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abiotrophy
adult polyglucosan body disease
advance directives
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
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, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anti IgLON5
apnea
areflexia
arm weakness
aspiration
autoantibodies
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
BiPAP
bladder dysfunction
botulinum toxin
brain atrophy
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
C9orf72
CAG repeats
camptocormia
CAT scan, abnormal
CAT scan, emission, abnormal
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
coma, episodic
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
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dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
disability, neurological
distal muscle weakness
DNA probes
drooling
dying
dysarthria
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electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
encephalitis
encephalitis, autoimmune
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epidemiology of neurology
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episodic unconsciousness
facial weakness
facial weakness, bilateral
falling
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fasciculation
fatigable chewing
fatigue
fibrillations
fine motor function, impaired
flaccid paralysis
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, spastic
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
gynecomastia
hand weakness
hearing loss
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
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hyperreflexia
hypersomnia
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hypophonia
hyporeflexia
hypotension, systemic
imbalance
immunotherapy
inclusion bodies
intellectual deficit
intellectual deterioration
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
laughing
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukoencephalopathy
life expectancy
liver disease
lobar atrophy
locked-in syndrome
masseter muscle weakness
memory, defect of recent
memory, impairment of
Mills syndrome
mimics
misdiagnosis
molecular genetics
mortality
motor neuron disease
motor neuron disease, misdiagnosis
MRI
MRI, abnormal
multiple sclerosis, differential diagnosis of
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muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
mutism
myelomalacia
myeloneuropathy
myocardial injury
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myocytolysis
myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurogenic bladder
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neurologic disease, diagnoses of
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neuronal migration disorder
neuronopathy
neuropathology
neuropathology, brain
neuropathy
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neuroprotective agents
optic atrophy
pain
pain, management of chronic
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paralysis, acute areflexic
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polyglucosan body
polyglucosan body disease
polymerase chain reaction
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practice guidelines
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
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pyramidal tract dysfunction
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quadriplegia
quality of life
radiculopathy
REM sleep behavior disorder
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
review article
riluzole
risk factors
saccadic eye movements, abnormal
salivation, excessive
sensorineural hearing loss
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
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spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
tandem gait, ataxic
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
vestibular function, tests of
vocalizations
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
West Nile fever
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 800 to 850 of 2707 << Previous Next >>

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
Adams & Victors Principles of Neurology, Chp 32, pg 721, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Neurosyphilis
Adams & Victors Principles of Neurology, Chp 32, pg 723, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Gliomatosis Cerebri
Adams & Victors Principles of Neurology, Chp 31, pg 654, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Ependymoma
Adams & Victors Principles of Neurology, Chp 31, pg 655, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Predicting Alzheimer Disease with �-Amyloid Imaging: Results from the Australian Imaging, Biomarkers, and Lifestyle Study of Ageing
Ann Neurol 74:905-913, Rowe, C.C.,et al, 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

Advanced MRI Morphologic Study Shows No Atrophy in Healthy Individuals with Hippocampal Hyperintensity
AJNR 34:1585-1588, Labate, A.,et al, 2013

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

MRI-Identified Pathology in Adults with New-Onset Seizures
Neurol 81:920-927, Hakami, T.,et al, 2013

Chiasmal Enlargement and Enhancement in Leber Hereditary Optic Neuropathy
Neurol 81:e126-e127, Ong, E.,et al, 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Isolated Bipallidal Lesions Caused by Extrapontine Myelinolysis
Neurol 81:1722-1723, Floris, G.,et al, 2013

Headache and Focal Neurologic Deficits in a 37-Year-Old Woman
JAMA Neurol 70:1445-1449, Ayodele, M.O.,et al, 2013

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

Clinical Features of MS Associated with Leber Hereditary Optic Neuropathy mtDNA Mutations
Neurol 81:2073-2081, Pfeffer, G.,et al, 2013

VZV Ischemic Optic Neuropathy and Subclinical Temporal Artery Infection without Rash
Neurol 80:220-222, Nagel, M.,et al, 2013

The Thalamus and Multiple Sclerosis
Neurol 80:210-219, Minagar, A.,et al, 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

Transglutaminase 6 Antibodies in the Diagnosis of Gluten Ataxia
Neurol 80:1740-1745, Hadjivassilou, M.,et al, 2013

Multifocal VZV Vasculopathy with Temporal Artery Infection Mimics Giant Cell Arteritis
Neurol 80:2017-2021, Nagel, M.,et al, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
Seizure 22:553-559, Caraballo, R.H.,et al, 2013

MRI findings in Post-operative Bilateral Posterior Ischemic Optic Neuropathy
J Ophthalmol 3:51-53, Bhatt, N.P.,et al, 2013

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

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

Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
Br J Radiol 85:e782-e792, Sureka, J. & Jakkani, R.K., 2012

Brain Atrophy is Related to Lacunar Lesions and Tissue Microstructural Changes in CADASIL
Stroke 38:1786-1790, Jouvent, E.,et al, 2012

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

Should we be nervous about coeliac disease? Brain abnormalities in patients with coeliac disease referred for neurologic opinion
JNNP 83:1216-1221, Currie, S.,et al, 2012

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
Neurol 79:2349-2354, Morita, M.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

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

Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
JAMA 307:1292-1301, Wahbi,K.,et al, 2012

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

Evidence-Based Path to Newborn Screening for Duchenne Muscular Dystrophy
Ann Neurol 71:304-313, Mendell,J.R.,et al, 2012

Clinicopathologic Conference, Neurocysticercosis Involving the Cerebral Ventricles and Spinal Meninges
NEJM 366:1924-1934, Case 15-2012, 2012

Endoscopic Treatment of Hydrocephalus
Arch Neurol 69:664, Walcott, B.P.,et al, 2012

Three-day CSF drainage barely reduces ventricular size in normal pressure hydrocephalus
Neurol 79:237-242, Lenfeldt, N.,et al, 2012

The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
Ann Neurol 72:9-17, Mercuri, E. & Muntoni, F., 2012

Visuospatial deficits in posterior cortical atrophy: structural and functional correlates
JNNP 83:860-863,855, Andrade, K.,et al, 2012

Distinct Lesion Morphology at 7-T MRI Differentiates Neuromyelitis Optica from Multiple Sclerosis
Neurol 79:708-714, Sinnecker, T.,et al, 2012



Showing articles 800 to 850 of 2707 << Previous Next >>