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acoustic nerve
adolescent medicine
advances in neurology
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
anosmia
anti GQ1b IgG antibody
anti IgLON5
anticholinergic drugs
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
areflexia
arm swing, reduced
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
ATP1A3 gene
attention span
autoantibodies
autoimmune basal ganglia encephalitis
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basilar impression
behavioral disorder
biologic markers
biopterin deficiency
bladder dysfunction
blepharospasm
bradykinesia
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
calcitonin
carbamazepine
carcinoembryonic antigen
carcinoma
cardiomyopathy
cataplexy
cataracts
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
compression fracture
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
crying, pathologic
cultured skin fibroblasts
degenerative diseases of CNS
delay in diagnosis
dementia
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonia, treatment of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalopathy
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
exophthalmus
eye movement, disorders of
facial nerve palsy
falling
familial
fine motor function, impaired
foam cells
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head circumference
headache
hearing loss
heart block
hemidystonia
hemifacial spasm
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
HLA
hoarseness
Hodgkin's disease
hydrocephalus
hyperreflexia
hypometric saccades
hypophonia
hyposmia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
inclusion bodies, intranuclear
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iron, brain
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
Kearns-Sayre syndrome
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia
limbic encephalitis
lipid storage disorder of CNS
liver disease
low back pain
lymphoma
macular degeneration
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, carcinomatous
mental retardation
mental status, abnormal
MERRF syndrome
microcephaly
midbrain
midbrain, atrophy
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
mortality
motor dysfunction
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
Niemann-Pick disease
NMDA antagonists
numb clumsy hands syndrome
nystagmus
nystagmus, monocular
ocular motility, disorders of
opened mouth
ophelia syndrome
ophthalmoplegia
optic atrophy
optic atrophy, unilateral
optic neuropathy
optokinetic nystagmus, abnormal
Paget's disease
Paget's disease, psychosis in
Paget's disease, spinal cord problem in
pain
palilalia
pancytopenia
PANK2 mutation
paraparesis
parasomnia
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penguin silhouette sign
personality change
personality disorder
pigmentary retinopathy
pitfalls
pleocytosis of cerebrospinal fluid
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
PRKN gene
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pull test
radiation hypersensitivity
radiculopathy
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
release phenomena
respirations in CNS disease
retinal artery occlusion
retinal hemorrhages
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
rituximab
root lesion, nerve
running
saccadic eye movements, abnormal
salivation, excessive
screening
seizure
sensorineural hearing loss
sensory loss, cortical
sequencing difficulty
serologic testing
serologic testing, false negative
seronegative
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
stare
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
suck reflex
superior orbital fissure syndrome
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tremor, psychogenic
trigeminal neuralgia
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vertebral-basilar insufficiency
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
Wolfram syndrome
Showing articles 300 to 350 of 8642 << Previous Next >>

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

Ophthalmologic Features of Parkinson's Disease
Neurol 62:177-180, Biousse,V.,et al, 2004

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

B- and T-cell Markers in Opsoclonus-Myoclonus Syndrome
Neurol 62:1526-1532,1466, Pranzatelli,M.R.,et al, 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

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

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

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

Post-Streptococcal Autoimmune Disorders of the Central Nervous System
Curr Opin Neurol 16:359-365, Snider,L. &Swedo,S., 2003

Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
Medicine 82:216-223, Rojas-Marcos,I.,et al, 2003

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Opsoclonus-myoclonus Syndrome Following Epstein-Barr Virus Infection
Neurol 58:1131-1132, Verma,A. &Brozman,B., 2002

Mycoplasma Pneumoniae Encephalitis in Childhood
J Microbiol Immunol Infect 35:173-178, Lin,W.-C., et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Drug-Induced Pisa Syndrome (Pleurothotomus)
CNS Drugs 10:166-174, Suzuki, T. & Matsuzaka, H., 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

Confusion After Antibiotics
Lancet 357:1410, Gavazzi,C.,et al, 2001

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Intrathecal Baclofen for the Treatment of Dystonia in Patients with Reflex Sympathetic Dystrophy
NEJM 343:625-630,654, van Hilten,B.J. et al, 2000

Relation Between Cholinesterase Inhibitor and Pisa Syndrome
Lancet 355:2222, Kwak,Y.T. et al, 2000

Abnormal White Matter Signal in Ataxia Telangiectasia
AJNR 21:1483-1485, Ciemins,J.J. & Horowitz,A.L., 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Progression of Parkinsonian Signs in Alzheimer's Disease
Neurol 54:1284-1289, Wilson,R.S.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Vertigo and Gait Ataxia Without Usual Signs of Lateral Medullary Infarction: A Clinical Variant Related to Rostral-dorsolateral Lesions
Cerebrovasc Dis 10:471-474, Kim,J.S., 2000

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.G.,et al, 1999

Effectiveness of Anticholinergics and Neuroleptic Dose Reduction on Neuroleptic-Induced Pleurothotonus (the Pisa Syndrome)
J Clin Psychopharmacol 19:277-280, Suzuki,T.,et al, 1999

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998



Showing articles 300 to 350 of 8642 << Previous Next >>