DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989
The Diagnostic Sensitivity of Electrophysiologic Testing in patients with Syncope Caused by Transient Bradycardia
NEJM 321:1703-1707, Fujimura,O.,et al, 1989
Renal Replacement Treatment in Patients with Spina Bifida or Spinal Cord Injury
BMJ 299:1506, Muralikrishna,G.S.,et al, 1989
Partial Seizures with Visual Disturbance Treated by Radiotherapy of Cavernous Hemangioma
Ann Neurol 26:782-785, Lance,J.W.&Smee,R.I., 1989
Electrocardiographic Changes During Electrographic Seizures
Arch Neurol 46:1169-1170, Keilson,M.J.,et al, 1989
The Importance of the Electrocardiogram in Ambulatory Electroencephalographic Recordings
Arch Neurol 46:1171-1174, Nousiainen,U.,et al, 1989
Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989
Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989
Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989
Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989
Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989
Perinatal Asphyxia and Cerebral Palsy
Am J Dis Child 143:1139-1140, Bedrick,A.D., 1989
Chiasmal Apoplexy:Haemorrhage from a Cavernous Malformation in the Optic Chiasm
JNNP 52:1095-1099, Regli,L.,et al, 1989
MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989
Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989
Upper Limb Emboli
J Cardiovasc Surg 30:165-168, Kaar,G.,et al, 1989
Advances in Neurology
JAMA 261:2859-2862, Joynt,R.J., 1989
REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989
Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989
Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989
Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989
Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989
Cerebrovascular Disorders of Infancy
In Handbk of Clin Neurol, Elsevier Sci Publ, NY, 2:3188., Salam-Adams,M.&Adams,R.D., 1988
Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988
Neuro-Ophthalmologic Complications of Cardiac Catheterization
Neurol 38:483-485, Kosmorsky,G.,et al, 1988
Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988
MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
Management of Aneurysmal Subarachnoid Hemorrhage
Stroke 19:1300-1305, Biller,J.,et al, 1988
Anticoagulant Drugs in the Elderly, Controversies in Therapeutics
BMJ 297:1260-1263, Lowe,G.D.O.&Scott,P.J.W., 1988
Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988
Risk of Brain Infarction in Familial Hypercholesterolemia
Stroke 19:1097-1100, Kaste,M.&Koivisto,P., 1988
Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988
Clinical Predictors of Electrophysiologic Findings in Pts with Syncope of Unknown Origin
Arch Int Med 148:1922-1928, Denes,P.,et al, 1988
Electrocerebral Accompaniments of Syncope Associated with Malignant Ventricular Arrhythmias
Ann Int Med 108:791-796, Aminoff,M.J.,et al, 1988
Minor Anomalies in Offspring of Epileptic Mothers
J Pediatr 112:521-529, 579-5811988., Gaily,E.,et al, 1988
MR Imaging of Intrachiasmatic Hemorrhage
J Comput Assist Tomogr 12:535-536, Moffit,B.,et al, 1988
Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988
Familial Parkinsonism, Apathy, Weight Loss & Central Hypoventilation:Successful Long-Term Management
Neurol 38:637-639, Roy,E.P.,et al, 1988
Parkinson's Disease in a Nationwide Twin Cohort
Neurol 38:1217-1219, Marttila,R.J.,et al, 1988
Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
Wertelecki. W. , et al, NEJM 319:276-2838., , 1988
Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988
Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988
Clinicopath Conf
Mastoiditis with Right Transverse-Sinus and Sigmoid-Sinus Thrombosis, Case Record 20-1988, NEJM 318:, 321328,1988., 1988
Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988
Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988
Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988
Characterization of Dystrophin in Muscle-Biopsy Spec from Pts with Duchenne's or Becker's Muscular Dystrophy
NEJM 318:1363-1368, 13921988., Hoffman,E.P.,et al, 1988
Dystrophin
Editorial, Lancet 2:429-4301988., , 1988
Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988