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acetylcholine
advances in neurology
alternating rapid movement
Alzheimer's disease
aniridia
anosmia
anti Yo antibody
anticholinesterase
apnea
apnea, primary central
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
diabetes mellitus, neurologic manifestations of
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
pretectal syndrome
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
rigidity
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
urinary incontinence
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 1431 << Previous Next >>

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

A Vertebral Artery Halo Sign Indicates Giant Cell Arteritis Affecting the Posterior Circulation of the Brain
Lancet 397:e6, Lambrechts, R.A.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Progressive Ataxia and Doenbeat Nystagmus in an Adult
JAMA Neurol 78:1018-10019, Fernandez, A.C.,et al, 2021

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

Nonalcoholic Wernicke Encephalopathy
Neurol 97:e1541-e1542, Hansen, G.,et al, 2021

Nocardial Brain Abscesses
NEJM 385:e53, Sherman, S.V., 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

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

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

Imaging Review of Paraneoplastic Neurologic Syndromes
AJNR 41:2176-2187, Madhavan, A.A.,et al, 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

An Underrecognized Etiology of New Daily Persistent Headache
Neurol 94:e114-e120, Duvall, J.R.,et al, 2020

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

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

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,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 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

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

Spontaneous Intracranial Hypotension: Atypical Radiologic Appearances, Imaging Mimickers, and Clinical Look-Alikes
AJNR 41:1339-1347, Bond, K.M.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

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

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

A Patient with a History of Weight Loss Presenting with Seizures
Neurol 95:e2038-e2042, Tang, G. & Benavides, D.R., 2020

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

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

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

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

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

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

Acute Lateral Medullary Infarct Due to Giant Cell Arteritis
Stroke 50:e290-e293, Dardick, J.M.,et al, 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 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



Showing articles 150 to 200 of 1431 << Previous Next >>