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Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.Memorias Do Instituto Oswaldo Cruz|January 1, 1994
Plasmodium falciparum proteinases: cloning of the putative gene coding for the merozoite proteinase for erythrocyte invasion (MPEI) and determination of hydrolysis sites of spectrin by Pf37 proteinaseI Florent, S Le Bonniec, B Carcy, et al.Transgenic Research|November 1, 1992
Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin geneG Grimber, C Galand, M Garbarz, et al.Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|June 6, 2012
Sarcoidosis and multiple sclerosis: systemic toxicity associated with the use of interferon-beta therapyC Carbonelli, S Montepietra, A Caruso, et al.American Journal of Hematology|October 1, 1989
Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in TunisiaA Mrad, J Kister, C Feo, et al.Blood|June 1, 1987
Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosisB Pothier, L Morlé, N Alloisio, et al.Scandinavian Journal of Haematology|November 1, 1981
Evidence for imbalanced furosemide-sensitive Na+, K+ cotransport in hereditary stomatocytosisB Chailley, C Feo, R Garay, et al.Annali Italiani Di Chirurgia|March 1, 1997
[New directions in the surgical treatment of gastroesophageal reflux. Review of the literature]V Bresadola, A P Murgia, P Zamboni, et al.European Journal of Haematology|September 1, 1987
Enrichment of blood units with young red cells (neocytes) with the IBM 2991 cell washerC Picot, R Girot, J Loutounda, et al.Gastroenterologie Clinique Et Biologique|May 1, 1984
[Primary lymphomas of the digestive tract. Therapeutic results of a series of 35 cases]A Herrera, P Solal-Celigny, P Gaulard, et al.Pageof 13