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advances in neurology
akinetic mute
algorithm
alien hand syndrome
Alzheimer's disease
anomic aphasia
anticonvulsants
anticonvulsants, selection of
aphasia
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
apolipoprotein E
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion, bilateral
blinking, reduced
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
Broca's aphasia
CAG repeats
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar vermis
cerebral cortical atrophy
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosome 12
Clinical Pathologic Conference(C.P.C.)
cognition
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diagnostic criteria
differential diagnosis
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspraxia
dystonia
dystonia, focal
ethics in neurology
eye movement, disorders of
falling
familial
fragile-X syndrome
Friedreich's ataxia
frontal behavioral spatial syndrome
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
huntingtin
Huntington's chorea
hyperreflexia
hypotonia
imbalance
imbalance, postural
inattention
incidence
intellectual deficit
Jakob-Creutzfeldt disease
jocularity
Lafora's disease
language disorder in adults
L-dopa
leukodystrophy
levitation
lobar atrophy
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental retardation
MERRF syndrome
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
multiple system atrophy
mutism
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myotonia dystrophica
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, total
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathology
personality change
Pick's disease
polymerase chain reaction
pontocerebellar atrophy
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
proteinopathy
psychiatric problems in neurologic disorders
psychological testing
rapidly progressing neurologic illness
release phenomena
review article
rigidity
rigidity, axial
risk factors
saccadic eye movements
saccadic eye movements, abnormal
seizure
seizure, paradoxical
seizure, treatment of
sensory loss
sensory loss, cortical
speech disorder
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
striatonigral degeneration
subthalamic nucleus
suck reflex
synucleinopathy
tau protein
tauopathy
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
visuospatial disturbance
Wernicke's aphasia
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 200 to 250 of 2224 << Previous Next >>

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

IGG4-Related Hypertrophic Pachymeningitis Coexpressing Antineutrophil Cytoplasmic Antibodies
Neurol 4:e341-e343, Massey, J., 2017

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

Posterior Ischemic Optic Neuropathy
UptoDate Aug, Tamhankar, M. & Volpe, N., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Neuropsychiatric Involvement of Behcets Disease
www.SMGEbooks.com Dec, Soyak, M., 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Acute Hydrocephalus Caused by Radiographically Occult Fourth Ventricular Outlet Obstruction
Neurol 88:e36-e37, Duran, D.,et al, 2017

Rheumatoid Pannus of the Cervical Spine
Neurol 88:e51, Weerasinghe, D.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

MRI Findings in Collet-Sicard Syndrome
Neurol 88:811, , 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

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

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

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

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

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

Subarachnoid Hemorrhage
NEJM 377:257-266, Lawton, M.T. & Vates, G.E., 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Alemtuzumab CARE-MS I 5-year follow-up
Neurol 89:1107-1116, Havrdova, E.,et al, 2017

Alemtuzumab CARE-MS II 5-year follow-up
Neurol 89:1117-1126, Coles, A.J.,et al, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Hydrocephalus as the Sole Presentation of Primary Diffuse Large B-cell Lymphoma of the Brain
Surg Neurol Internatl 8:165, Boshrabadi, A.P.,et al, 2017

Intraventricular Neurocysticercosis and Bruns Syndrome: A Review
WWW.rarediseasejournal.com, Campbell,B.R., et al, 2017

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

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

Emerging Cases of Powassan Virus Encephalitis in New England:Clinical Presentation, Imaging, and Review of the Literature
CID 62:707-713, Piantadosi,A.,et al, 2016

Syphilitic Optic Neuropathy: Re-Emerging Cases Over a 2-Year Period
Neuro-Ophthalmol 40:69-73, Apinyawasisuk, S.,et al, 2016



Showing articles 200 to 250 of 2224 << Previous Next >>