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  1. 1821
    “…Defects in genes encoding ribosomal proteins cause Diamond Blackfan Anemia (DBA), a red cell aplasia often associated with physical abnormalities. …”
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    Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia
  2. 1822
    “…OBJECTIVE: To find out the prevalence and relationship of anemia in reproductive age women in rural area of Tabas, center of Iran. …”
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    Prevalence of Anemia and Correlated Factors in the Reproductive Age Women in Rural Areas of Tabas
  3. 1823
    “…A deficiency of some ribosomal proteins (RPs) impairs processing and causes Diamond Blackfan anemia (DBA), which is associated with anemia, congenital malformations and cancer. p53 mediates many features of DBA, but the mechanism of p53 activation remains unclear. …”
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    The role of the DNA damage response in zebrafish and cellular models of Diamond Blackfan anemia
  4. 1824
    “…INTRODUCTION: The management of patients with aplastic anemia, to an extent, depends on the etiology i.e., inherited or acquired. …”
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    Clinicohematological correlation and chromosomal breakage analysis in suspected Fanconi anemia patients of India
  5. 1825
    “…We report a case of t(8;21) acute myeloid leukemia presenting as severe aplastic anemia. While initial bone marrow biopsy lacked any cytogenetic abnormalities in 20 analyzed metaphases, repeat bone marrow biopsy eight days later demonstrated this translocation. …”
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    Translocation (8;21) acute myeloid leukemia presenting as severe aplastic anemia
  6. 1826
    por Meznar, M, Pareznik, R, Voga, G
    Publicado 2009
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    Effect of anemia on tissue oxygenation saturation and the tissue deoxygenation rate during ischemia
  7. 1827
    “…Over 12 months, the proportion of asymptomatic carriers with anemia (mild, moderate, or severe) was reduced in both arms. …”
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    Treatment of Asymptomatic Carriers of Plasmodium falciparum with Artemether–Lumefantrine: Impact on the Prevalence of Anemia
  8. 1828
    “…Five years later, he developed an autoimmune hemolytic anemia (AIHA), anti-IgG positive, with reduced reticulocyte count, leukopenia, and thrombocytopenia with antiplatelet antibodies. …”
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    Alemtuzumab Plus Cyclosporine Treatment of the Autoimmune Hemolytic Anemia in an Adult Bowel Transplant
  9. 1829
    “…Individuals with Fanconi anemia (FA) are susceptible to bone marrow failure, congenital abnormalities, cancer predisposition and exhibit defective DNA crosslink repair. …”
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    Fanconi anemia signaling and Mus81 cooperate to safeguard development and crosslink repair
  10. 1830
    “…OBJECTIVE: To investigate the clinical characteristics of seronegative hepatitis-associated aplastic anemia (AA) (SNHAA) and hepatitis B virus (HBV) infection complicating AA (HBVAA), and thereby compare the efficacy of immunosuppressive therapy (IST). …”
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    Efficacy and safety of immunosuppressive therapy in the treatment of seronegative hepatitis associated aplastic anemia
  11. 1831
    “…Objective: The study explores the association between the household environment and the prevalence of anemia among children under the age of 5 years in India. …”
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    Association of Household Environment and Prevalence of Anemia Among Children Under-5 in India
  12. 1832
    por Brosh, Robert M., Cantor, Sharon B.
    Publicado 2014
    “…The FANCJ DNA helicase is mutated in hereditary breast and ovarian cancer as well as the progressive bone marrow failure disorder Fanconi anemia (FA). FANCJ is linked to cancer suppression and DNA double strand break repair through its direct interaction with the hereditary breast cancer associated gene product, BRCA1. …”
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    Molecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemia
  13. 1833
    “…Infection of poultry with chicken anemia virus (CAV) is implicated in several field problems in broiler flocks due to the immunosuppression generated and, consequently, the increased susceptibility to secondary infections. …”
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    Comparative histopathological and immunological study of two field strains of chicken anemia virus
  14. 1834
    “…OBJECTIVE: To assess the prevalence of anemia and associated factors in older adults. METHODS: The prevalence and factors associated with anemia in older adults were studied on the basis of the results of the Saúde, Bem-Estar e Envelhecimento (SABE – Health, Welfare and Aging) study. …”
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    Prevalence of anemia and associated factors in older adults: evidence from the SABE Study
  15. 1835
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    Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania
  16. 1836
    “…FANCD2 is a product of one of the genes associated with Fanconi anemia (FA), a rare recessive disease characterized by bone marrow failure, skeletal malformations, developmental defects, and cancer predisposition. …”
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    Defective FANCI Binding by a Fanconi Anemia-Related FANCD2 Mutant
  17. 1837
    “…Cumulative information from randomized, controlled, multicenter trials on a diverse range of indications, including patients with chronic heart failure, postpartum anemia/abnormal uterine bleeding, inflammatory bowel disease, NDD-CKD, and those undergoing hemodialysis, supports the efficacy of FCM for iron replacement in patients with iron deficiency and iron-deficiency anemia. …”
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    Optimizing iron delivery in the management of anemia: patient considerations and the role of ferric carboxymaltose
  18. 1838
    “…Hospitalized patients frequently have considerable volumes of blood removed for diagnostic testing which could lead to the development of hospital-acquired anemia. Low hemoglobin levels during hospitalization may result in significant morbidity for patients with underlying cardiorespiratory and other illnesses. …”
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    A Retrospective Study Investigating the Incidence and Predisposing Factors of Hospital-Acquired Anemia
  19. 1839
    “…Left untreated, hemorrhage from necrotic bowel tissue will lead to severe fetal anemia and even intrauterine death. We encountered a case of fetal intestinal volvulus causing severe anemia, which was diagnosed postnatally and successfully treated with surgical intervention.…”
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    A Case of Fetal Intestinal Volvulus Without Malrotation Causing Severe Anemia
  20. 1840
    “…OBJECTIVES: To analyze the frequency of β(S)-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia. METHOD: The frequency of β(S)-globin haplotypes and alpha-thalassemia and any association with clinical and laboratorial manifestations were determined in 117 sickle cell anemia children aged 3–71 months. …”
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    Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia
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