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Differential
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abortion, spontaneous
acetylcholine receptor
acetylcholine receptor antibody
advances in neurology
adverse drug reaction
agenesis of corpus callosum
Aicardi's syndrome
alpha-fetoprotein
Alzheimer's disease
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ANA
anesthesia, general
anesthesia, local
anti basal ganglia antibodies
anti MAG antibodies
antimetabolite
antistreptolysin titer
antithyroid antibodies
aphasia
areflexia
arthrogryposis multiplex
asymptomatic
ataxia
ataxia, truncal
atidarsagene autotemcel
autism
autoantibodies
autoimmune disease
axonal spheroid
azathioprine
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bilateral periventricular nodular heterotopia
brain atrophy
brain biopsy
breast feeding
burst suppression pattern, electroencephalogram
CAT scan, abnormal
catatonia
central core disease
cerebellar degeneration
cerebral cortex
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cesarean section
Charcot-Marie-Tooth
cherry red spot
cherry red spot-myoclonus syndrome
children
chorioretinitis
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coloboma
complications
confusion
confusional state, acute
congenital malformation
congenital malformation, non CNS
congenital myasthenic syndromes
corpus callosum
cortical dysplasia, focal
cyst, porencephalic
deep gray nuclei
degenerative diseases of CNS
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
drug induced neurologic disorders
dyskinesia
dysphagia
dystonia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, Hashimoto's
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
eye movement, disorders of
Fabry's disease
facial asymmetry
falling
familial
Fazio-Londe's disease
fever
FLAMES
floppy infant
Friedreich's ataxia
gammaglobulin therapy, intravenous
gangliosidosis GM2
gaze palsy
gaze palsy, supranuclear
gene
gene therapy
genetic neurologic disorders
genetic screening
hallucination
headache
heavy metal intoxication
hemihypertrophy, congenital
hemiparesis
hemispherectomy
hepatomegaly
heterotopia
hexosaminidase-A
hexosaminidase-A and B
histopathology
Huntington's chorea
hyperreflexia
hypomelanosis of Ito
hypomyelination
hypopigmentation of skin
hypotonia
hypotonia, infants
immunologic disease
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infantile bilateral striatal necrosis
infantile neuronal degeneration
infantile spasm
insomnia
intellectual deficit
intellectual deterioration
iron, brain
Jewish
Kugelberg-Welander syndrome
labor, complicated
lactic acidemia
Leigh's disease
lethargy
leukodystrophy
level of consciousness, decreased
lipid storage disorder of CNS
lysosomal storage disease
macrocephaly
magnesium sulfate
malabsorption
malformation, CNS, congenital
Mary Walker phenomenon
megalencephaly
meningeal enhancement
mental retardation
mental status, abnormal
mesial temporal sclerosis
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
microcephaly
micropthalmia
misdiagnosis
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, cortical enhancement
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, negative
MRI, paramagnetic effect
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, congenital
myasthenia gravis, infantile and juvenile
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, passive transfer of
myasthenia gravis, receptor site in
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic crisis
myoclonus
myoclonus, epilepsy
myopathy
myopathy, metabolic
myotonia dystrophica
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
nerve conduction studies, motor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neuronal cell death
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal migration disorder
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
night sweats
NMDA antagonists
nystagmus
nystagmus, rotary
opisthotonus
optic atrophy
optic nerve
optic nerve, lesion of
optic neuritis
PANK2 mutation
paraparesis, familial spastic
Parkinson disease
paroxysmal neurologic disorder
patient information and support
pediatric neurology
perineural invasion
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
poison, mercury
poison, neurologic problems with
Pompe's disease of glycogen storage
Pompe's disease, infantile
postural abnormality
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis, childhood
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
recurrent
respiratory depression
respiratory failure
respiratory tract infection
retinal degeneration
retropulsion
review article
rigidity
rituximab
safety
Sandhoff's disease
segmental demyelination
seizure
seizure, adult onset
seizure, children
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, neonatal
seizure, prognosis in childhood
seizure, psychomotor-temporal lobe
seizure, surgical treatment of
seizure, treatment of
serologic testing
serologic testing, false negative
seronegative
skin, biopsy
skin, lesions in neurologic disorders
SMN1 gene
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
startle reaction
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stillbirth
storage disease of CNS
streptococcal infection
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
survival motor neuron gene
symmetric brain lesions
systemic lupus erythematosus
systemic lupus erythematosus, neonatal
systemic lupus erythematosus, neurologic complications with
Tay-Sachs disease
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
thymectomy
thymus and neuromuscular function
thyroiditis
titubation
tone, muscle, increased
treatment of neurologic disorder
tremor
tremor, intention
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
ventricular enlargement
visual acuity, decreased
visual fields, constricted
visual loss
weakness
weakness, generalized
Werdnig-Hoffman disease
West disease
white matter disease
wide based gait
Showing articles 700 to 750 of 1511 << Previous Next >>

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Death in Children with Epilepsy: A Population-based Study
Lancet 359:1891-1985, Camfield,C.S.,et al, 2002

Hemodynamic Studies in Early Ischemic Stroke
Stroke 33:1274-1279, Akopov,S. &Whitman,G.T., 2002

