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Differential
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abducens nerve paralysis
abscess, intracerebral
achilles tendon, enlarged
acoustic nerve
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
addiction, heroin
addiction, heroin-neurologic complications with
akinetic mute
alopecia
aneurysm, berry
angiography, posterior fossa
angiotensin-converting enzyme
anterior commissure
anterior inferior cerebellar artery
anti Ma
anti MAG antibodies
antibodies to measles
aphasia
aphonia
apraxia of eye movements
aqueduct of Sylvius, enlargement
arbovirus
areflexia
arterial dissection
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteritis, temporal
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
atypical
autism
autoantibodies
autoimmune disease
autonomic dysfunction
autosomal dominant leukodystrophy
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Benedikt's syndrome
Bickerstaff's brainstem encephalitis
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, dysfunction
brainstem, glioma
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
brainstem, syndrome
cachexia
CAG repeats
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cauda equina
cauda equina, enhancement
cauda equina, lesion of
central nervous system, infection of
centrum semiovale
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hemorrhage
cerebellar hypoplasia
cerebellar infarction
cerebellar infarction, bilateral
cerebellar lesion
cerebellar peduncle
cerebellum
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral cortical encephaliis
cerebral edema, cytotoxic
cerebral edema, vasogenic
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral peduncle
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, location of
children
chorea
chromosomal abnormality
chromosome 11
Claude's syndrome
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel pursuit movements
Collier's sign
coma
comorbidities
complications
confusion
congenital malformation
congenital ocular motor apraxia
conjunctivitis
conus medullaris, lesion of
corpus callosum
corpus callosum, atrophy of
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve palsies
crying, pathologic
cyst, parenchymal
cystatin C mutation
deafness, bilateral
deep gray nuclei
degenerative diseases of CNS
dementia
demyelinating disease
Dengue fever
developmental retardation
diagnostic criteria
diaschisis
differential diagnosis
diplopia
down-beat nystagmus
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram, periodic complexes
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, progressive
epicanthal folds
epidemiology of neurology
Erdheim-Chester disease
erectile dysfunction
exome sequencing
eye movement, disorders of
eye, pain in
face, numbness of
facial appearance, abnormal
facial nerve palsy
facial pain
facial weakness
falling
familial
finger nose finger test
Fisher's syndrome
fluorescein angiography
foam cells
fourth ventricle, enlargement of
fourth ventricle, floor
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
gadolinium
gait disorder
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
giant cell arteritis
glioma
glutamic acid decarboxylase, antibody
gray matter
hammertoes
head injury
head injury, brain stem lesion after
head jerks
headache
headache, recurrent
headache, severe
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
heel swelling
hemiparesis
heralding manifestation
herniation syndromes, intracranial
herpes simplex encephalitis
herpes simplex encephalitis, atypical
herpes simplex encephalitis, extra temporal
HGPPS
hiccoughs
highly active antiretroviral therapy
histiocytosis
Horner's syndrome
H-sign, spinal cord
human immunodeficiency virus type 1
hydrocephalus
hyperactivity
hyperreflexia
hypodontia
hypometric saccades
hypomyelination
hyponatremia
hypothalamus
hypothalamus, lesion of
hypotonia
imbalance
immune reconstitution inflammatory syndrome
immune-mediated pathogenesis
immunocompetent
immunologic disease
immunosuppression
impulsivity
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
infection
infertility
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intracerebral hemorrhage
JC virus
joint hypermobility
Joubert syndrome
Kearns-Sayre syndrome
lactic acidemia
lacunar infarction
lateral medullary syndrome
lateropulsion
laughing, pathologic
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
listeria monocytogenes
listeriosis, CNS
locked-in syndrome
low back pain
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malformation, CNS, congenital
malformation, vascular, cerebral
mammillary bodies
Marchiafava-Bignami disease
medulla oblongata
medulla oblongata, infarction of
medulla oblongata, lesion of
medulla oblongata, malformation
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
mental status, abnormal
metabolic acidosis
microdontia
microhemorrhage, intracerebral
midbrain
midbrain, infarction of
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
MNGIE syndrome
molar tooth sign
molecular genetics
monoclonal antibodies
mortality
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, contrast enhanced, cloud-like
MRI, contrast enhanced, subependymal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, mass effect on
MRI, optic nerve
MRI, snowball lesions
MRI, spinal cord
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle weakness, proximal
mycoplasma
mycoplasma pneumoniae
myelitis, longitudinal
myelitis, transverse
myelomalacia
myoclonus
nausea and vomiting
neoplasm, posterior fossa
neoplasm, primary of CNS
nerve root enhancement
nerve root, lumbar, lesion of
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuroophthalmology
neuropathology
next-generation sequencing
nonverbal
Nothnagel's syndrome
nutritional deficiency
nystagmus
nystagmus, cerebellar
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, retractorius
nystagmus, rotary
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular dysmetria
ocular motility, disorders of
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, bilateral, acute
opportunistic infection, CNS
opsoclonus
opsoclonus, differential diagnosis of
optic chiasm
optic chiasm, lesion of
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
orthostatic hypotension
ovarian insufficiency
pain, back
paraparesis
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
periaqueductal lesion
periodic alternating gaze
personality change
pes cavus
pituitary
pituitary stalk, lesion of
pituitary, lesion of
PLEDs
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
POLG1 gene
POLR3B
polymerase chain reaction
polymerase chain reaction, false negative
pons, hypoplasia
pons, infarction of
pons, lesion of
pontine glioma
positional head-hanging test
posterior fossa, arteriovenous malformation
posterior fossa, mass of
posterior inferior cerebellar artery syndrome
precipitating factors
pregnancy, neurologic complications in
pretectal syndrome
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudoabducens palsy
pseudobulbar palsy
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, ectopic-acquired
pupil, midposition and fixed, bilateral
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract, uncrossed
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
reading disorder, acquired
recurrent
Red flags
regional enteritis
release phenomena
remote effect of cancer on the nervous system
renal failure
renal failure, acute
respiratory tract infection
restiform body
reticular activating system
retinal branch artery occlusion
reversible neurologic disorder
review article
rigidity
root lesion, nerve
rubeola virus
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
scoliosis
scoliosis, neurologic association with
screening
seizure
sensorineural hearing loss
sensory loss
sensory loss, crossed pattern
serologic testing
seronegative
skew deviation
skin, biopsy
snout reflex
spastic ataxia
spasticity
speech, delayed development of
spinal cord, lesion of
spinocerebellar ataxia
splenium of corpus callosum
spondylolysis
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
striatum, lesion of
striatum, lesion of, bilateral
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
subcortical U fibers
succinate dehydrogenase deficiency
superior cerebellar peduncle
Susac's syndrome
symmetric brain lesions
syncope
syndactyly
systemic illness
tandem gait, ataxic
tantrum
teeth, abnormal
teeth, number of in infants
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular enlargement
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve
third nerve lesions, nuclear
third nerve palsy
third nerve palsy, bilateral
third nerve palsy, partial
third ventricle, wall
tinnitus
titubation
treatment of neurologic disorder
tremor
tremor, intention
tremor, rubral
tremor, thalamic
tremor, writing
trigeminal artery, persistent
trinucleotide repeats
tropical disease
tumefactive lesion
upward transtentorial herniation
urinary incontinence
uveitis
vaccination, neurologic complications with
vertebral artery
vertebral artery occlusion
vertigo
viral infection
viral infection, CNS
visual loss
visuospatial disturbance
walking, difficulty with
Wallerian degeneration
weakness
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
white matter disease, pattern
white matter disease, periventricular
white matter disease, subcortical
wide based gait
writing
x-linked intellectual deficit
x-linked mental retardation
 		Showing articles 650 to 700 of 1502 << Previous Next >>

