Results 301 to 310 of about 1,740,227 (374)

Combinations of beta chain abnormal hemoglobins with each other or with beta-thalassemia determinants with known mutations: influence on phenotype.

, 1997
T. H. J. Huisman
openalex  

Some of the next articles are maybe not open access.

Related searches:

Abnormal Hemoglobins in Japan

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, Yuzo Ohba, Takaoki Miyaji
openaire   +4 more sources

Radioimmunoassay for Abnormal Hemoglobins

Science, 1977
A 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.
Titus H.J. Huisman, M. E. Gravely, M. B. Baker, G. Altay, Fred A. Garver, C. S. Jones   +5 more
openaire   +4 more sources

Diagnosis and screening of abnormal hemoglobins

Clinica Chimica Acta, 2023
Hemoglobin (Hb) abnormalities, such as thalassemia and structural Hb variants, are among the most prevalent inherited diseases and are associated with significant mortality and morbidity worldwide. However, there were not comprehensive reviews focusing on different clinical analytical techniques, research methods and artificial intelligence (AI) used ...
Ali, Sani, Muhammad, Idrees Khan, Saud, Shah, Youli, Tian, Genhan, Zha, Liuyin, Fan, Qiang, Zhang, Chengxi, Cao   +7 more
openaire   +3 more sources

Interaction of Hemoglobin E with Other Abnormal Hemoglobins

Acta Haematologica, 2011
Mammen Chandy, Ramachandran V Shaji, Eunice Sindhuvi Edison, Alok Srivastava   +3 more
openaire   +4 more sources

Abnormal hemoglobins in mauritius Island [PDF]

American Journal of Hematology, 1995
Solange Lee Kwai Yan, Sanjay Beesoon, Rajagopal Krishnamoorthy, Rajendranath Ramaswamy, Nathalie Kok Shun, Navaratnam Kotea, Dominique Labie, Ronald L. Nagel, Sarajoni Jankee, Soorianarain Baligadoo, Soondal Koomar Surrun, Rolande Ducrocq   +11 more
openaire   +4 more sources

The incidence of -thalassemia and abnormal hemoglobins in Turkey.

Acta Haematologica, 1971
The present study has been carried out to estimate the gene frequency of thalassemia and abnormal hemoglobins in a random Turkish population.
A. Çavdar, A. Arcasoy
semanticscholar   +1 more source

Thalassemia and abnormal hemoglobin

International Journal of Hematology, 2002
Thalassemia 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
Pranee Winichagoon, Suthat Fucharoen
openaire   +3 more sources

The Hematuria of Abnormal Hemoglobin Diseases

Archives of Surgery, 1955
The property of the red blood cell to sickle is a manifestation of abnormal molecular arrangement of that cell's hemoglobin. This was established by Pauling and co-workers in 1949. 1 Since then, other abnormal hemoglobins have been discovered by electrophoretic methods.
Sidney M. Goldman, Roland R. Cross, A. Zerne Chapman   +2 more
openaire   +4 more sources

Abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Dayaks of Sarawak.

Human Heredity, 1975
A survey of abnormal hemoglobins, G6PD deficiency and hereditary ovalocytosis was carried out among the Dayaks of Sarawak. The only abnormal hemoglobin found was Hb Co Sp, which occurred in 0.35% of the Land Dayaks and 0.83% of the Sea Dayaks.
J. Ganesan, L. Lie-injo, P. Ong Beng
semanticscholar   +1 more source