Pharmacy workload benchmarking: Establishing a health-system outpatient infusion productivity metric von Reichard, Jeffrey S, Garbarz, David M, Teachey, Amanda L, Allgood, Jonathan, Brown, M Jay

Volltext

Heatwave von Garbarz, Michel

Volltext

Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis von Garbarz, M., Devaux, I., Bournier, O., Grandchamp, B., Dhermy, D.

Volltext

Comparison of Hospital Mortality During ST-Segment Elevation Myocardial Infarction in the Era of Reperfusion Therapy in Women Versus Men and in Older Versus Younger Patients von Juliard, Jean-Michel, MD, Golmard, Jean Louis, MD, PhD, Himbert, Dominique, MD, Feldman, Laurent J., MD, PhD, Delorme, Laurent, MD, Ducrocq, Gregory, MD, Descoutures, Fleur, MD, Sorbets, Emmanuel, MD, Garbarz, Eric, MD, Boudvillain, Olivier, MD, Aubry, Pierre, MD, Vahanian, Alec, MD, Steg, Philippe Gabriel, MD

Volltext

Polymorphisms of the Tissue Factor Pathway Inhibitor (TFPI) Gene in Patients With Acute Coronary Syndromes and in Healthy Subjects: Impact of the V264M Substitution on Plasma Level... von Moatti, Didier, Seknadji, Patrick, Galand, Colette, Poirier, Odette, Fumeron, Frederic, Desprez, Sophie, Garbarz, Michel, Dhermy, Didier, Arveiler, Dominique, Evans, Alun, Luc, Gerald, Ruidavets, Jean-Bernard, Ollivier, Veronique, Hakim, Jacques, Aumont, Marie Claude, de Prost, Dominique

Volltext

Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis von Boulanger, L, LeCompte, M C, Dhermy, D, Garbarz, M

Volltext

Spectrin αIIa variant in dominant and non-dominant spherocytosis von BOIVIN, P, GALAND, C, DEVAUX, I, LECOMTE, M. C, GARBARZ, M, DHERMY, D

Volltext

Erythroid expression of the human alpha-spectrin gene promoter is mediated by GATA-1- and NF-E2-binding proteins von Boulanger, Laurent, Sabatino, Denise E, Wong, Ellice Y, Cline, Amanda P, Garrett, Lisa J, Garbarz, Michel, Dhermy, Didier, Bodine, David M, Gallagher, Patrick G

Volltext

Spectrin beta-chain variant associated with hereditary elliptocytosis von Dhermy, D, Lecomte, M C, Garbarz, M, Bournier, O, Galand, C, Gautero, H, Feo, C, Alloisio, N, Delaunay, J, Boivin, P

Volltext

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 domain von Morle, L, Morle, F, Roux, AF, Godet, J, Forget, BG, Denoroy, L, Garbarz, M, Dhermy, D, Kastally, R, Delaunay, J

Volltext

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects von Dhermy, Didier, Galand, Colette, Bournier, Odile, Boulanger, Laurent, Cynober, Thérèse, Schismanoff, Pierre Olivier, Bursaux, Elisabeth, Tchernia Boivin, Gil, Pierre, Garbarz, Michel

Volltext

Erythroid Expression of the Human [alpha]-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins von Boulanger, L, Sabatino, DE, Wong, E Y, Cline, A P, Garrett, L J, Garbarz, M, Dhermy, D, Bodine, D M, Gallagher, P G

Volltext

The Characterization of Protein 4.1 Presles, a Shortened Variant of RBC Membrane Protein 4.1 von Morle, L., Garbarz, M., Alloisio, N., Girot, R., Chaveroche, I., Boivin, P., Delaunay, J.

Volltext

Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-association von TSE, W. T, LECOMTE, M.-C, COSTA, F. F, GARBARZ, M, FEO, C, BOIVIN, P, DHERMY, D, FORGET, B. G

Volltext

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis von Garbarz, M, Lecomte, MC, Dhermy, D, Feo, C, Chaveroche, I, Gautero, H, Bournier, O, Picat, C, Goepp, A, Boivin, P

Volltext

Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis von Garbarz, M, Dhermy, D, Bournier, O, Bezeaud, A, Boivin, P

Volltext

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis von Jenkins, P B, Abou-Alfa, G K, Dhermy, D, Bursaux, E, Féo, C, Scarpa, A L, Lux, S E, Garbarz, M, Forget, B G, Gallagher, P G

Volltext

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis von Garbarz, M, Dhermy, D, Lecomte, MC, Feo, C, Chaveroche, I, Galand, C, Bournier, O, Bertrand, O, Boivin, P

Volltext

Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family: transmission of the same molecular defect in spectrin through three generations with different clinical expr... von LECOMTE, M. C, DHERMY, D, GARBARZ, M, FEO, C, GAUTERO, H, BOURNIER, O, PICAT, C, CHAVEROCHE, I, GALAND, C, BOIVIN, P

Volltext

Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis von DHERMY, D, GARBARZ, M, LECOMTE, M.-C, CHAVEROCHE, I, BOURNIER, O, GAUTERO, H, BLOT, I, BOIVIN

Volltext