Search Results - "ANGUS MUIR, W"

HLA B27 in Ankylosing Spondylitis: Differences in Frequency and Relative Risk in American Blacks and Caucasians by Khan, M A, Braun, W E, Kushner, I, Grecek, D E, Muir, W Angus, Steinberg, A G

“…Twenty-eight HLA alleles of the A and B loci were determined in 23 American Blacks and 50 Caucasians with primary ankylosing spondylitis (AS). The prevalence…”
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Magnetic-susceptibility measurement of human iron stores by Brittenham, G M, Farrell, D E, Harris, J W, Feldman, E S, Danish, E H, Muir, W A, Tripp, J H, Bellon, E M

“…We made direct noninvasive magnetic measurements of hepatic iron stores with a specially designed superconducting quantum-interference-device (SQUID)…”
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Iron overload disorders: natural history, pathogenesis, diagnosis, and therapy by McLaren, G D, Muir, W A, Kellermeyer, R W

“…Hemochromatosis is a syndrome which, when fully expressed, is manifested by melanoderma , diabetes mellitus, and liver cirrhosis, with iron overload involving…”
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Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine families by Muir, W A, McLaren, G D, Braun, W, Askari, A

“…Hereditary hemochromatosis is an autosomal recessive disease in which the gene is linked to the HLA system. Investigation of nine unrelated probands and their…”
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Iron transport across brush-border membranes from normal and iron-deficient mouse upper small intestine by Muir, W A, Hopfer, U, King, M

“…We have studied Fe(III)-citrate and Fe(II)-ascorbate uptake by purified intestinal brush-border membrane vesicles from normal (iron-replete) and iron-deficient…”
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Protracted infusion of 5-FU with weekly low-dose cisplatin as second-line therapy in patients with metastatic colorectal cancer who have failed 5-FU monotherapy by Ahlgren, J D, Trocki, O, Gullo, J J, Goldberg, R, Muir, W A, Sisk, R, Schacter, L

“…Forty four patients who had documented progression of metastatic colorectal cancer while receiving 5-fluorouracil (5-FU) monotherapy were treated with…”
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Erythrocyte pyruvate kinase deficiency in the Ohio Amish: origin and characterization of the mutant enzyme by ANGUS MUIR, W, BEUTLER, E, WASSON, C

“…We have identified eight individuals in an Amish population in Geauga County, Ohio, who have a congenital hemolytic anemia and red cell pyruvate kinase (PK)…”
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Arthritis of hemochromatosis. Clinical spectrum, relation to histocompatibility antigens, and effectiveness of early phlebotomy by Askari, A D, Muir, W A, Rosner, I A, Moskowitz, R W, McLaren, G D, Braun, W E

“…Five patients who presented with arthritis as the sole manifestation of hereditary hemochromatosis and 51 family members were studied. Studies included…”
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Diagnostic workup bias in the evaluation of a test. Serum ferritin and hereditary hemochromatosis by Ransohoff, D F, Muir, W A

“…Two studies report markedly divergent results about the usefulness of serum ferritin in diagnosing iron overload in relatives of patients with hereditary…”
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Prenatal diagnosis of classic hemophilia by Firshein, S I, Hoyer, L W, Lazarchick, J, Forget, B G, Hobbins, J C, Clyne, L P, Pitlick, F A, Muir, W A, Merkatz, I R, Mahoney, M J

“…Prenatal diagnosis of classic hemophilia (hemophilia A) in mid-trimester was achieved by means of immunoradiometric assays for factor VIII on fetal plasma and…”
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The Prevalence of Plasma Thromboplastin Antecedent (PTA, Factor XI) Deficiency by Muir, W. Angus, Ratnoff, Oscar D.

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Methyprylon-Induced Bone Marrow Suppression in Siblings: An Inherited Defect? by McLaren, Gordon D, Doukas, Michael A, Muir, W. Angus

“…Transient bone marrow suppression in two sisters followed ingestion of the sedative-hypnotic drug methyprylon. No other pharmacologic or environmental inciting…”
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Bullous pemphigoid as a manifestation of chronic lymphocytic leukemia by Goodnough, L T, Muir, W A

“…We describe a patient with chronic lymphocytic leukemia (CLL) and bullous pemphigoid. Initial treatment with high-dose prednisone (60 mg/day for 14 days)…”
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Glucosephosphate-isomerase (GPI) deficiency: GPI elyria by Beutler, E, Sigalove, W H, Muir, W A, Matsumoto, F, West, C

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Hemochromatosis. Pathophysiologic and genetic considerations by Ross, C E, Muir, W A, Alan, B P, Graham, R C, Kellermeyer, R W

“…The clinical, genetic, and pathologic findings, and the pertinent case histories in two families with idiopathic hemochromatosis are presented. These studies…”
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Premature cataracts in a family with hidrotic ectodermal dysplasia by Hazen, P G, Zamora, I, Bruner, W E, Muir, W A

“…In a family with hidrotic ectodermal dysplasia affecting five members in three generations, bilateral premature cataracts have developed in four of the five…”
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