Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acrocyanosis
Adies pupil
adult polyglucosan body disease
advances in neurology
adverse drug reaction
agenesis of corpus callosum
Aicardi-Goutieres syndrome
Alexanders disease
alpha glucosidase
alveolar hypoventilation
Alzheimer's disease
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anesthesia, general
angiography, cerebral, false negative
angiography, cerebral, negative
ankylosing spondylitis
anterior horn cell disease
anterior tibial muscle weakness
antibodies to measles
antiviral agents
apnea
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthralgia
arylsulfatase A
ascending paralysis
aspartate aminotransferase
aspartocyclase
aspiration
aspirin
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
atypical
audiogram
auditory evoked brainstem potentials
autoimmune disease
autonomic dysfunction
autonomic neuropathy
axonal degeneration
B 12 deficiency
Babinski sign
bacterial infection
baldness
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basement membrane
basement membrane thickening
biologic markers
BiPAP
bladder dysfunction
bone marrow biopsy
bradycardia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
bulbar palsy, progressive
burning skin
cachexia
CAG repeats
calcification, intracranial
Canavan's disease
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, spine
cataracts
cataracts, congenital
cauda equina, enhancement
CD4 counts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, women
cervical spine
Charcot-Marie-Tooth
chilbran skin lesions
children
chorea
choreoathetosis
chromosome 12
chromosome 19
chromosome 3
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cognition
coma
complications
confusion
congestive heart failure
consanguinity
copper deficiency
corona radiata
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cortical blindness, transient
cortical infarction
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
cyanosis
cyst
cyst, parenchymal
deafness
deafness, bilateral
deafness, sudden
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delayed dentition
dementia
dementia, childhood
dementia, frontotemporal
denervation of muscle
denervation potentials
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
diffuse idiopathic skeletal hyperostosis
diplopia
diplopia, transient
disability, neurological
distal muscle weakness
disulfiram
drooling
dural sinus thrombosis
dying
dysarthria
dysdiadochokinesia
DYSF gene
dysferlinopathy
dysmetria
dysphagia
dyspnea
dystonia
dystonia, children
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
electron microscopy
emotional lability
encephalitis
encephalitis, focal
encephalopathy
encephalopathy, acute
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, post anoxic
enzyme treatment
enzyme, defect
enzyme, muscle disease
episodic neurologic deficits
evoked potentials
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
fibrillations
flail arm syndrome
foot deformity
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, atrophy
frontal lobe, pathologic signs of
fundus, abnormality of
funduscopic exam
gait disorder
gait, spastic
gastric partitioning
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
genu of corpus callosum
globus pallidus, hemorrhage
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycogen storage disease
GM1 ganglioside antibodies
gray matter
Guillain Barre syndrome, differential diagnosis of
hand weakness
head bobbing
head circumference
head lag
headache
headache, positional
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
heart block
hemiparesis
hemiparesis, transient
hepatomegaly
heralding manifestation
high arched feet
high arched palate
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hypercapnia
hyperhomocysteinemia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypodontia
hypoglycorrhachia
hypomyelination
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
incoordination
infection
intellectual deficit
intellectual deterioration
interferon alpha
intestinal pseudoobstruction
intrauterine
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
Japan
Jewish
Kernig's sign
Krabbe's disease
laminar necrosis, cortical
laughing
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
Lewy body disease, diffuse
life expectancy
life support, withdrawal of
lobar atrophy
lymphoma
lymphoma involving CNS
lysosomal storage disease
lysosomes, abnoral
macrocephaly
Marinesco-Sjogren syndrome
masseter muscle wasting
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningismus
meningitis, melanomatous
mental retardation
merosin
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
microangiopathy, brain
microangiopathy, retina
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Middle east
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoclonal gammopathy
monoparesis
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, functional
