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Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1972 T, Gjemdal, K, Rootwelt
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Causes and Pathophysiology of Acquired Sideroblastic Anemia [PDF]
Genes, 2022 The sideroblastic anemias are a heterogeneous group of inherited and acquired disorders characterized by anemia and the presence of ring sideroblasts in the bone marrow.
Xavier Calvo +2 more
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Sideroblastic Anemia Terminating in Myelofibrosis
American Journal of Hematology, 1982AbstractTwo patients with primary acquired sideroblastic anemia who eventually developed myelofibrosis with myeloid metaplasia are reported. Splenectomy was performed in one patient because of increasing blood transfusion requirements, and splenic histology revealed both myeloid metaplasia and ringed sideroblasts.
T J Myers +2 more
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Sideroblasts, Siderocytes, and Sideroblastic Anemia
New England Journal of Medicine, 1975SMALL iron-containing granules, demonstrable by means of the Prussian blue reaction, have been recognized in erythrocytes and their precursors for at least 30 years.1 2 3 4 5 Only recently, through the use of electron microscopy,6 7 8 have two distinct series of iron-containing erythroid cells been distinguished: one in which the iron consists of ...
G E, Cartwright, A, Deiss
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Therapeutische Umschau. Revue therapeutique, 2006 Sideroblastic anemias are a heterogenous group of disorders characterized by the presence of sideroblasts in the bone marrow aspirate. Current classification schemes distinguish between diseases of the heme synthesis pathway and diseases of other mitochondrial pathways which can either be of primary origin (defects in mitochondrial DNA) or of secondary
CAZZOLA, MARIO, INVERNIZZI, ROSANGELA
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Sideroblastic Anemia: Molecular Analysis of the ALAS2 Gene in a Series of 29 Probands and Functional Studies of 10 Missense Mutations [PDF]
Human Mutation, 2011 X-linked Sideroblastic Anemia (XLSA) is the most common genetic form of sideroblastic anemia, a heterogeneous group of disorders characterized by iron deposits in the mitochondria of erythroid precursors.
Hervé Puy +2 more
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Meme biosynthesis in sideroblastic anemia
International Journal of Biochemistry, 1980Abstract The activities of δ-aminolevulinic acid synthase (ALA-S), δ-aminolevulinic acid dehydratase (ALA-D), uroporphyrinogen I synthase (Uro-I-S), uroporphyrinogen decarboxylase (Uro-DC) and heme synthase have been studied in peripheral red blood cells of 9 patients with hereditary sideroblastic anemia (HSA) and 8 patients with refractory ...
A V, Pasanen +3 more
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