Home > Node > Subnode Stomatocytosis Lo, S.S.; Hitzig, W.H.; Marti, H.R. Schweizerische Medizinische Wochenschrift 100(46): 1977-19791970ISSN/ISBN: 0036-7672 PMID: 5507841 Document Number: 27682 Document emailed within 1 workday Purchase for $29.90 Secure & encrypted paymentsRelated DocumentsKurnolski, I. 1973: A case of anemia with stomatocytosis Vutreshni Bolesti 12(3): 99-101Carella, M.; Stewart, G.W.; Ajetunmobi, J.F.; Schettini, F.; Delaunay, J.; Iolascon, A. 1999: Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia Haematologica 84(9): 862-863Rix, M.; Bjerrum, P.J.; Wieth, J.O.; Frandsen, B. 1991: Congenital stomatocytosis with hemolytic anemia--with abnormal cation permeability and defective membrane proteins Ugeskrift for Laeger 153(10): 724-726Vives-Corrons, J.L.; Carrera, A.; Triginer, J.; Kahn, A.; Rozman, C. 1975: Haemolytic anaemia due to congenital deffect in phosphohexoseisomerase. Report of a new variant (PHI-Barcelona) with stomatocytosis and increased osmotic fragility Sangre 20(2): 197-206Smith, J.E.; Moore, K.; Boyington, D.; Potter, K.A. 1983: Glutathione metabolism in canine hereditary stomatocytosis with mild erythrocyte glutathione deficiency Journal of Laboratory and Clinical Medicine 101(4): 611-616Yawata, Y. 1983: Recent progress in research on red cell membrane disorders in Japan: pathogenesis of microspherocytosis in hereditary spherocytosis, sodium transport abnormalities in stomatocytosis, and homeo-adaptive compensatory mechanism for membrane fluidity in red cell membrane lipid abnormalities Nihon Ketsueki Gakkai Zasshi: Journal of Japan Haematological Society 46(7): 1426-1440