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Differential
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agraphia
akinesia
akinesia of eyelid function
alexia
alpha-fetoprotein
Alzheimer's disease, visual variant
aminoacidurias
ANA
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, occlusion, language disorder with
aphasia
aphasia, children
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia of eye movements
apraxia of eyelid closure
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
attention deficit disorder with hyperactivity
autism
automobile accidents
Benedict's solution test
bifid uvula
blepharospasm
brain biopsy
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral arteries, territory of
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, bilateral
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cleft palate
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
confusion
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
diabetes mellitus
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
drooling
dysarthria
dysphagia
dysplasia of C.N.S.
dystonia
ecchymoses
electroencephalogram
encephalitis
encephalitis, viral
executive dysfunction
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
familial
ferric chloride test
fever
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gait, apraxic
gaze palsy
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
growth retardation
handwriting
hearing problems in children
hemianopia, homonymous
hemiparesis
hypertension
hypotonia
immunodeficiency
immunosuppression
immunosuppressive agents
in situ hybridization
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jaw jerk, abnormal
karyotyping
klippel feil syndrome
language disorder in adults
language disorders in children
L-dopa
leukemia
lid
lid abnormalities
lobar atrophy
lymphoma
maple syrup urine disease
masked facies
memory, impairment of
mental retardation
microaneurysm, retinal
micrographia
midline defect in children
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
multiple system atrophy
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
nasal speech
neglect
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
palatopharyngeal incompetence
Parkinson disease
Parkinsonism syndrome
pathology
personality change
phenylketonuria
Pick bodies
Pick's disease
pneumonia
polymerase chain reaction
posterior cortical atrophy
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
pure akinesia
radiation hypersensitivity
release phenomena
respirations in CNS disease
retropulsion
Rett's syndrome
review article
rigidity
rocking
scoliosis
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
semantic dementia
simultanagnosia
single photon emission computed tomography
skin, lesions in neurologic disorders
somnolence
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
spinal muscular atrophy
steroid therapy, CNS treatment and complications with
stuttering
systemic lupus erythematosus
tachycardia
tauopathy
telangiectases
temporal lobe, atrophy
thrombocytopenia
urinary incontinence
urine test for metabolic disorders
visual field defect
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
Showing articles 50 to 100 of 605 << Previous Next >>

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Functional Neurological Disorder
Stroke 51:1629-1635, Popkirov, S., et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
Neurol 94:843-848, Van Ommeren, R.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Tapia Syndrome at the Time of the COVID-19 Pandemic
Neurol 95:312-313, Decavel, P.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

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

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

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

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

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

Wilson Disease
NIDDK Oct2018, , 2018

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

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

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

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

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

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

A 54-year-old woman with Confusion and Visual Disturbances
Neurol 91:363-367, Rossi, K.C.,et al, 2018

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



Showing articles 50 to 100 of 605 << Previous Next >>