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agitation
aminoacidopathies
aminoacidurias
aneurysm
aneurysm, intracranial
anosognosia
antiviral agents
aphasia
aphasia, global
aphasia, transcortical
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
athetosis
atypical
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basilar artery stenosis
behavioral disorder
bilirubin encephalopathy
blindness, sudden
brain atrophy
brain damage
brainstem, lesion of
breast feeding
bulbar palsy
CAG repeats
CAT scan
CAT scan, abnormal
catalepsy
cataplexy
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrospinal fluid, glycine
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
choreoathetosis
chromosomal abnormality
chromosome 6
Clinical Pathologic Conference(C.P.C.)
congenital myasthenic syndromes
conjugate gaze, forced
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
developmental retardation
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
disease modifying agents
downward gaze, paralysis of
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
emtricitabine
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
epidemiology of neurology
executive dysfunction
exercise intolerance
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
false negative
familial
fever
floppy infant
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
Guillain Barre syndrome, infantile and childhood form
hallucination
hallucination, visual
head injury
headache
hearing loss
hemiparesis
hemorrhage, thalamic
hepatomegaly
hepatosplenomegaly
hoarseness
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypophonia
hyporeflexia
iatrogenic neurologic disorders
imbalance
impulsivity
inattention
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, location of
intracerebral hemorrhage, volume
intraventricular hemorrhage
jaundice
kernicterus
lactic acidemia
leucine
lid closure, weakness of
life expectancy
lipid storage disorder of CNS
lysosomal storage disease
maple syrup urine disease
MELAS syndrome
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
metabolic disorder, primary
miglustat
migraine
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
moro reflex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, muscle
MRI, negative
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myoclonus
myopathy
myopathy, drug-induced
myopathy, mitochondrial
nasal speech
nausea and vomiting
neglect
neoplasm, primary of CNS
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neurotoxic
neurotoxin
Niemann-Pick disease
nystagmus
ocular motility, disorders of
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, head injury causing
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
ophthalmoplegia, total
ophthalmoplegic migraine
opisthotonus
organomegaly
paranoia
Parkinsonism syndrome
personality change
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
ragged-red fibers
rapidly progressing neurologic illness
renal failure
retinal degeneration
retropulsion
review article
salivation, excessive
schizophrenia
screening
seizure
seizure, children
seizure, laughing as manifestation
sensorimotor stroke
sensorineural hearing loss
setting sun phenomena
short stature
skew deviation
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
strokelike episodes
subthalamic nucleus
suck, poor
systemic illness
temporal lobe, lesion
term infant
thalamic aphasia
third nerve palsy
third nerve palsy, childhood
third nerve palsy, congenital
third nerve palsy, cyclic
transverse smile
treatment of neurologic disorder
tremor
trinucleotide repeats
upgaze, paralysis of
ventricular enlargement
vertical gaze
viral infection
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
visuospatial disturbance
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
wheelchair
whole genome sequencing
wide based gait
Showing articles 650 to 700 of 1791 << Previous Next >>

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Diabetic Gustatory Sweating Successfully Treated with Topical Glycopyrrolate, Report of a Case and Review of the Literature
Arch Int Med 159:877-878, Urman,J.D.&Bobrove,A.M., 1999

Varicella as a Risk Factor for Cerebral Infarction in Childhood:A Case-Control Study
Ann Neurol 45:679-680, Sebire,G.,et al, 1999

Cat-Scratch Disease Encephalopathy:A Cause of Status Epilepticus in School-Aged Children
J Pediatrics 134:635-638, Armengol,C.E.&Hendley,J.O., 1999

Brain Tumors in Children
Arch Neurol 56:421-425, Packer,R.J., 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Open Comparative Long-Term Study of Vigabatrin vs Carbamazepine in Newly Diagnosed Partial Seizures in Children
Arch Neurol 56:605-607, Zamponi,N.&Cardinali,C., 1999

Vagus Nerve Stimulation for Medication-Resistant Generalized Epilepsy
Neurol 52:1510-1512, Labar,D.,et al, 1999

Left Vagal nerve Stimulation in Children with Medically Refractory epilepsy
J Pediatr 134:563-566, 532, Murphy,J.V.&Pediatric VNS Study Group, 1999

Vagal Nerve Stimulation in epileptic Encephalopathies
Pediatrics 103:778-782, 821, Parker,A.P.J.,et al, 1999

A Double-Blind, Randomized Trial of Topiramate as Adjunctive Therapy for Partial-Onset Seizures in Children
Neurol 52:1338-1344, Elterman,R.D.,et al, 1999

Intractable Epilepsy
Lancet 353:1238, Shuper,A.,et al, 1999

Chromatic Sensitive Epilepsy:A Variant of Photosensitive Epilepsy
Ann Neurol 45:790-793, Tobimatsu,S.,et al, 1999

