HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY (Q76926084)

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1 December 2019

title

HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY (English)

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1 December 2019

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H E HUTCHISON

1

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P H PINKERTON

2

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P WATERS

3

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H LEHMANN

4

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D BEALE

5

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A S DOUGLAS

6

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publication date

1 October 1964

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language of work or name

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volume

2

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issue

5417

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page(s)

1099-1103

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A new case of congenital hemolytic anemia with intra-erythrocytic inclusions and dark urines. The importance of splenectomy in the appearance of these inclusions

1 December 2019

cites work

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12 December 2020

The use of the isotope 51Cr as a label for red cells

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12 December 2020

Properties and Inheritance of Hæmoglobin by Asymmetric Recombination

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12 December 2020

Autohemolysis and other changes resulting from the incubation in vitro of red cells from patients with congenital hemolytic anemia

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12 December 2020

A new technique for differentiation of hemoglobin

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12 December 2020

Starch Gel Electrophoresis in a Discontinuous System of Buffers

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12 December 2020

HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES

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12 December 2020

Congenital hemolytic anemia with intra-erythrocytic inclusions and dark urines. Report of a new case with electron microscope study

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12 December 2020

Tris buffer for the demonstration of haemoglobin A2 by paper electrophoresis

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12 December 2020

HEREDITARY HEINZ-BODY ANAEMIA. A REPORT OF STUDIES ON FIVE PATIENTS WITH MILD ANAEMIA

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12 December 2020

A Method for the Estimation of the Concentration of Haemoglobin Variants with Particular Reference to Haemoglobins A2 and S and the Recognition of Thalassaemia Minor

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12 December 2020

Congenital hemolytic disease associated with red cell inclusion bodies, abnormal pigment metabolism and an electrophoretic hemoglobin abnormality

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12 December 2020

An improved method for the fingerprinting of human hemoglobin

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12 December 2020

On the recombination of canine and human haemoglobins

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12 December 2020

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

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12 December 2020

Congenital hemolytic anemia with abnormal pigment metabolism and red cell inclusion bodies: a new clinical syndrome

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12 December 2020

Phenacetin-induced haemolytic anaemia

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12 December 2020

Abnormal human haemoglobins. I. The comparison of normal human and sickle-cell haemoglobins by fingerprinting

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12 December 2020

The hemolytic effect of primaquine and related compounds: a review

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12 December 2020

Hemoglobin Zurich. I. A new hemoglobin anomaly associated with acute hemolytic episodes with inclusion bodies after sulfonamide therapy

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12 December 2020

HAEMOGLOBIN LEPORE TRAIT; AN ANALYSIS OF THE ABNORMAL HAEMOGLOBIN

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12 December 2020

Thalassemia in the West Indies

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12 December 2020

Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice

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12 December 2020

CONGENITAL HEINZ-BODY ANAEMIA. FURTHER EVIDENCE ON THE CAUSE OF HEINZ-BODY PRODUCTION IN RED CELLS

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12 December 2020

Identifiers

DOI

10.1136/BMJ.2.5417.1099

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1 December 2019

PubMed publication ID

14198723

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