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Issues
1987
ISSN 0001-5792
EISSN 1421-9662
Acta Haematologica 1987, Vol. 78, No. 2-3
Special Section
Professor Hermann Lehmann: A Personal Tribute
Acta Haematol (1987) 78 (2-3): 71–73.
https://doi.org/10.1159/000205847
Molecular Variation
A Short Review of Human γ-Globin Gene Anomalies
Acta Haematol (1987) 78 (2-3): 80–84.
https://doi.org/10.1159/000205850
Structure, Function
X-Ray Crystallographic and Functional Studies of Human Haemoglobin Mutants Produced in Escherichia coli
Acta Haematol (1987) 78 (2-3): 85–89.
https://doi.org/10.1159/000205851
Deformability of the Hemoglobin Molecule as the Basis of Its Functional Behavior
Acta Haematol (1987) 78 (2-3): 90–94.
https://doi.org/10.1159/000205852
Structure, Physiology
Reduction and Spectroscopic Properties of Hemoglobins M
Acta Haematol (1987) 78 (2-3): 95–98.
https://doi.org/10.1159/000205853
Modification of Hemoglobin with Site-Directed Bifunctional Reagents
Acta Haematol (1987) 78 (2-3): 99–104.
https://doi.org/10.1159/000205854
Role of Membrane-Bound Haemoglobin Products in Oxidative Damage in Sickle Cell Membranes
Acta Haematol (1987) 78 (2-3): 105–108.
https://doi.org/10.1159/000205855
Diagnosis, Distribution
Structure and Function of a New Hemoglobin Variant, Hb Meilahti (α2β2 36(C2)Pro→Thr), Characterized by Mass Spectrometry
Acta Haematol (1987) 78 (2-3): 109–113.
https://doi.org/10.1159/000205856
Neonatal Screening and Mass-Spectrometric Analysis of Hemoglobin Variants in Japan
Acta Haematol (1987) 78 (2-3): 114–118.
https://doi.org/10.1159/000205857
Characterization Approach of ‘Silent’ Beta-Chain Hemoglobin Variants
Acta Haematol (1987) 78 (2-3): 119–122.
https://doi.org/10.1159/000205858
High-Performance Liquid Chromatography as a Method to Identify Haemoglobin Abnormalities
Acta Haematol (1987) 78 (2-3): 123–126.
https://doi.org/10.1159/000205859
Strategy for Structural Characterization of Haemoglobin Variants
Acta Haematol (1987) 78 (2-3): 127–129.
https://doi.org/10.1159/000205860
Haemoglobinopathies, Thalassaemias and Enzymopathies in Saudi Arabia: The Present Status
Acta Haematol (1987) 78 (2-3): 130–134.
https://doi.org/10.1159/000205861
Haemoglobin Disorders among Southeast-Asian Refugees in France
Acta Haematol (1987) 78 (2-3): 135–136.
https://doi.org/10.1159/000205862
Screening
Prenatal Diagnosis of Hematologic Diseases, 1986 Update
Acta Haematol (1987) 78 (2-3): 137–141.
https://doi.org/10.1159/000205863
Neonatal Haemoglobinopathy Screening
Acta Haematol (1987) 78 (2-3): 142–143.
https://doi.org/10.1159/000205864
Haemoglobin A/F Ratio in Neonates at 7 Days Correlated with Birth Weight and Estimated Gestational Age
Acta Haematol (1987) 78 (2-3): 144–148.
https://doi.org/10.1159/000205865
Haemoglobinopathy Screening in a ‘Low-Risk’ Area of the United Kingdom: South Glamorgan, Wales
D.P. Bentley; I. Cavill; M.J. Choiseul; D. Evans; R.D. Hutton; A. Jacobs; K. Jobbins; D. McLellan; A. May; B.S. Walpole; C.A. Wardrop
Acta Haematol (1987) 78 (2-3): 149–153.
https://doi.org/10.1159/000205866
Thalassaemia
The Origin of Mutant β-Globin Genes in Human Populations
Acta Haematol (1987) 78 (2-3): 154–158.
https://doi.org/10.1159/000205867
Approach to the Diagnosis of β-Thalassaemia by DNA Analysis
Acta Haematol (1987) 78 (2-3): 159–167.
https://doi.org/10.1159/000205868
Prevention of Thalassaemia and Haemoglobin S Syndromes in Greece
Acta Haematol (1987) 78 (2-3): 168–172.
https://doi.org/10.1159/000205869
α-Thalassaemia and the Malaria Hypothesis
Acta Haematol (1987) 78 (2-3): 173–179.
https://doi.org/10.1159/000205870
Can Automated Haematology Analysers Discriminate Thalassaemia from Iron Deficiency?
Acta Haematol (1987) 78 (2-3): 180–183.
https://doi.org/10.1159/000205871
Sickle Cell Disease
Genetic Heterogeneity of Sickle Mutations
Acta Haematol (1987) 78 (2-3): 184–185.
https://doi.org/10.1159/000205872
Avascular Necrosis of the Femoral Head in Sickle Cell Syndrome: A Report of 5 Cases
Acta Haematol (1987) 78 (2-3): 186–192.
https://doi.org/10.1159/000205873
Clinical Management of Severe Sickle Cell Disease
Acta Haematol (1987) 78 (2-3): 193–197.
https://doi.org/10.1159/000205874
Transfusion and Exchange Transfusion in Sickle Cell Anaemias, with Particular Reference to Iron Metabolism
Acta Haematol (1987) 78 (2-3): 198–205.
https://doi.org/10.1159/000205875
Iron Overload and Iron Chelation Therapy in Thalassaemia and Sickle Cell Haemoglobinopathies
Acta Haematol (1987) 78 (2-3): 206–211.
https://doi.org/10.1159/000205876
Iron Overload
Orally Active Alpha-Ketohydroxypyridine Iron Chelators: Effects on Iron and Other Metal Mobilisations
Acta Haematol (1987) 78 (2-3): 212–216.
https://doi.org/10.1159/000205877
In vivo Evaluation of Hydroxypyridone Iron Chelators in a Mouse Model
Acta Haematol (1987) 78 (2-3): 217–221.
https://doi.org/10.1159/000205878
