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Differential
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abdominal distention
abducens nerve paralysis
acetazolamide
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
adrenal crisis, acute
adverse drug reaction
agenesis of corpus callosum
alcohol
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
algorithm
alopecia
alpha-fetoprotein
alveolar hypoventilation
Alzheimer's disease
amenorrhea
aminoacidopathies
aminoacidurias
ammonia
amniocentesis
amphetamines
amyotrophic lateral sclerosis
anemia
Angelman syndrome
angiokeratoma
ankle edema
anorexia nervosa
anticonvulsants
aphasia
apnea
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arteriovenous malformation
arteriovenous malformation, cerebral
arthralgia
arthritis
arylsulfatase B
ascending paralysis
ascites
astrogliopathy
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atlanto-axial subluxation
atrial enlargement
attention deficit disorder with hyperactivity
autism
autoimmune disease
autonomic dysfunction
axonal degeneration
basal ganglia, calcification of
basilar impression
battered child syndrome
behavior modification
behavior, combative
behavioral disorder
biologic markers
bitemporal visual field defect
blepharophimosis
blepharospasm
blind spot, enlarged
blindness, sudden
bone age
bone biopsy
bone marrow transplantation
brachial plexus neuropathy
brachial plexus neuropathy, familial
bradycardia
brain atrophy
brain biopsy
brainstem, atrophy
breech delivery
Brown-Vialetto-Van Laere syndrome
bruit
bruit, cranial
bruxism
bulbar palsy
cachexia
calcification, intracranial
carbonic anhydrase II deficiency
carcinoembryonic antigen
carcinoma
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cauda equina, enhancement
cavernous sinus
cavernous sinus, metastasis to
celiac disease, adult
celiac disease, childhood
central hypoventilation, congenital
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral palsy
cerebral vasculature
cerebral venous thrombosis
cerebrospinal fluid, biochemical markers of CNS tumors
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
chemotherapy, CNS treatment and complications with
child abuse
children
chorea
choreoathetosis
chorionic gonadotropin
chorioretinitis
chromophobe adenoma
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 15
chromosome 8
chronic graft versus host disease
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clonus
Cockayne's syndrome
codfish vertebrae
cold hands sign
collagen vascular disease
coma
complications
compression fracture
congenital heart disease
congenital heart disease, CNS complications with
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital malformation, non CNS
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
Cornelia de Lange syndrome
corpus callosum, atrophy of
corpus callosum, hypoplastic
corpus callosum, thinning
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniopharyngioma
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cryopyrin-associated periodic syndrome
cryptorchidism
cultured skin fibroblasts
cyanosis
cystinosis
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
degenerative diseases of CNS
dementia
dementia, childhood
dementia, rapidly progressive
dermatitis herpetiformis
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
digits, abnormal
diplopia
dislocated hip, congenital
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
drooling
dural sinus thrombosis
dysarthria
dyslexia
dysmorphic
dysostosis multiplex
dysphagia
dyspraxia
dystonia
ear, abnormal
ears, low set
eating disorder
echocardiogram
echocardiogram, transesophageal
ectopic pinealoma
ejection fraction
ejection fraction, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emergencies, neurologic
empty sella
encephalopathy
encephalopathy, progressive
endovascular therapy
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
episodic disorders
evoked potentials
exercise
exercise intolerance
exome sequencing
exostosis
eye movement, disorders of
eyebrows, abnormal
eyes, sunken
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial nerve palsy
facial weakness, bilateral
failed medical management
failure to thrive
false negative
familial
FARS2 deficiency
fatigue
feeding disorder
fetal alcohol syndrome
fetus
fever
fever, recurrent
fibrillations
fine motor function, impaired
finger tapping
floppy infant
foam cells
follicle stimulating hormone
fontanel, bulging
foot drop
foot drop, bilateral
foot numbness
fracture, pathologic
frontal bossing
fucosidosis
gadolinium
gait disorder
gait, apraxic
gait, spastic
gangliosidosis GM1
gangliosidosis GM2
gastrointestinal disease, neurologic complications
gastrointestinal motility
gender
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genital hypoplasia
genu valgum
GFAP gene
glucose tolerance test, abnormal
gluten ataxia
gluten sensitivity
gluten-free diet
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
Gowers maneuver
gray hair
growth hormone
growth hormone deficiency
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, infantile and childhood form
hair, darkening of
hair, loss
hamartoma
hand deformity
hand flapping
hand weakness
head bobbing
head circumference
head injury
head injury, hypothalamic and pituitary damage
head injury, pediatric
headache
headache, recurrent
hearing loss
heart block
heart murmur
hemiparesis
hemoglobin abnormality, neurologic complications of
hemorrhage, intracranial, newborn
hemorrhagic diathesis
hepatitis
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary multiple exostoses
herpes simplex virus
herpes simplex virus infection, newborn
herpes simplex virus, human nervous system and
high arched palate
hip dysplasia
Hirschprung's disease
hirsutism
HLA
homocystinuria
human immunodeficiency virus type 1
Hunter's syndrome
hydrocephalus
hydrocephalus, communicating
hydrocephalus, congenital
hydrocephalus, etiology
hydrocephalus, fetal
hydrocephalus, infants and children
hydrocephalus, intrauterine
hydrocephalus, treatment of
hypercapnia
hyperhomocysteinemia
hypernatremia
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertelorism
hypertonia
hypertrophic cardiomyopathy
hypertrophic intracranial pachymeningitis
hypodontia
hypoglycemia
hypogonadism
hypomagnesemia
hypomyelination
hypoparathyroidism
hypopigmentation of skin
hypopituitarism
hyporeflexia
hypotelorism
hypothalamus
hypothalamus, disturbance of
hypothalamus, lesion of
hypothalamus, neoplasm of
hypothermia
hypothermia, causes of
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
imperforate anus
impotence
impulsivity
inability to stand on tiptoes
inclusion bodies, intranuclear
infection
