Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abiotrophy
adult polyglucosan body disease
advances in neurology
algorithm
Alzheimer's disease
aminoacidopathies
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, conjugal
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, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm weakness
arthrogryposis multiplex
ataxia
ataxia, progressive
autonomic dysfunction
axonal degeneration
Babinski sign
behavioral disorder
bladder dysfunction
brain atrophy
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central core disease
cerebellar atrophy, primary
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
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
chromosome 5
cognition
congenital heart disease
crying, pathologic
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dermatomyositis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dyspnea
dystonia
electromyogram
emotional lability
epidemiology of neurology
episodic neurologic deficits
exercise
exercise intolerance
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
fluency
foot drop
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Guillain Barre syndrome
gynecomastia
hallucination
hand weakness
hearing loss
heavy metal intoxication
hemiparesis
heralding manifestation
history of neurology
hoarseness
Huntington's chorea
hyperpigmentation of skin
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinentia pigmenti
infant, evaluation of
inflexibility, mental
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Isaacs syndrome
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Jewish
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lathyrism
laughing
laughing, pathologic
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
leukoencephalopathy
Lewy body
life expectancy
lobar atrophy
lysosomal storage disease
malformation, CNS, congenital
memory, defect of recent
memory, impairment of
mental retardation
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelomalacia
myeloneuropathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic bladder
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuromyotonia
neuronal degeneration
neuronopathy
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
next-generation sequencing
nusinersen
optic atrophy
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
paroxysmal neurologic deficits
patient information and support
peroneal muscle atrophy, causes of
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
recombinant DNA
Refsum's disease
release phenomena
respirator
respiratory failure
review article
RFLPs
riluzole
risk factors
Roussy Levy syndrome
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stereotyped behavior
stiff man syndrome
superoxide dismutase
survival motor neuron gene
temporal lobe, atrophy
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
torticollis
trauma
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
urea-cycle enzymopathies
urinary incontinence
vestibular function, tests of
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 850 to 900 of 4485 << Previous Next >>

A 52-year-old Man with Diplopia and Ataxia
Neurol 87:e140-e143, Bradshaw, M.J.,et al, 2016

The Contemporary Spectrum of Multiple Sclerosis Misdiagnosis
Neurol 87:1393-1399, Solomon, A.J.,et al, 2016

Superior MRI Outcomes with Alemtuzumab Compared with Subcutaneous Interferon �-1a in MS
Neurol 87:1464-1472, Arnold, D.L.,et al, 2016

Clinicopathologic Conference, IgG4-Related Hypophysitis
NEJM 375:1469-1480, Case 31-2016, 2016

A 20-year-old Man with Headache and Double Vision
Neurol 87:e162-e167, Moussawi, K.,et al, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Acute Disseminated Encephalomyelitis in 228 Patients
Neurol 86:2085-2096, Koelman, D.L.H.,et al, 2016

Malignancies after Mitoxantrone for Multiple Sclerosis
Neurol 86:2203-2207, Buttmann, M.,et al, 2016

Fulminant Central Nervous System Nocardiosis in a Patient Treated with Alemtuzumab for Relapsing-Remitting Multiple Sclerosis
JAMA Neurol 73:757-759, Penkert, H.,et al, 2016

A Young Man with Progressive Vision and Hearing Loss
JAMA Neurol 73:880-883, Kung, N.H.,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

Rebound Syndrome in Patients with Multiple Sclerosis after Cessation of Fingolimod Treatment
JAMA Neurol 73:790-794, Hatcher, S.E.,et al, 2016

Incidence of Radiologically Isolated Syndrome: A Population-Based Study
AJNR 37:1017-1022, Forslin, Y.,et al, 2016

Reversible Corticospinal Tract Hyperintensities in Neurologic Lyme Disease
Neurol 87:548-548, Pruvost-Robieux, E.,et al, 2016

MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
Neurol 86:e71-e72, Saeedan, M.B. & Dogar, M.A., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Neuromyelitis Optica: Evaluation of 871 Attacks and 1,153 Treatment Courses
Ann Neurol 79:206-216,204, Kleiter, I.,et al, 2016

Cystic Lesions as a Rare Complication of Deep Brain Stimulation
Mov Disord Clin Pract 3:87-90, Sharma, V.D.,et al, 2016

