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abdominal protrusion
abdominal x-ray
abducens nerve paralysis
abiotrophy
achilles tendon, enlarged
adult polyglucosan body disease
advance directives
advances in neurology
adverse drug reaction
agnosia
agnosia, visual
akinesia of eyelid function
algorithm
alpha coma
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anisocoria
anomic aphasia
anti GQ1b IgG antibody
anti IgLON5
anti Ri antibody
antitoxin
aphasia
aphasia, progressive, primary
apnea
applause sign
apraxia
apraxia of eyelid opening
areflexia
arm swing, reduced
arm weakness
arthralgia
aspiration
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autonomic dysfunction
autonomic dysfunction, acute
autonomic neuropathy
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
Bickerstaff's brainstem encephalitis
biologic markers
BiPAP
bismuth
bladder dysfunction
blepharospasm
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brain atrophy
brainstem
brainstem, dysfunction
brainstem, lesion of
bulbar dysfunction
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, juvenile
bulbar palsy, progressive
C0ORF72
CAG repeats
calcification, intracranial
camptocormia
carcinoma
carcinoma of bladder
carotid angiogram
CAT scan, abnormal
CAT scan, emission, abnormal
central hypoventilation
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction, subcortical
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
Charcot's sign
chewing, impaired
choking
chorea
clam poisoning
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cogwheel rigidty
coma
coma, episodic
compulsivity
confusion
corpus callosum, lesion of
corpus callosum, thinning
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cystatin C mutation
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
depression
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
diplopia
disorientation
distal muscle weakness
DNA probes
downward gaze
drooling
drowsiness
dying
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dyspnea
dystonia
dystonia, cervical
ears of the Lynx MR sign
electromyogram
electromyogram, decremental response
emergencies, neurologic
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalomyelitis
encephalopathy
enterovirus
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
Erdheim-Chester disease
executive dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
Fabry's disease
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
feeding disorder
fever
fibrillations
fine motor function, impaired
fish poisoning
Fisher's syndrome
flaccid paralysis
flail arm syndrome
foam cells
food poisoning
food-borne infection
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, apraxic
gait, spastic
gastroparesis
gastrostomy
gastrostomy, percutaneous endoscopic
gaze palsy
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
glycogen storage disease
granulomatosis with polyangiitis
granulomatous disease
grasp reflex
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, variant forms of
gynecomastia
hand weakness
head bobbing
headache
hearing loss
heel swelling
hemianopia
hemifacial spasm
hemiparesis
heralding manifestation
histiocytosis
histochemistry of muscle
HLA
hoarseness
honey
hospice
hyperreflexia
hypersomnia
hypertension
hypometric saccades
hypophonia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
ideomotor apraxia
imbalance
immunotherapy
impulsivity
inclusion bodies
inclusion bodies, intracytopasmic
infant, evaluation of
insomnia
intellectual deficit
intellectual deterioration
internal capsule
intracerebral hemorrhage
intrinsic hand muscles, wasting of
irritability
irritable baby
jaw clonus
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
lacunar infarction
language disorder in adults
laughing
laughing, pathologic
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukoencephalopathy
leukopenia
lid closure, weakness of
life expectancy
lip, biting
lobar atrophy
loss of sympathy
lymphoma involving CNS
lymphomatoid granulomatosis
malignancy screen
masked facies
memory, defect of recent
memory, impairment of
meningitis, aseptic
mental status, abnormal
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
middle cerebellar peduncle, lesion
migraine
Mills syndrome
mimics
misdiagnosis
mitochondrial disease
monoclonal gammopathy
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
MRI
MRI, abnormal
MRI, mouse ears
MRI, negative
MRI, serial
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle spasm, face
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis
myasthenia gravis, presenting manifestations
myasthenic syndrome
myelitis
myelomalacia
myeloneuropathy
myoclonic jerks
myoclonus
myokymia
myokymia, facial
myopathy
myopathy, mitochondrial
myorhythmia
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
nerve injury
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuroprotective agents
neurotoxic
neurotoxin
next-generation sequencing
nystagmus
nystagmus, dissociated
nystagmus, vertical
obsessive-compulsive disorder
ocular myopathy
ocular myopathy, differential diagnosis
oculocephalic reflex
opened mouth
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
pain
pain, abdominal
pain, management of chronic
palate, paralysis
palliative care
paralysis
paralysis, acute
paralysis, acute areflexic
paraneoplastic brainstem encephalitis
paraparesis
paraparesis, familial spastic
paraparesis, spastic
parasomnia
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathologic reflex
penguin silhouette sign
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis vaccine
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
post infectious polyneuropathy
post polio syndrome
postural abnormality
practice guidelines
prevention of neurologic disorders
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
progressive supranuclear palsy
proximal muscle atrophy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, oval
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, CNS treatment and complications with
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
rash
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
repetitive nerve stimulation
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retrocollis
retropulsion
review article
rigidity
rigidity, axial
riluzole
risk factors
saccadic eye movements, abnormal
salivation, excessive
saxitoxin
seizure
semantic dementia
sequencing difficulty
shell fish poisoning
sinemet
skin, lesions in neurologic disorders
sleep
sleep apnea, obstructive
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
spastic paraplegia, type 11
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
splenomegaly
standing difficulty
startle reaction
stem cell transplantation
steroid therapy, CNS treatment and complications with
stooped posture
subarachnoid hemorrhage
suck, poor
systemic illness
tachycardia
tandem gait, ataxic
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporalis muscle wasting
thrombocytopenia
tinnitus
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
toxins, nervous system
transverse smile
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
urinary retention
vertigo
vestibular function, tests of
viral infection
viral infection, CNS
vision, blurred
visual symptoms
vocal cord paralysis
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, fatiguable
weakness, focal
weakness, generalized
weakness, infant
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
West Nile fever
wheelchair
white matter disease
white matter disease, subcortical
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 250 to 300 of 3938 << Previous Next >>

