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Differential
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achilles tendon, enlarged
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
algorithm
angiography, neurologic complications with
ankle reflex, absent
areflexia
artery of Adamkiewicz
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
bladder dysfunction
bone marrow transplantation
brainstem, atrophy
brainstem, lesion of
burning paresthesia
CAG repeats
cane
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chenodeoxycholic acid
children
chromosomal abnormality
chromosome 2
chromosome 6
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
consanguinity
corpus callosum, thinning
cultured skin fibroblasts
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diet
differential diagnosis
distal muscle atrophy
distal muscle weakness
Dravet syndrome
drug induced neurologic disorders
dysarthria
dysmetria
dysmorphic
dysphagia
ears of the Lynx MR sign
electroencephalogram, inflammatory disease
encephalopathy
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial appearance, abnormal
failure to thrive
falling
familial
FARS2 deficiency
fatty acid, elevated plasma content
fever
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
frataxin
Friedreich's ataxia
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
hammertoes
hand weakness
hearing loss
hepatomegaly
high arched feet
hyperreflexia
hypogonadism
hypomyelination
hypotonia
iatrogenic neurologic disorders
imbalance
impulsivity
inborn errors of metabolism
incoordination
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Jewish
lactic acidemia
leg weakness, bilateral
Leigh's disease
leukodystrophy
liver disease
Lorenzo's oil
meningitis, CSF cell count-normal
mental retardation
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
myelin protein zero gene
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoclonus, epilepsy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
next-generation sequencing
night blindness
numbness, extremity
nystagmus
nystagmus, rotary
ocular motility, disorders of
oculodentodigital dysplasia
optic ataxia
optic atrophy
orthostatic hypotension
pain, foot
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraplegia
paraplegia, acute
paraplegia, neonatal
paresthesias
past pointing
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
polyglucosan body disease
polyneuropathy
pons, lesion of
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
release phenomena
review article
Romberg's sign
scissors gait
SCN1A gene
scoliosis
screening
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, tonic-clonic
skin, darkening of
sodium channel dysfunction
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spasticity
speech, loss of
spinal cord, infarction of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
status epilepticus
steppage gait
stiff legs
striatonigral degeneration
striatonigral degeneration, infantile
subcortical U fibers
symmetric brain lesions
syndactyly
teeth, abnormal
testicular atrophy
titubation
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
umbilical artery catheterization
urinary incontinence
visual impairment
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
xanthoma, tendon
Showing articles 350 to 400 of 1537 << Previous Next >>

Low-Dose Recombinant Tissue-Type Plasminogen Activator Enhances Clot Resolution in Brain Hemorrhage
Stroke 42:3009-3016,2999, Naff, N.,et al, 2011

Oral Acyclovir Suppression and Neurodevelopment after Neonatal Herpes
NEJM 365:1284-1292,1338, Kimberlin, D.W.,et al, 2011

Warfarin-Related Intraventricular Hemorrhage
Neurol 77:1840-1846, Biffi, A.,et al, 2011

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Intraventricular Hemorrhage
UpToDate, Sept, Cucchiara B.L. and Pacelli, J.P., 2011

Chronic Granulomatous Herpes Encephalitis: A Rare Entity Posing a Diagnostic Challenge
J Neurosurg Pediatrics 8:402-406, Adamo, M.A.,et al, 2011

Cervical Carotid Artery Disease in Sickle Cell Anemia: Clinical and Radiological Features
Blood 118:6192-6199, Telfer, P.T.,et al, 2011

Athletics, Minor Trauma, and Pediatric Arterial Ischemic Stroke
Eur J Pediatr 169:557-562, Sepelyak, K.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

New-Onset Aferbrile Seizures in Infants: Role of Neuroimaging
Neurol 74:150-158, Hsieh,D.,et al, 2010

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy
NEJM 362:790-799, Glauser,T.A.,et al, 2010

Prospective Study of New-Onset Seizures Presenting as Status Epilepticus in Childhood
Neurol 74:636-642, 624, Singh,R.K.,et al, 2010