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial hemorrhage
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intraventricular hemorrhage
joint hypermobility
Kearns-Sayre syndrome
Klinefelter's syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic acidemia
laminar necrosis, cortical
language disorders in children
L-dopa
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
lens, dislocation of
lens, ectopic
lethargy
leukemia
leuko-araiosis
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
leukotrienes
level of consciousness, decreased
libido, decreased
lid
lid abnormalities
life expectancy
lip, abnormal
lipid storage disorder of CNS
livedo reticularis
liver disease
liver nodules
low birth weight
Lowe's syndrome
lumbar puncture
luteinizing hormone
lymphadenopathy
lymphoma
lysosomal storage disease
macrocephaly
malabsorption
malabsorption syndrome
malformation, vascular
malformation, vascular, cerebral
malformation, Vein of Galen
meconium staining
melanomatosis, primary malignant
MELAS syndrome
meningitis, aseptic
meningitis, CSF cell count-normal
menses
mental retardation
mental status, abnormal
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
microcephaly
micrognathia
micromelia
microspherophakia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
molybdenum cofactor deficiency
monoclonal gammopathy
Morquio syndrome
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, angiography
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRS
mucopolysaccharidoses
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myelomeningocele
myelopathy
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, vacuolar
myopia
myotonia
nasal bridge, wide
nausea and vomiting
neck, webbed
negative
neoplasm, intracranial with metastasis extracranially
neoplasm, intracranial, congenital
neoplasm, intracranial, infants
neoplasm, pituitary
neoplasm, primary intracranial
neoplasm, primary intracranial-treatment of
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-incidence of
neoplasm, primary of CNS-survival
neoplasm, primary of CNS-treatment of
nerve biopsy
nerve growth factor
nerve growth stimulating activity
nerve root enhancement
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory, hereditary
neuroprotective agents
Niemann-Pick disease
Noonan Syndrome
normal
nose, abnormal
numbness, ascending
numbness, extremity
nutritional deficiency
nystagmus
nystagmus, see-saw
obesity
ocular motility, disorders of
oligodactyly
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
optic atrophy
optic atrophy, bilateral
optic foramina
optic foramina, abnormal
optic nerve sheath fenestration
optic nerve, decompression of
optic nerve, hypoplasia of
optic neuropathy
oral ulcerations
orthostatic hypotension, idiopathic
osteogenesis imperfecta
osteopetrosis
osteoporosis
otosclerosis
P300
palatal myoclonus
Pallister-Hall syndrome
palpebral fissure, short
pancytopenia
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinsonism syndrome
parotitis
paroxysmal neurologic deficits
PAS positive
patent ductus arteriosus
pathology
pectus carinatum
pectus excavatum
pediatric neurology
perceptual-motor dysfunction
personality change
pheochromocytoma
philtrum, hypoplastic
philtrum, tented
phocomelia
photophobia
photosensitivity, skin
pigmentary retinopathy
pinched face
pitfalls
pituitary, adenoma
pituitary, dysfunction
pituitary, enlargement
pituitary, hormones of
pituitary, lesion of
plasmacytoma
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
pleocytosis of cerebrospinal fluid
POEMS syndrome
polydactyly
polyhydramnios
polyneuropathy
polyps, gastrointestinal tract
pons, atrophy
postural abnormality
Prader-Labhart-Willi syndrome
precocious puberty
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
pretectal syndrome
prevention of neurologic disorders
primitive neuroectodermal tumors
progeria
prognathism
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychosocial aspects
ptosis
puberty
puberty, delayed
pulmonary stenosis
pupil, ectopic-congenital
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly progressing neurologic illness
rash
reading problem, causes of
recurrent
red eye
renal failure
renal tubular acidosis
ReNU syndrome
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retinal degeneration
retinitis pigmentosa
retinopathy
Rett's syndrome
review article
riboflavin transporter deficiency
rickets
Riley-Day syndrome
risk factors
ritalin
rocking
root lesion, nerve
Rosenthal fibers
saddle nose
Sanfilippo syndrome
Schwartz-Jampel syndrome
sclerae, blue
scoliosis
scoliosis, neurologic association with
screaming
seizure
seizure, children
seizure, drug resistance
seizure, focal
seizure, injury following
seizure, intractable
seizure, neonatal
sella turcica, enlargement of
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
serologic testing
short neck
short stature
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
Shy-Drager syndrome
sickle cell trait
simian crease
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull bone, thickening
skull x-ray
skull x-ray, abnormal
sleep
sleep pathology and physiology
small vessel disease
somatosensory evoked potentials
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, absence of
speech, delayed development of
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
splenomegaly
spongy degeneration of brain
standing difficulty
stem cell transplantation
stent, venous sinus
steppage gait
stereotyped behavior
stimulant drugs
stooped posture
strabismus
strokelike episodes
subarachnoid hemorrhage
subdural hematoma
subdural hematoma, neonates and infants
subgaleal fluid collection
suck, poor
superior sagittal sinus thrombosis
suprasellar lesion
syndactyly
synophrys
systemic illness
teeth, abnormal
telangiectases
temper tantrums
temporal lobe, lesion
teratoma
term infant
third ventricle, mass of
thrombophlebitis
thyroid function tests
toe walking
tongue, enlarged
tongue, protrusion of
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
trichopoliodystrophy
upgaze, paralysis of
urea-cycle enzymopathies
uric acid, low
urinary 17 hydroxycorticosteroids
urinary 17 ketosteroids
valvulopathy
vascular endothelial growth factor
vein of Galen
ventriculostomy, endoscopic
viral infection, CNS
visual acuity, decreased
visual field defect
visual field testing
visual impairment
visual loss
visual tracking
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight gain
weight loss
Werner's syndrome
wheelchair
white matter disease
whole genome sequencing
wide based gait
wrist drop
xeroderma pigmentosa
x-linked mental retardation
x-ray, cervical spine
Showing articles 900 to 950 of 1868 << Previous Next >>

