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Hemoglobin|June 27, 2006
Iron-chelating and free-radical scavenging activities of microwave-processed green tea in iron overloadSomdet Srichairatanakool, Sakaewan Ounjaijean, Chonthida Thephinlap, et al.Hemoglobin|July 27, 2007
Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletionCornelis L Harteveld, Florens G A Versteegh, Eduard H G van Leer, et al.Hemoglobin|July 27, 2007
Globin chain synthesis is a useful complementary tool in the differential diagnosis of thalassemiasShohreh Khatami, Soghra Rouhi Dehboneh, Sedigheh Sadeghi, et al.Hemoglobin|January 1, 1991
Hb Isehara (or Hb Redondo) [beta 92 (F8) His----Asn]: an unstable variant with a proximal histidine substitution at the heme contactT Harano, K Harano, Y Kushida, et al.Hemoglobin|January 1, 1990
Hb F-Catalonia or alpha 2G gamma(2)15(A12)Trp----ArgD Plaseska, J B Wilson, F Kutlar, et al.Hemoglobin|January 1, 1990
Hb F-Charlotte, an A gamma variant with a threonine residue in position gamma 75 and a glycine residue in position gamma 136D Plaseska, F Kutlar, J B Wilson, et al.Hemoglobin|June 9, 2004
Safety of purified poloxamer 188 in sickle cell disease: phase I study of a non-ionic surfactant in the management of acute chest syndromeSamir K Ballas, Beatrice Files, Lori Luchtman-Jones, et al.Hemoglobin|June 9, 2004
Spectrum of hemoglobinopathies in Orissa, IndiaGuru Prasad Chhotray, Bisnu Prasad Dash, Manoranjan RanjitHemoglobin|June 9, 2004
Cardiac involvement in beta-thalassemia major and beta-thalassemia intermediaMara Ferrara, Sofia M R Matarese, Barbara Borrelli, et al.Hemoglobin|June 9, 2004
Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in ThailandLukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, et al.Pageof 238