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Differential
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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
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebral palsy
cerebrospinal fluid, lactic acid concentration
Charcot-Marie-Tooth
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
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
dysmorphic
dysphagia
ears of the Lynx MR sign
electroencephalogram, inflammatory disease
encephalopathy
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
exome sequencing
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
Showing articles 550 to 600 of 1502 << Previous Next >>

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

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 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

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

Course and Treatment of Myasthenia Gravis During Pregnancy
Neurol 52:447-452, Batocchi,A.P.,et al, 1999

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

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Early Prognostic Indicators of Outcome in Infants with Neonatal Cerebral Infarction:A Clinical,Electroencephalogram,and Magnetic Resonance Imaging Study
Pediatrics 103:39-46, Mercuri,E.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Buccal Midazolam and Rectal Diazepam for Treatment of Prolonged Seizures in Childhood and Adolescence:A Randomised Trial
Lancet 353:623-626,650, Scott,R.C.,et al, 1999

Lorazepam for the Prevention of Recurrent Seizures Related to Alcohol
NEJM 340:915-919, D'Onofrio,G.,et al, 1999

Diffusion- and Perfusion-Weighted Magnetic Resonance Imaging in Deep Cerebral Venous Thrombosis
Stroke 30:1144-1146, Keller,E.,et al, 1999

Hemorrhage After an Acute Ischemic Stroke
Stroke 30:761-764, Motto,C.,et al, 1999

Varicella as a Risk Factor for Cerebral Infarction in Childhood:A Case-Control Study
Ann Neurol 45:679-680, Sebire,G.,et al, 1999

Cat-Scratch Disease Encephalopathy:A Cause of Status Epilepticus in School-Aged Children
J Pediatrics 134:635-638, Armengol,C.E.&Hendley,J.O., 1999

Brain Tumors in Children
Arch Neurol 56:421-425, Packer,R.J., 1999

Clinicopath Conf:Burkitt-Like B-Cell Lymphoma, Nocardiosis
NEJM 340:1188-1196, Case 11-1999, 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Open Comparative Long-Term Study of Vigabatrin vs Carbamazepine in Newly Diagnosed Partial Seizures in Children
Arch Neurol 56:605-607, Zamponi,N.&Cardinali,C., 1999

Vagus Nerve Stimulation for Medication-Resistant Generalized Epilepsy
Neurol 52:1510-1512, Labar,D.,et al, 1999

Left Vagal nerve Stimulation in Children with Medically Refractory epilepsy
J Pediatr 134:563-566, 532, Murphy,J.V.&Pediatric VNS Study Group, 1999

Vagal Nerve Stimulation in epileptic Encephalopathies
Pediatrics 103:778-782, 821, Parker,A.P.J.,et al, 1999

A Double-Blind, Randomized Trial of Topiramate as Adjunctive Therapy for Partial-Onset Seizures in Children
Neurol 52:1338-1344, Elterman,R.D.,et al, 1999

Intractable Epilepsy
Lancet 353:1238, Shuper,A.,et al, 1999

Chromatic Sensitive Epilepsy:A Variant of Photosensitive Epilepsy
Ann Neurol 45:790-793, Tobimatsu,S.,et al, 1999

Measurement of the Urinary Lactate:Creatinine Ratio for the Early Identification of Newborn Infants at Risk for Hypoxic-Ischemic Encephalopathy
NEJM 341:328-335,364, Huang,C.,et al, 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,M.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Phenobarbital Compared with Phenytoin for the Treatment of Neonatal Seizures
NEJM 341:485-489, Painter,M.J.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

When to Start and Stop Anticonvulsant Therapy in Children
Arch Neurol 56:1073-1077, Greenwood,R.S.&Tennison,M.B., 1999

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

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,et al, 1999

Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
Hum Pathol 30:978-981, Abdulkader, I.,et al, 1999

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Antepartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1549-1553,1537, Badawi,N.,et al, 1998

Intrapartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1554-1558,1537, Badawi,N.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998

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

Response to External Ventricular Drainage in Spont Intracerebral Hemorr with Hydrocephalus
Neurol 50:519-523, Adams,R.E.&Diringer,M.N., 1998

Clinicopath Conf
Sarcoidosis, Involving the Spinal Cord & Mediastinal Lymph Nodes, Case 8-1998, NEJM 338:747-754., , 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Neurologic Manifestations of Spinal Epidural Arteriovenous Malformations
Neurol 50:517-519, Hemphill III,J.C.,et al, 1998

Risk of Recurrent Seizures After Two Unprovoked Seizures
NEJM 338:429-434, Hauser,W.A.,et al, 1998

Epilepsy in Young People:23 Year Follow Up of the British National Child Development Study
BMJ 316:339-342, Kurtz,Z.,et al, 1998

Amyloid Neuropathy Simulating Lower Motor Neuron Disease
Neurol 51:600-602, Quattrini,A.,et al, 1998

Hydrocephalus:A Previously Unrecognized Predictor of Poor Outcome from Supratentorial Intracerebral Hemorrhage
Stroke 29:1352-1357, Diringer,M.N.,et al, 1998



Showing articles 550 to 600 of 1502 << Previous Next >>