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Blood|November 1, 1976
Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesisA Kahn, D Cottreau, C Boyer, et al.Human Genetics|September 1, 1993
Spectrin alpha IIa variant in dominant and non-dominant spherocytosisP Boivin, C Galand, I Devaux, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1988
[Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants]M C Lecomte, D Dhermy, H Gautero, et al.Acta Haematologica|January 1, 1984
Hereditary elliptocytosis with a spectrin molecular defect in a white patientM C Lecomte, D Dhermy, M Garbarz, et al.British Journal of Haematology|November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variantsM C Lecomte, M Garbarz, H Gautero, et al.British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.Blood|July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact siteN Parquet, I Devaux, L Boulanger, et al.Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.Pageof 34