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Preliminary NINDS Neuropathologic Criteria for Steele-Richardson-Olszewski Syndrome (Progressive Supranuclear Palsy)
Neurol 44:2015-2019, Hauw,J.-J., 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

Rapidly Progressing Atrophy of Medial Temporal Lobe in Alzheimer's Disease
Lancet 343:829-830, Jobst,K.A.,et al, 1994

Acute Pseudobulbar Mutism with Good Functional Recovery
Neurol 44:176-177, Chesser,M.Z.,et al, 1994

Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
Ann Neurol 35:237-239, Polo,K.B.&Jabbari,B., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Olfactory Testing Differentiates Between Progressive Supranuclear Palsy & Idiopathic Parkinson's Dis
Neurol 43:962-965, Doty,R.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Pontine and Extrapontine Myelinolysis:A Neurologic Disorder Following Rapid Correction of Hyponatremia
Medicine 72:359-373, Karp,B.I.&Laureno,R., 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Detection in Life of Confirmed Alzheimer's Disease, Medial Temporal Lobe Atrophy by Computed Tomography
Lancet 340:1179-1183, Jobst,K.A.,et al, 1992

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

The Apomorphine Test in Parkinsonian Syndromes
JNNP 54:870-872, D'Costa,D.F.,et al, 1991

Autonomic Nervous Function in Progressive Supranuclear Palsy
Arch Neurol 48:1083-1084, vanDijk,J.G.,et al, 1991

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Acute Pseudobulbar or Suprabulbar Palsy
Arch Neurol 48:501-507, Besson,G.,et al, 1991

Idazoxan Treatment in Progressive Supranuclear Palsy
Neurol 41:986-991, Ghika,J.,et al, 1991

Positron Emission Tomography in Progressive Supranuclear Palsy
Arch Neurol 48:389-391, Bhatt,M.H.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Relapse of Infant Botulism
Ann Neurol 28:187-189, Glauser,T.A.,et al, 1990

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990



Showing articles 250 to 300 of 3938 << Previous Next >>