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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 1000 to 1050 of 1243 << Previous Next >>

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Abnormal Visual Evoked Potentials in Myotonic Dystrophy
Neurol 33:1622-1625, Cott,P.S.,et al, 1983

Families with Myotonic Dystrophy with & without Cardiac Involvement
Arch Int Med 143:2134-2136, Hawley,R.J.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

ACTH & Prednisone in Childhood Seizure Disorders
III, et al, Neurol 33:966-970983., Snead,O.C., 1983

Temporal Lobe Astrocytoma with Infantile Spasms
Ann Neurol 14:695-696, Mimaki,T.,et al, 1983

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Radionuclide Angiocardiographic Analysis of Myocardial Function in Myotonic Muscular Dystrophy
Neurol 33:657-660, Hartwign,G.B.,et al, 1983

The Treatment of Myotonia:Evaluation of Chronic Oral Taurine Therapy
Neurol 33:599-603, Durelli,L.,et al, 1983

Myasthenia Gravis In Children:Long-Term Follow-up
Ann Neurol 13:504-510, Rodriguez,M.,et al, 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Cyanotic Congenital Heart Disease with Suspected Stroke, Should All Patients Receive Antibiotics
Arch Neurol 40:209-212, Kurlan,R.,et al, 1983

Capsular Stroke as a Cause of Hemiplegia in Infancy
Neurol 33:1044-1046, Young,R.S.K.,et al, 1983

Pyridoxine-Dependency Seizure:Report of a Rare Presentation
Ann Neurol 13:103-104, Krishnamoorthy,K.S., 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Hypoxic-Ischemic Encephalopathy in the Newborn
Arch Neurol 40:261-266, Fenichel,G.M., 1983

Epilepsies of Infancy & Childhood
Ann Neurol 13:113-124, Gomez,M.R.,et al, 1983

High Dose Gammaglobulin for Intractable Childhood Epilepsy
Lancet 2:162-163, Ariizumi,M.,et al, 1983

Long-Term Prognosis in Two Forms of Childhood Epilepsy:Absence Seizures & Epilepsy with Rolandic EEG Foci
Ann Neurol 13:642-648, Loiseau,P.,et al, 1983

Corpus Callosotomy for Control of Intractable Epilepsy in Children
Neurol 33:891-897, Geoffroy,G.,et al, 1983

High Intravenous Phenytoin Dosage Requirement in a Newborn Infant
Neurol 33:106-108, Whelan,H.T.,et al, 1983

Paraldehyde Therapy in Childhood Status Epilepticus
Arch Neurol 40:477-480, Curless,R.G.,et al, 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Early Prognosis of Epilepsy
BMJ 285:1699-1701, Shorvon,S.D.,et al, 1982

Efficacy of Phenobarbital Monotherapy in Treatment of Neonatal Seizures-relationship to Blood Levels
Neurol 32:1401-1404, Gal,P.,et al, 1982

Prognosis In Childhood Epilepsy
NEJM 306:831-836, Thurston,J.H.,et al, 1982

Prognosis Of Childhood Epilepsy-Another Look
NEJM 306:861-862, Berg,B.O., 1982

Seizure Recurrence After A First Unprovoked Seizure
NEJM 307:522-528, Hauser,W.A.,et al, 1982

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

Use of Valproic Acid in Treatment of Infantile Spasms
Arch Neurol 39:49-52, Bachman,D.S., 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Progressive Dyskinesia Due to Internal Cerebral Vein Thrombosis
Neurol 32:769-772, Solomon,G.E.,et al, 1982

Middle Cerebral Artery Occlusion with Migraine
Stroke 13:308-311, Castaldo,J.E.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Acute Neurological Dysfunction Associated with Destructive Lesions of the Basal Ganglia in Children
Ann Neurol 12:328-332, Goutieres,F.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Fenfluramine In Autism
NEJM 307:1450-1451, Ruttenberg,B.A., 1982

Infantile Autism Associated with the Fragile-X Syndrome
Journal of Autism & Developmental Disorders 12:295-301982., Meryash,D.L.,et al, 1982



Showing articles 1000 to 1050 of 1243 << Previous Next >>