Results 201 to 210 of about 4,170 (243)
Evaluation of Heavy Menstrual Bleeding in Adolescents [PDF]
J Clin Res Pediatr EndocrinolKontbay Çetin T, Keskin Sarılar Z.
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Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families. [PDF]
Ann HematolAmri Y +7 more
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Validation of Noninvasive Methemoglobin and Carboxyhemoglobin Measurements Using Pulse Co-Oximeter in Healthy Dogs. [PDF]
Vet Med (Auckl)Her J, Roh J, Keys DA.
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Hemoglobin, 1980
The incidence of abnormal hemoglobins among the Japanese is estimated at one per 2,700 through systematic surveys (chiefly by use of electrophoresis of hemolysates) of 160,000 people, which have been carried out for these twenty years. About 40 variants of abnormal hemoglobins were detected and identified by chemical analysis.
S, Shibata, T, Miyaji, Y, Ohba
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The incidence of abnormal hemoglobins among the Japanese is estimated at one per 2,700 through systematic surveys (chiefly by use of electrophoresis of hemolysates) of 160,000 people, which have been carried out for these twenty years. About 40 variants of abnormal hemoglobins were detected and identified by chemical analysis.
S, Shibata, T, Miyaji, Y, Ohba
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ABNORMAL HEMOGLOBINS: LABORATORY METHODS
Hemoglobin, 2001Laboratory methods allowing the detection and characterization of hemoglobin variants are reviewed. Protein chemistry techniques such as isoelectrofocusing, electrophoreses under various experimental conditions, cation exchange and reversed phase high performance liquid chromatography, are the most frequently used for the detection of variants.
H, Wajcman +8 more
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The American Journal of the Medical Sciences, 1961
Summary and ConclusionsSickle cell trait can be separated from hemoglobin S-C disease, S-thalassemia, and even sickle cell anemia only on the basis of careful hematologic and electrophoretic studies, even after necropsy has been performed.
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Summary and ConclusionsSickle cell trait can be separated from hemoglobin S-C disease, S-thalassemia, and even sickle cell anemia only on the basis of careful hematologic and electrophoretic studies, even after necropsy has been performed.
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Radioimmunoassay for Abnormal Hemoglobins
Science, 1977A sensitive and specific radioimmunoassay has been developed for the identification or quantification of the human hemoglobin variants S, C, D-Los Angeles, E, G Philadelphia, Russ, O Arab, Beograd, J Paris I, G San Jose, Q Iran, Korle Bu, and F Malta I.
F A, Garver +5 more
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Thalassemia and abnormal hemoglobin
International Journal of Hematology, 2002Thalassemia and abnormal hemoglobins are common genetic disorders in Asia. Thalassemia is not only an important public health problem but also a socio-economic problem of many countries in the region. The approach to deal with the thalassemic problem is to prevent and control birth of new cases. This requires an accurate identification of the couple at
Suthat, Fucharoen, Pranee, Winichagoon
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Abnormal human hemoglobins IX. Chemistry of hemoglobin JBaltimore
Biochimica et Biophysica Acta, 1963A human abnormal hemoglobin with the electrophoretic mobility of hemoglobin J has been isolated and studied. The amino acid substitution in this abnormal hemoglobin has been investigated. It has been found that an aspartic acid residue substitutes in this hemoglobin J the glycine residue present in position 16 of the β peptide chain.
C, BAGLIONI, D J, WEATHERALL
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