Results 151 to 160 of about 25,303 (208)

Frailty phenotype in adults with sickle cell disease. [PDF]

J Gerontol A Biol Sci Med Sci
Oyedeji CI, Mohamed RE, Faldowski R, Callaway T, Poole T, Denis Oliva F, Mathis V, Subramaniam A, Whitson H, Reeve BB, Pieper C, Telen MJ, Ashley-Koch A, Cohen HJ, Hall K, Strouse JJ.   +15 more
europepmc   +1 more source

Daprodustat augments red cell and γ-globin production in models of sickle cell disease. [PDF]

Blood Red Cells Iron
Sharma M, Ishfaq M, Mondal P, Mohideen A, Chowdhury FA, Taiclet S, Philips BJ, Crosby D, Wood KC, Straub AC, Ghosh S, Yien YY, Xu JZ.   +12 more
europepmc   +1 more source

Blood, Brain, and Bypass: Moyamoya Syndrome Unmasked During Hematologic Optimization in an Adult With Sickle Cell Disease. [PDF]

Cureus
Memari K, Reinoso E, Rodriguez SA, Alvarez NP, Lazo LP, Williams S, Cohen P.   +6 more
europepmc   +1 more source

Lower efficacy of transfusion of red blood cells from donors with sickle cell trait. [PDF]

Hemasphere
Dzieciatkowska M, Stephenson D, Hay A, Wang X, Keele GR, Nemkov T, Deng X, Stone M, Hansen KC, Kleinman S, Norris PJ, Busch MP, Page GP, Spitalnik SL, Roubinian N, Zimring JC, Thein SL, D'Alessandro A.   +17 more
europepmc   +1 more source

Distribution of Abnormal Hemoglobins in Saudi Arabia: Analysis of Private Sector Laboratory Data. [PDF]

J Epidemiol Glob Health
Raslan OM, Radhwi OO, Al Mahdi HB, Mansory EM.   +3 more
europepmc   +1 more source

Sickle cell hemoglobin, primaquine sensitivity and their correlation. 1. Sickle cell hemoglobin.

Journal of postgraduate medicine, 1966
openaire   +1 more source

An AI-enabled tool for quantifying overlapping red blood cell sickling dynamics in microfluidic assays.

Lab Chip
Kadivar N, Li G, Zheng J, Dao M, Karniadakis GE, Xu M.   +5 more
europepmc   +1 more source

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Effect of piracetam on sickle erythrocytes and sickle hemoglobin

Biochimica Et Biophysica Acta (BBA) - Protein Structure, 1981
Piracetam, 2-oxo-1-pyrrolidine acetamide, inhibits sickling of red cells containing sickle hemoglobin (Hb S). The concentration required for 50% inhibition is about 300 mM. Addition of piracetam into the supersaturated Hb S solution in concentrated phosphate buffer prolongs the delay time prior to gelation.
Toshio Asakura, S Tsuyoshi Ohnishi, Kazuhiko Adachi   +2 more
exaly   +3 more sources

Sickle Cell Anemia and Fetal Hemoglobin

American Journal of the Medical Sciences, 1994
Fetal hemoglobin, the predominant hemoglobin of the fetus, is good for sickle cell anemia. This hemoglobin inhibits the polymerization of sickle hemoglobin. Clinical studies have shown that at any level of fetal hemoglobin, the more that is present, the better off is the patient.
Martin H Steinberg
exaly   +3 more sources