Portosystemic Encephalopathy in Hereditary Hemorrhagic Telangiectasia
Am J Med 85:858-860, Fagel,W.J.,et al, 1988
The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988
MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988
Transient Tic Disorder and the Spectrum of Tourette's Syndrome
Arch Neurol 45:1200-1201, Kurlan,R.,et al, 1988
Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988
Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 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
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
Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988
Improvement of Cerebral CT Abnor Following Liver Transplant in a Patient with Wilson Disease
J Comput Assist Tomogr 12:138-149, Rothfus,W.E.,et al, 1988
Efficacy of Alprazolam for Essential Tremor
Neurol 38:241-243, Huber,S.J.&Paulson,G.W., 1988
Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988
Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988
Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988
Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988
Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988
Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988
Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988
Neurofibromatosis
Conference Statement, National Institutes of Health Consensus Development Conference, Arch Neurol 45, 57578,1988., 1988
Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
Lancet 1:1263-1265, Burton,J.L., 1988
Diagnosis and Treatment of Presymptomatic Wilson's Disease
Lancet 2:435-437, Walshe,J.M., 1988
Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988
The Familial Nature of Multiple Sclerosis:Age-Correlated Empiric Recurrence Risks for Children & Siblings of Pts
Neurol 38:990-991, Sadovnick,A.D.,et al, 1988
Treatment of Essential Tremor with Arotinolol
Neurol 38:650-652, Kuroda,Y.,et al, 1988
Essential Tremor Cured by Infarction Adjacent to the Thalamus
JNNP 51:591-592, Duncan,R.,et al, 1988
Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988
Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988
Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988
Risk of Dementia in Relatives of Patient with Alzheimer's Disease
Neurol 38:786-790, Huff,F.J.,et al, 1988
Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988
Mollaret's Meningitis, A Variant of Recurrent Hereditary Polyserositis, Both Provoked by Metaraminol
Arch Neurol 45:926-927, Barakat,M.H.,et al, 1988
Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,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
Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,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
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
Lack of Association Between Essential Tremor and Parkinson's Disease
Ann Neurol 24:23-26, Cleeves,L.,et al, 1988
Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988
Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988
Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988
McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988
Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988