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W A Muir

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Medical Decision Making : an International Journal of the Society for Medical Decision Making|January 1, 1982
Diagnostic workup bias in the evaluation of a test. Serum ferritin and hereditary hemochromatosisD F Ransohoff, W A Muir
Archives of Internal Medicine|November 1, 1980
Bullous pemphigoid as a manifestation of chronic lymphocytic leukemiaL T Goodnough, W A Muir
The Journal of Biological Chemistry|April 25, 1984
Iron transport across brush-border membranes from normal and iron-deficient mouse upper small intestineW A Muir, U Hopfer, M King
American Journal of Human Genetics|May 1, 1984
Erythrocyte pyruvate kinase deficiency in the Ohio Amish: origin and characterization of the mutant enzymeW A Muir, E Beutler, C Wasson
American Journal of Hematology|January 1, 1981
Labile anticoagulant in a patient with lymphomaG H Goldsmith, H Saito, W A Muir
JAMA|October 13, 1978
Methyprylon-induced bone marrow suppression in siblings. An inherited defect?G D McLaren, M A Doukas, W A Muir
Critical Reviews in Clinical Laboratory Sciences|January 1, 1983
Iron overload disorders: natural history, pathogenesis, diagnosis, and therapyG D McLaren, W A Muir, R W Kellermeyer
The American Journal of Medicine|May 1, 1984
Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine familiesW A Muir, G D McLaren, W Braun, et al.
American Journal of Medical Genetics|January 1, 1983
Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levelsW A Muir, J Knoke, A Martin, et al.
Archives of Dermatology|December 1, 1980
Premature cataracts in a family with hidrotic ectodermal dysplasiaP G Hazen, I Zamora, W E Bruner, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Medical Decision Making : an International Journal of the Society for Medical Decision Making|January 1, 1982
Diagnostic workup bias in the evaluation of a test. Serum ferritin and hereditary hemochromatosisD F Ransohoff, W A Muir
Archives of Internal Medicine|November 1, 1980
Bullous pemphigoid as a manifestation of chronic lymphocytic leukemiaL T Goodnough, W A Muir
The Journal of Biological Chemistry|April 25, 1984
Iron transport across brush-border membranes from normal and iron-deficient mouse upper small intestineW A Muir, U Hopfer, M King
American Journal of Human Genetics|May 1, 1984
Erythrocyte pyruvate kinase deficiency in the Ohio Amish: origin and characterization of the mutant enzymeW A Muir, E Beutler, C Wasson
American Journal of Hematology|January 1, 1981
Labile anticoagulant in a patient with lymphomaG H Goldsmith, H Saito, W A Muir
JAMA|October 13, 1978
Methyprylon-induced bone marrow suppression in siblings. An inherited defect?G D McLaren, M A Doukas, W A Muir
Critical Reviews in Clinical Laboratory Sciences|January 1, 1983
Iron overload disorders: natural history, pathogenesis, diagnosis, and therapyG D McLaren, W A Muir, R W Kellermeyer
The American Journal of Medicine|May 1, 1984
Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine familiesW A Muir, G D McLaren, W Braun, et al.
American Journal of Medical Genetics|January 1, 1983
Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levelsW A Muir, J Knoke, A Martin, et al.
Archives of Dermatology|December 1, 1980
Premature cataracts in a family with hidrotic ectodermal dysplasiaP G Hazen, I Zamora, W E Bruner, et al.
Pageof 2