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abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
acetazolamide
aciduria
Adies pupil
adolescent medicine
advances in neurology
adverse drug reaction
algorithm
alpha-fetoprotein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
amyloidosis
amyotrophic lateral sclerosis
anemia
ankle edema
anti GQ1b IgG antibody
anticholinergic drugs
apraxia of eye movements
areflexia
artane
arthralgia
arthrogryposis multiplex
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic-dystonia syndromes
athetosis
athetosis, causes of
atlanto-axial subluxation
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
biopterin deficiency
bladder dysfunction
blepharospasm
botulinum toxin
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
burning skin
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, isodense lesion with acute hemorrhage
cataracts
catecholamine
cavernous sinus, syndrome
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebral cortical atrophy
cerebral hypoperfusion
cerebral ischemia
cerebral palsy
cerebral palsy, associated problems with
cerebral vasculature, calcification
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
ceruloplasmin, serum
cervical spine
Charcot-Marie-Tooth
chelation therapy
children
chorea
chorea, causes of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
cognition
cogwheel rigidty
complications
compression fracture
contractures, joint
cornea, opacity of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
deferiprone
degenerative diseases of CNS
delay in diagnosis
dementia
dental procedure, neurologic complications with
depression
dermatomyositis
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diphenhydramine
diplopia
diurnal variation
DNA probes
donut sign
dopa responsive dystonia
dopamine
drooling
drop attacks
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia musculorum deformens, carrier
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, painful
dystonia, segmental
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
edema, pedal
efficacy
empyema, epidural
empyema, subdural
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalopathy
encephalopathy, progressive
endarterectomy, carotid
enzyme, defect
episodic neurologic deficits
equinovarus
esophageal varices
exome sequencing
eye movement, disorders of
facial expression abnormality
facial movement disorder
facial nerve palsy
Fahr disease
familial
fatigue
fine motor function, impaired
foot deformity
frontal lobe, pathologic signs of
fungal infection, CNS
gait disorder
galactorrhea
gamma amino butyric acid
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, stimulation
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
granuloma, pulmonary
grasp reflex
growth retardation
Guillain Barre syndrome
hands, fisted
head nodding
headache, positional
hearing loss
heparin, subcutaneous
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
Hodgkin's disease
homovanillic acid
hospitalization
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperreflexia
hypertonia
hypoalbuminemia
hypocalcemia
hypoglycorrhachia
hypoparathyroidism
hypoparathyroidism, idiopathic
hyporeflexia
hyposmia
hypotonia
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
iron, brain
jugular foramen syndrome
Kayser-Fleischer ring
klippel feil syndrome
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukopenia
Lhermitte's sign
limbic encephalitis
lithium
liver function enzymes
lymphoma
masked facies
mastoiditis
memory, impairment of
meningismus
meningitis
meningitis, carcinomatous
meningitis, fungal
meningitis, syphilitic
meningitis, TB
mental retardation
mental status, abnormal
microcephaly
mimics
misdiagnosis
molecular genetics
monoamines
monoclonal antibodies
mononeuropathy
mortality
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI pattern
MRI, abnormal
MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
multiple sclerosis
multiple system atrophy
Munchausen syndrome
muscle diseases, characteristics of
muscle pain
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelitis
myelitis, transverse
myelitis, transverse, idiopathic
myelitis, transverse, prognosis
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal stuffiness
neck pain
neuritis, causes of
neurochemistry
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
neuropathy, diabetic
neuropsychiatry
neurotomy
neurotransmitter
next-generation sequencing
NMDA antagonists
norepinephrine
numb clumsy hands syndrome
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
ocular motility, disorders of
ophelia syndrome
ophthalmoplegia
optic atrophy
optic neuropathy
osteomyelitis
osteomyelitis, skull
otitis, neurologic complications with
pain
pallidotomy
PANK2 mutation
paraparesis
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal neurologic deficits
parsidol
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
personality change
phenylketonuria
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
pons, lesion of
porphyria
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
primary familial brain calcification
PRKN gene
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
pseudohypoparathyroidism
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychosis
pupil, abnormality in neurologic disorders
pupil, tonic
quadriparesis
quality of life
radiation hypersensitivity
radiculopathy
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
renal stones
respiratory failure
retinopathy
reversible neurologic disorder
review article
RFLPs
rigidity
Riley-Day syndrome
risk factors
rituximab
safety
sarcoidosis
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory level
sensory tricks
serologic testing
serologic testing, false negative
seronegative
sexual dysfunction in neurologic disease
shaking
short stature
sicca syndrome
sinemet
sinusitis
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, childhood
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotaxic surgery
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stimulation, deep brain
stimulation, deep brain, bilateral
striatal encephalitis
striopallidodentate calcifications, familial idiopathic
substantia nigra
symmetric brain lesions
tardive dyskinesia
tardive dystonia
telangiectases
tetrahydrobiopterin
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
thrombophlebitis, prophylaxis
toe walking
tonic foot response
tonic spasms
torticollis
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trigeminal neuralgia
tripping
tyrosine hydroxylase deficiency
unconsciousness
unconsciousness, transient
urinary incontinence
urinary retention
urinary urgency
valium
vasospasm, cerebral
visual loss
walking
walking frame
walking, difficulty with
Werdnig-Hoffman disease
wheelchair
white matter disease
Wolfram syndrome
workup
wrist drop
writers cramp
xerophthalmia
xerostomia
zinc
Showing articles 1050 to 1100 of 2609 << Previous Next >>

