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addiction, heroin
addiction, heroin-neurologic complications with
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
alcoholism
ammonia
anoxia
arterial dissection
arterial dissection, bilateral
arterial dissection, carotid
arterial dissection, spontaneous
ataxia
ataxia, cerebellar
ataxia, progressive
athetosis
auditory evoked brainstem potentials
autism
autoimmune basal ganglia encephalitis
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, hemorrhage
basal ganglia, hemorrhage, bilateral
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bilirubin encephalopathy
blepharospasm
blindness
bone marrow transplantation
bradykinesia
brain atrophy
brain damage
brainstem, lesion of
breast feeding
calcification, intracranial
carbon monoxide poisoning
carotid artery disease
carotid artery stenosis
carotid artery stenosis, bilateral
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, contrast enhanced
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
centrum semiovale
cerebellar degeneration
cerebellar infarction
cerebellar infarction, bilateral
cerebellar lesion
cerebellum
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral infarction
cerebral infarction, hemorrhagic
cerebral palsy
cerebrotendinous xanthomatosis
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
cholesterol
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
claustrum
cognition
coma
complications
confusion
congenital malformation
consanguinity
copper
corpus callosum, lesion of
corpus callosum, thinning
cranial neuropathy
Cree leukoencephalopathy
cry, abnormal
cry, high-pitched
cryoglobulinemia
cyanide poison
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental retardation
disability rating scale, neurological
disorientation
disseminated intravascular coagulation(DIC)
disulfiram
dizziness
drug abuse
drug abuse, neurologic complications of
drug induced neurologic disorders
drug overdose
dysarthria
dyskinesia
dysphagia
dyspnea
dyssynergia cerebellaris myoclonica
dystonia
ecstasy
efficacy
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
encephalopathy, delayed
encephalopathy, neonatal
encephalopathy, post anoxic
enzyme, defect
epidemiology of neurology
equinovarus
familial
fever
frontal lobe, behavior with disease of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus focused ultrasound ablation
globus pallidus, hemorrhage
globus pallidus, infarction
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, swelling
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hamartoma
hanging
headache
headache, recurrent
hearing loss
hemianopia
hemianopia, homonymous
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration, non-Wilsonian
heterotopia
high altitude sickness
hippocampus
human immunodeficiency virus type 1
hyperalimentation
hyperammonemic encephalopathy
hyperbaric oxygen
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperreflexia
hyponatremia
hyporeflexia
hypotension, systemic
hypothermia
hypotonia
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunosuppression
immunotherapy
inborn errors of metabolism
industrial neurologic disorders
infection
intellectual deficit
intellectual deterioration
internal capsule
intracerebral hemorrhage
intravenous
iodine deficiency
iron, brain
jaundice
kernicterus
ketoacidosis
Latvia
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukoencephalopathy
liver disease
liver function enzymes
liver transplantation
manganese intoxication
maple syrup urine disease
memory, impairment of
mental retardation
metabolic acidosis
metabolic disorder, primary
methanol intoxication
methcathinone
methylmalonic acidemia
methylmalonic aciduria
midbrain
midbrain, infarction of
midbrain, lesion of
mild cognitive impairment
mimics
moro reflex
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, ADC maps
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, paramagnetic effect
MRI, perfusion
MRI, serial
MRI, susceptibility weighted
MRI, T1 weighted fat suppression
MRI, T1 weighted high signal foci
MRS
mutism
myelinolysis, extrapontine
myelopathy
myelopathy, hepatic
myoclonus
myoclonus, epilepsy
Native Americans
neurofibromatosis 1
neurofilaments
neurologic complications
neurologic complications of, surgery
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neurotoxic
neurotoxicity, acute
neurotoxin
nystagmus
occupational neurologic disorders
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, neonatal
opisthotonus
optic atrophy
organ transplantation
osmotic demyelination syndrome
palilalia
pallidotomy
PANK2 mutation
papilledema
paraparesis, spastic
parenteral alimentation
Parkinson disease
Parkinson disease, familial
Parkinson disease, fluctuations in
Parkinson disease, on-off phenomena in
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
personality change
pigmentary retinopathy
pituitary
poison, neurologic problems with
portal caval shunt
postural abnormality
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
progressive pallidum atrophy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quality of life
radiation therapy, CNS treatment and complications with
renal failure
renal failure, acute
retinal degeneration
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
rigidity
Russia
safety
sea-blue histiocytes
seizure
seizure, children
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
septicemia
setting sun phenomena
skin, cherry-red
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
static encephalopaty of childhood with neurodegeneration in adulthood
stereotaxic surgery
stimulant drugs
striatum, lesion of
substantia nigra
subthalamic nucleus
suck, poor
suicide
symmetric brain lesions
systemic illness
term infant
thalamus, lesion of
thalamus, lesion of-bilateral
toxic encephalopathy
toxins, nervous system
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
upgaze, paralysis of
uremia
uremic encephalopathy
urinary incontinence
urine test for metabolic disorders
vasculitides
vertical gaze
visual acuity, decreased
visual evoked response
visual field defect
watershed infarcts
welder
wheelchair
white matter disease
white matter disease, periventricular
Showing articles 400 to 450 of 3801 << Previous Next >>

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

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

Generalised Motor Neuron Disease as an Unusual Manifestation of Borrelia Burgdorferi Infection
JNNP 63:257-258, Hemmer,B.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
JNNP 62:88-91, Waragai,M.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Riluzole
Lancet 348:795-799, Wokke,J., 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995



Showing articles 400 to 450 of 3801 << Previous Next >>