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agitation
aminoacidopathies
aminoacidurias
aneurysm
aneurysm, intracranial
anosognosia
antiviral agents
aphasia
aphasia, global
aphasia, transcortical
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
athetosis
atypical
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basilar artery stenosis
behavioral disorder
bilirubin encephalopathy
blindness, sudden
brain atrophy
brain damage
brainstem, lesion of
breast feeding
bulbar palsy
CAG repeats
CAT scan
CAT scan, abnormal
catalepsy
cataplexy
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrospinal fluid, glycine
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
choreoathetosis
chromosomal abnormality
chromosome 6
Clinical Pathologic Conference(C.P.C.)
congenital myasthenic syndromes
conjugate gaze, forced
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
developmental retardation
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
disease modifying agents
downward gaze, paralysis of
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
emtricitabine
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
epidemiology of neurology
executive dysfunction
exercise intolerance
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
false negative
familial
fever
floppy infant
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
Guillain Barre syndrome, infantile and childhood form
hallucination
hallucination, visual
head injury
headache
hearing loss
hemiparesis
hemorrhage, thalamic
hepatomegaly
hepatosplenomegaly
hoarseness
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypophonia
hyporeflexia
iatrogenic neurologic disorders
imbalance
impulsivity
inattention
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, location of
intracerebral hemorrhage, volume
intraventricular hemorrhage
jaundice
kernicterus
lactic acidemia
leucine
lid closure, weakness of
life expectancy
lipid storage disorder of CNS
lysosomal storage disease
maple syrup urine disease
MELAS syndrome
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
metabolic disorder, primary
miglustat
migraine
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
moro reflex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, muscle
MRI, negative
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myoclonus
myopathy
myopathy, drug-induced
myopathy, mitochondrial
nasal speech
nausea and vomiting
neglect
neoplasm, primary of CNS
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neurotoxic
neurotoxin
Niemann-Pick disease
nystagmus
ocular motility, disorders of
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, head injury causing
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
ophthalmoplegia, total
ophthalmoplegic migraine
opisthotonus
organomegaly
paranoia
Parkinsonism syndrome
personality change
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
ragged-red fibers
rapidly progressing neurologic illness
renal failure
retinal degeneration
retropulsion
review article
salivation, excessive
schizophrenia
screening
seizure
seizure, children
seizure, laughing as manifestation
sensorimotor stroke
sensorineural hearing loss
setting sun phenomena
short stature
skew deviation
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
strokelike episodes
subthalamic nucleus
suck, poor
systemic illness
temporal lobe, lesion
term infant
thalamic aphasia
third nerve palsy
third nerve palsy, childhood
third nerve palsy, congenital
third nerve palsy, cyclic
transverse smile
treatment of neurologic disorder
tremor
trinucleotide repeats
upgaze, paralysis of
ventricular enlargement
vertical gaze
viral infection
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
visuospatial disturbance
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
wheelchair
whole genome sequencing
wide based gait
Showing articles 200 to 250 of 1791 << Previous Next >>

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

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

T2*-Based MR imaging of hyperglycemia-induced hemichorea-hemiballism
J Neuroradiol 44:31-37, Yu, F.,et al, 2017

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

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

Palsy of Conjugate Horizontal Gaze and Face due to Isolated Abducens Nuclear Infarction
Neurol 89:e180-e181, Kim, J.S.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,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

Thrombolytic Removal of Intraventricular Haemorrhage in Treatment of Severe Stroke: Results of the Randomised, Multicentre, Multiregion, Placebo-Controlled CLEAR III Trial
Lancet 389:603-611,575, Hanley, D.F.,et al, 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 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

Prehospital Emergency Care in Childhood Arterial Ischemic Stroke
Stroke 48:1095-1097, Stojanovski, B.,et al, 2017

Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
Stroke 48:e126-e129, Sajja, A.,et al, 2017

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

Dont Fall for Pseudo-INO
Neurol 88:e205-e206, Traber, G.L.et al, 2017

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

Buprenorphine for the Treatment of the Neonatal Abstinence Syndrome
NEJM 376:2341-2348, Kraft, W.K.,et al, 2017

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

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Endovascular Therapies for Acute Ischemic Stroke in Children
Stroke 48:2026-2030, Huang, M.I.,et al, 2017

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

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

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
Orphanet J Rare Dis 12:166, Heitz, C., et al, 2017

Listeria infections in Neonates
Neoreviews 17:e515-e520, McKinney, J.S., 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Congenital Zika Virus Syndrome in Brazil: A Case Series of the first 1501 livebirths with complete investigation
Lancet 388:891-897, Franca, G.V.A.,et al, 2016

Zika Virus: An Emergent Neuropathological Agent
Ann Neurol 80:479-489, White, M.K.,et al, 2016

A 20-year-old Man with Headache and Double Vision
Neurol 87:e162-e167, Moussawi, K.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Chikungunya Virus-Associated Encephalitis
Neurol 86:94-102, Gerardin, P.,et al, 2016

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

A 62-Year-Old Woman with Bizarre Behavior and Recurrent Episodes of Behavioral Arrest
Neurol 86:e62-e65, Briglia, H.,et al, 2016

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016

Diabetic Sensory and Motor Neuropathy
NEJM 374:1455-1464, Vinik, A.I.,et al, 2016

Minimally Invasive Surgery for Intracerebral and Intraventricular Hemorrhage
Stroke 47:1399-1406, Fiorella, D.,et al, 2016

Thiamine Deficiency Presenting as Intraventricular Hemorrhage
Stroke 47:e95-e97, Al-Bayati, A.R.,et al, 2016

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

Candida Infections of the Central Nervous System
UptoDate Jan, Kauffman, C.A., 2016

Neurological, Respiratory, Musculoskeletal, Cardiac and Ocular Side-Effects of Anti-PD-1 Therapy
Eur J Cancer 60:210-225, Zimmer, L.,et al, 2016

Moyamoya Disease Presenting with Subarachnoid Hemorrhage: Clinical Features and Neuroimaging of a Case Series
Brit J Neurosurg 29:804-810, Wan, M.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Magnetic Resonance Neurography Detects Diabetic Neuropathy Early and with Proximal Predominance
Ann Neurol 78:939-948, Pham, M.,et al, 2015

Community Based Case-Control Study of Childhood Stroke Risk Associated with Congenital Heart Disease
Stroke 46:336-340, Fox, C.K.,et al, 2015

Acute Ischemic Stroke in Pediatric Patients
Stroke 46:e32-e33, Mittal, S.O.,et al, 2015

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015



Showing articles 200 to 250 of 1791 << Previous Next >>