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	COVID-19: Daily Top 10 Papers

Anemia

Free Subscription 15.03.2021 4 Blood 6 Br J Haematol 13 Hemoglobin 1 J Pediatr Hematol Oncol 1 Kidney Int 3 N Engl J Med 1 Nature 1 Nephron 1 Pediatrics 1 PLoS One 1 Transfusion

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Single Articles

Blood

1. KIM-SHAPIRO DB, Gladwin MT
   Arginine for mitochondrial oxidative enzymopathy.
   Blood. 2020;136:1376-1378.
   PubMed        
   
   
2. BROUSSE V, Connes P
   Vasomotor hyperresponsiveness in SCD.
   Blood. 2020;136:1120-1121.
   PubMed        
   
   
3. VOIT RA, Grace RF
   Pyruvate kinase deficiency in a newborn with extramedullary hematopoiesis in the skin.
   Blood. 2020;136:770.
   PubMed        
   
   
4. LUZZATTO L, Ally M, Notaro R
   Glucose-6-phosphate dehydrogenase deficiency.
   Blood. 2020;136:1225-1240.
   PubMed         Abstract available
   
   

   
   Br J Haematol

5. BELLO-MANGA H, Galadanci AA, Abdullahi S, Ali S, et al
   Low educational level of head of household, as a proxy for poverty, is associated with severe anaemia among children with sickle cell disease living in a low-resource setting: evidence from the SPRING trial.
   Br J Haematol. 2020;190:939-944.
   PubMed         Abstract available
   
   
6. DE SANTIS GC, Costa TCM, Santos FLS, da Silva-Pinto AC, et al
   Blood transfusion support for sickle cell patients during haematopoietic stem cell transplantation: a single-institution experience.
   Br J Haematol. 2020;190:e295-e297.
   PubMed        
   
   
7. MCGINNIS E, Smith TW
   Clostridium perfringens sepsis with spherocytosis and green neutrophil inclusions.
   Br J Haematol. 2020;190:641.
   PubMed        
   
   
8. LIAPIS K, Vrachiolias G, Spanoudakis E, Kotsianidis I, et al
   Vacuolation of early erythroblasts with ring sideroblasts: a clue to the diagnosis of linezolid toxicity.
   Br J Haematol. 2020;190:809.
   PubMed        
   
   
9. GERARD D, Bourin S, Phulpin A, Picard V, et al
   Previously misdiagnosed red cell membrane disorder and familial consequences.
   Br J Haematol. 2020;190:810.
   PubMed        
   
   
10. WOUTERS HJCM, Stam SP, van der Klauw MM, Bakker SJL, et al
    The association between haemoglobin concentrations and muscle mass determined from urinary creatinine excretion rate: a population-based cohort study.
    Br J Haematol. 2020;190:e349-e352.
    PubMed        
    
    

    
    Hemoglobin

11. SAJADPOUR Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, et al
    Association between Different Polymorphic Markers and beta-Thalassemia Intermedia in Central Iran.
    Hemoglobin. 2020;44:27-30.
    PubMed         Abstract available
    
    
12. SHOUJAA A, Moasses F, Mukhalalaty Y, Murad H, et al
    Genotype/Phenotype Correlation of beta-Thalassemia in Syrian Patients: A Cross-Sectional Study.
    Hemoglobin. 2020;44:42-46.
    PubMed         Abstract available
    
    
13. SAKAMOTO A, Nakadate H, Tada K, Yamashiro Y, et al
    A Japanese Family with the Unstable Hb Sydney (HBB: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation.
    Hemoglobin. 2020;44:58-60.
    PubMed         Abstract available
    
    
14. CHEN X, Luo S, Huang J, Yuan D, et al
    Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare alpha-Thalassemia Gene HBA2: c.1A>G Mutation.
    Hemoglobin. 2020;44:51-54.
    PubMed         Abstract available
    
    
15. LUO H, Zou Y, Liu Y
    A Novel beta-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family.
    Hemoglobin. 2020;44:55-57.
    PubMed         Abstract available
    
    
16. VAN GAMMEREN AJ, Pelkmans L, Endschot CCWV, Roelofsen-de Beer RJAC, et al
    An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C).
    Hemoglobin. 2020;44:61-63.
    PubMed         Abstract available
    