Paraneoplastic Chorea Associated with CRMP-5 Neuronal Antibody and Lung Carcinoma
Ann Neurol 51:625-630, Vernino,S.,et al, 2002

Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
Neurol 58:1013-1018,997, Suzuki,M.,et al, 2002

Neonatal Cerebral Infarction Diagnosed by Diffusion-Weighted MRI
Stroke 33:1142-1145, Mader,I.,et al, 2002

Dopamine Transporter Brain Imaging to Assess the Effects of Pramipexole vs Levodopa on Parkinson Disease Progression
JAMA 287:1653-1661, Parkinson Study Group, 2002

Sudden Death in Epilepsy: A Wake-up Call for Management
Lancet 359:1790-1791, Pedley, T.A. &Hauser,W.A., 2002

Deaths from Stroke in US Children, 1979-1998
Neurol 59:34-39,6, Fullerton,H.J.,et al, 2002

Minor Head Injury as Cause and Co-Factor in the Aetiology of Stroke in Childhood: A Report of Eight Cases
JNNP 73:13-16, Kieslich,M.,et al, 2002

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

A Painful Hip as a Presentation of Guillain-Barre Syndrome in Children
BMJ 322:149-150, Tang,T. &Noble-Jamieson,C., 2001

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Encephalitis Associated with Glutamic Acid Decarboxylase Autoantibodies
Neurol 56:814, Marchiori,G.C.,et al, 2001

Neurodegenerative Diseases and Prions
NEJM 344:1516-1526,1548, Prusiner,S.B., 2001

Stroke Prevention and Treatment in Sickle Cell Disease
Arch Neurol 58:565-568, Adams,R.J., 2001

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Enzyme Replacement Therapy in Fabry Disease
JAMA 285:2743-2749, Schiffmann,R.,et al, 2001

CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
Neurol 56:1528-1533, Burkhard,P.R.,et al, 2001

Chickenpox and Stroke in Childhood
Stroke 32:1257-1262, Askalan,R.,et al, 2001

Stem-Cell Research: Drawing the Line
Lancet 358:163,217, Greenberg,D.S., 2001

Cerebral Sinovenous Thrombosis in Children
NEJM 345:417-423, DeVeber,G.,et al, 2001

Sudden Unexplained Death in Children With Epilepsy
Neurol 57:430-434, Donner,E.J.,et al, 2001

Arterial Dissection and Stroke in Children
Neurol 57:1155-1160, Fullerton,H.J.,et al, 2001

Positron Emission Tomography in Evaluation of Dementia
JAMA 286:2120-2127,2194, Silverman,D.H.S.,et al, 2001

Silent Infarcts in Children With Sickle Cell Anemia and Abnormal Cerebral Artery Velocity
Arch Neurol 58:2017-2021, Pegelow,C.H.,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

High-dose Intravenous Immune Globulin for Stiff-person Syndrome
NEJM 345:1870-1876, Dalakas,M.B.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,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

Morvans Syndrome: Peripheral and Central Nervous System and Cardiac Involvement With Antibodies to Voltage-Gated Potassium Channels
Brain 124:2417-2426, Liguori,R., et al, 2001

Morvans Syndrome Associated With Voltage-Gated K+ Channel Antibodies
Neurol 54:771-772, Barber,P.A., et al, 2000

Immune Cytopenias as the Presenting Finding in Primary Sjogrens Syndrome
QJM 93:825-829, Schattner,A.,et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Antiphospholipid and Antinuclear Antibodies in Patients with Epilepsy or New-onset Seizure Disorders
Am J Med 109:712-717, Peltola,J.T.,et al, 2000

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

Early Identification of Refracvtory Epilepsy
NEJM 342:314-319, Kwan,P.&Brodie,M.J., 2000

Psychogenic Status Epilepticus in Children: Psychiatric and Other Risk Factors
Neurol 54:969-970, Pakalnis,A.,et al, 2000

Subdural Hematoma During Low-Dose ACTH Therapy in Patients with West Syndrome
Neurol 54:2346-2347, Ito,M.,et al, 2000

Factor V Leiden and Antiphospholipid Antibodies Are Significant Risk Factors for Ischemic Stroke in Children
Stroke 31:1283-1288, Kenet,G.,et al, 2000

Intravenous Valproate in Pediatric Epilepsy Patients with Refractory Status Epilepticus
Neurol 54:2188-2189, Uberall,M.A.,et al, 2000

Early Diffusion-Weighted MR Imaging Abnormalities in Sustained Seizure Activity
AJR 174:1304-1306, Kassem-Moussa,H.K.,et al, 2000

Measles,MMR, and Autism: The Confusion Continues
Lancet 355:1379, , 2000

Predictors of Multiple Seizures in a Cohort of Children Prospectively Followed from the Time of their First Unprovoked Seizure
Ann Neurol 48:140-147, 137, Shinnar,S. et al, 2000

Management of Epilepsy in Adolescents and Adults
Lancet 356:323-329, Brodie,M.J. & French,J.A., 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



Showing articles 700 to 750 of 1511 << Previous Next >>