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Ineffective erythropoiesis
Known as:
Defective erythropoiesis
National Institutes of Health
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Related topics
Related topics
6 relations
5q-syndrome
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IV
Congenital dyserythropoietic anemia, type II
HYPERBILIRUBINEMIA, SHUNT, PRIMARY
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Broader (1)
Dyserythropoiesis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Recent trends in treatment of thalassemia.
A. El‐Beshlawy
,
M. El-Ghamrawy
Blood Cells, Molecules & Diseases
2019
Corpus ID: 73466628
Review
2014
Review
2014
Sideroblastic anemia: diagnosis and management.
S. Bottomley
,
M. Fleming
Hematology/Oncology Clinics of North America
2014
Corpus ID: 36751110
2014
2014
Erythropoiesis‐driven regulation of hepcidin in human red cell disorders is better reflected through concentrations of soluble transferrin receptor rather than growth differentiation factor 15
K. Fertrin
,
C. Lanaro
,
+10 authors
F. Costa
American journal of hematology/oncology
2014
Corpus ID: 25099548
Growth differentiation factor 15 (GDF‐15) is a bone marrow‐derived cytokine whose ability to suppress iron regulator hepcidin in…
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Review
2012
Review
2012
Mechanisms of defective erythropoiesis and anemia in pediatric acute lymphoblastic leukemia (ALL)
M. Steele
,
A. Narendran
Annals of Hematology
2012
Corpus ID: 20894647
Anemia frequently accompanies the diagnosis of acute lymphoblastic leukemia (ALL) in children and is considered to be one of the…
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2012
2012
Bone marrow mesenchymal stem cells in patients with beta thalassemia major: molecular analysis with attenuated total reflection-Fourier transform infrared spectroscopy study as a novel method.
C. Aksoy
,
A. Guliyev
,
E. Kılıç
,
D. Uçkan
,
F. Severcan
Stem Cells and Development
2012
Corpus ID: 21004637
Bone marrow mesenchymal stem cells (BM-MSCs) are the main cellular components of the bone marrow, providing a supportive cellular…
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2012
2012
An unusual cause for recurrent jaundice in an otherwise healthy male.
S. Dasari
,
K. Naha
,
M. Prabhu
Australasian Medical Journal
2012
Corpus ID: 207437159
A 41-year-old Asian-Indian male presented with recurrent episodes of jaundice over the past six months. Physical examination was…
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2011
2011
Prospects for a hepcidin mimic to treat β-thalassemia and hemochromatosis
N. Parrow
,
Sara Gardenghi
,
S. Rivella
Expert Review of Hematology
2011
Corpus ID: 207211413
Iron is required for numerous functions in the human body. However, iron utilization in biological systems is challenging because…
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Review
2009
Review
2009
Pathophysiology of Transfusional Iron Overload: Contrasting Patterns in Thalassemia Major and Sickle Cell Disease
J. Porter
Hemoglobin
2009
Corpus ID: 21558567
The pathophysiological consequences of transfusional iron overload largely reflect the pattern of excess iron distribution and…
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2009
2009
Use of Jak2 Inhibitors to Limit Ineffective Erythropoiesis and Iron Absorption in Mice Affected by β-Thalassemia and Other Disorders of Red Cell Production.
L. Melchiori
,
Sara Gardenghi
,
+6 authors
S. Rivella
2009
Corpus ID: 208436277
Abstract 2020 Poster Board I-1042 β-thalassemia intermedia (TI) and major (TM) are characterized by Ineffective Erythropoiesis…
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1992
1992
Identifying the Substance Abuser in Clinical Practice
K. Bell
Orthopedic Nursing
1992
Corpus ID: 26256380
Illicit drugs are used regularly by 14.5 million Americans. By identifying patients who abuse substances, the nurse will be…
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