    
17. ROPERO P, Arbeteta J, Nieto JM, Gonzalez FA, et al
    Nondeletional alpha-Thalassemia: Two New Mutations on the alpha2 Gene.
    Hemoglobin. 2020;44:17-19.
    PubMed         Abstract available
    
    
18. AL-RIYAMI AZ, Daar S, Kindi SA, Madhani AA, et al
    alpha-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
    Hemoglobin. 2020;44:20-26.
    PubMed         Abstract available
    
    
19. NAZ S, Rehman SU, Shakeel M, Rehman H, et al
    Molecular Heterogeneity of beta-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan.
    Hemoglobin. 2020;44:37-41.
    PubMed         Abstract available
    
    
20. MIR SA, Alshehri BM, Alaidarous M, Banawas SS, et al
    Prevalence of Hemoglobinopathies (beta-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.
    Hemoglobin. 2020;44:47-50.
    PubMed         Abstract available
    
    
21. MASHON RS, Das R, Dhawan R, Kakkar N, et al
    Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography.
    Hemoglobin. 2020;44:64-66.
    PubMed         Abstract available
    
    
22. BELISARIO AR, Carneiro-Proietti AB, Sabino EC, Araujo A, et al
    Hb S/beta-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Hemoglobin. 2020;44:1-9.
    PubMed         Abstract available
    
    
23. SARIHI R, Amirizadeh N, Oodi A, Azarkeivan A, et al
    Distribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent beta-Thalassemia Patients in Different Population of Iran: Effect of Ethnicity.
    Hemoglobin. 2020;44:31-36.
    PubMed         Abstract available
    
    

    
    J Pediatr Hematol Oncol

24. OZDEMIR ZC, Duzenli Kar Y, Bor O
    Whole Blood miR-210, miR-122, miR-223 Expression Levels and Their Relationship With Iron Status Parameters and Hypercoagulobility Indices in Children With Iron Deficiency Anemia.
    J Pediatr Hematol Oncol. 2021 Mar 12. pii: 00043426-900000000-96945.
    PubMed         Abstract available
    
    

    
    Kidney Int

25. FUCHS MAA, Broeker KAE, Schrankl J, Burzlaff N, et al
    Inhibition of transforming growth factor beta1 signaling in resident interstitial cells attenuates profibrotic gene expression and preserves erythropoietin production during experimental kidney fibrosis in mice.
    Kidney Int. 2021 Mar 8. pii: S0085-2538(21)00278.
    PubMed         Abstract available
    
    

    
    N Engl J Med

26. TAHER AT, Musallam KM, Cappellini MD
    beta-Thalassemias.
    N Engl J Med. 2021;384:727-743.
    PubMed        
    
    
27. MENON BS, Teh KH
    Gum Hypertrophy from Cyclosporine.
    N Engl J Med. 2021;384:744.
    PubMed        
    
    
28. OGUNWOLE SM
    Without Sanctuary.
    N Engl J Med. 2021;384:791-793.
    PubMed        
    
    

    
    Nature

29. WONKAM A
    Sequence three million genomes across Africa.
    Nature. 2021;590:209-211.
    PubMed        
    
    

    
    Nephron

30. ALFANDARY H, Rinat C, Gurevich E, Eisenstein I, et al
    Hemolytic Uremic Syndrome: A Contemporary Pediatric Experience.
    Nephron. 2020;144:109-117.
    PubMed         Abstract available
    
    

    
    Pediatrics

31. APPAVU B, Deng D, Dowling MM, Garg S, et al
    Arteritis and Large Vessel Occlusive Strokes in Children After COVID-19 Infection.
    Pediatrics. 2021;147.
    PubMed         Abstract available
    
    

    
    PLoS One

32. KUSHITOR SB, Owusu L, Kushitor MK
    The prevalence and correlates of the double burden of malnutrition among women in Ghana.
    PLoS One. 2020;15:e0244362.
    PubMed         Abstract available
    
    

    
    Transfusion

33. NGUYEN TN, Maenulein E, Fihman V, Vinatier I, et al
    Serologic characteristics of oxaliplatin antibodies in 15 patients with drug-induced immune hemolytic anemia.
    Transfusion. 2021 Mar 9. doi: 10.1111/trf.16360.
    PubMed         Abstract available
    
    

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