Results 171 to 180 of about 298,625 (226)

Pyruvate Kinase Deficiency: Markedly Decreased Reticulocyte PK Activity and Limited Specificity of the PK/HK Ratio. [PDF]

Int J Mol Sci
Koleva L, Dolgikh IA, Kryukova AV, Prudinnik DS, Bovt EA, Shakhidzhanov SS, Mann SG, Smetanina NS, Ataullakhanov FI, Sinauridze EI.   +9 more
europepmc   +1 more source

Epigenetic Regulation of Erythropoiesis: From Developmental Programs to Therapeutic Targets. [PDF]

Int J Mol Sci
Vasiloudis NI, Paschoudi K, Beta C, Georgolopoulos G, Psatha N.   +4 more
europepmc   +1 more source

Molecular Mechanisms of Iron Metabolism and Overload. [PDF]

Biomedicines
Tayal A, Kaur J, Sadeghi P, Maitta RW.
europepmc   +1 more source

Luspatercept for the treatment of anemia in allo-HSCT for patients with hematological diseases. [PDF]

Blood Cancer J
Xin X, Zhang W, Li Z, Gui R, Wang J, Ji L, Zhang Y, Fang B, Song Y, Zu Y, Zhou J.   +10 more
europepmc   +1 more source

Iron Overload Cardiomyopathy in Myelodysplastic Syndrome: A Fatal Outcome After 20 Years of Chronic Transfusions. [PDF]

JACC Case Rep
Hayashida M, Nohara S, Yamakawa R, Nishikido A, Matsushima Y, Yanai T, Ishimatsu T, Otsuka M, Fukumoto Y.   +8 more
europepmc   +1 more source

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Three siblings with variable degrees of neuromuscular involvement and congenital sideroblastic anemia: A peculiar phenotype and a surprise genotypic explanation

Annals of Human Genetics, 2023
Introduction: Congenital sideroblastic anemias (CSAs) are a group of inherited bone‐marrow disorders manifesting with erythroid hyperplasia and ineffective erythropoiesis.
M. Salam, K. Salama, Yasmeen M. M. Selim, M. Saad, Rasha Rady, Salem Alawbathani, S. Schroeder, M. A. Elmonem, N. Elkhateeb   +8 more
semanticscholar   +1 more source

Myopathy with Lactic Acidosis and Sideroblastic Anemia Caused By a Novel PUS1mutation

Blood, 2023
Mutations in the mitochondrial aminoacyl tRNA synthetases (ARSs) are associated with various clinical phenotypes, including myopathy, lactic acidosis, and sideroblastic anemia (MLASA), which is a rare autosomal recessive disorder.
Y. Xiong, Wenrui Yang, H. Fan, Li Zhang, Xin Zhao, L. Jing, Fengkui Zhang   +6 more
semanticscholar   +1 more source