Why Would You Remove Half a Brain? Outcome of 58 Children after Hemispherectomy-Johns Hopkins 1968-96
Pediatrics 100:163-171, Vining,E.P.G.,et al, 1997

Clinicopath Conf
Dysembryoplastic Neuroepithelial Tumor, Case 14-1997, NEJM 336:1373-1379997., , 1997

Gabapentin Monotherapy:An 8-Day, Study in Hosp Pts with Refractory Complex Partial or Secondarily Gen Seizures
Neurol 49:739-745, Bergey,G.K.,et al, 1997

Assessment of Vagus Nerve Stimulation for Epilepsy
Neurol 49:293-297, Fisher,R.S.,et al, 1997

Focal Cortical Dysplasia:Appearance on MR Images
Radiology 203:553-559, Yagishita,A.,et al, 1997

Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
Am J Med 102:67-77, Fraser,C.L.,et al, 1997

Coma Induced by Abuse of Gamma-Hydroxybutyrate (GBH or Liquid Ecstasy) :A Case Report
BMJ 314:35-36, Thomas,G.,et al, 1997

Stroke Associated with Cardiac Surgery, Determinants, Timing, & Stroke Subtypes
Arch Neurol 54:83-87, Libman,R.B.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Adult-Onset Temporal Lobe Epilepsy Associated with Smoldering Herpes Simplex 2 Infection
Neurol 48:425-430, Cornford,M.E.&McCormick,G.F., 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

