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The Journal of Clinical Investigation|September 1, 1990
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-associationW T Tse, M C Lecomte, F F Costa, et al.Endocrinology|July 18, 2009
Absence of estrogen receptor-related-alpha increases osteoblastic differentiation and cancellous bone mineral densityI Delhon, S Gutzwiller, F Morvan, et al.Annales De Chirurgie|January 1, 1989
[Multiple primary lung cancers. The importance of early diagnosis and survival after a new surgical excision]X Mousset, J Deslauriers, M Beaulieu, et al.Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 16, 2013
Demonstration of a 13-keV Kr K-shell x-ray source at the National Ignition FacilityK B Fournier, M J May, J D Colvin, et al.Acta Anaesthesiologica Belgica|January 1, 1986
The peroperative management in multiple organ donors: a crucial phase in organ transplantationJ P Squifflet, M Carlier, B Gribomont, et al.British Journal of Cancer|February 6, 2003
Cell cycle checkpoint status in human malignant mesothelioma cell lines: response to gamma radiationC Vivo, C Lecomte, F Levy, et al.Blood|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.Journal of Visceral Surgery|March 14, 2021
Management of abdominal emergencies in adults using telemedicine and artificial intelligenceG Gorincour, O Monneuse, A Ben Cheikh, et al.The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, et al.Pageof 35