Zobrazeno 1 - 10
of 36
pro vyhledávání: '"M, Boussiou"'
Autor:
Renzo Galanello, Antonino Giambona, A. Loutradi, Aurelio Maggio, L. Macioni, F. Locati, Jimmie D. Lowery, Luis A. Ugozzoli, Ching-I Patsy Lin, M. Boussiou, Antonio A. Reyes, R. Bruce Wallace, A. Re
Publikováno v:
American Journal of Hematology. 59:214-222
We describe the evaluation of the Bio-Rad BeTha Gene 1 kit (Bio-Rad Laboratories, Hercules, CA), a DNA-probe assay designed for the qualitative determination of the eight most common Mediteranean β-thalassemia mutations. The kit utilizes the princip
Autor:
Ph. Karababa, D. Mavroudis, Helen A. Papadaki, Z. Repapinou, George D. Eliopoulos, A. Loutradi-Anagnostou, V. Kafarakis, M. Boussiou
Publikováno v:
International journal of laboratory hematology. 29(1)
An improved method for the diagnostic approach of alpha(+)-thalassaemia is described. The method is based on five common parameters: absence of iron deficiency, mild morphological abnormalities of erythrocytes, normal or slightly reduced erythrocytic
Autor:
L A, Ugozzoli, J D, Lowery, A A, Reyes, C I, Lin, A, Re, F, Locati, R, Galanello, L, Macioni, A, Maggio, A, Giambona, A, Loutradi, M, Boussiou, R B, Wallace
Publikováno v:
American journal of hematology. 59(3)
We describe the evaluation of the Bio-Rad BeTha Gene 1 kit (Bio-Rad Laboratories, Hercules, CA), a DNA-probe assay designed for the qualitative determination of the eight most common Mediterranean beta-thalassemia mutations. The kit utilizes the prin
Publikováno v:
Hemoglobin. 15(6)
Study of the Hpa I polymorphism 3' to the beta-globin gene in the Greek population revealed absence of the site in 238 beta S chromosomes, in contrast to a much larger sample of chromosomes carrying the beta A gene, where this site was consistently p
Autor:
Yves Blouquit, M. Boussiou, Nicole Arous, Frédéric Galactéros, Phaedon Fessas, Dimitris Loukopoulos, M. Sellaye, George Komis, Jean-Philippe Rosa
Publikováno v:
FEBS Letters. (2):247-250
A new electrophoretically silent hemoglobin variant is described that produces the classical phenotype of β thalassemic intermedia in association with β° thalassemia trait. This variant has the expression of a silent β thalassemia trait. The abno
Autor:
N, Arous, F, Galacteros, P, Fessas, D, Loukopoulos, Y, Blouquit, G, Komis, M, Sellaye, M, Boussiou, J, Rosa
Publikováno v:
FEBS letters. 147(2)
A new electrophoretically silent hemoglobin variant is described that produces the classical phenotype of beta thalassemic intermedia in association with beta thalassemia trait. This variant has the expression of a silent beta thalassemia trait. The
Autor:
J, Rosa, P, Fessas, F, Galacteros, N, Monplaisir, D, Loukopoulos, Y, Blouquit, G, Komis, N, Arous, M, Boussiou
Publikováno v:
Progress in clinical and biological research. 134
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Akademický článek
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