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activated protein C resistance
advances in neurology
agitation
agnosia
algorithm
aluminum
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, conjugal
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Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
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Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amnesia
amyloid angiopathy, cerebral
amyloid beta protein
amyloid imaging
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
aneuploidy
aneurysm, intracranial, familial
anomic aphasia
anticholinesterase
antiphospholipid antibodies
antithrombin III deficiency
aphasia
aphasia, progressive
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
apraxia, constructional
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
attention span
behavioral disorder
benign essential tremor
biologic markers
blood dyscrasias, neurologic findings with
blood transfusion
brain transplantation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cell fusion test
central core disease
central nervous system, infection of
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral glucose metabolism
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, biochemical markers of CNS disease
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
Charcot-Marie-Tooth
children
choline acetyltransferase
chromosomal abnormality
chromosome 1
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chromosome 21
chromosome 9
cigarette smoking
clindamycin
coagulopathy
cognition
cost
crying, pathologic
cultured skin fibroblasts
D-dimer
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depression
developmental milestones, loss of
diagnostic criteria
differential diagnosis
DNA probes
donepezil
dural sinus thrombosis
dysarthria
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dysphagia
dystonia
echolalia
epidemiology of neurology
ethics in neurology
executive dysfunction
Factor V Leiden
false negative
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fluency
foam cells
Friedreich's ataxia
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hallucination
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heavy metal intoxication
hemiparesis
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hepatic failure
hepatosplenomegaly
hippocampus
human genome
Huntington's chorea
hyperpyrexia, CNS disorder causing
hyperreflexia
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
infantile hemiplegia
inflexibility, mental
intellectual deficit
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, medical precaution with
jaundice
Kugelberg-Welander syndrome
language disorder in adults
lipid storage disorder of CNS
lobar atrophy
lupus anticoagulant
lymphoma involving CNS
manic-depressive
medical-legal aspects of neurology
memory, impairment of
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mild cognitive impairment
misdiagnosis
molecular genetics
mongolism
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, false negative
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MRI, negative
MRI, serial
muscular dystrophy
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myotonia dystrophica
nausea and vomiting
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy, amyloid
neurotransmitter
nicotine
Niemann-Pick disease
obsessive-compulsive disorder
pain, increased response
paranoia
paraparesis, spastic
paratonia
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Parkinson disease, familial
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive material in the brain
personality change
Pittsburgh Compound B
poison, mercury
poison, neurologic problems with
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prethrombotic state
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pulmonary embolism
recombinant DNA
release phenomena
research
review article
RFLPs
risk factors
seizure
senile plaques
single photon emission computed tomography
slow virus infection of CNS
spinal muscular atrophy
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spongy degeneration of brain
stereotyped behavior
stimulation, deep brain
straight sinus
subarachnoid hemorrhage
subdural hematoma
superior sagittal sinus thrombosis
tau protein
thrombophlebitis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
twins
ubiquilin 1
viral infection, CNS
visuospatial disturbance
Werdnig-Hoffman disease
Wernicke's aphasia
word-finding difficulty
Showing articles 150 to 200 of 2374 << Previous Next >>

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

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

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Cost-Effectiveness and Value-Based Pricing of Aducanumab for Patients with Early Alzheimer Disease
Neurol 98:e968-e977, Whittington, M.D.,et al, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Controversy and Progress in Alzheimers Disease - FDA Approval of Aducanumab
NEJM 385:doi:10.1056/NEJMp2111320, Rabinovici, G.D., 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

Aducanumab: What About the Patient?
Ann Neurol 90:334-335, Petersen, R.C., 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,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 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

The Effects of Long-Term Medication Use in Alzheimer Disease
Neurol 96:e2247-e2250, Karceski, S., 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

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

Smoking Causes Fatal Subarachnoid Hemorrhage
Stroke 51:3018-3022, Rautalin, I.,et al, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

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

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

Application of Deep Learning to Predict Standardized Uptake Value Ratio and Amyloid Status on 18F-Florbetapir PET Using ADNI Data
AJNR 41:980-986, Reith, F.,et al, 2020

High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
AJNR 41:1126-1130, Mabray, M.C.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

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

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Clinical Epidemiology of Familial Sarcoidosis
Respir Med 149:36-41, Terwiel, M. & Van Moorsel, C.H.M., 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

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

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

Debate Sparks Over LATE, a Recently Recognized Dementia
JAMA 322:914-916, Abbasi, J., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019



Showing articles 150 to 200 of 2374 << Previous Next >>