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Differential
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abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
Alexanders disease
Alexanders disease, adult onset
ammonia
amniocentesis
Angelman syndrome
anorexia
aspartate aminotransferase
astrogliopathy
ataxia
ataxic gait
auditory and vestibular pathways
autonomic dysfunction
B 12 deficiency
B 12 deficiency, infants
bacterial infection
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
biologic markers
bone age
brain biopsy
brainstem, lesion of
breast feeding
Brown-Vialetto-Van Laere syndrome
bulbar palsy
calcification, intracranial
carbonic anhydrase II deficiency
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
cataracts, congenital
celiac disease, childhood
cerebellar atrophy, secondary
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonarterial territory
cerebrovascular accident, recurrent
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 19
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clubbing of fingers
coma
complications
compression fracture
congenital infection, CNS
congenital infection, viral
congenital malformation
consanguinity
contractures, joint
Cornelia de Lange syndrome
cortical blindness
cortical infarction
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cultured skin fibroblasts
cystic fibrosis, neurologic complications with
cystinosis
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diarrhea
diencephalic syndrome
differential diagnosis
digits, abnormal
disability, neurological
drooling
dysarthria
dysmorphic
dysphagia
dystonia
eating disorder
electroencephalogram, abnormalities of
encephalomyelitis
encephalopathy
encephalopathy, neonatal
enzyme, defect
epileptic encephalopathy
evoked potentials
eye movement, disorders of
eyebrows, abnormal
facial appearance, abnormal
failure to thrive
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
floppy infant
fracture, pathologic
gait disorder
galactosemia
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genital hypoplasia
GFAP gene
glioma
gluten-free diet
growth hormone deficiency
growth retardation
hand deformity
hand flapping
head circumference
hearing loss
hemianopia
hemiparesis
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
hirsutism
human immunodeficiency virus type 1
hydrocephalus
hyperammonemic encephalopathy
hyperbilirubinemia
hyperphagia
hyperreflexia
hypogonadism
hypopigmentation of skin
hyporeflexia
hypothalamus, neoplasm of
hypothermia
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
infection
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
irritability
jaundice
Leigh's disease
lens, dislocation of
lenticular nucleus, lesion of, bilateral
lethargy
leukodystrophy
leukotrienes
life expectancy
liver disease
low birth weight
lymphadenopathy
lymphocytic interstitial pneumonitis
lymphoma
macrocephaly
malabsorption
MELAS syndrome
meningitis, CSF cell count-normal
mental retardation
metabolic acidosis
metabolic disorder, primary
microcephaly
micrognathia
micromelia
migratory lesion pattern
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
molybdenum cofactor deficiency
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, serial
muscle biopsy
myelination of nervous system
myoclonus
nasal bridge, wide
nausea and vomiting
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathy
nose, abnormal
nutritional deficiency
nystagmus
obesity
occipital lobe, infarction
occipital lobe, lesion of
oligodactyly
opisthotonus
opportunistic infection
optic atrophy
ornithine transcarbamylase deficiency
osteoporosis
pain, leg
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
parotitis
paroxysmal neurologic deficits
partial thromboplastin time, prolonged
patient information and support
peripheral blood smear
peroxisomal disease
personality change
phocomelia
photophobia
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prothrombin time, prolonged
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pulmonary infiltrates
pupil, ectopic-congenital
pyramidal tract dysfunction
quadriparesis
recurrent
renal failure
renal tubular acidosis
respiratory failure
review article
rhabdomyosarcoma
riboflavin transporter deficiency
Rosenthal fibers
saddle nose
screaming
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
seizure, neonatal
serum alanine aminotransferase
short stature
simian crease
skin, hematoma
skin, lesions in neurologic disorders
spastic diplegia
spasticity
spinal cord, compression of
strabismus
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuporous
suck, poor
symmetric brain lesions
syndactyly
synophrys
systemic illness
temper tantrums
thalamus, lesion of
thalamus, lesion of-bilateral
toe walking
tongue, protrusion of
transplacental virus infections
treatment of neurologic disorder
tremulousness
trichopoliodystrophy
urea-cycle enzymopathies
uric acid, low
urine test for metabolic disorders
vegetarianism
vertebral erosion
vitamin deficiency
vitamin K
vitamin K deficiency
weakness
weakness, generalized
weakness, progressive
white matter disease
wide based gait
Wolff-Parkinson-White syndrome
wrist drop
Showing articles 850 to 900 of 1673 << Previous Next >>

