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Differential
(Click to cross reference)
affect, flat
agitation
agnosia, visual
Alice in Wonderland syndrome
alternating rapid movement, impaired
anorexia
arm weakness
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
Balint's syndrome
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bedridden
bradykinesia
CAT scan, emission, abnormal
caudate nucleus, lesion of, bilateral
cerebellar lesion
cerebral cortex
cerebrospinal fluid
cerebrospinal fluid, abnormal
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
color vision, impaired
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
delay in diagnosis
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
depression
difficulty climbing stairs
diplopia
dissociated sensory loss
dizziness
dysarthria
dyschromatopsia
dysdiadochokinesia
dysmetria
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
episodic disorders
eye movement, disorders of
falling
false negative
false positive
familial
fibrillations
finger nose finger test
gait disorder
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hallucination, visual
handwriting
headache
headache, episodic
heel-knee-shin test
hemianopia, homonymous
heralding manifestation
hot cross bun sign
hyporeflexia
imbalance
immunohistochemistry
incoordination
insomnia
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
life expectancy
linear lesion
macropsia
memory, defect of recent
memory, impairment of
mental status, abnormal
metamorphopsia
micropsia
Mini Mental Status Examination
monoparesis
mortality
motor cortex
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, negative
MRI, punctate pattern
MRI, spinal cord
MRI, susceptibility weighted
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
nasal brushings
nerve conduction studies
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
nystagmus
occipital cortex
occipital lobe, lesion of
pathognomonic
perseveration
PLEDs
PLEDs, bilateral independent
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
prion disease
prognosis
progressive neurologic disorder
proprioception
prosopagnosia
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
pursuit eye movements, abnormal
rapidly progressing neurologic illness
real-time quaking-induced conversion
Romberg's sign
saccadic eye movements, abnormal
skin, biopsy
spinal cord
spinal cord, lesion of
spongy degeneration of brain
square wave jerks
startle myoclonus
symmetric brain lesions
tandem gait, ataxic
tau protein
thalamus, lesion of-bilateral
vertigo
vertigo, episodic
vibratory sensation
vision, blurred
visual distortions
visual loss
visual loss, progressive
walking frame
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wide based gait
workup
Showing articles 0 to 50 of 4652 Next >>

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

RT-QuIC: A New Test for Sporadic CJD
Pract Neurol 19:49-55, Green, A.J.E., 2019

Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples
JAMA Neurol 74:155-162,144, Bongianni, M.,et al, 2017

A 64-year-old Man with Visual Distortions
Neurol 87:e252-e256, McGrath, E.R.,et al, 2016

Cerebrospinal Fluid Real-Time Quaking-Induced Conversion is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study
Ann Neurol 80:160-165, McGuire, L.I.,et al, 2016

Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid
mBio 6:e02451-14, Orru,C.D.,et al, 2015

A Test for Creutzfeldt-Jakob Disease Using Nasal Brushings
NEJM 371:519-529, Orru, C.D.,et al, 2014

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Long-Term Follow-Up of Psychogenic Pseudosyncope
Neurol 87:2214-2219, Saal, D.P.,et al, 2016

Stiff-Man Syndrome and Variants
Arch Neurol 69:230-238, McKeon,A.,et al, 2012

Diagnosis and Treatment of Psychogenic Parkinsonism
JNNP 82:1300-1303, Jankovic, J., 2011

Asymptomatic Spinal Cord Lesions Predict Disease Progression in Radiologically Isolated Syndrome
Neurol 76:686-692, 680, Okuda,D.T.,et al, 2011

Baseline MRI Predicts Future Attacks and Disability in Clinically Isolated Syndromes
Neurol 67:968-972, Tintore,M.,et al, 2006

Infratentorial Lesions Predict Long-term Disability in Patients with Initial Findings Suggestive of Multiple Sclerosis
Arch Neurol 61:217-221, Minneboo,A.,et al, 2004

The Outcome of Neurology Outpatients with Medically Unexplained Symptoms: A Prospective Cohort Study
JNNP 74:897-900,842, Carson,A.J.,et al, 2003

The 12 Year Prognosis of Unilateral Functional Weakness and Sensory Disturbance
JNNP 74:591-596,557, Stone,J.,et al, 2003

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Cognitive Complaints in Patients with Whiplash Injury:The Impact of Malingering
JNNP 64:339-343, Schmand,B.,et al, 1998

Mild Traumatic Brain Injury,Toward Understanding Manifestations and Treatment
Arch Int Med 158:90-97, Kushner,D., 1998

Outcome in Conversion Disorder:A Follow Up Study
JNNP 58:750-752, Couprie,W.,et al, 1995

Eye Movement Abnormalities in Systemic Lupus Erythematosus
Arch Neurol 52:1145-1149, Keane,J.R., 1995

Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
JNNP 59:406-412, Factor,S.A.,et al, 1995

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Amyloid-Related Imaging Abnormalities (ARIA) in Clinical Trials of Gantenerumab in Early Alzheimer Disease
JAMA Neurol 92:19-29, Salloway,S.,et al, 2025

Palliative and End-of-Life Care in Stroke:A Scientific Statement from the American Heart Association
Stroke 56;e75-e86, Creutzfeldt,C.J.,et al, 2025

Spontaneous Spinal Cord Infarction in a Young Patient: An Overview of Clinical Features and Management
Stroke 56:58-61, Chornay,C.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Polka Dot Intracerebral Hemorrhage in Leukemia
Stroke 56:e49-e50, Rebchuk,A.D.,et al, 2025

Clinical Presentation, Investigation Findings, and Outcomes of IgG4-Related Pachymeningitis,A Systematic Review
JAMA Neurol 82:193-199, Terrim,S.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Functional Outcome in Patients with Carotid Artery Dissection Undergoing Thrombectomy or Standard Medical Treatment
Neurol 104:e213465, Sykora,M.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Calcitonin Gene-Related Peptide-Targeted Therapy in Migraine: Current Role and Future Perspectives
Lancet 405:1014-1026, Versijpt,J.,et al, 2025

Endovascular Therapy for Patients with Low NIHSS Scores and Large Vessel Occlusion in the 6- to 24-Hour Window
Neurol 104:e213442, Marto,J.P.,et al, 2025



Showing articles 0 to 50 of 4652 Next >>