Randomized Trial of Adjunctive Topiramate Therapy in Infants with Refractory Partial Seizures
Neurol 74:714-720, Novotny,E.,et al, 2010

Neurological Outcomes at 18 Months of Age After Moderate Hypothermia for Perinatal Hypoxic Ischaemic Encephalopathy: Synthesis and Meta-Analysis of Trial Data
BMJ 340:c363, Edwards,A.D.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Intracerebral Hemorrhage in Cocaine Users
Stroke 41:680-684, Martin-Schild,S., et al, 2010

Frequency and Prognosis of Convulsive Status Epilepticus of Different Causes: A Systematic Review
Arch Neurol 67:931-940, Neligan,A., et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

Neonatal Cerebral Sinovenous Thrombosis From Symptom to Outcome
Stroke 41:1382-1388, Berfelo,F.J., et al, 2010

Recent Advances in Neuroblastoma
NEJM 362:2202-2011, Maris,J.M., et al, 2010

Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
Neurol 74:e97-e100, Nguyen,T.P. &El-Hakam,L.M., 2010

Painful Paraplegia Caused by Spontaneous Abdominal Compartment Syndrome
Neurol 74:1833-1834, Hermann,A., et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Childhood Posterior Circulation Arterial Ischemic Stroke
Stroke 41:2201-2209, Mackay,M.T.,et al, 2010

Clinical and Neuroimaging Findings of Cree Leukodystrophy: A Retrospective Case Series
AJNR 31: 1418-1423, Harder,S.,et al, 2010

Guidelines for the Management of Spontaneous Intracerebral Hemorrhage
Stroke 41:2108-2129, Morgenstern,L.B.,et al, 2010

Long-Term Mortality in Childhood-Onset Epilepsy
NEJM 363:2522-2529, Sillanp��,M. &Shinnar,S., 2010

Personalized Approaches to Clopidogrel Therapy: Are We There Yet?
Stroke 41:2997-3002, Anderson,C.D.,et al, 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Clinicopath Conf. Rickets Due to Vitamin D Deficiency
NEJM 360:398-407, Case 3-2009, 2009

Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
Neurol 72:469-471, Liguori,M.,et al, 2009

Practice Parameter: Evaluation of Distal Symmetric Polyneuropathy: Role of Laboratory and Genetic Testing (An Evidence-Based Review)
Nuerol 72:185-192, England,J.D.,et al, 2009

Thrombolysis in Childhood Stroke: Report of 2 Cases and Review of the Literature
Stroke 40:801-807, Arnold,M.,et al, 2009

Genetic Aspects of Alzheimer Disease
The Neurologist 15:80-86, Williamson,J.,et al, 2009

Unexplained Seizures in an Infant
Lancet 373:94, Astuto,M.,et al, 2009

Intraventricular Hemorrhage: Severity Factor and Treatment Target in Spontaneous Intracerebral Hemorrhage
Stroke 40:1533-1538, Hanley,D.F., 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

Spinal Dural Arteriovenous Fistulas
AJNR 30:639-648, Krings,T. &Geibprasert,S., 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Resuscitation at Birth and Cognition at 8 Years of Age: A cohort Study
Lancet 373:1615-1622,1581, Odd,D.E.,et al, 2009

Disclosure of APOE Genotype for Risk of Alzheimers Disease
NEJM 361:245-254,298, Green,R.C.,et al, 2009

Moderate Hypothermia to Treat Perinatal Asphyxial Encephalopathy
NEJM 361:1349-1358, Azzopardi,D.,et al, 2009

Intraventricular Fibrinolysis and Lumbar Drainage for Ventricular Hemorrhage
Stroke 40:3275-3280, Staykov,D.,et al, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Epilepsy in Children with Infantile Thiamine Deficiency
Neurol 73:828-833, Fattal-Valevski,A.,et al, 2009

Obesity Is a Common Comorbidity for Pediatric Patients with Untreated, Newly Diagnosed Epilepsy
Neurol 73:658-664, 654, Daniels, Z.S.,et al, 2009

Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
Neurol 73:2071-2078, 2054, Debette,S.,et al, 2009



Showing articles 350 to 400 of 1537 << Previous Next >>