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Blood Disorders

Exhibiting 35 entries found in the GMN corpus.

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YearTitle & TagsAuthor(s)
1519Liber theoricae nec non practicae Alsaharavii.
1803An account of an haemorrhagic disposition existing in certain families.
1855Die Haemophilie oder die Bluterkrankheit.
1865Glycosurie, diabète sucré. In his Clinique médicale de l’Hôtel-Dieu, 2me. éd., 2, 663-98.
1871De la microcythémie
1886A case of haemophilia: pedigree through five generations.
1889Ueber Haemochromatose.
1890Die Gelenkerkrankungen bei Blutern mit Berücksichtigung der Diagnose.
1904Elliptical human red cell corpuscles.
1910Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia.
1911Haemophilia.
1922Sickle-cell anemia.
1925Familial icterus gravis of the new-born and its treatment.
1926Hereditär pseudohemofili.
1927Anemia in children, with splenomegaly and peculiar changes in the bones.
1927Familiäre infantile perniziösaartige Anämie (perniziöses Blutbild und Konstitution).
1934The haemostatic possibilities of snake-venom.
1935The prothrombin in hemophilia and in obstructive jaundice.
1936Mediterranean disease – thalassemia (erythroblastic anemia of Cooley); associated pigment abnormalities simulating hemochromatosis.
1937Hemophilia. II. Some properties of a substance obtained from normal human plasma effective in accelerating the coagulation of hemophilic blood.
1938Recherches sur l’anémie érythroblastique infantile des peuples de la Méditerranée orientale. Étude anthropologique, étiologique et pathogénique. La transmission héréditaire de la maladie.
1948The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia.
1949Sickle cell anemia, a molecular disease.
1949The inheritance of sickle cell anemia.
1952Christmas disease, a condition previously mistaken for haemophilia.
1954Protection afforded by sickle-cell trait against subtertian malarial infection.
1957Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.
1959Genetic basis of the thalassaemia diseases.
1961Stomatocytosis: a hereditary red cell anomaly associated with haemolytic anaemia.
1966Man’s haemoglobins: including the haemoglobinopathies and their investigation.
1968Molecular pathology of human haemoglobin.
1985Enzymatic amplication of B-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.
2001Dying in the City of the Blues: Sickle cell anemia and the politics of race and health.
2011The bleeding disease: Hemophilia and the unintended consequences of medical progress.
2021CRISPR-Cas9 gene editing for sickle cell disease and ß-thalassemia.