Measurement of the Urinary Lactate:Creatinine Ratio for the Early Identification of Newborn Infants at Risk for Hypoxic-Ischemic Encephalopathy
NEJM 341:328-335,364, Huang,C.,et al, 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,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

Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
Hum Pathol 30:978-981, Abdulkader, I.,et al, 1999

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

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

Sneddon's Syndrome:Neuro-Ophthalmologic Manifestations in a Possible Autosomal Recessive Pattern
Neurol 51:1185-1187, Rehany,U.,et al, 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Incidence of Status Epilepticus in Rochester, Minnesota, 1965-1984
Neurol 50:735-741, Hesdorffer,D.C.,et al, 1998

Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
Ann Neurol 43:514-520, Hayman,M.,et al, 1998

Concurrent Medical Disease in Work-Relatede Carpal Tunnel Syndrome
Arch Int Med 158:1506-1512, 14961998., Atcheson,S.G.,et al, 1998

Clinicopath Conf
Demyelinating Process Consistent with Multiple Sclerosis, Case 26-1998, NEJM 339:542-549998., , 1998

Temporal Lobe Epilepsy in Childhood:Clin, EEG, & Neuroimag Findings & Synd Class in a Cohort with New-Onset Szres
Neurol 49:960-968, Harvey,A.S.,et al, 1998

Magnetic Resonance Imaging Evidence of Hippocampal Injury After Prolonged Focal Febrile Convulsions
Ann Neurol 43:413-426, 4111998., VanLandingham,K.E.,et al, 1998

Long-Term Intellectual and Behavioral Outcomes of Children with Febrile Convulsions
NEJM 338:1723-1728, Verity,C.M.,et al, 1998

Long-Term Prognosis of Seizures with Onset in Childhood
NEJM 338:1715-1722, Sillanpaa,M.,et al, 1998

A Comparison of Rectal Diazepam Gell and Placebo for Acute Repetitive Seizures
NEJM 338:1869-1875, 19161998., Dreifuss,F.E.,et al, 1998

Medical Causes of Seizures
Lancet 352:383-390, Delanty,N.,et al, 1998

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

An Optimality Score for the Neurologic Examination of the Term Newborn
J Pediatr 133:406-416, Dubowitz,L.,et al, 1998

Second Malig in Young Children with Prim Brain Tumors Following Trtm with Prolonged Postop Chemo & Delay Irrad
Ann Neurol 44:313-316, 3001998., Duffner,P.K.,et al, 1998

Recombinant Human Nerve Growth Factor in the Treatment of Diabetic Polyneuropathy
Neurol 51:695-702, 6621998., Apfel,S.C.,et al, 1998

Response to External Ventricular Drainage in Spont Intracerebral Hemorr with Hydrocephalus
Neurol 50:519-523, Adams,R.E.&Diringer,M.N., 1998

Spontaneous Dural Carotid Cavernous Sinus Fistula Pres Isolat Ophthalmoplegia:Eval with MR Angiogr
Neurol 50:814-816, Uehara,T.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Risk of Recurrent Seizures After Two Unprovoked Seizures
NEJM 338:429-434, Hauser,W.A.,et al, 1998

Epilepsy in Young People:23 Year Follow Up of the British National Child Development Study
BMJ 316:339-342, Kurtz,Z.,et al, 1998

Hydrocephalus:A Previously Unrecognized Predictor of Poor Outcome from Supratentorial Intracerebral Hemorrhage
Stroke 29:1352-1357, Diringer,M.N.,et al, 1998

Prevent of a 1st Stroke by Transfusions in Children/Sickle Cell Anemia & Abnorm Results on Transcr Doppler Ultrasonog
NEJM 339:5-11, Adams,R.J.,et al, 1998

Stroke in Children and Sickle-Cell Disease, Baltimore-Washington Cooperative Young Stroke Study
Neurol 51:169-176, Earley,C.J.,et al, 1998

Clinical Features of Moyamoya Disease in the United States
Stroke 29:1347-1351, Chiu,D.,et al, 1998

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

Pupil Involvement in Patients with Diabetes-Associated Oculomotor Nerve Palsy
Arch Ophthalmol 116:723-727, 7981998., Jacobson,D.M., 1998

Managing Oculomotor Nerve Palsy
Arch Ophthalmol 116:798, Trobe,J.D., 1998

Most Diabetic Third Nerve Palsies are Peripheral
Neurol 51:1510, Keane,J.R.&Ahmadi,J., 1998

Binocular Vertical Diplopia
Mayo Clin Proc 73:55-66, Brazis,P.W.&Lee,A.G., 1998



Showing articles 650 to 700 of 1791 << Previous Next >>