Familial Haemolytic Anaemia with Erythrocyte Inclusion Bodies, Bilifuscinuria and Abnormal Haemoglobin (Haemoglobin Galliera Genova)
- 1 September 1965
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 11 (5) , 511-517
- https://doi.org/10.1111/j.1365-2141.1965.tb00095.x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Abnormal human haemoglobins: I. The comparison of normal human and sickle-cell haemoglobins by “fingerprinting”Published by Elsevier ,2003
- Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Koln) in a Glasgow FamilyBMJ, 1964
- Hæmoglobin–LeporeHollandiaNature, 1962
- An improved method for the fingerprinting of human hemoglobinBiochimica et Biophysica Acta, 1961
- Congenital Hemolytic Disease Associated with Red Cell Inclusion Bodies, Abnormal Pigment Metabolism and an Electrophoretic Hemoglobin AbnormalityBlood, 1960
- Normal Functions of the Spleen Relative to Red Blood Cells: A ReviewBlood, 1959
- An improved procedure for starch-gel electrophoresis: further variations in the serum proteins of normal individualsBiochemical Journal, 1959
- Congenital Hemolytic Anemia with Abnormal Pigment Metabolism and Red Cell Inclusion Bodies: a New Clinical SyndromeBlood, 1958
- Trypsin-catalysed transpeptidationsBiochemical Journal, 1954
- Autohemolysis and Other Changes Resulting from the Incubation in Vitro of Red Cells from Patients with Congenital Hemolytic AnemiaBlood, 1954