MRI, high signal foci on
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
multiple organ failure
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, congenital
muscular dystrophy, limb-girdle
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, acute
myopathy, critically ill
myopathy, drug-induced
myopathy, steroid induced
myopia
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve root enhancement
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic evaluation
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal degeneration
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
neuroprotective agents
neurotoxic
neurotoxicity, acute
next-generation sequencing
nutritional deficiency
nystagmus
obesity
occipital lobe, lesion of
old age, neurology of
ophthalmoplegia
optic atrophy
optic nerve, hypoplasia of
optic neuropathy
optic neuropathy, nutritional
pain
pain, abdominal
pain, foot
paralysis
paralysis, recurrent
paraparesis
paraparesis, spastic
paresthesias
Parkinson disease
pathology
patient information and support
pediatric neurology
percussion induced muscle contraction
persistent vegetative state
personality change
pes cavus
pleocytosis of cerebrospinal fluid
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, critically ill
polyneuropathy, critically ill, children
polyradiculoneuropathy
Pompe's disease of glycogen storage
pons, atrophy
pons, lesion of
posterior column disease
posterior longitudinal ligament, ossification of
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pupil, abnormality in neurologic disorders
pupil, tonic
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
reading disorder, acquired
recurrent
respirator
respiratory failure
retina, abnormal
retinal artery occlusion
retinal branch artery occlusion
retinal infarction
retinal lesion
retinopathy
retrovirus
reversible neurologic disorder
review article
rigidity
riluzole
risk factors
Rosenthal fibers
rubeola virus
saccadic eye movements, abnormal
Schilder's disease
sedimentation rate, elevated
seizure
seizure, children
sensorineural hearing loss
sensory loss
septicemia
serologic testing
sicca syndrome
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
slit lamp examination
slow virus infection of CNS
small vessel disease
SMN1 gene
spasticity
speech disorder, childhood
spinal cord
spinal cord degeneration
spinal cord, cervical
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
spinal stenosis
spinal stenosis, cervical canal
splenium of corpus callosum
spondylosis
spongy degeneration of brain
spontaneous remission
staggering
standing difficulty
startle reaction
steroid
steroid therapy, CNS treatment and complications with
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural hematoma
superior sagittal sinus thrombosis
sural nerve
survival motor neuron gene
Susac's syndrome
symmetric brain lesions
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
temporal lobe, atrophy
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
titubation
toe walking
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
toxic encephalopathy
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trigeminal neuralgia
trinucleotide repeats
tripping
urinary incontinence
urine test for metabolic disorders
vasculopathy
vein of Galen
vertigo
viral infection
viral infection, CNS
virus, slow
visual acuity, decreased
visual loss
visual tracking
visuospatial disturbance
vitamin deficiency
vitamin E deficiency
Waldenstrom's macroglobulinemia
walking, delayed
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
white matter disease, periventricular
white matter disease, subcortical
wide based gait
winging of scapula
word-finding difficulty
workup
xerophthalmia
xerostomia
X-linked neuropathy
Showing articles 200 to 250 of 4781 << Previous Next >>

Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Progressive Parkinsonism, Balance Difficulties, and Supranuclear Gaze Palsy
JAMA Neurol 71:104-107, Erro, R.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Primary Sjogren Syndrome
BMJ 344:e3821, Ramos-Casals, M.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Pure Motor Monoparesis Due to Ischemic Stroke
The Neurologist 17:301-308, Hiraga, A., 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Neuroimaging in Cockayne Syndrome
AJNR 31:1623-1630, Koob,M.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Clinical and Neuroimaging Findings of Cree Leukodystrophy: A Retrospective Case Series
AJNR 31: 1418-1423, Harder,S.,et al, 2010

Imaging-Pathologic Correlation in Corticobasal Degeneration
AJNR 30:1884-1892, Tokumaru,A.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Ischemic Stroke of the Cortical "Hand Knob" Area: Stroke Mechanisms and Prognosis
J Neurol 256:1146-1151, Peters, N.,et al, 2009

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009



Showing articles 200 to 250 of 4781 << Previous Next >>