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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 700 to 750 of 1537 << Previous Next >>

Status Epilepticus in Children with Epilepsy:The Role of Antiepileptic Drug Levels in Prevention
Pediatrics 98:1119-1121, Maytal,J.,et al, 1996

The Babinski Sign:100 Years On
BMJ 313:1029-1030, Ditunno,J.F.&Bell,R., 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Cerebrovascular Complications of HIV in Children
AJNR 17:1913-1917, Shah,S.S.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
Ann Neurol 39:132-136, Furtado,S.,et al, 1996

Clinicopath Conf
Chronic Schistosoma Mansoni Infection Involving Large Intestine and Spinal Cord, Case 4-1996, NEJM 3, 4:2-389,1996., 1996

Intracranial Abnor in Infants Treated with Extracorporeal Membrane Oxygenation:Update on Sonographic & CT Findings
AJNR 17:287-294, Bulas,D.I.,et al, 1996

Subarachnoid Fluid Collections:A Cause of Macrocrania in Preterm Infants
J Pediatr 128:234-236, AlSaedi,S.A.,et al, 1996

Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
Neurol 46:527-531, Brandt,J.,et al, 1996

A 64-Year-Old Man with Diabetes and Ascending Paraplegia
Lancet 347:516, Gliemroth,J.,et al, 1996

High-Dose Corticotropin (ACTH) vs. Prednisone for Infantile Spasms:A Prospective, Randomized, Blinded Study
Pediatrics 97:375-379, Baram,T.Z.,et al, 1996

Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
Arch Neurol 53:493-497, Zappacosta,B.,et al, 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996

The Spectrum of Brain MR Abnormalities in Sickle-Cell Disease:A Report from the Cooperative Study of Sickle Cell Disease
AJNR 17:965-972, Moser,F.G.,et al, 1996

Celiac Disease with Cerebral Calcium and Silica Deposits:X-ray Spectroscopic Findings, An Autopsy Study
Neurol 46:1088-1092, Toti,P.,et al, 1996

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996

Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
Arch Neurol 53:940-942, Kompoliti,A.,et al, 1996

The Management of Brainstem Gliomas in Patients with Neurofibromatosis 1
Neurol 46:1652-1660, Pollack,I.F.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Childhood Chronic Inflammatory Demyelinating Neuropathies:Clinical Course and Long-term Follow-up
Neurol 47:98-102, Nevo,Y.,et al, 1996

Prevention of Brain Haemorrhage and Ischaemic Injury in Premature Babies
Lancet 348:208-209, Koppe,J.G., 1996

Antenatal Phenobarbital Therapy and Neonatal Outcome I:Effect on Intracranial Hemorrhage
Pediatrics 97:644-648, Shankaran,S.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

Discontinuation of Anticonvulsant Therapy in Children Free of Seizures for 1 Year:A Prospective Study
Neurol 46:969-974, Dooley,J.,et al, 1996

Random Comp Monother Trial of Phenobarb, Phenytoin, Carbamazepine, or Sod Valp for Newly Dx Child Epilep
Lancet 347:709-713, deSilva,M.,et al, 1996

Startle Provoked Epileptic Seizures:Features in 19 Patients
JNNP 61:151-156, Manford,M.R.A.,et al, 1996

The Risk of Seizure Recurrence After a First Unprovoked Afebrile Seizure in Childhood:An Extended Follow-up
Pediatrics 98:216-225, Shinnar,S.,et al, 1996

Efficacy of Gabapentin Therapy in Children with Refractory Partial Seizures
J Pediatr 128:829-833, Khurana,D.S.,et al, 1996

The Use of Parenteral Antiepileptic Drugs & The Role of Fosphenytoin
(Suppl Editor) , Neurol 46:S1-S2896., Wilder,B.J., 1996

Accidental Injury is a Serious Risk in Children with Typical Absence Epilepsy
Arch Neurol 53:929-932, Wirrell,E.C.,et al, 1996

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995

Neurologic Complications of Lumbar Epidural Anesthesia and Analgesia
Neurol 45:1795-1801, Yuen,E.C.,et al, 1995

Elevated Serum lactate Correlates with Intracranial Hemorrhage in Neonates Treated with Extracorporeal Life Support
Pediatrics 96:914-917, Grayck,E.N.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Treatment for Children with Brain Tumours
BMJ 311:1213-1214, Stevens,M.C.G.,et al, 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Lamotrigine for the Treatment of Epilepsy in Childhood
J Pediatr 127:991-997, Besag,F.M.C.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Cranial Ultrasound Predict of Disabling & Nondisabling Cerebral Palsy at Age Two in Low Birth Wt Population
Pediatrics 95:249-254, Pinto-Martin,J.A.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995



Showing articles 700 to 750 of 1537 << Previous Next >>