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Differential
(Click to cross reference)
akinetic mute
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, familial
amyloid plaques
aneuploidy
animal exposure
arm weakness
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atypical
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blood transfusion
bovine spongiform encephalopathy
brain biopsy
central nervous system, infection of
cerebellar lesion
cerebral cortex
cerebrospinal fluid, abnormal
cerebrospinal fluid, protein of
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
corneal transplant
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
diet
difficulty climbing stairs
dizziness
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
encephalopathy
epidemiology of neurology
eye movement, disorders of
falling
familial
fasciculation
fatal familial insomnia
finger nose finger test
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
growth hormone
hallucination
handwriting
head turning
heel-knee-shin test
hockey stick sign
iatrogenic neurologic disorders
imbalance
insomnia
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, conjugal
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
life expectancy
linear lesion
lymphoma involving CNS
molecular genetics
mongolism
monoparesis
mortality
motor cortex
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, indications for
MRI, negative
MRI, punctate pattern
MRI, susceptibility weighted
mutism
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
neurologic disease, diagnoses of
neurologic signs
neuropathology
nystagmus
occupational neurologic disorders
pituitary, hormones of
polymerase chain reaction
prion disease
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
psychosis
psychotic behavior
pulvinar sign
rapidly progressing neurologic illness
real-time quaking-induced conversion
review article
risk factors
Romberg's sign
roving eye movements
scrapie
seizure
skin, biopsy
sleep pathology and physiology
slow virus infection of CNS
spongy degeneration of brain
startle myoclonus
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tandem gait, ataxic
thalamus, lesion of
thalamus, lesion of-bilateral
trauma
tremor
upgaze, paralysis of
urinary incontinence
viral infection, CNS
walking frame
walking, difficulty with
weakness, acute
weakness, focal
wheelchair
wide based gait
workup
Showing articles 450 to 500 of 2016 << Previous Next >>

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

CRAO and Silent Brain Infarcts caused by Cardiac Myxomas in Carney Complex
Neurol 92:e286-e287, Huang, L-T.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

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

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

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

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Chronic Meningitis Investigated via Metagenomic Next-Generation Sequencing
JAMA Neurol 75:947-955,915, Wilson,M.R.,et al, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Adult-Onset Vanishing White Matter Disease
Neurol 90:e1091-e1092, Villar-Quiles, R.N.,et al, 2018

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

Cranial Cavernous Malformations
Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,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

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
Neuropsych Dis Treat 13:2175-2179, Wang,J.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

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

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

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

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

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

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

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

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

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

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

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



Showing articles 450 to 500 of 2016 << Previous Next >>