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advances in neurology
algorithm
allodynia
Alzheimer's disease
aminoacidopathies
amyloid
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
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, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
angiostrongylus cantonensis
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm atrophy
arm weakness
ascending paralysis
aspiration
asthma
asthma, poliomyelitis-like syndrome with
ataxia
ataxia, progressive
Babinski sign
behavioral disorder
biologic markers
BiPAP
brain atrophy
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
children
chorea
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cognition
concussion
confusion
congenital heart disease
constipation
controversies in neurology
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
diplegia, atonic
diplegia, brachial
disability, neurological
disorientation
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dystonia
electromyogram
emotional lability
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic neurologic deficits
evidence-based research
evoked potentials
exercise intolerance
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
finger weakness
flaccid paralysis
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
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
head injury
headache
headache, progressive
health insurance
helminthic infection of CNS
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
hospice
Huntington's chorea
hyperreflexia
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, ubiquitin
inclusion body myositis
inflexibility, mental
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
lactic acidemia
laminectomy, cervical
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
Lewy body disease, diffuse
life expectancy
lobar atrophy
locked-in syndrome
lysosomal storage disease
meningismus
meningitis, eosinophilic
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
mobility
mobility aids
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, functional
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
mutism
myasthenia gravis
myelopathy
myelopathy, ischemic
myopathy
myopathy, autoimmune
myopathy, quadriceps
myositis
nasal speech
neck weakness
nerve biopsy
neurologic complications of, surgery
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neurologic testing
neuronal degeneration
neuropathology
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
next-generation sequencing
nusinersen
owl's eye sign of spinal cord
pain
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
parasitic infection
parasitic infection, CNS
paresthesias
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
patient information and support
peroxisomal disease
personality change
pes cavus
physical therapy
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
practice guidelines
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
raw fish ingestion
release phenomena
respirator
respiratory failure
review article
riluzole
risk factors
saccadic eye movements, abnormal
scoliosis
scoliosis, neurologic association with
scooters
screening
seizure
shoulder, subluxation
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
SMN1 gene
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid therapy, CNS treatment and complications with
stiff legs
superoxide dismutase
survival motor neuron gene
sushi
syringomyelia
tau protein
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
trauma
travel history
travel, foreign
treatment of neurologic disorder
trinucleotide repeats
tripping
ubiquitin
urea-cycle enzymopathies
urinary incontinence
viral infection
viral infection, CNS
viral isolation
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 150 to 200 of 4573 << Previous Next >>

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

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

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

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,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

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

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

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

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

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 4573 << Previous Next >>