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Differential
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acetazolamide
adverse drug reaction
agnosia, color
akathisia
akinesia of eyelid function
alexia without agraphia
algorithm
alien hand syndrome
alpha-fetoprotein
Alzheimer's disease
amnesic stroke
anatomy of
anemia
ankle edema
anti IgLON5
anticholinergic drugs
anticholinesterase
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
arm swing, reduced
arylsulfatase A
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
athetosis
autoantibodies
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bent spine syndrome
biologic markers
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
botulinum toxin
bradykinesia
brain biopsy
brain damage
brainstem, dysfunction
brainstem, lesion of
bruxism
bulbar dysfunction
bulbar palsy
CAG repeats
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
caudate nucleus, atrophy
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar pontine angle
cerebellar pontine angle tumor
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebral peduncle
cerebrovascular accident
ceruloplasmin, serum
channelopathy
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
cirrhosis
cisterna magna
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
cold intolerance
coma
coma, episodic
comorbidities
complications
conjugate gaze, forced
consanguinity
conversion reaction
cortical-basal ganglionic degeneration
cranial nerve palsies
creatine phosphokinase(CPK)elevated
crying, pathologic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diplopia
diurnal variation
donepezil
dopa responsive dystonia
down-beat nystagmus
downward gaze
drooling
drug induced neurologic disorders
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
dysmetria
dysphagia
dysphasia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, post traumatic
dystonia, treatment of
dystonia, truncal
dystonic reaction, acute
DYT1 mutation
edema, pedal
electromyogram
emotional lability
employment
encephalitis, autoimmune
enzyme, defect
ependymoma
episodic disorders
episodic neurologic deficits
equinovarus
esophageal varices
ethics in neurology
exercise
exercise-induced neurologic dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial expression abnormality
falling
familial
fever
fine motor function, impaired
fluctuate
foot deformity
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
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
gests antagoniste
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head nodding
headache
health insurance
hearing loss
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemidystonia
hemifacial spasm
hemiplegia
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
HLA
hoarseness
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hyperreflexia
hypoalbuminemia
hypometric saccades
hypophonia
hypotonia
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
internet
intracranial pressure, increased
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kayser-Fleischer ring
kyphosis
laughing, pathologic
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
lenticular nucleus, lesion of, bilateral
leukemia
leukodystrophy
leukopenia
levitation
lithium
liver disease
liver function enzymes
low back pain
lymphoma
lysosomal storage disease
manganese intoxication
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
midbrain
midbrain, atrophy
midbrain, infarction of
migraine
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, extrapyramidal-treatment of
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
MRI, T1 weighted high signal foci
MRS
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle hypertrophy
muscle spasm, face
muscle weakness
muscular dystrophy
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myokymia
myopathy
myopathy, metabolic
myorhythmia
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neurocutaneous disease
neuroendocrinology
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromyotonia
neuroophthalmology
neuropathology
neuropathy
numb clumsy hands syndrome
nystagmus
nystagmus, vertical
obsessive-compulsive disorder
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
pain
palilalia
palinopsia
PANK2 mutation
paraparesis
parasomnia
paraspinal muscle
paraspinal muscle weakness
parkin gene
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
penguin silhouette sign
penicillamine
personality change
pigmentary retinopathy
Pisa syndrome
pitfalls
pleocytosis of cerebrospinal fluid
polycythemia, secondary
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
postural abnormality
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pull test
pure sensory stroke
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
renal stones
respirations in CNS disease
retinal degeneration
retinitis pigmentosa
retinopathy
retrocollis
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
running
saccadic eye movements, abnormal
salivation, excessive
Saudi Arabia
screening
sea-blue histiocytes
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
sensory tricks
sequencing difficulty
short stature
shoulder, elevation
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
somnolence
spasticity
speech disorder
speech disorder, childhood
spinal cord
spinal cord, lesion of
spinal muscular atrophy
splenomegaly
stare
stem cell transplantation
stimulation, deep brain
stimulation, deep brain, bilateral
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
substantia nigra
suck reflex
suicide
swallow evaluation
symmetric brain lesions
tardive dystonia
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
thalamus, infarction of
thrombocytopenia
toe walking
tonic foot response
torticollis
trauma
treatment of neurologic disorder
treatment, empirical
tremor
tremor, intention
tremor, jaw
tremor, postural
tricyclic antidepressant
trientine dihydrochloride
trinucleotide repeats
tripping
upgaze
upgaze, paralysis of
urinary incontinence
urinary sulfatidase excretion
vision, blurred
visual evoked response
visual field defect
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
zinc
Showing articles 550 to 600 of 1183 << Previous Next >>

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

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

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

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

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,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

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

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

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

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

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Ptosis, Blepharospasm, and Apraxia of Eyelid Opening Secondary to Putaminal Hemorrhage
Neurol 53:652, Verghese,J.,et al, 1999

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

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

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

Globus Pallidus Deep Brain Stimulation for Generalized Dystonia:Clinical and PET Investigation
Neurol 53:871-874, Kumar,R.,et al, 1999

Catalepsy After Stroke
Neurol 53:1132-1135, Saposnik,G.,et al, 1999

Acute Dystonia Induced by Drug Treatment
BMJ 319:623-626, vanHarten,P.N.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Optimality Score for the Neurologic Examination of the Infant at 12 and 18 Months of Age
J Pediatr 135:153-161,140, Haataja,L.,et al, 1999

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

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

A Case-Controlled MRI/MRA Study of Neurovascular Contact in Hemifacial Spasm
Neurol 53:2132-2139, Ho,S.L.,et al, 1999

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Hemifacial Spasm:Clinical Findings and Treatment
Muscle & Nerve 21:1740-1747, Wang,A & Jankovic,J, 1998

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Aggressive Approach in the Treatment of Acute Lead Encephalopathy with an Extraordinarily High Concentration of Lead
Arch Pediatr Adolesc Med 152:1100-1104, Gordon,R.A.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Acute Vestibular Syndrome
NEJM 339:680-685, Hotson,J.R.&Baloh,R.W., 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Long Term Results of Botulinum Toxin Type A (Dysport) in the Treatment of Hemifacial Spasm:A Report of 175 Cases
JNNP 64:751-757, Jitpimolmard,S.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

An Open-Label Trial of Gabapentin Treatment of Paroxysmal Symptoms in Multiple Sclerosis Patients
Neurol 51:609-611, Solaro,C.,et al, 1998

Tardive Dyskinesia:Diagnosis, Pathogenesis, and Management
The Neurologist 4:180-187, Trugman,J.M., 1998

Long-Term Effect of Botulinum Toxin in Impairment and Functional Health in Cervical Dystonia
Neurol 50:1461-1463, Brans,J.W.M.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998



Showing articles 550 to 600 of 1183 << Previous Next >>