Renal Manifestations of Angiotrophic Lymphoma: Clinicopathological Features
Nephrol Dial Transplant 12:190-194, Sepandj, F.,et al, 1997
Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996
Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996
Clinicopath Conf
Hypertension, MI, and Cerebral Infarctions with Pheochromocytoma, Am J Med 100:357-36496., , 1996
Clinicopath Conf
Qunidine-Induced Thrombocytopenia, Cerebral Hemorrhage, Case 15-1995, NEJM 332:1363-137095., , 1995
Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995
Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995
Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994
Anticoagulant-Related Bleeding:Clinical Epidemiology, Prediction, and Prevention
Am J Med 95:315-328, Landefeld,C.S.&Beyth,R.J., 1993
McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992
Clinicopath Conf
Multiple Myeloma, Presenting as Plasmacytoma of Bone Extending into Sphenoid Sinus, Case 21-1992, NE, M 31417-1424,1992., 1992
Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992
Uses and Technique of Pediatric Lumbar Puncture
Am J Dis Child 146:1160-1165, Ward,E.&Gushurst,C.A., 1992
Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991
Cranial Neuropathy Associated with Primary Amyloidosis
Ann Neurol 29:451-454, Traynor,A.E.,et al, 1991
Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991
Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991
VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991
Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
J Pediatr 119:42-45, Riviello,J.J.,et al, 1991
Intellectual Outcome in Children with Maple Syrup Urine Disease
J Pediatr 119:46-50, Kaplan,P.,et al, 1991
Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991
Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991
Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990
Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989
Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989
Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989
Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989
CT & MRI in Maple Syrup Urine Disease
Neurol 38:486-488, Uziel,G.,et al, 1988
Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988
Clinicopath Conf
Pheochromocytoma with Hemorrhagic Infarct, Catecholamine-Induced Dilated Cardiomyopathy, Case Record, 15988,NEJM 318:970-981,1988., 1988
The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988
McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988
An Adolescent with Intermittent Headache, Transient Hemiparesis, and Urinary Abnormalities
J Pediatr 113:769-776, Gruskin,A.B.&Chang,C., 1988
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987
Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987
Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986
GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985
Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985
McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985
Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984
Cerebral Computed Tomography in Maple Syrup Urine Disease
J Comput Assist Tomogr 8:410-411, Romero,F.J.,et al, 1984
Acute Ventilatory Failure & Myoglobinuria
Neurol 34:369-371, Taverner,D.,et al, 1984
Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983
Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983
Acute Myopathy Associated with Gasoline Sniffing
Neurol 33:629-631, Kovanen,J.,et al, 1983
Severe Dystonia & Myoglobinuria
Neurol 32:1195-1197, Jankovic,J.,et al, 1982
Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982
The Spectrum of Peripheral Neuropathy in Myeloma
Neurol 31:24-31, Kelly,J.J.,et al, 1981
Acute Rhabdomyolysis Associated With An Echovirus 9 Infection
Arch Int Med 140:1671-1672, Josselson,J.,et al, 1980
Rhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Arch Neurol 37:187-188, Britt,C.W.,et al, 1980