A Prospective Study on Sudden Unexpected Death in Epilepsy
Ann Neurol 26:195-203, Leestma,J.E.,et al, 1989
Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989
Radiologic Screening for von Hippel-Lindau Disease:Role of Gd-DTPA Enhanced MR Imaging of the CNS
J Comput Assist Tomogr 13:743-755, Filling-Katz,M.R.,et al, 1989
Serial Electrocardiographic Recording in Aneurysmal Subarachnoid Hemorrhage
Stroke 20:1162-1167, Brouwers,P.J.A.M.,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
A Prospective Study of Atrial Fibrillation and Stroke
Stroke 20:1648-1652, D'Olhaberriague,L.,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
The Rational Management of Idiopathic Intracranial Hypertension
Arch Neurol 46:1049-1051, Corbett,J.J.&Thompson,H.S., 1989
The Cost to the Central Nervous System of Climbing to Extremely High Altitude
NEJM 321:1714-1719, 1989,, Hornbein,T.F.,et al, 1989
Problems in Genetic Prediction for Huntington's Disease
Lancet 2:601-603, Morris,M.J.,et al, 1989
Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,et al, 1989
Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989
The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989
The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989
Fatigue Syndrome:Neurasthenia Revived, Psychiatric Illnesses are Worth Considering
BMJ 298:1199-1200, White,P., 1989
Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989
Reversibility of CT and MR Findings in Neuro-Bechet Disease
J Comput Assist Tomogr 13:669-673, Patel,D.V.,et al, 1989
Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989
Multiple Pyogenic Brain Abscesses:An Analysis of 21 Patients
JNNP 52:591-594, Basit,A.S.,et al, 1989
Delayed Neurologic Display in Murine Typhus, Report of Two Cases
Arch Int Med 149:949-951, Samra,Y.,et al, 1989
Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989
Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 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
Rippling Muscle Disease
Arch Neurol 46:405-408, Ricker,K.,et al, 1989
Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989
Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989
Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.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
A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
NEJM 320:1331-1333, Parker,W.D.,et al, 1989
Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989
Neurological and Developmental Findings in Children with Cataracts
Am J Dis Child 13:706-710, Pike,M.G.,et al, 1989
Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989
Clinicopath Conf
Metastatic Adenocarcinoma Compatible with Breast Origin of Mastoid and Temporal Bone, Case Record 14, 189,NEJM 320:924-930,1989., 1989
Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
NEJM 320:1735-1740, Schindler,D.,et al, 1989
Experience with Anencephalic Infants as Prospective Organ Donors
NEJM 321:344-350, Peabody,LJ.L.,et al, 1989
Anencephalic Newborns, Can Organs be Transplanted Before Brain Death?
NEJM 321:388-391, Truog,R.D.&Fletcher,J.C., 1989
On the Use of Anencephalic Infants as Organ Donors
et al, NEJM 321:391-3931989., Medearis,D.N.&Holmes,L.B., 1989
Neurologic Complications in Long-Standing Nephropathic Cystinosis
Arch Neurol 46:543-548, Fink,J.K.,et al, 1989
Epilepsy in Women of Childbearing Age, If Anticonvulsants Cannot be Avoided Use Carbamazepine
BMJ 298:581, Saunders,M., 1989
Pattern of Malformations in the Children of Women Treated with Carbamazepine During Pregnancy
NEJM 320:1661-1666, Jones,K.L.,et al, 1989
Aicardi Syndrome in Two Sisters
J Pediatr 115:282-283, Molina,J.A.,et al, 1989
Valproate and Spina Bifida
BMJ 298:1300-1301, Oakeshott,P.&Hunt,G.M., 1989
Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
Arch Neurol 46:184-187, Allard,J.C.,et al, 1989
Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989
Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989
Placebo-Controlled, Randomised Trial of Warfarin & ASA for Prevention of Thromboembolic Complic in Chronic A Fib
Lancet 1:175-179, Petersen,P.,et al, 1989
Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989