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,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

Neurology of the Vasculitides and Connective Tissue Diseases
JNNP 65:10-22, Moore,P.M.&Richardson,B., 1998

Angiographically Defined Primary Angiitis of the CNS, Is It Really Benign
Neurol 51:183-188, Woolfenden,A.R.,et al, 1998

Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation
Brain 121:127-133, Lugaresi,E.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Meningoencephalomyelitis Caused by Herpes Simplex Virus-1 in Pt with Idiopathic T CD4+Lymphocytopenia
Neurol 50:569-570, Tumbarello,M.,et al, 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Bilateral Optic Disk Pallor After Unilateral Internal Carotid Artery Occlusion
Neurol 50:809-811, Archer,J.S.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,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

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Guillain-Barre Syndrome
Lancet 352:635-641, Hahn,A.F., 1998

Guillain-Barre Syndrome:MR Imaging Findings of the Spine in Eight Patients
Radiology 208:137-141, Byun,W.M.,et al, 1998

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Effects of Weight Loss on the Course of Idiopathic Intracranial Hypertension in women
Neurol 50:1094-1098, Kupersmith,M.J.,et al, 1998

Anticardiolipin Antibodies are Frequently Present in Patients with Idiopathic Intracranial Hypetension
Arch Neurol 55:817-820, Leker,R.R.&Steiner,I., 1998

Idiopathic Intracranial Hypertension Without Papilledema, A Case-Control Study in Headache Center
Neurol 51:245-249, Wang,S-J.,et al, 1998

Familial Idiopathic Intracranial Hypertension with Spinal and Radicular Pain
Arch Neurol 55:854-856, Santinelli,R.,et al, 1998

Permanent Visual Loss and Cerebrovascular Accidents in Giant Cell Arteritis: Predictors and Response to Treatment
Arthritis Rheum 41:1497-1504, Gonzalez-Gay,M.,et al, 1998

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

Dural Arteriovenous Fistulas as a Cause of Intracranial Hypertension Due to Impairment of Cranial Venous Outflow
JNNP 65:308-316, Cognard,C.,et al, 1998

Stroke After a Visit to the Hairdresser
Lancet 350:866,1777-1778, Nwokolo,N. &Bateman,D.E., 1997

Idiopathic CD4+ T Lymphocytopenia Presenting as Progressive Multifocal Leukoencephalopathy: Case Report
CID 24:526-527, Chikezie,P.U. &Greenberg,A.L., 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Enhanced MR Imaging of Hypertrophic Pachymeningitis
AJR 169:1425-1428, Friedman,D.P.&Flanders,A.E., 1997

Chronic Inflammatory Demyelinating Polyradiculoneuropathy in Children
Muscle & Nerve 20:1569-1575997., Simmons,Z.,et al, 1997

Optic Nerve Sheath Fenestration for Pseudotumor Cerebri
J Neuro-Ophthalmol 17:86-91, Goh,K.Y.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Imaging Appearance of Pachymeningeal Tuberculosis
AJR 169:1421-1424, Goyal,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Ticlopidine and Thrombotic Thrombocytopenic Purpura
NEJM 337:1245, Kupfer,Y.&Tessler,S., 1997

Cocaine-Associated Dystonic Reaction
Am J Emerg Med 15:513-516, Fines,R.E.,et al, 1997

Fulminant Demyelinating Neuropathy Mimicking Cerebral Death
Muscle & Nerve 20:1595-1597997., Bakshi,N.,et al, 1997

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

An Acute Neurologic Syndrome Temporally Associated with Postexposure Trtm of Rabies
Pediatrics 100:720-721, Mortiere,M.D.&Falcone,A.L., 1997

Guillain-Barre Syndrome Following Allogeneic Bone Marrow Transplantation
Neurol 49:1711-1714, Wen,P.Y.,et al, 1997

Fou Rire Prodromique Hearlding a Left Internal Carotid Artery Occlusion
Stroke 28:2081-2083, Carel,C.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

A 9-Year-Old With Fever and Severe Muscle Pains
Lancet 349:1666, Punda-Polic,V.,et al, 1997

Treatment of Inflammatory Myopathies
Muscle & Nerve 20:651-664997., Mastaglia,F.L.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

A Boy with Heart Failure, A Thick Tongue, and Double Vision
Lancet 349:1516, Karstein,J.,et al, 1997



Showing articles 1050 to 1100 of 2609 << Previous Next >>