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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 500 to 550 of 1431 << Previous Next >>

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

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

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

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

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

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Brainstem Involvement in Hypertensive Encephalopathy
Neurol 62:1417-1419, Cruz-Flores,S.,et al, 2004

Plasmapheresis Improves Outcome in Postinfectious Cerebellitis Induced by Epsteiin-Barr Virus
Neurol 62:1443, Schmahmann,J.D., 2004

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Early Diagnosis of Central Pontine Myelinolysis with Diffusion-Weighted Imaging
AJNR 25:210-213, Ruzek,K.A.,et al, 2004

The Clinical Significance of Diffusion-Weighted MR Imaging in Infratentorial Strokes
Neurol 62:574-580, Englelter,S.T.,et al, 2004

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

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Five New Cases of a Recently Described Leukoencephalopathy with High Brain Lactate
Neurol 63:688-692, Linnankivi,T.,et al, 2004

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Diffusion-Weighted and Conventional MR Imaging Findings of Neuroaxonal Dystrophy
AJNR 25:1269-1273, Sener,R.N., 2004

MR Imaging of Brain-Stem Hypoplasia in Horizontal Gaze Palsy with Progressive Scoliosis
AJNR 25:1046-1048, Rossi, A.,et al, 2004

MR Imaging Presentation of Intracranial Disease Associated with Langerhans Cell Histiocytosis
AJNR 25:880-891, Prayer, D.,et al, 2004

Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
Am J Surg Pathol 27:487-493, George, D.H.,et al, 2003

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Serial Proton MR Spectroscopy and Diffusion Imaging Findings in HIV-Related Herpes Simplex Encephalitis
AJNR 24:2015-2019, S�mann,P.G., et al, 2003

Clinicopath Conf., Meningencephalitis and Sepsis Due to Neisseria Meningitidis Infection
NEJM 349:2341-2349, Case 38-2003, 2003

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Prevalence of Antigliadin Antibodies in Ataxia Patients
Neurol 60:1674-1675,1566, Abele,M.,et al, 2003

Nodulus Infarction Mimicking Acute Peripheral Vestibulopathy
Neurol 60:1700-1702, Lee,H.,et al, 2003

Neurologic Manifestations of Vitamin B12 Deficiency
NEJM 348:2208, Scherer,K., 2003

Clinicopath Conf., West Nile Virus Meningoencephalitis
NEJM 348:2239-2247, Case17-2003, 2003



Showing articles 500 to 550 of 1431 << Previous Next >>