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Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Source of elevated serum mitochondrial creatine kinase activity in patients with malignancyK Okano, K Yamamoto, Y Ohba, et al.Hemoglobin|January 1, 1987
Hyperunstable hemoglobin Toyama [alpha 2 136(H19)Leu----Arg beta 2]: detection and identification by in vitro biosynthesis with radioactive amino acidsY Ohba, K Yamamoto, Y Hattori, et al.Hemoglobin|January 1, 1989
Characterization of beta-thalassemia mutations among the JapaneseY Hattori, A Yamane, Y Yamashiro, et al.Hemoglobin|January 1, 1988
A beta+-thalassemia (codon 24, GGT----GGA) found in a JapaneseY Hattori, Y Yamashiro, Y Matsuno, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|February 1, 1990
[A Japanese family with hereditary HbH disease--a case report and its gene analysis]Y Hattori, Y Yamashiro, K Yamamoto, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 1, 1989
[Refractory anemia with ringed sideroblasts complicated with delta beta-thalassemia-like hemoglobinopathy]Y Aoyagi, H Akimoto, K Yamaoka, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|April 15, 1985
Frequency of alkaline phosphatase-immunoglobulin complex among diseased and healthy populationsY Hattori, K Yamamoto, C Urabe, et al.Hemoglobin|January 1, 1977
Hemoglobin Karatsu: beta 120 (GH 3) lysine leads to asparagine, an example of HB Riyadh in JapanT Miyaji, Y Ohba, M Matsuoka, et al.International Journal of Hematology|February 1, 1991
Further cases of Hb Hirosaki in two Japanese familiesY Ohba, K Yamamoto, Y Hattori, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|June 1, 1990
[Present and future of physiological examinations]T MiyajiPageof 616