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abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alternating rapid movement
aluminum
anorexia
anti IgLON5
anticonvulsants
anticonvulsants, selection of
antithyroid antibodies
apnea
apraxia
arm swing, reduced
arm weakness
asterixis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bismuth
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
CAG repeats
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebral glucose metabolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
chewing movements
children
choking
chorea
chorea, familial
choreoathetosis
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonus
coenzyme Q10 deficiency
cognition
color vision, impaired
coma
coma, episodic
confabulation
confusion
congenital infection, CNS
congenital paresis
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, transmissible
dementia, treatment of
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
diabetes mellitus
dialysis
dialysis dementia
diet
differential diagnosis
diplopia
doll's head maneuver
Dravet syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
faciobrachial dystonic seizure
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
gait disorder
gait, apraxic
gaze palsy, vertical
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
granular osmiphilic material
grasp reflex
gray matter
gyrus, abnormal
hallucination
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
heel-knee-shin test
hemimyoclonic jerks
hepatosplenomegaly
heralding manifestation
hoarseness
hyperreflexia
hypersomnia
hyperthyroidism
hypometric saccades
hyponatremia
hypophonia
hypothyroidism
hypotonia
imbalance
imbalance, postural
immunohistochemistry
immunotherapy
inattention
incontinence, fecal
incoordination
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intrauterine infection
intrauterine infection, viral of CNS
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
juvenile paresis
Kearns-Sayre syndrome
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
limbic encephalitis
linear lesion
maculopathy
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningoencephalitis
mental retardation
MERRF syndrome
micrographia
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, susceptibility weighted
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic ataxia
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoclonus, treatment of
myoclonus-ataxia syndrome
myopathy
myopathy, mitochondrial
nausea and vomiting
neuroaxonal leukodystrophy
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurotoxic
neurotoxin
next-generation sequencing
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
ovarian tumor
palatal myoclonus
pancytopenia
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polyneuropathy
pontocerebellar atrophy
potassium channel antibodies
prion disease
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pursuit eye movements, abnormal
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
retinopathy
review article
rigidity
Romberg's sign
rooting reflex
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
seizure
seizure, children
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
short stature
sleep pathology and physiology
slow virus infection of CNS
slurred speech
snout reflex
sodium valproate
somnolence
spasticity
speech disorder
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 7
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suicide
symmetric brain lesions
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
teratoma, ovarian
thalamus, lesion of-bilateral
thyroiditis
toxins, nervous system
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze, paralysis of
urinary incontinence
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
visual acuity, decreased
visual impairment
vocalizations
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 150 to 200 of 3352 << Previous Next >>

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 80:629-632, Zanusso, G.,et al, 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

Lafora Periodic Acid-Schiff Inclusion Bodies
Neurol 85:e130-e131, de Assis Franco, I.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Clinical Reasoning: An Unusual Case of Subacute Encephalopathy
Neurol 84:e33-e37, Parikh, N.,et al, 2015

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

A 28-year-old Man with Progressive Gait Disturbance and Encephalopathy
Neurol 83:e204-e207, Massaro, A.M. & Pruitt, A., 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014

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

Progressive Cerebellar Ataxia and New-Onset Diabetes
Lancet 383:186, Kong, M.,et al, 2014

IgG4-Related Leptomeningitis: A Reversible Cause of Rapidly Progressive Cognitive Decline
Neurol 82:540-542, Mehta, S.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Dialysis Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
Adams & Victors Principles of Neurology Chp 40, pg 1155, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lithium
Adams & Victors Principles of Neurology Chp 43, pg 1212, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
Adams & Victors Principles of Neurology, Chp 30, pg 624, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
Adams & Victors Principles of Neurology, Chp 31, pg 668, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 973, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 748, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Subacute Sclerosing Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

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

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



Showing articles 150 to 200 of 3352 << Previous Next >>