Biomedical subjects
R G Huntsman
Publications and source records attributed to R G Huntsman.
The use of the cord blood sample for the detection of sickle-cell anaemia in the newborn.
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An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples.
Agar gel, cellulose acetate, and starch gel electrophoresis are all capable of diagnosing sickle-cell anaemia, sickle-cell haemoglobin C disease, and haemoglobin C disease in cord blood samples. Of these three electrophoretic techniques, agar gel is the easiest to interpret.Paper electrophoresis can reliably and rapidly detect sickle haemoglobin and haemoglobin C in cord blood samples. Being incapable of differentiating foetal and normal adult haemoglobin, the value of paper electrophoresis is limited to an initial screening procedure.
An assessment of Sickledex as an alternative to the sickling test.
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A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anaemia.
A simple and rapid screening test which differentiates sickle-cell trait and sickle-cell anaemia is described. The test utilizes 0.1 ml of whole blood and is based on the low solubility of reduced sickle haemoglobin. Results intermediate between the sickle-cell trait and sickle-cell anaemia are obtained in unusual cases of sickle-cell anaemia with high foetal haemoglobin. The need to supplement the results with haematological and electrophoretic techniques is discusses.
Thalassemia research and abnormal hemoglobins.
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Abnormal human myoglobin: 53 (D4) glutamic acid--lysine.
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Do pregnant women take their iron?
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Haemoglobin F Texas II (alpha-2 gamma-2, 6 Glu-Lys), the second of the haemogloin F Texas variants.
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Blood groups and enzymes of human red cells after five years' storage in liquid nitrogen.
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Haemoglobin F Hull (gamma-121 glutamic acid--lysine), homologous with haemoglobins O Arab and O Indonesia.
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The serum folic acid levels of grass-fed and stabled horses.
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The Talbot fingers: a study in symphalangism.
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Haemoglobin O Arab in Egypt and Aden: possible errors resulting from the use of haemoglobin variants as genetic markers in population surveys.
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Simple test for ingested iron in hospital and domiciliary practice.
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Thrombotic microangiopathy. Recovery of a case after heparin and magnesium therapy.
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