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acetylcholine
advances in neurology
alternating rapid movement
Alzheimer's disease
aniridia
anti Yo antibody
anticholinesterase
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
ataxia
ataxia, cerebellar
ataxia, congenital
ataxia, hereditary
ataxia, progressive
ataxic gait
auditory evoked brainstem potentials
autism
autoantibodies
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, calcification of
bladder dysfunction
blindness
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, hypoplasia
brainstem, infarction of
brainstem, malformation
Brazil
CAG repeats
calcification, intracranial
calcification, intraventricular
calcification, periventricular
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebellum
cerebral cortical atrophy
cerebral palsy
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular disease, infant and childhood
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 28
chromosome 6
Clinical Pathologic Conference(C.P.C.)
clinodactyly
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital ocular motor apraxia
contractures, joint
controversies in neurology
cornea, opacity of
corpus callosum, hypoplastic
cyst
cyst, porencephalic
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
depression
developmental abnormality of brain
developmental retardation
diabetes insipidus
diabetes mellitus
digits, abnormal
dizziness
down-beat nystagmus, primary position of gaze
dysarthria
dysdiadochokinesia
dysmetria
dystonia
ear, abnormal
electroretinograph
ELISA
encephalitis, viral
encephalocele
enzyme, defect
evoked potentials
excitotoxin
eye movement, disorders of
familial
flavivirus
foot deformity
fourth ventricle, enlargement of
fragile-X syndrome
Friedreich's ataxia
gait disorder
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
Gillespie syndrome
glutamate dehydrogenase deficiency
glutamic acid
head jerks
head nodding
hearing loss
heel-knee-shin test
heterotopia
HGPPS
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydrocephalus
hydrocephalus, congenital
hydroxytryptophan L-5(L-5 HTP)
hyposmia
hypotonia
hypotonia, infants
hypoxia
imbalance
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iris, abnormal
jittery baby
Joubert syndrome
L-dopa
Leber's congenital amaurosis
life expectancy
lissencephaly
lymphocytic choriomeningitis
macular degeneration
malformation, CNS, congenital
Marinesco-Sjogren syndrome
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
memory, impairment of
mental retardation
microcephaly
molar tooth sign
molecular genetics
mortality
mosquito
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
multiple system atrophy
myelomalacia
myoclonic jerks
myoclonus
myopathy
myotonia dystrophica
nausea and vomiting
neurologic disease
neurologic disease, diagnoses of
neuronal migration disorder
neuroophthalmology
neuropathology
neurotoxin
neurotransmitter
nystagmus
nystagmus, pendular
ocular motility, disorders of
old age, neurology of
oligophrenin 1
ophthalmoplegia
optic atrophy
orthostatic hypotension
pachygyria
palatal myoclonus
paraneoplastic cerebellar degeneration
Parkinson disease
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal nonkinesigenic dyskinesia
physostigmine
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pons, atrophy
pons, hypoplasia
pontocerebellar atrophy
posterior cerebral artery territory infarction
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyramidal tract, uncrossed
remote effect of cancer on the nervous system
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
risk factors
rubella encephalitis
rubella syndrome
rubella virus
saccadic eye movements, abnormal
scoliosis
scoliosis, neurologic association with
seizure
sensorineural hearing loss
Shy-Drager syndrome
sleep apnea
sleep pathology and physiology
spasticity
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
startle myoclonus
striatonigral degeneration
superior cerebellar peduncle
syndactyly
titubation
trazodone
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
vertebral artery
vertebral artery hypoplasia
vertebral-basilar insufficiency
vertigo
viral infection
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual loss
Walker-Warburg syndrome
walking, difficulty with
white matter disease
white matter disease, periventricular
white matter disease, subcortical
Wolfram syndrome
X-linked bulbospinal neuronopathy
x-linked mental retardation
Zika virus infection
Showing articles 150 to 200 of 1054 << Previous Next >>

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Isolated and Persistent Hiccup by Tiny Ischemia at Dorsolateral Medulla
Neurol 93:e934, Seo,J.H., 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

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

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

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

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

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Cerebellar Microbleed Distribution Patterns and Cerebral Amyloid Angiopathy
Stroke 50:1727-1733, Pasi, M.,et al, 2019

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

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

Gasperini Syndrome
Neurol 90:e261, Lorio, R., 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

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

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

Brain Imaging in Cases with Positive Serology for Dengue with Neurologic Symtoms: A Clinicoradiologic Correlation
AJNR 39:699-703, Vanjare, H.A.,et al, 2018

Facial Ulceration in stroke
Neurol 90:e1448-e1449, May, L.M.,et al, 2018

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

Coma
Neurol 90:e1638-e1645, Schievink, W.I.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Autoimmune Pancerebellitis Associated with Pembrolizumab Therapy
Neurol 91:91-93, Vitt, J.R.,et al, 2018

Cerebrovascular Manifestations of Neurosarcoidosis: An Underrecognized Aspect of the Imaging Spectrum
AJNR 39:1194-1200, Bathla, G.,et al, 2018

Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

Bow Hunter Syndrome:A Rare Cause of Posterior Circulation Stroke
Neurol 91:329-331, Jadeja,N. and Nalleballe,K., 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

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

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Imaging Characteristics of Venous Parenchymal Abnormalities
Stroke 48:3258-3265, Arnoux, A.,et al, 2017

Human Immunodeficiency Virus Presenting as Progressive Multifocal Leukoencephalopathy Restricted to the Posterior Fossa
JAMA Neurol 74:597-598, Schubert, R.D. & Richie, M.B., 2017

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

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,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

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

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,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

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 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 Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
AJNR 37:1256-1261, Capizzano, A.A.,et al, 2016

Imaging Signs in Spontaneous Intracranial Hypotension: Prevalence and Relationship to CSF Pressure
AJNR 37:1374-1378, Kranz, P.G.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016



Showing articles 150 to 200 of 1054 << Previous Next >>