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Acta Haematologica|January 1, 1992
Potential for treatment of anaemia of prematurity with recombinant human erythropoietin: preliminary resultsR H Phibbs, K M Shannon, W C Mentzer
Pediatric Neurology|January 1, 1995
Nontraumatic fat embolism syndrome in sickle cell anemiaD P Horton, D M Ferriero, W C Mentzer
The Journal of Clinical Investigation|December 1, 1982
Missing band 7 membrane protein in two patients with high Na, low K erythrocytesW M Lande, P V Thiemann, W C Mentzer
The Journal of Biological Chemistry|September 25, 1991
Purification of band 7.2b, a 31-kDa integral phosphoprotein absent in hereditary stomatocytosisD Wang, W C Mentzer, T Cameron, et al.
Blood|November 11, 1975
Hereditary stomatocytosis: membrane and metabolism studiesW C Mentzer, W B Smith, J Goldstone, et al.
Blood|February 1, 1980
G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemiaW C Mentzer, R Warner, J Addiego, et al.
The Journal of Pediatrics|October 1, 1976
Developmental change in red blood cell volume: implication in screening infants and children for iron deficiency and thalassemia traitM A Koerper, W C Mentzer, G Brecher, et al.
The American Journal of Pediatric Hematology/Oncology|February 1, 1994
Availability of related donors for bone marrow transplantation in sickle cell anemiaW C Mentzer, S Heller, P R Pearle, et al.
Biochimica Et Biophysica Acta|November 21, 1984
Two-dimensional electrophoretic analysis of human erythrocyte cylindrinW M Lande, P V Thiemann, K A Fisher, et al.
American Journal of Medical Genetics|April 1, 1984
Prenatal diagnosis of chronic granulomatous diseaseK K Matthay, M S Golbus, D W Wara, et al.
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