Functional Abilities at Age 4 Years of Children Born Before 29 Weeks of Gestation
BMJ 306:1715-1718, Johnson,A.,et al, 1993
Prevention of Congenital Abnormalities by Periconceptional Multivitamin Supplementation
BMJ 306:1645-1648, Czeizel,A.E., 1993
A Predictive Model for Delirium in Hospitalized Elderly Medical Patients Based on Admission Characteristics
Ann Int Med 119:474-481, Inouye,S.K.,et al, 1993
Syncope After Eating
NEJM 328:1572, Schima,W.,et al, 1993
Low Back Pain
BMJ 306:901-909, Frank,A., 1993
Epilepsy and Pregnancy
BMJ 307:492-495, O'Brien,M.D.&Gilmour-White,S., 1993
Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993
Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993
The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993
Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
JAMA 270:2321-2325, Babul,R.,et al, 1993
Secondary Prevention in Non-Rheumatic Atrial Fib After TIA or Minor Stroke
European Atrial Fibrillation Trial Study Group, Lancet 342:1255-1262, 1251-1252993., , 1993
A Model for Management of Patients with Stroke During the Acute Phase Outcome and Economic Implications
Stroke 24:1823-1827, Odderson,I.R.&McKenna,B.S., 1993
Cranial Nerve Palsies in Spontaneous Carotid Artery Dissection
JNNP 56:1191-1199, Sturzenegger,M.&Huber,P., 1993
Fetal Alcohol Syndrome and Fetal Alcohol Effects
Comm of Substance Abuse & Comm on Children with Disabilitites, Pediatrics 91:1004-100693., , 1993
Visual Failure and Optic Atrophy Associated with Chlorambucil Therapy
BMJ 306:109, Yiannakis,P.H.&Larner,A.J., 1993
Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993
Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993
Periconceptional Folic Acid Exposure and Risk of Occurrent Neural Tube Defects
JAMA 269:1257-1261, 12921993., Werler,M.M.,et al, 1993
Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993
The Neurological Complciations of Sepsis
Ann Neurol 33:94-100, Bolton,C.F.,et al, 1993
Reduction in Incidence of Optic Nerve Disease with Annual Ivermectin to Control Onchocerciasis
Lancet 341:130-134, 153-1541993., Abiose,A.,et al, 1993
Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993
Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993
Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993
Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993
Idiopathic Intracranial Hypertension (Pseudotumor Cerebri) Descriptive Epidemiology in Rochester, MN, 1976-90
Arch Neurol 50:78-80, Radhakrishnan,K.,et al, 1993
Pseudotumor Cerebri:CT Findings and Correlation with Vision Loss
AJR 160:143-146, Gibby,W.A.,et al, 1993
Reversible Neurologic Toxicity with Fludarabine Phosphate for Mycosis Fungiodes & Chronic Lymphocytic Leukemia
Ann Int Med 118:114-116, Cohen,R.B.,et al, 1993
Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993
Guillain-Barre Syndrome (GBS) with Bilateral Optic Neuritis and Central White Matter Disease
Neurol 43:842-843, Nadkarni,M.&Lisak,R.P., 1993
Catastrophic Visual Loss Due to Cryptococcus Neoformans Meningitis
Medicine 72:207-224, Rex,J.H.,et al, 1993
Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993
Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993
Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993
Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993
Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993
Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993
Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993
Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993
Visual Evoked Potential in Adrenoleukodystrophy:Glycerol Trioleate and Lorenzo Oil
Ann Neurol 34:169-174, 1211993., Kaplan,P.W.,et al, 1993
Klippel-Feil Syndrome:CT and MR of Acquired & Congen Abnormal of Cervical Spine & Cord
J Comput Assist Tomogr 17:215-244, Ulmer,J.L.,et al, 1993
Aicardi's Syndrome:MR Appearance of Unusual Orbital and Ventricular Cystic Lesions
AJR 160:601-603, Mehta,r.C.,et al, 1993
Association of Facial Hemangiomas with Dandy-Walker and Other Posterior Fossa Malformations
J Pediatr 122:379-384, Reese,V.,et al, 1993
Neuroradiological Manifestations of Focal Polymorphic Delta Activity in Children
Arch Neurol 50:181-184, Maytal,J.,et al, 1993
Magnetic Resonance Imaging
NEJM 328:708-716, 785-7911993., Edelman,R.R.&Warach,S., 1993
Effects of Stimulus Intensity & Electrode Placement on Efficacy & Cognition of ECT
NEJM 328:839-846, 8821993., Sackeim,H.A.,et al, 1993
Permanent Global Amnesia with Unknown Etiology
Neurol 43:326-332, Kritchevsky,M.&Squire,L.R., 1993
Brief Report:Treatment of Vasospastic Amaurosis Fugax with Calcium-Channel Blockers
NEJM 329:396-398, 4261993., Winterkorn,J.M.S.,et al, 1993
Reflex Anoxic Seizures
BMJ 307:214-215, Appleton,R.E., 1993
Medicare Hospital Utilization Review for Ischemic Cerebrovascular Disease
Neurol 43:650-654, Lanska,D.J., 1993