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Differential
(Click to cross reference)
ataxia, cerebellar
axonal spheroid
basal ganglia
basal ganglia, lesion of
blindness
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
children
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
dental pulp biopsy
dentate nuclei
dentate nuclei, lesion of
developmental retardation
electromyogram
electron microscopy
gait disorder
genetic neurologic disorders
Hallervorden Spatz disease
hypotonia
intellectual deficit
iron, brain
lysosomal storage disease
MRI
MRI, abnormal
MRI, eye of tiger sign
MRI, gradient-echo
MRI, high signal foci on
MRI, paramagnetic effect
myoclonus
myoclonus, epilepsy
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neurologic disease, diagnoses of
neuronal cell death
optic atrophy
PANK2 mutation
quadriplegia
skin, biopsy
vision, failure of in childhood
visual evoked response
visual impairment
Showing articles 800 to 850 of 1243 << Previous Next >>

Cerebral Vasculopathy Associated with Primary Varicella Infection
Arch Neurol 47:1033-1035, Caekebeke,J.F.V.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Febrile Status Epilepticus
Pediatrics 86:611-616, Maytal,J.&Shinnar,S., 1990

National General Practice Study of Epilepsy:Recurrence After a First Seizure
Lancet 336:1271-1274, Hart,Y.M.,et al, 1990

Changing View of Prognosis of Epilepsy
BMJ 301:1112-1114, Reynolds,E.H., 1990

A Follow-up Study of Intractable Seizures in Childhood
Ann Neurol 28:699-705, Huttenlocher,P.R.&Hapke,R.J., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Acute Neuro Dysfun Assoc with Lesions of the Basal Ganglia:Benign Form of Infantile Bilateral Striatal Necrosis
J Pediatr 117:578-581, Roig,M.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989

Duchenne Muscular Dystrophy Carrieris
Neuroradiology 31:373-376, Matsumura,K., 1989

Generalized Seizures in an Infant Due to Environmentally Acquired Cocaine
Pediatrics 84:1110-1102, Rivkin,M.&Gilmore,H.E., 1989

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Transmission of Alpers'Disease (Chr Prog Encephalopathy) Produces Exper Creutzfeldt-Jakob Disease in Hamsters
Neurol 39:615-621, Manuelidis,E.E.,et al, 1989

Rapid Sequential Phenobarbital Treatment of Neonatal Seizures
Pediatrics 83:674-678, Gilman,J.T.,et al, 1989

Neonatal Seizures:Current Concepts and Revised Classification
Pediatrics 84:422-428, Volpe,J.J., 1989

Neonatal Seizures
Editorial, Lancet 2:135-1371989., , 1989

Treatment of Infantile Spasms with High-Dose ACTH:Efficacy and Plasma Levels of ACTH and Cortisol
Neurol 39:1027-1031, Snead,O.C.,et al, 1989

A Randomized Study of Carbamazepine Versus No Medication after a First Unprovoked Seizure in Childhood
Neurol 39:851-852, Camfield,P.,et al, 1989

A Five-Year-Old Girl with Acute Renal Failure and Multiple Cerebral Infarctions
J Pediatr 115:816-823, Mauro,R.D.,et al, 1989

Surgery for Intractable Epilepsy:Issues and Outcome
Pediatrics 84:886-894, Duchowny,M.S., 1989

Convulsions in the Older Infant
BMJ 299:1331-1333, Valman,H.B., 1989

Unilateral Moya-Moya Disease:MRI Findings
Neuroradiology 31:442, Wilms,G.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Oligoantigenic Diet Treatment of Children with Epilepsy and Migraine
J Pediatr 114:51-58, Egger,J.,et al, 1989

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

Low Morbidity and Mortality of Status Epilepticus in Children
Pediatrics 83:323-331, Maytal,J.,et al, 1989

Status Epilepticus:It's Not What We've Thought or Taught
Pediatrics 83:444-445, Freemen,J.M., 1989

Etiology and Mortality of Status Epilepticus in Children, A Recent Update
Arch Neurol 46:74-76, Phillips,S.A.&Shanahan,R.J., 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
NEJM 320:1592-1597, 1621-16231989., Mendell,J.R.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Vomiting as an Ictal Manifestation of Epileptic Seizures and Syndromes
JNNP 51:1448-1451, Panayiotopoulos,C.P., 1988

When to Start Anticonvulsant Treatment in Childhood Epilepsy:The Case for Avoiding or Delaying Treatment
BMJ 297:1529-1530, Mellor,D., 1988



Showing articles 800 to 850 of 1243 << Previous Next >>