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Blood
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May 1, 1976
Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin S
B Tatsis, K Sofroniadou, C I Stergiopoulos
Blood
|
June 1, 1977
Frequencies of thalassemia in American blacks
H I Pierce, S Kurachi, K Sofroniadou, et al.
European Journal of Internal Medicine
|
April 12, 2001
Visceral leishmaniasis in a patient with acquired hypogammaglobulinemia
D Voutsinas, L Foudoulaki, K Sofroniadou, et al.
British Journal of Haematology
|
January 1, 1975
Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin
K Sofroniadou, W G Wood, P E Nute, et al.
British Medical Journal
|
April 7, 1973
Thalassaemia in Cyprus
T Ashiotis, Z Zachariadis, K Sofroniadou, et al.
Drug Safety
|
March 1, 1990
Acute bone marrow aplasia associated with intravenous administration of deferoxamine (desferrioxamine)
K Sofroniadou, M Drossou, L Foundoulaki, et al.
Clinical Endocrinology
|
April 1, 1984
Pituitary and thyroid insufficiency in thalassaemic haemosiderosis
D P Livadas, K Sofroniadou, A Souvatzoglou, et al.
British Journal of Haematology
|
December 1, 1979
Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia
J B Clegg, A Metaxatou-Mavromati, C Kattamis, et al.
Clinical Endocrinology
|
October 1, 1987
A study of beta-cell function after glucagon stimulation in thalassaemia major treated by high transfusion programme
D P Livadas, E Economou, K Sofroniadou, et al.
Blood
|
February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks
P G Waber, M A Bender, R E Gelinas, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Blood
|
May 1, 1976
Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin S
B Tatsis, K Sofroniadou, C I Stergiopoulos
Blood
|
June 1, 1977
Frequencies of thalassemia in American blacks
H I Pierce, S Kurachi, K Sofroniadou, et al.
European Journal of Internal Medicine
|
April 12, 2001
Visceral leishmaniasis in a patient with acquired hypogammaglobulinemia
D Voutsinas, L Foudoulaki, K Sofroniadou, et al.
British Journal of Haematology
|
January 1, 1975
Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin
K Sofroniadou, W G Wood, P E Nute, et al.
British Medical Journal
|
April 7, 1973
Thalassaemia in Cyprus
T Ashiotis, Z Zachariadis, K Sofroniadou, et al.
Drug Safety
|
March 1, 1990
Acute bone marrow aplasia associated with intravenous administration of deferoxamine (desferrioxamine)
K Sofroniadou, M Drossou, L Foundoulaki, et al.
Clinical Endocrinology
|
April 1, 1984
Pituitary and thyroid insufficiency in thalassaemic haemosiderosis
D P Livadas, K Sofroniadou, A Souvatzoglou, et al.
British Journal of Haematology
|
December 1, 1979
Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia
J B Clegg, A Metaxatou-Mavromati, C Kattamis, et al.
Clinical Endocrinology
|
October 1, 1987
A study of beta-cell function after glucagon stimulation in thalassaemia major treated by high transfusion programme
D P Livadas, E Economou, K Sofroniadou, et al.
Blood
|
February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks
P G Waber, M A Bender, R E Gelinas, et al.
Page
of 1