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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 350 to 400 of 1054 << Previous Next >>

Causative Factors and Epidemiology of Bilateral Vestibulopathy in 255 Patients
Ann Neurol 61:524-532, Zingler,V.C.,et al, 2007

Distinct Imaging Patterns and Lesion Distribution in Posterior Reversible Encephalopathy Syndrome
AJNR 28:1320-1327, Bartynski,W.S.,et al, 2007

Clinicopath Conf., Left Atrial Myxoma with Systemic Embolization
NEJM 357:1137-1145, Case 28-2007, 2007

Hypoplastic Vertebral Artery: Frequency and Associations With Ischaemic Stroke Territory
JNNP 78:954-958, Park-J.-H.,et al, 2007

Shotgun Pellet Embolization to the Posterior Cerebral Circulation
AJNR 27:261-263, deCosta,L.B.,et al, 2006

Remote Cerebellar Hemorrhage
AJNR 27:387-390, Amini,A.,et al, 2006

Benign Tremulous Parkinsonism
Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006

Bilateral Cerebellar Infarction Caused by Dominant Medial Posterior Inferior Cerebellar Artery
Neurol 66:1125-1126, Han,S.W.,et al, 2006

Transient Hemiageusia in Cerebrovascular Lateral Pontine Lesions
JNNP 77:680-683, Landis,B.N.,et al, 2006

Progressive Multifocal Leukoencephalopathy Revisited: Has the Disease Outgrown Its Name?
Ann Neurol 60:162-173, Koralnik,I.J., 2006

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

Cerebellar Infarction Presenting Isolated Vertigo: Frequency and Vascular Topographical Patterns
Neurol 67:1178-1183, Lee,H.,et al, 2006

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Cerebellar Infarction int he Territory of the Medial Branch of the Superior Cerebellar Artery
Neurol 66:115-117, Sohn,S.-I.,et al, 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Spontaneous Spinal Cerebrospinal Fluid Leaks and Intracranial Hypotension
JAMA 295:2286-2296, Schievink,W.I., 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Location and Outcome of Anticoagulant-Associated Intracerebral Hemorrhage
Neurocrit Care 05:197-201, Flaherty, M.L.,et al, 2006

Upside Down Reversal of Vision Due to an Isolated Acute Cerebellar Ischemic Infarction
J Neurol 253:953-954, Hern�ndez,A.H.,et al, 2006

Chasing "Chasing the Dragon" with MRI: Leukoencephalopathy in Drug Abuse
Br J Radiol 78:997-1004, Bartlett,E. &Mikulis,D.J., 2005

Cerebral Embolism from Left Atrial Myxoma Leading to Cerebral and Retinal Aneurysms
AJNR 26:666-669, Herbst, M.,et al, 2005

Brainstem Auditory Evoked Potential Monitoring
Neurol 65:1551-1555,1522, James,M.L. &Husain,A.M., 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Methyl Bromide Intoxication Causes Reversible Symmetric Branstem and Cerebellar MRI Lesions
Neurol 64:1279-1281, Geyer,H.L.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Cerebellar Ataxia and Central Nervous System Whipple Disease
Arch Neurol 62:618-620, Matthews,B.R.,et al, 2005

Management of Acute Cerebellar Stroke
Arch Neurol 62:537-544, Jensen,M.B. &St. Louis,E.K., 2005

Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
Neurol 64:1461-1464, Wolf,N.I.,et al, 2005

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

JC Virus Granule Cell Neuronopathy: A Novel Clinical Syndrome Distinct from Progressive Multifocal Leukoencephalopathy
Ann Neurol 57:576-580, Koralnik,I.J.,et al, 2005

Clinicopath Conf., Pheochromocytoma
NEJM 352:2223-2231, Case 16-2005, 2005

Vertebrobasilar Disease
NEJM 352:2618-2626, Savitz,S.I.&Caplan,L.R., 2005

Vagal Nerve Stimulation Effect on Cerebellar Tremor in Multiple Sclerosis
Neurol 65:499, Marrosu,F.,et al, 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

West Nile Virus Meningoencephalitis:MR Imaging Findings
AJNR 26:1986-1995, Petropoulou,K.A.,et al, 2005

Autoantibodies in Postinfectious Acute Cerebellar Ataxia
Neurol 65:1114-1116, Uchibori,A.,et al, 2005

Cerebellar Hemorrhage after Angioplasty
NEJM 352:6, Riecker,A.,et al, 2005

West Nile Virus Infection: MR Imaging Findings in the Nervous System
AJNR 26:289-297, Ali,M., et al, 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005

Upward Transtentorial Herniation, Hydrocephalus, and Cerebellar Edema in Hypertensive Encephalopathy
Neurologist 11:171-175, Adamson, C.D.,et al, 2005

Cerebellar Endometriosis
AJR 182:1543-1546, Sarma,D.,et al, 2004

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
Arch Neurol 61:953-956, Umashankar,G.,et al, 2004



Showing articles 350 to 400 of 1054 << Previous Next >>