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Journal Articles

Characterization of the Underlying Molecular Defect in Hereditary Spherocytosis Associated With Spectrin Deficiency

H. Hassoun, J.N. Vassiliadis, J. Murray, P.R. Njolstad, John J. Rogus, S.K. Ballas, F. Schaffer, P. Jarolim, V. Brabec, J. Palek

Blood (1997) 90 (1): 398–406.

https://doi.org/10.1182/blood.V90.1.398

Published: 1997

Journal Articles

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

P Jarolim, JL Murray, HL Rubin, WM Taylor, JT Prchal, SK Ballas, LM Snyder, L Chrobak, WD Melrose, V Brabec, J Palek

Blood (1996) 88 (11): 4366–4374.

https://doi.org/10.1182/blood.V88.11.4366.4366

Published: 1996

Journal Articles

Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis

P Jarolim, HL Rubin, V Brabec, J Palek

Blood (1995) 85 (11): 3278–3282.

https://doi.org/10.1182/blood.V85.11.3278.bloodjournal85113278

Published: 1995

Journal Articles

Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis

P Jarolim, HL Rubin, V Brabec, L Chrobak, AS Zolotarev, SL Alper, C Brugnara, H Wichterle, J Palek

Blood (1995) 85 (3): 634–640.

https://doi.org/10.1182/blood.V85.3.634.bloodjournal853634

Published: 1995

Journal Articles

Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia

C Lenzner, P Nurnberg, BJ Thiele, A Reis, V Brabec, A Sakalova, G Jacobasch

Blood (1994) 83 (10): 2817–2822.

https://doi.org/10.1182/blood.V83.10.2817.2817

Published: 1994

Journal Articles

Red Cell Lipids in Autoimmune Hemolytic Anemia

V. BRABEC, M.D., Č. MICHALEC, M.D., J. PALEK, M.D., M. KOUT, M.D.

Blood (1969) 34 (4): 414–420.

https://doi.org/10.1182/blood.V34.4.414.414

Published: 1969

NARROW

Characterization of the Underlying Molecular Defect in Hereditary Spherocytosis Associated With Spectrin Deficiency

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis

Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis

Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia

Red Cell Lipids in Autoimmune Hemolytic Anemia

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ASH Publications

American Society of Hematology

Characterization of the Underlying Molecular Defect in Hereditary Spherocytosis Associated With Spectrin Deficiency

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis

Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis

Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia

Red Cell Lipids in Autoimmune Hemolytic Anemia

Email alerts

ASH Publications

American Society of Hematology

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