency Virus-Associated Meningitis, Clinical Course & Correlations
Am J Med 83:813-816, Hollander,H.&Stringari,S., 1987

Alteration in the Natural History of Neurosyphilis by Concurrent Infection with the HIV
NEJM 316:1569-1572, 1600-16011987., Johns,D.R.,et al, 1987

Neurologic Relapse after Benzathine Penicillin Therapy for Secondary Syphilis in a Patient with HIV Infection
NEJM 316:1587-1589, 1600-16011987., Berry,C.D.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

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

Spinal Myoclonus Associated with HTLV-III/LAV Infection
Arch Neurol 43:1203-1204, Berger,J.R.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

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

Subacute Encephalopathy Associated with Human Immunodeficiency Virus in Haemophilia A
BMJ 293:993, Rahemtulla,A.,et al, 1986

Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986

Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986

Preventive Screening for the Fragile X Syndrome
NEJM 315:607-609, Turner,G.,et al, 1986

Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986

Benign Sexual Headach within a Family
Arch Neurol 43:1158-1160, Johns,D.R., 1986

Virus Isolation From & Identification of HTLV-III/LAV-Producing Cells in Brain Tissue From a Pt. with AIDS
JAMA 256:2365-2371, 2390-23911986., Gartner,S.,et al, 1986

Human T-Cell Lymphotropic Virus Type III Infection of the CNS, A Preliminary in Situ Analysis
JAMA 256:2360-2364, 2390-23911986., Stoler,M.H.,et al, 1986

Expressions of Human Immunodeficiency Virus Antigen (HIV-Ag) in Serum & CSF During Acute & Chronic Infection
Lancet 2:177-180, Goudsmit,J.,et al, 1986

Immunohistochemical Identification of HTLV-III Antigen in Brains of Patients with AIDS
Ann Neurol 20:289-295, Gabuzda,D.H.,et al, 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Vacuolar Encephalopathy of AIDS
NEJM 315:1549-1550, delaMonte,S.,et al, 1986

Recommended Infection-Control Policies for Patients with Human Immunodeficiency Virus Infection
NEJM 315:1562-1564, Gerberding,J.L., 1986

Preventing Possible HTLV-III Contamination from EEG Electrodes
NEJM 315:1167, Shukla,D., 1986

Neurological Manifestations of Human Immunodeficiency Virus Infection
BMJ 293:462-463, Carne,C.A.&Adler,M.W., 1986



Showing articles 1550 to 1600 of 1944 << Previous Next >>