Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
advance directives
advances in neurology
algorithm
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, complications with
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, hospitalization
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
analgesic
anterior horn cell disease
anti Hu antibody
anticonvulsants
antiviral agents
anxiety
aphasia
aphasia, progressive, primary
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
asthma
asthma, poliomyelitis-like syndrome with
ataxia
ataxia, progressive
autoantibodies
Babinski sign
behavioral disorder
benzodiazepine
BiPAP
bulbar palsy
bulbar palsy, progressive
cachexia
camptocormia
cane
carbon monoxide poisoning
carcinoma of lung
caregiver
CAT scan, abnormal
CAT scan, emission, abnormal
CD4 counts
central nervous system, infection of
cerebellar atrophy, primary
cerebral death
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cervical spine
cervical spine injury
cervical spine injury, treatment of
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
children
chills
chromosomal abnormality
chromosome 5
climate change
Clinical Pathologic Conference(C.P.C.)
cognition
coma
confusion
congenital heart disease
constipation
cost
cost effectiveness
cough
CPAP
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
depression
developmental milestones
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diarrhea
differential diagnosis
diplegia, brachial
disability rating scale, neurological
distal muscle atrophy
distal muscle weakness
drooling
drowning
dying
dysarthria
dysphagia
dyspnea
efficacy
electromyogram
emotional lability
encephalitis
encephalitis, central European
encephalitis, Powassan
encephalitis, viral
encephalomyelitis
encephalomyeloneuritis
encephalopathy
encephalopathy, post anoxic
enterovirus
enterovirus infection of CNS
epidemiology of neurology
ethics in neurology
euthanasia
exercise
facial weakness, bilateral
familial
fasciculation
fatigue
fever
fibrillations
flaccid paralysis
flail arm syndrome
fluency
foot drop
football neurologic injuries
frontotemporal dementia, behavioral variant
F-wave response
gait disorder
ganglionitis
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
hallucination
hand weakness
hanging
headache
hemiparesis
heralding manifestation
highly active antiretroviral therapy
hospice
human immunodeficiency virus type 1
hunger
hypercapnia
hyperreflexia
hypogammaglobulinemia
hyporeflexia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
immunohistochemistry
immunosuppression
inclusion body myositis
infection
inflexibility, mental
insomnia
intellectual deficit
intermittent positive pressure breathing
internal capsule
intrinsic hand muscles, wasting of
jaw jerk, abnormal
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
laminectomy, cervical
laughing, pathologic
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukemia
leukemia, neurologic findings assoc.with
leukoencephalopathy
lid closure, weakness of
life expectancy
life support, withdrawal of
life sustaining treatment
limbic encephalitis
lobar atrophy
locked-in syndrome
medical-legal aspects of neurology
meningismus
mental status, abnormal
Mills syndrome
mimics
minimally conscious state
misdiagnosis
molecular genetics
monomelic amyotrophy
monoparesis
morphine
mortality
motor neuron disease
motor neuron disease, spontaneous recovery
motor system
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, ischemic
myeloradiculitis
myocardial infarction
myopathy
narcotic analgesics
nausea and vomiting
neck pain
neck weakness
nerve conduction studies
neurologic complications
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuronal degeneration
neuronopathy
neuronopathy, sensory
neuropathology
neuropathology, brain
neuroprotective agents
next-generation sequencing
nusinersen
old age, neurology of
opiate
owl's eye sign of spinal cord
oxygen therapy
pain
pain, back
pain, increased response
pain, management of chronic
palliative care
paralysis, acute
paralysis, acute areflexic
paraneoplastic ganglionopathy
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, flaccid
paraparesis, spastic
paraplegia
paraspinal muscle
Parkinsonism syndrome
Parkinsonism-dementia complex
patient information and support
persistent vegetative state
personality change
phrenic nerve pacemaker
physician assisted suicide
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poliomyelitis
poliomyelitis-like illness
polymerase chain reaction
positive sharp waves
practice guidelines
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
public health
pulmonary embolism
pulmonary function tests
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quality of life
radiculitis
rapidly progressing neurologic illness
release phenomena
remote effect of cancer on the nervous system
repetitive nerve stimulation
respirator
respiratory arrest
respiratory failure
respiratory tract infection
retrovirus
review article
right to die
riluzole
risk factors
rodents
safety
salivation, excessive
scoliosis
scoliosis, neurologic association with
screening
sedation
sensory symptoms
serologic testing, false negative
single photon emission computed tomography
sleep
sleep pathology and physiology
SMN1 gene
spastic ataxia
spasticity
speech disorder
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spirometry
spondylosis
stereotyped behavior
strangulation
suicide
superoxide dismutase
survival motor neuron gene
syringomyelia
thalamus, lesion of
tick bite
tick-borne encephalitis
tongue, atrophy
tongue, fasciculations of
tracheostomy
trauma
treatment of neurologic disorder
tripping
unconsciousness
valium
viral infection
viral infection, CNS
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West Nile fever
wheelchair
word-finding difficulty
Showing articles 150 to 200 of 6941 << Previous Next >>

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

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

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

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

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

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 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

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

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

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

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

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

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

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

Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
JNNP 59:38-44, Bouche,P.,et al, 1995

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

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

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Recent Developments in the Drug Treatment of Motor Neurone Disease
BMJ 309:140-141, , 1994

Sequences Specific for Enterovirus Detected in Spinal Cord from Patients with Motor Neurone Disease
BMJ 308:1541-1543, Woodall,C.J.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
Neurol 44:547-548, Camu,W.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Intravenous Immunoglobulin Trtm in Pts with Motor Neuron Syndromes Assoc with Anti-GM Antibodies:A Contrld Study
Neurol 44:429-432, Azulay,J-P.,et al, 1994

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Clinical Significance of Hypointensity in the Motor Cortex on T2-Weighted Images
Neurol 44:1181, Iwasaki,Y.,et al, 1994

Extent of Pontine Pyramidal Tract Wallerian Degeneration and Outcome after Supratentorial Hemorrhagic Stroke
Stroke 25:1207-1210, Fukui,K.,et al, 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
Lancet 341:265-268, Couratier,P.,et al, 1993



Showing articles 150 to 200 of 6941 << Previous Next >>