Intravenous Immune Globulin Therapy for Neurologic Diseases
Ann Int Med 126:721-730, Dalakas,M.C., 1997

Erythropoietin-Associated Hypertensive Posterior Leukoencephalopathy
Neurol 49:686-689, Delanty,N.,et al, 1997

Seizures in Medically Complex Patients
Epilepsia 38:S55-S59, Boggs,J.G., 1997

Anhidrosis:An Unusual Presentation of Diabetes Insipidus
Neurol 49:1708-1710, Shimizu,H.,et al, 1997

Long-Term Effects of Pancreatic Transplantation on Diabetic Neuropathy
Ann Neurol 42:727-736, Navarro,X.,et al, 1997

Epilepsy in Childhood
BMJ 315:924-930, Neville,B.G.R., 1997

Electroconvulsive Therapy for Treatment of Intractable Seizures, Initial Findings in Two Children
Neurol 49:1389-1392, Greisemer,D.A.,et al, 1997

If First AED Fails to Control Child's Epilepsy, What Are the Chances of Success with Next Drug
J Pediatr 131:821-824, 7941997., Camfield,P.R.,et al, 1997

Topiramate Placebo-Controlled Dose-Ranging Trial in Refractory partial Epilepsy Using 200-, 400-, and 600-mg Daily Dosages
Neurol 46:1684-1690, Faught,E.,et al, 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Treatment of Rasmussen's Syndrome with Ganciclovir
Neurol 47:925-928, McLachlan,R.S.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Lambert-Eaton Myasthenic Syndrome Presenting with Severe Respiratory Failure
Muscle & Nerve 19:1328-1333996., Nicolle,M.W.,et al, 1996

Nonmotor Fluctuations in Patients with Parkinson's Disease
Neurol 47:1180-1183, Hillen,M.E.&Sage,J.I., 1996

Nerve Growth Factor and Diabetic Neuropathy
Lancet 348:1044-1045, Dyck,P.J., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

New Antiepileptic Drugs:A Systematic Review of Their Efficacy and Tolerability
BMJ 313:1169-1174, 1157, 1158996., Marson,A.G.,et al, 1996

Long Term Use of Lamotrigine & Vigabatrin in Severe Refractory Epilepsy:Audit of Outcome
BMJ 313:1184-1185, 11571996., Walker,M.C.,et al, 1996

Refractory Epilepsy:Comparison of MR Imaging, CT, and Histopathologic Findings in 117 Patients
Radiology 201:97-105, Bronen,R.A.,et al, 1996

Vagus Nerve Stimulation for the Treatment of Medically Intractable Seizures
Arch Neurol 53:1176-1180, Salinsky,M.C.,et al, 1996

Abnormal Heart Rate Variability as a Manifestation of Autonomic Dysfunction in Hemispheric Brain Infarction
Stroke 27:2058-2063, Korpelainen,J.T.,et al, 1996

Treatment of End Stage Dilated Cardiomyopathy
Br Heart J 72:S52-S56, O'Connell,J.B.,et al, 1996

The Treatment of Postprandial Hypotension in Autonomic Failure with 3, 4-DL-Threo-Dihydroxyphenylserine
Neurol 47:1414-1420, 13701996., Freeman,R.,et al, 1996

Stimulus-Evoked Sinus Arrest in Severe Guillain-Barre Syndrome:A Case Report
Neurol 47:1239-1242, Minahan,R.E.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Spinal Cord Infarction:Etiology and Outcome
Neurol 47:321-330, Cheshire,W.P.,et al, 1996

Temporal Lobectomy for Refractory Epilepsy
JAMA 276:470-475, Sperling,M.R.,et al, 1996

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

Felbamate-Associated Fatal Acute Hepatic Necrosis
Neurol 46:1457-1459, O'Neil,M.G.,et al, 1996

Clinical Profile of Patients with Epileptic and Nonepileptic Seizures
Neurol 46:1530-1533, Devinsky,O.,et al, 1996

Epstein-Barr Virus-Associated Acute Autonomic Neuropathy
Ann Neurol 40:453-455, Bennett,J.L.,et al, 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
Lancet 347:28-29, Heafield,M.T.E.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

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

Brain Damage and Postoperative Hyponatremia:The Role of Gender
Neurol 46:323-328, Aruy,J.C.&Arieff,A.I., 1996



Showing articles 900 to 950 of 1868 << Previous Next >>