Results 131 to 140 of about 3,469 (181)

[Siderocytes, sideroblasts and sideroblastic anemia].

Lijecnicki vjesnik, 1968
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[Sideroblastic anemia].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1972
T, Gjemdal, K, Rootwelt
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Sideroblastic anemia.

Indian pediatrics, 2002
J, Menon, L, Mathews
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The molecular genetics of sideroblastic anemia.

Blood, 2019
Ducamp S, Fleming MD.
europepmc   +1 more source

A diagnostic pitfall in iron-refractory microcytic hypochromic anemia with acquired ring sideroblasts initially treated as iron deficiency anemia-a case report. [PDF]

Front Med (Lausanne)
Liu X, Ma J, Song A, Yang S, Li M, Yang J.   +5 more
europepmc   +1 more source

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Sideroblastic anemia terminating in myelofibrosis

American Journal of Hematology, 1982
AbstractTwo 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.
Thomas J Myers, Joseph A Grasso
exaly   +3 more sources

[Sideroblastic anemias].

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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Sideroblasts, Siderocytes, and Sideroblastic Anemia

New England Journal of Medicine, 1975
SMALL 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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Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations

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.
Caroline Kannengiesser, Agnes Guerci-Bresler, Gérard Tertian   +2 more
exaly   +3 more sources

Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation

Blood Cells, Molecules, and Diseases, 2017
The most frequent germline mutations responsible for non syndromic congenital sideroblastic anemia are identified in ALAS2 and SLC25A38 genes. Iron overload is a key issue and optimal chelation therapy should be used to limit its adverse effects on the ...
Cyrielle Fouquet, Karim Maloum, Fabienne Toutain   +2 more
exaly   +2 more sources