Complications of Intravenous Immune Globulin Treatment in Neurologic Disease
Neurol 47:674-677, Brannagan III,T.H.,et al, 1996

Fever, Convulsions and Coma in Scleromyxedema:A"Dermato-Neuro Syndrome"
Neurol 46:1778-1779, River,Y.,et al, 1996

Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 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

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

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

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

Magnetic Resonance Imaging of Brain Iron in Health and Disease
J Neurol Sci 134:19-26,1, Vymazal,J.,et al, 1995

Site of Autonomic Dysfunction in a Patient with Ross'Syndrome and Postganglionic Horner's Syndrome
Neurol 45:2094-2096, Wolfe,G.I.,et al, 1995

Conditions That Mimic Stroke in the Emergency Department
Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995

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

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

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Tailored Ant Temporal Lobectomy:Relation Between Extent of Resec of Mesial Structures & Postsurg Sz Outcome
Arch Neurol 52:173-178, Kanner,A.M.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

The Effect of Intensive Diabetes Therapy on Development & Progression of Neuropathy
The Diabetes Control & Compl Trial Res Gr, Ann Int Med 122:561-56895., , 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Fatal Infantile Polyarteritis Nodosa with Predominant Central Nervous System Involvement
Stroke 26:699-701, Engel,D.G.,et al, 1995

Complications with Shunts in Adults with Spina Bifida
BMJ 311:286-287, Tomlinson,P.&Sugarman,I.D., 1995

Panic Attacks and Panic Disorder:The Great Neurologic Imposters
Semin Neurol 15:126-132, Stahl,S.M.&Soefje,S., 1995

Occupational Outcome After Temporal Lobectomy for Refractory Epilepsy
Neurol 45:970-977, Sperling,M.R.,et al, 1995

Surgical Treatment of Temporal Lobe Epilepsy:Clinical, Radiological and Histopathological Findings in 178 Patients
JNNP 58:666-673, Zentner,J.,et al, 1995

Bilaterally Symmetric Hippocampi and Surgical Outcome, Jack
Neurol 45:1353-1358, Jr,C.R.,et al, 1995

Hippocampal Volumetrics Differentiate Pts with Temporal Lobe Epilepsy & Extratemporal Lobe Epil
Arch Neurol 52:819-824, Gilmore,R.L.,et al, 1995

Preoperative MRI Predicts Outcome of Temporal Lobectomy:An Actuarial Analysis
Neurol 45:1358-1363, 12481995., Berkovic,S.F.,et al, 1995

Psychiatric Classification of Nonconversion Nonepileptic Seizures
Arch Neurol 52:199-201, Alper,K.,et al, 1995

A Randomized Controlled Trial of Chronic Vagus Nerve Stimulation for Treatment of Medically Intractable Seizures
Neurol 45:224-230, Cereghino,J.,et al, 1995

Rational Polypharmacy in the Treatment of Epilepsy
(Ed) , Neurol (suppl) 45:S1-S38., Wilder,B.J., 1995

Contralateral Hyperhidrosis after Cerebral Infarction:Clinicoanatomic Correlations in Five Cases
Stroke 26:896-899, Kim,B.S.,et al, 1995

Visual System Abnormalities in Adrenomyeloneuropathy
Ann Neurol 37:550-552, Kaplan,P.W.,et al, 1995

Autonomic and Thermal Sensory Symptoms and Dysfunction After Stroke
Stroke 26:1379-1385, Naver,H.,et al, 1995

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Diminished Nocturnal Blood Pressure Decline and Lesion Site in Cerebrovascular Disease
Stroke 26:829-833, Yamamoto,Y.,et al, 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Fulminant Hepatic Failure Induced by Lamotrigine
BMJ 311:292, Makin,A.J.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
Neurol 45:995-997, Kulisevsky,J.,et al, 1995

Manganese and Chronic Hepatic Encephalopathy
Lancet 346:270-274, Krieger,D.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995



Showing articles 850 to 900 of 1673 << Previous Next >>