Magnetic Resonance Imaging of Cerebral Aspergillosis: Imaging and Pathological Correlations
PLoS ONE 11:DOI:10.1371/Journal.pone.0152474, Marzoif, G.,et al, 2016

MRI Characteristics of Neuromyelitis Optica Spectrum Disorder
Neurol 84:1165-1173, Jin Kim, H.,et al, 2015

Very Late-Onset Neuromyelitis Optica Spectrum Disorder Beyond the Age of 75
J Neurol 262:1379-1384, Krumbholz, M.,et al, 2015

Cardiovascular Dysfunction in Multiple Sclerosis
Neurologist 20:108-114, Kaplan, T.B.,et al, 2015

A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Spinal Cord Ischemia: Practical Imaging Tips, Pearls, and Pitfalls
AJNR 36:825-830, Vargas, M.I.,et al, 2015

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

Outcome after Resuscitation Beyond 30 Minutes in Drowned Children with Cardiac Arrest and Hypothermia: Dutch Nationwide Retrospective Cohort Study
BMJ 350:h418, Kieboom, J.K.,et al, 2015

Acute Idiopathic Transverse Myelitis in Children
Neurol 84:341-349,332, Deiva, K.,et al, 2015

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
Neurol 84:226-230,218, Wolf, N.I.,et al, 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Varicella-Zoster Virus Infections in Patients Treated with Fingolimod
JAMA Neurol 72:31-39,10, Arvin, A.M.,et al, 2015

Short Myelitis Lesions in Aquaporin-4-IgG-Positive Neuromyelitis Optica Spectrum Disorders
JAMA Neurol 72:81-87, Flanagan, E.P.,et al, 2015

Clinical Reasoning: A 51-Year-Old Woman with Acute Foot Drop
Neurol 84:e48-e52, Rallis, D.,et al, 2015

Investigation of Leptomeningeal Enhancement in MS
Neurol 84:770-775, Eisele, P.,et al, 2015

Cyclical Konzo Epidemics and Climate Variability
Ann Neurol 77:371-380, Oluwole, O.S.A., 2015

Two Cases of Congenital Myasthenic Syndrome with Vocal Cord Paralysis
Neurol 84:1281-1282, Al-Shahoumi, R.,et al, 2015

Characteristics of Lumbar Disc Herniation with Exacerbation of Presentation Due to Spinal Manipulative Therapy
Medicine 94:e661, Huang, S.L.,et al, 2015

Paroxysmal Dystonia as a Manifestation of Multiple Sclerosis
Neurologist 19:132-134, Machado, C.,et al, 2015

Bionic Reconstruction to Restore Hand Function After Brachial Plexus Injury: A Case Series of Three Patients
Lancet 385:2183-2189, Aszmann, O.C.,et al, 2015

Comparing 3T and 1.5T MRI for Mapping Hippocampal Atrophy in the Alzheimers Disease Neuroimaging Initiative
AJNR 36:653-660, Chow, N.,et al, 2015

Short Stature, Imperforate Anus, and Polydactyly
Neurol 84:e117, Dumitrascu, O.,et al, 2015

Relapse in Multiple Sclerosis
BMJ 350:h1765, Galea, I.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:DOI:10.1056/NEJMoa1415061, DOI:10.1056 NEJM e1503217, Saver, J.L.,et al, 2015

Thrombectomy within 8 Hours after Symptom Onset in Ischemic Stroke
NEJM 372:DOI:10.1056 NEJMoa1503780, DOI:1056NEJM e1503217, Jovin, T.G.,et al, 2015

Tonic Eye Deviation in Stiff-Person Syndrome
Neurol 84:e124-e127, Chakravarthi, S.,et al, 2015

Newer Agents in the Treatment of Multiple Sclerosis
Neurologist 19:104-117, Pawate, S. & Bagnato F., 2015

A Case of Refractory Nocturnal Seizures
Neurol 84:e134-e136, Pavlakis, P.P. & Douglass, L.M., 2015

Neurological Manifestations of Scrub Typhus
JNNP 86:761-766, Misra, U.K.,et al, 2015



Showing articles 850 to 900 of 4485 << Previous Next >>