Delayed Cerebellar Disease and Death After Accidental Exposure to Dimethylmercury
NEJM 338:1672-1676, 16921998., Nierenberg,D.W.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Cerebellum in Attention-Deficit Hyperactivity Disorder
Neurol 50:1087-1093, Berquin,P.C.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Acute Vestibular Syndrome
NEJM 339:680-685, Hotson,J.R.&Baloh,R.W., 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Dilemma of Discontin of Anticoag Therapy for Pts with Intracran Hem & Mech Heart Valves
Neurosurg 42:769-773, Eelco,F.M.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Predicting Neurologic Deterioration in Patients with Cerebellar Hematomas
Neurol 511:1364-1369, St. Louis,E.K.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Patterns of Lateral Medullary Infarction, Vascular Lesion-MR Imaging Correl of 34 Cases
Stroke 29:645-652, Kim,J.S.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Vertigo
Lancet 352:1841-1846, Baloh,R.W., 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

The Variable MR Appearance of Primary Lymphoma of the Central Nervous System:Comparison with Histopathologic Features
AJNR 18:563-572, Johnson,B.A.,et al, 1997

Horner's Syndrome Due to First-Order Neuron Lesions of the Oculosympathetic Pathway
AJR 169:581-584, Nagy,A.N.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Causes and Mechanisms of Cerebellar Infarction in Young Patients
Stroke 28:2400-2404, Barinagarrementeria,F.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

von Hippel-Lindau Disease
Medicine 76:381-391, Maher,E.R.&Kaelin,W.G., 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Brainstem CMV Encephalitis in AIDS:Clinical Case and MRI Features
Neurol 48:529-530, Pierelli,F.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Central Poststroke Pain & Wallenberg's Lateral Medullary Infarction:Freq, Charact & Determinants in 63 Pts
Neurol 49:120-125, MacGowan,D.J.L.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997



Showing articles 650 to 700 of 1502 << Previous Next >>